Mbbs students

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Guidelines for the MBBS
Students during their
Paediatric Posting
Department of Child Health
Maharajgunj Campus
Institute of Medicine
Department of Paediatrics
Maharajgunj Campus
MBBS Programme
Faculty Members:
Dr. Ramesh K Adhikari Professor, Dean, Institute of
Medicine
Dr. Prakash S Shrestha Professor; Head of the
Department
Dr. Pushpa R Sharma Professor, Co-Ordinator MD
(Paediatric) Programme
Dr. Fakir C Gami Associate Professor; Co-Ordinator
MBBS Programme
Dr. Laxman Shrestha Assistant Professor
Dr. Shiva Shrestha Assistant Professor
Dr. Sudha Basnet Assistant Professor
Activities:
a. Theory classes.
b. Bedside clinical classes.
c. Problem based seminars.
A. Theory Classes:
Theory classes will be held every Sunday, Tuesday and
Thursday in the academic building room no 3 between
12 .00 to 1.00 PM. These theory classes will be taken by
respective teachers as follows:

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Topic headings Teachers
CNS disorders
Nutritional disorders Prof. Ramesh
Adhikari
Respiratory disorders
Gastrointestinal disorders Prof. PR Sharma
Hepatobiliary disorders
Neonatology including birth injuries Prof. PS Shrestha
Chromosomal disorders
Congenital malformations
Collagen disorders
Endocrinal disorders
Genitourinary disorders
Dr. Fakir C Gami
Cardiovascular disorders
Rheumatic heart disease Dr. Siva Shrestha
Haematological disorders
Infectious diseases (except Respiratory) Dr. Sudha
Basnet
Preventive paediatrics
Emergencies (including poisoning)
Childhood disabilities
School health programme
B. Bedside clinical classes:
TOTAL WEEKS:12
COURSE OBJECTIVES:
During the Paediatric posting, it is anticipated that the
student will consolidate the paediatric knowledge with
the skills which will be acquired in this posting. On
completion of the Paediatric posting, the student should
be able to:
1. Obtain a comprehensive and focused history from a
child and his/her family regarding the health and illness
of infants, children and adolescents
2. Perform comprehensive and focused physical
examinations of infants, children and adolescents
3. Synthesize the data derived from the history, physical
and laboratory assessments and formulate a problem-
oriented approach to the child's presenting problems
4. Apply an understanding of the normal growth and
development of infants, children and adolescents to
clinical problems and appreciate the impact of illness on
that growth and development
5. Apply knowledge of basic science and clinical
epidemiology to the diagnosis and management of
clinical paediatric problems
6. Demonstrate an approach to the common health
problems of infants, children and adolescents including
their assessment, diagnosis and management
7. Implement the important strategies of health
supervision that pertain to infants, children and
adolescents, including disease and injury prevention,
anticipatory guidance and screening
8. Demonstrate an understanding of the influence of
family, community and society on the child in health
and disease
9. Demonstrate the attitudes and professional behaviours
appropriate for clinical paediatric practice
Bedside clinical classes will be conducted in Kanti
Children’s Hospital daily between 9.00-11.30 AM.

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Students should wear apron and they should have name
tag. Student should bring with them stethoscope,
clinical thermometer, measuring tape, hammer and
torch light. They should not bring small pocket note
book given by drug companies. Each student will be
given respective bed numbers. Students will be
responsible to write case history, examination findings
and suggested investigations in the note book. At least
12 case summaries should be submitted to the
department at the end of their posting.
In the first day of the posting students will be oriented
about: teaching/learning activities, Kanti Children’s
Hospital, distribution of beds, principles in paediatric
clinical examination, and materials needed to bring
during this posting. In the first week students will be
demonstrated in history taking and clinical examination
skills. Special emphasis will be given in formulating
questions for history taking. Following examination skill
will be demonstrated:
Methods of performing clinical examination in child with:
Nervous system Prof RK Adhikary
Respiratory problem Prof. PR Sharma
Cardiovascular problem Dr. S Basnet
Gastrointestinal problem. Prof. PS Shrestha
Urinary problem Dr. Fakir C Gami
Musculoskeletal problem Dr. Fakir C Gami
And evaluation of a neonate. Prof. Prakash S Shrestha
From the second week onwards students will present the
cases in rotation for discussion. During the discussion
special emphasis will be given in eliciting the clinical signs
and correlating the findings of history with it. In every case
the appropriate investigations will be discussed. Each
students will present at least three cases. Students will
attend the neonatal unit of TUTH at the 10th week of their
paediatric posting.
Teaching faculties and weekly schedule
Following teachers are responsible for conducting the
clinical bedside classes in Kanti Children’s Hospital in the
following week days:
Days Teachers
Sunday Dr. S Shrestha
Problem oriented approach
seminar
Monday: Dr. FC Gami
Tuesday: Dr. S Basnet
Wednesday: Prof. PR Sharma
Thursday: Prof. R K Adhikari
Friday: Prof. PS Shrestha
Format for the presentation in the bedside clinical
discussion by students:
A. Presenting complaints: in chronological order.
B. Medical history and its subcomponents:
a. History of present illness; b. Past illnesses, treatment
and allergy history; c. birth history; d. immunization
history;
e. developmental history;
C. Nutritional history
D. Family and socio-economic history
E. Clinical examination: Vital signs; anthropometric
measurements; general surveys (pallor, cyanosis,
jaundice, etc)
F. Regional examination
G. Specific system examination
METHOD OF EVALUATION:

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Student evaluations will be based on clinical performance
assessments and a written examination at the end of the
rotation (see Annex A). Students are required to pass the
clinical evaluations to obtain a pass in Paediatrics Posting
which will be held during the 11th week of their posting. In
this examination students will have clinical examination (
one long case and one short case).
During the clinical examination following points will
be observed:
1. Approach to patient.
2. Correlating symptoms/signs with pathophysiology.
3. Demonstration of clinical signs.
4. Suggested investigations to reach the diagnosis.
5. Plan of treatment.
C. Problem based seminars:
Every Sunday there will be a seminar on a given problem.
Students will be given a problem case three days prior to
the date. Remaining parts of history, examination findings
and investigations will be supplied in the seminar in the
triple jump methodology. In this seminar students will
discuss the hypothetical diagnosis, differential diagnosis,
important historical questions, examination findings,
investigations and treatment. This seminar will be held at
the meeting hall of the Health Learning Materials Centre
between 9.00 – 11.30 AM. Following problems will be
discussed in the Problem oriented approach seminar: a
child with cough or difficulty in breathing, a child with low
weight for age; a child with swelling of feet, a child with
convulsion and fever; a child with diarrhoea; a child with
weakness of limbs; a child with rash; a child with severe
pallor a child with joint pain; a child with fever, a neonate
with jaundice; a neonate with poor sucking
RECOMMENDED TEXTBOOKS
1. Nelson Essentials of Paediatrics, Richard E. Behrman,
Robert Kliegman, W.B. Saunders Company, Third
Edition, 1998, 846 pages
2. Ghai’s Text Book Of Paediatrics
3. Care of new born. Meharban Singh
4. Pocket Book of Practical Paediatric Problmes; Sharma
PR; Health Learning Material Center; 4th Ed.
GENERAL REFERENCE TEXTBOOKS
1. Nelson Textbook of Paediatrics, Behrman, Saunders,
Fifteenth Edition, 1996,
2. Paediatric Medicine, Mary Ellen Avery and Lewis R.
First, 1994, Second Edition, Williams, and Wilkins,
3. Principles and Practice of Paediatrics, Oski et al, 1994,
Second Edition, J.B. Lippincott, 2368 pages
4. Primary Paediatric Care, Hoekelman et al, Mosby, 1992,
1795 pages.
5. Rudolph's Paediatrics, Rudolph, Twentieth Edition,
Appleton & Lange, 1996, 2337 pages
6. Fundamentals of Pediatrics, Rudolph’s, First Edition,
Rudolph & Kamei, 1994 701 pages
GUIDE TO PAEDIATRIC HISTORY-TAKING AND
EXAMINATION
HISTORY-TAKING
Hospital is very often a new and worrying experience for
parents and children. Often children are given fear of a
doctor for injection and white apron syndrome is known
case. Allow for this and for limitation in their vocabulary of

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illness. The child has few if any standards against which to
measure his new experience. Diagnosis in many system
rests mainly on what you learn from listening to and
talking with a parent about his/her child’s illness. The
process of obtaining an account of that illness—commonly
called “the history taking”—is most productive if you treat it
as a conversation. As in most conversations, the process
works best if discourse is friendly, takes place between
people who respect each other, is unhurried and has a
focus or direction.
SOME TACTICS IN PREPARING FOR THE CONVERSATION
A clinical conversation rarely starts out easily. The parent
wants help and understanding but he/she may be impeded
by unexpressed fears or guilts. The history taker wants
information but he/she may be impeded by haste or
distractions. You, the history taker, normally control the
conversation and it is your responsibility to minimize such
impediments. You can achieve this by several simple
maneuvers. These may seem to be no more than common
sense and courtesy (as indeed they are) but it is surprising
how often they are neglected.
Arrangement of the Conversants
You should see to it that you and the patient/parent are
situated in the position that is normal in people who are
talking seriously with each other. This means that you
must both be seated comfortably with your heads at the
same level. When one conversant’s head is far above the
other’s it implies a dominance that can inhibit easy talking.
People who are conversing as equals rarely talk face-to-face,
with their faces parallel. Such a position is associated with
confrontation, interrogation, interview, and intimate
conversation but not with formal conversation. A slight
obliquity in the faces of the participants is natural and
important. Conversations are rarely easy over barriers like
desks and tables. The participants should be separated
only by empty space. The amount of space is important-
about 3 feet seems right. More or less separation of the
participants impedes good conversation.
These important arrangements can be established by the
positions of tables and chairs in the examining room. At the
bedside they must be improvised. You should sit down to
put your head close to the level of that of the parent. It is
better to sit on a low stool. It is not at all bad manners for
you to sit on the edge of a bed: It imparts a familiarity and
informality that can facilitate conversation.
The Presence of Other People
The clinical conversation is essentially one-on-one, and it
normally involves matters that the patient/parent may
consider private, so other people should usually be
excluded from the room. When patients/parent request
that another person be present you should honor the
request; relatives can be helpful in adding or confirming
elements of the history. In case of older children, please
ask the child if he/she needs to be seen alone. In such a
case you should not hesitate to arrange for a later interview
with the patient alone to clear up specific points if you
think that is necessary.
In teaching hospitals, the presence of students, who are
strangers to the patient, may impede communication. This
problem can be reduced if you introduce these people and
explain the reason for their presence. You must always ask
permission for the presence of such neutral observers (it is
rarely denied). If you sense that observers are significantly
interfering with the conversation you should ask them to
leave. As in the case when relatives are present you may
want to arrange for a subsequent interview alone. As a
student you must introduce and give reason for history
taking . You have to decide whom you will listen?
THE ELEMENTS OF THE CONVERSATION
The Opening Conversation: it leads to presenting
complaint

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After you are seated you should begin the conversation in
such a way as to indicate that you are not in a hurry. In
paediatrics, most of the time the history will be given by
the parent. It is the parental observation that will be
narrated to you. The points parent want to highlight may
not be important for you. You should then lead to the
matter of concern by asking the parent/patient an open-
ended question indicating that you want to know why
he/she has come to this health facility. Is this is the new
visit or the follow-up visit?
The phrasing of this opening question is important, for it
may shape the whole subsequent conversation. If you don’t
know why the patient has come, ask “What can I do for
you?” If you already have an idea of the nature of the
complaint bring that up at once by forming your question
appropriately. If you ask the usual neutral question when
you already know the general complaint, you risk making
the parent/patient, who usually knows if you already have
some preliminary information, think that you are forgetful
or distracted. if you know anything at all of the reason for
the visit, make it clear at the beginning that you know or
remember at least a little.
Once you have indicated that you expect the patient/parent
to tell his story most parents/patients will launch some
kind of an account of the illness. This is occasionally quite
long and detailed, but it is usually brief or incomplete.
Some people will ramble off course. If this happens you
should interrupt, picking up the thread of the story and
getting the parent/patient back on course.
Parents/patients will rarely volunteer to you all you need or
want to know. Usually this opening account will give only a
general idea of the major complaint with an incomplete
chronology. Bedside logic requires far more information
than most patients volunteer. They cannot be expected to
know what may be important to you. You should allow the
patient/parent to complete the opening statement as far as
he seems to want to go, for it will contain at least the
skeleton of the present illness. Let him finish what he has
to say. The flesh of the present illness must be obtained in
a subsequent part of the conversation, the Middle
Conversation.
The Middle Conversation: leads to history of present
illness
The Middle Conversation is impossible to describe or to
dictate, since it must be shaped to fit each case, but three
general principles are often neglected.
First, you must maintain a normal degree of eye contact
with the parent/patient as you would do in any other
focused and personal conversation. Second, you must never
take notes in the Opening and the Middle Conversations.
Note taking converts a conversation into an interrogation
and it makes the parent/patient think that you aren’t
interested enough to try to remember his story, even for a
brief time ( during your final examination this may take a
long time) Third, you must not tolerate any interruptions
during the Opening and middle Conversations.
Interruptions will be interpreted as an indication that you
are distracted or in haste.
During the Middle Conversation you determine many
important features of the present illness, outlined below.
These features are the critical ones in bedside logic and it
works best if you obtain them fully at the first opportunity,
so you must not neglect or truncate the Middle
Conversation. Most errors in bedside logic arise from
neglect of the Middle Conversation.
In the Middle Conversation you ask specific questions that
you need an answer to. Here, you begin to test your
hypotheses about the disease process. You explore your
ideas of the organ systems involved, the nature of the
pathological process and the extent of that process. You
generate questions to test your ideas as they develop: This
is the essence of bedside logic.

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It is important to avoid asking leading questions, those in
which the form of the question implies an expected answer,
since some paernts tend to tell you what they think you
want to hear. Your questions must be put in such a way
that the patient understands that the possible responses,
“yes,” “no,” and “sometimes” are all equally important. Thus
a specific question about common cold accompanying an
ear pain might be stated, “I need to know whether or not
your child ever get common cold with pain. Tell me if it ever
occurs or never occurs or sometimes occurs.” It works well
to offer the patient choices to show that you have no
preference for the response.
There is another problem with leading questions of the kind
that are formed to indicate the expectation of a negative
answer. When you ask, for example, “Your child never have
vomiting with the pain does he?” you may be misled by the
answer. If vomiting does not accompany the pain the usual
native Nepali-speaker will respond “No,” meaning “No – he
does not have vomiting with the pain.” The other-speaker
(for example) may respond “Yes,” meaning “Yes-I agree with
you when you say that he does not have nausea with the
pain.” This problem may well exist as a linguistic variant in
other languages
The End Conversation
When you believe that you have exhausted the possibilities
of the Middle Conversation you begin the End
Conversation. This consists of a recitation by you of the
story of the illness as you understand it so far. You repeat
your understanding of the story of the illness, asking the
parent/patient to correct you when you are wrong. Give the
parent/patient the chance to add anything. Ask “Have I
missed anything?” or “Is there anything I have said that is
not quite correct?”
In this End Conversation not only are you trying to
establish the complete story as you understand it, but also
you are letting the parent/patient know that you are
beginning to formulate your ideas of what may be wrong.
Your positions are temporarily reversed: He is listening and
you are talking.
For this reason you must be careful to recognize the
unexpressed fears and guilts of the patient/parent, for in
the End Conversation he is beginning to find out what you
think. There are two important things to keep in mind in
this connection.
First, parent/patients who have complaints that they
themselves do not understand often fear that their child
have a fatal illness.
Second, patients often conceal information from you that
may be important, usually related to something that they
are ashamed of like peculiar dietary practices or giving
medicines by themselves.
It is useful to introduce such matters at this time. If
appropriate, it is helpful for you to say, for example, that
the story suggests to you that the problem might be related
to some drugs or medicines that the patient might be
taking and that you want to know about them. If such
sensitive matters are brought up by you in this End
Conversation in a matter-of-fact way and you indicate why
you are asking about them, most parent will respond freely.
It is much better to get into such things in the End
Conversation than to reserve them for the more
interrogatory or confrontational setting of the routine
questioning of the drug history
In this way, the End Conversation can be used to lead into
the other elements of the history that are usually organized
as the drug history, the past history, the family history, the
developmental history, and so on. It does not matter in
what order these latter elements of the history are obtained.
It is easiest if they are explored in whatever order seems
natural.
In patients with respiratory illness there is often a past
history of several similar illnesses. Getting these straight in
the Middle and End Conversations can sometimes be

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difficult, in such cases you may find it helpful to review
nasal polyp or abnormal shape of the chest during the
physical examination, when each findings point to the past
illnesses that led to it.
You should use the End Conversation to begin to bring the
parent/patient into your thinking process so far as you
think that to be desirable at this point. Here you tell the
parent, in effect, what other matters are important to you.
This will lead naturally to a discussion of other matters that
otherwise might seem to him to be unimportant.
The Rest of the History
The most important elements of the other parts of the
history—the Past History, the Family History and so on—
will emerge in the three Conversations described above. You
should, however, cover the routine elements that have not
come up. This should be done after the End Conversation.
WHAT IS IMPORTANT TO THE PARENT/PATIENT, AND WHY?
parents want problems solved. You must learn what these
problems are. The main problem is usually the major
symptom. In general a patient/parent will only volunteer to
you what concerns him most. This may not be what most
concerns you, but you must listen to what the
parent/patient says first, for this tells you both what he
considers to be important and what most bothers him. This
is the function of the Opening Conversation.
At some point you must discover why a particular aspect of
the history concerns the patient most and you should not
hesitate to ask why. “Why does this diarrhoea concern you
so much?” or “Why do you worry so much about this
diarrhoea?” are questions that often yield answers which
illustrate the magnitude of the problem or reveal specific
fears or hitherto-concealed elements of the history. You
may ask “What do you think is causing your problem?” This
question often brings out previously unexpressed fears and
sometimes give you an unsuspected lead to correct
understanding.
WHAT IS IMPORTANT TO YOU?
Patients/parent rarely appreciate what is important to you.
You uncover this in the Middle Conversation.
In talking with patients you should pay attention not only
to the answers to your questions but also to specific
nonverbal communications. The meanings of some
behavioral responses—not making an eye contact (autistic
child), unstable child (ADHD) and the like—are obvious.
Others are more subtle: head nodding, wheeze, stridor, hair
changes, severe malnutrition, swollen face. By constantly
watching the patient, you may pick up many important
clues in “body language” like chorea, tremor, crossing of
legs .
Simple format for history taking
Date: History taken from:
Place of residence within last one month:
Child's name: age: sex:
Race (can be very relevant, e.g. in haemolytic anaemias):
Presenting complaint:
Allow parents to tell the story in their own words. Practise
making notes while looking in the witness's eyes. It is
important to look really interested and not just to sound it.
Be aware also of the child at this stage: his activity, sounds,
expressions, interest. Then extend the story in the context
of the range of possible diagnoses which the initial remarks
suggest. Have any drugs been given, and with what
response? If parents use ”feverish” "wheezy", "diarrhoea",
"constipation" ask them to describe what is meant. Be
precise about dates. Very often older children can tell you

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their complaints in their own words more precisely than
their parent, so do not forget to ask children using simple
children language.
Systemic enquiry
Central nervous system:
change in activity or mood, floppiness, posture, walk, co-
ordination, vision, onset of headaches. "Fits" must be
described in great detail, including time of episode,
triggered by temper or temperature? colour change,
associated incontinence, tonic, clonic, etc.
Alimentary system:
appetite, feeding pattern, evidence of weight loss, vomiting
(amount? nature? effortless? projectile? Salivation? Difficult
to swallow? how far does it go? stained with blood? bile?),
constipation, diarrhoea, character of stools (bulk,
frequency, colour, mucus, blood, etc.), apparent pain, any
excess thirst.
Cardiovascular system:
cough, breathlessness on exertion, central cyanosis, apathy
and (in babies) slow feeding and weight loss; fainting
episodes and palpitations in older children.
Respiratory system:
discharge from eyes, ears or nose, sore throat, cough and
its characteristics; breathlessness, stridor, wheeze and
observed precipitating factors (e.g. exercise, dust, animals);
cyanosis.
Haemopoietic system:
pallor, listlessness, breathlessness, bleeding, bruising,
lumps.
Genito-urinary system:
change in urinary frequency, pain on micturition, force and
continuity of stream, loin pain, character of urine
(including unusual smell or colour), late onset of enuresis,
rash, itch, bleeding PV.
Endocrine system:
growth; need of new clothes and shoes; build - getting
stouter or slimmer; head-aches; abnormal thirst and urine
volume; breast or genital changes; apathy; vision; birth-
marks.
Skin:
new marks or spots: eczema; superficial lumps.
Past History:
Mother's health during pregnancy
Place of birth
Gestational age at birth (full-term or number of weeks pre-
term)
Mode of delivery
Birth weight
Problems around time of birth
Breast- or bottle-fed
Achievement of developmental milestones
Previous illnesses (in chronological order)
Infectious disease contacts
Details of immunisations
Allergies and drug hypersensitivities
If the child has been in a hospital elsewhere
Family History should be taken eg:
Father 32 years (plumber) asthma and hayfever
Mother 29 years (housewife) no health problems but has
younger brother with Down's syndrome
Children -

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The child being examined aged 8
twins aged 4
spontaneous abortion at 14 weeks
N.B. Consanguinity may be relevant to recessively inherited
conditions and is much more common in certain racial and
religious groups.
Social History:
Type of house/flat, including number of rooms, number of
occupants (including relatives and lodgers), nature of
heating, existence of damp, mode of cooking, animals near
the place of residence
Parent(s) employed or not.
Tactful attitudes and questions may elicit a history of single
parenthood, partners, alcoholism, drug abuse.
Cigarette smokers: number and how many a day (relevant
to children's respiratory infections).
Name of school: is the child happy there? does he have
particular friends or enemies? is he bullied on way to and
from school? what does he enjoy best: games or studies?
Document culture, including race and religion.
Hepatosplenomegaly
Examples of questions for history of present illness:
How old is the child? Congenital infections, storage
disorders.
Where is the place of residence? Malaria, kalazar,
Does the child have fever?
For how long? Malaria, kalazar, typhoid, TB,
Does it come every day? Infectious mononucleosis and
Is fever associated with rash, other viral infections, leptospi
runny eyes or red eye? roicterohaemorrhagica.
Infective hepatitis
Is it associated with purpura? Malignant diseases, sepsis.
Does the child have jaundice? Infective hepatitis, Hodgkin’s.
Delayed developmental mile
stones of life? Lipid storage disorders.
Is the child plump? Glycogen storage disorders.

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Is the child pale? Thalassaemia, malignancies
Does the child have joint pain?Rheumatoid arthritis, other collagen diseases.
Does the child have difficulty
in breathing? CCF, visceral larva migrans
Examples of questions for past medical history:
Did mother had illnesses
during pregnancy? Congenital infections
Does the child have umbilical
sepsis? Portal hypertension
Any history of rheumatic fever? Cardiac failure, subacute
bacterial infections
Did the child have dysentery? Amoebic liver.
Is the child vaccinated with BCG? Miliary tuberculosis.
Did the child have jaundice? Cirrhosis.thalassaemia
Did the child vomited blood? Cirrhosis.
Is there consanguinity of marriage?Thalassaemia, metabolic disorders.
CLINICAL EXAMINATION OF CHILDREN
Preliminary guidelines:
If possible, avoid having children separated from parents, forcibly undressed and measured. All of these are threats and may make
subsequent examination much more difficult. Never rush into an examination and never place a child flat on a couch or bed without
careful preparation. Unless the condition is very acute and/or co-operation is unnecessary, quiet friendly contact is time well spent.

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Make sure the room and your hands are warm.
Try to keep on the same level physically and in the words and tone used.
Always talk to the child before touching. Talk about toys,
clothes, other siblings, etc., until many of the child's fears
are overcome. Possibly start with gently holding and looking
at his hands or feet and continue to talk quietly and gently
through the examination.
Contrary to past teaching, it may be possible to examine a
partly clothed child provided all the body is seen (step by
step).
Use blankets/sheets to cover legs while chest is being
examined and trunk while external genitalia are being
examined.
Sensitive children may best be examined initially on a
parent's knee, until they become more confident. With
frightened or uncooperative children be opportunist in
examining whatever part is offered or available.
Leave uncomfortable procedures (otoscopy, throat, rectal
examination*, etc.) to the end. Be aware of the child's
response to you.
* Rectal examination should only be undertaken with the
agreement and presence of a senior staff member.
Inspection and General Assessment:
Paediatric examination begins as the child enters the room:
disproportion; dysmorphism; unusual walk; strange
behaviour. A child asleep in a parent's arms is a gift from
heaven: do not move or waken him. Look at the frequency
and depth of breathing; feel the fontanelle; slip a warm
stethoscope below clothes to auscultate the heart; ask
mother to adjust her position to attempt flexion of the
child's neck; very gently palpate the abdomen for
organomegaly and other lumps.
Height
Weight plot on appropriate centile chart
Head circumference
State of hydration - general condition, eagerness to drink,
skin pinch and sunken eyes. Skin - texture, colour,
birthmarks, spots, bruises, oedema, rash: describe
distribution, colour, and whether macular, papular,
macuiopapular, vesicular, bullous, pustular, petechial.
Mucous membranes (as an approximate estimate of
haemoglobin). Very occasionally helpful with profound
anaemia.
State of nutrition - axillae, abdomen, thighs, loose skin and
creasing; "skin suit too big for child"; skinfolds., oedema
Pulse
Temperature
Blood pressure, using an appropriate cuff (i.e. the width of
the cuff should cover 2/3 of distance from shoulder to
elbow).
Examples of examination findings:
Propped-up position Cardiac failure, portal hypertension (huge ascitis)
Thin built Tuberculosis, malignancy
Plump Glycogen storage disorder.

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Pallor Malignancy, thalassaemia
Cyanosis CCF
Jaundice Infective hepatitis, cirrhosis,
Thalasaemia.
Oedema CCF, cirrhosis, malignancy
Clubbing Cirrhosis, SBE, tuberculosis
Purpuric rashes Malignancies, cirrhosis. congenital infections.
Lymphadenopathy Malignancy, kalazar.
High fever Typhoid, malaria, kalazar, malignancy, SBE, infective
Hepatitis. Infectious mononucleosis
Maculo-papular rash viral infections, typhoid,
Joint swelling, bony tenderness Malignancy, collagen disease
Eyes: congestion Viral infections, infectious mononucleosis, leptospirosis
Cherry red spots Lipid storage disorders
Keysherfisher ring Wilson’s disease
Mouth
Bleeding gum Malignancy, kalazar
Chest:
Murmur CCF, Glycogen storage, SBE rheumatic
Basal creps CCF, visceral larva migrants
Effusions CCF, visceral larva migrans, collagen.
Abdomen:
Tender liver viral hepatitis, amoebic, bacterial, CCF
Non tender malignancy, thalassaemia
storage disorders, kalazar, malaria

14
Ascitis Cirrhosis, tubercular, visceral larva migrans, malignancy.
Prominent abdominal
veins cirrhosis.

15
Abdominal pain:
Acute onset: Intestinal / ureteric colic
Worms, food allergy, diabetic ketoacidosis, obstructions, calculus, visceral
infarctions
Chronic onset Organomegaly, ulcers, constipation, functional
Associated symptoms:
Rash urticaria, HS purpura, collagen diseases, leukaemias, HUS
Fever shigellosis, hepatitis, UTI, basal pneumonia, tuberculosisis, typhoid,
pyelonephritis
Diarrhoea enteritis,
Vomiting gastroenteritis, hepatitis, colic
Difficulty breathing, cough cardiac failure, pneumonia, asthma
Constipation Chronic functional, intestinal tuberculosis, hirshprung, hypothyroidism,
intussusception, volvulus.
Jaundice infective hepatitis, sickle cell anaemia, cholangitis,
Haematemesis PUS, portal hypertension, Malignancy
Distension of abdomen intestinal obstruction, ascitis,
Visceromegaly,
Scar marks Trauma, past operations- bands, faith healers applications of heat for colic.
Dark coloured urine trauma, porphyria, haemoglobinuria,
Severe dehydration renal vein thrombosis
.

16
Eyes - bitots spot, xerophthalmia, strabismus,
conjunctivitis, cataract, fundoscopy, comment on visual
acuity.
Respiratory Examination:
Mouth-breathing: check nasal airway.
Inspect again for central cyanosis and finger/toe-clubbing.
Record rate of respiration. Are accessory muscles of
respiration being used? Is there chest indrawing?
Nostril-flaring? Describe the chest shape, including pigeon-
chest, hyperinflation, Harrison's sulci, sternal recession,
and pectus excavatum. Is indrawing present? Where?
Listen - especially for the predominantly inspiratory sound
of croup, or the prolonged expiratory wheeze of asthma;
record any cough.
Careful percussion, comparing opposite sides, MAY
occasionally identify extensive consolidation or effusion,
and may confirm the hyper-resonance on the side of a
pneumothorax. There is local stony dullness with a pleural
effusion or empyema.
Auscultation: Are breath sounds equal bilaterally?
Rhonchi? Where? What pitch? What phase of respiration?
Crepitations? Where? What quality? When? Altering with
coughing? Vocal resonance may help in the co-operative
older child. The inexperienced may suspect that signs are
asymmetrical but cannot judge which side is abnormal.
Gentle careful palpation of chest movement will often help
the examiner identify the abnormal one.
It is often helpful to leave the following part of the
examination until last BUT IT IS ESSENTIAL.
Palpate the whole neck and occiput for masses, especially
for enlarged lymph nodes. Is there a goitre? Look closely at
both eardrums Do not ask "Could I look in your ear
please?" Ask "which ear would you like me to look in first?"
Record any discharge, and appearance of tympanic
membranes.
Obtain a brief but adequate view of the oropharynx. This is
often best done on a parent's knee (depending on the child's
age). If a spatula should prove necessary, then a mother's
hand firmly on the child's forehead may help while the
child's hands are restrained by her other arm. Note
appearance of buccal mucosae, gums and dentition: look
for clefts, (including submucous), thrush, Koplik's spots,
ulcers or erythema over soft palate and palatofaucial pillar
Cardiovascular Examination:
Inspect for central and peripheral cyanosis (the latter may
be quite reliable if skin is warm and veins well filled), record
any tachypnoea or tachycardia and look for old operation
scars. Palpate both radial pulses and note any disorder of
rhythm. Feel both femoral pulses and the right radial and
femoral pulses together: low volume femoral pulses and
radio-femoral delay may indicate coarctation of the aorta.
Palpate the apex beat and (using the palm of the hand)
check for a praecordial heave or thrill.* Blood pressure
should be measured in all children: in those with CVS
disease, it should be recorded in all 4 limbs.
* Also slip a finger in the suprasternal notch - a thrill is
commonly present here in the presence of aortic stenosis.
Auscultate at the apex to identify the heart sounds - you
may need to feel the carotid pulse simultaneously to be
sure of the timing. ALWAYS listen at the apex, left lower
sternal edge, aortic area, pulmonary area, left
infraclavicular region, AND POSTERIORLY. Listen to the
right arterior chest to exclude dextrocardia; should
dextrocardia be suspected, try to answer the question: "is it
really so or has the mediastinum been displaced by
pressure or traction?".
Examples of commonly heard murmurs are:

17
1. Benign flow murmur - heard centrally in early and
systole and may be musical or vibrating in quality. If
quiet may be localised.
2. Venous hum - heard in the neck and infraclavicular
regions, but alters with position of the patient and may
disappear on compression of the jugular veins.
3. Ventricular septal defect - may be loud and heard widely
over the chest especially LLSE to apex, and filling the
whole of systole.
4. Persistent ductus arteriosus - often a musical cadence,
spilling from systole into diastole, and associated with
full, bounding pulses.
Note 1. The best signs of cardiac failure are tachycardia and
tachypnoea. Peripheral oedema and hepatomegaly are LATE
signs. Growth rate, general demeanour and exercise
tolerance (e.g. during feeding) are valuable indices of
cardiac status.
Note 2. Heart murmurs are often graded as follows:
Grade 1 very soft
Grade 2 Soft
Grade 3 easily heard
Grade 4 easily heard, plus a thrill
Grade 5 very loud
Grade 6 audible without a stethoscope
Abdominal Examination:
Inspect for distension, movement with respiration, visible
peristalsis, skin laxity or dryness, or any superficial
abnormalities, e.g. umbilical hernia. Palpate the abdomen
gently with warm hands and using the WHOLE flat of the
hand. At no time is reassuring talk so important as now,
and if possible have parents close by. Watch the child's face
closely for apprehension or reaction to pain, particularly as
gentle but deep palpatation begins. Crying children relax
the abdomen briefly during inspiration, allowing a fraction
of a second to obtain information. Palpate with gentle
fingertips for the liver (1 cm below the costal margin may be
normal), the spleen (which tends to enlarge down the left
flank, particularly in younger children) and both kidneys
(which are often felt in slim co-operative children). Record
local tenderness guarding, or the size, position and quality
of any mass. This is often best done by a simple diagram of
the child's abdomen. Percuss for a distended bladder, and
auscultate the bowel sounds. Rectal examination with 5th
finger but only if indicated and with supervision from
trained staff.
Genitalia:
Female: external inspection only, looking for stage of
puberty enlargement of clitoris (e.g. adrenogenital
syndrome)
perineal rash or excoriation
vaginal discharge (on pants)
Male: size and shape of penis
hypospadias +/- chordee
balanitis
position of testes
inguinal hernia (reducible?), hydrocele (check
trans-illumination to
differentiate from haematocele).
Pubertal development grading:
Stages 1 and 5 are fully infantile and fully adult
respectively. You need remember only stages 2, 3 and 4.
a) Boys: Genital (penis) development
Stage
1:
testes, scrotum and penis as in early childhood,
testes 2 ml.

18
Stage
2:
some enlargement of testes and scrotum, testes
>3ml.
Stage
3:
early lengthening of penis
Stage
4:
enlarged penis in length and breadth, with glans
development
Stage
5:
adult genitalia
b) Girls: breast development
Stage
1:
As in early childhood
Stage
2:
Breast bud
Stage
3:
Breast and areola enlarging
Stage
4:
Areola and papilla form a secondary mound
distinct from enlarging breast
Stage
5:
Mature
c) Boys and girls: pubic hair
Stage
1:
no pubic hair
Stage
2:
sparse growth of hair each side of penile root or
on labia
Stage
3:
darker coarse hair meeting on symphysis
Stage
4:
adult hair, no spread to medial surface of thighs
Stage
5:
adult in quantity and type with spread to medial
surface of thighs
Examination of Central Nervous System:
Observe closely the child's alertness, willingness to play,
happiness, irritability.
With an unconscious child record response to stimuli, e.g.
light touch, firm stroke to skin, shining of bright light.
Write down examples of his capabilities, e.g. pursues ball
under table, plays peek-a-boo, imitates car engine, enjoys
make-believe, talks articulately ("mummy, look at the doll"),
etc.
Record apparent asymmetry, unsteadiness while walking/
running/ sitting, or any inco-ordinaition when reaching for
toys. Is the gait abnormal? Are there abnormal added
movements, e.g. jerks, athetoid writhing movements,
salaam attacks, episodes of blankness, or unusual
postures?
Assess tone. Does he feel floppy? Is there muscle-wasting or
fasciculation? Is there hypertonia of a particular muscle
group, e.g. high adductor spasm (scissoring) in spastic
diplegia? Is there associated clonus?
Test power. Informally by observing child kick a football, lift
a box of bricks i.e. effortful activity appropriate to age. More
formally a systematic documentation of neck, trunk and
limb power may be necessary, including flexion, extension,
rotation; where appropriate compare right with left.
Assess reflexes, including jaw, biceps, supinator, triceps,
knee, ankle, plantar. Sensation is often difficult to test
reliably and consistently, particularly in younger children.
Record any cranial nerve defects. N.B. Optic atrophy,
strabismus and palatal weakness may be caused either by
local defects, or as part of the spectrum of cerebral palsy.

19
Steps in making a diagnosis and identifying
the treatment
Presenting complaints
Probable pathophysiological causes
Formulation of questions for history
of present illness
Formulations of questions for past
illness
Formulations of questions for medical
history
Formulations of questions for family
and social history
Making of a historical diagnosis
Formulations of signs that may be
present in-relation to the diagnosis
Examination of the patient
Correlating the historical data with
examination data
Clinical diagnosis
Listing of clinical conditions that may
have similar signs
List of differential diagnoses
(Not more than three)
List of investigations
All junior and senior interns should report to Dr. Siva
Shrestha upon their arrival in the department.
What the Junior interns should do ?
1. Take complete histories/ perform complete clinical
examination in OPD and indoor and present to senior
intern.
2. Attend MCH immunization clinic in Wednesdays and
attend Nutrition clinic on Mondays.
3. Attend clinical/ Journal club meetings.

20
What the Senior interns should do?
1. Take histories/ do complete clinical examination if there
are no junior interns. Supervise the junior interns on
history writing and examination.
2. Fill up the lab. report forms/ draw blood as required for
investigations.
3. Present cases with above mentioned investigations when
appropriate to MD resident/Medical officer
4. Attend clinical/ journal club meetings.
5 Assist MD resident /house officer in resuscitation of
Newborn once a week by staying as a first on call with
MD residents/ house officers. They should make their
own roster and it should be approved by respective
consultant.
6. Keep log book of their daily activities and present to
consultant before getting certificate of their posting as
intern
7. Follow-up of admitted patients
USE the SOAP, SOAPIE, or SOAPIER documentation
formats, you should follow a structured method to write
narrative progress notes. These formats are part of the
problem-oriented medical record system of documentation,
which describes patient problems on multidisciplinary
progress notes. If you use the SOAP format, you'll
document the following information for each problem
Subjective data: information the patient or family members
tell you, such as the chief complaint. Objective data:
factual, measurable data you gather during the
assessment, such as observed signs and symptoms, vital
signs, and lab test values. Assessment data: conclusions
based on the collected subjective and objective data and
formulated as patient problems or nursing diagnoses Plan:
your strategy for relieving the patient's problem, including
immediate or short-term actions and long-term measures.
In all clinical settings, They will be responsible for taking
complete paediatric histories and performing physical
examinations, as well as formulating differential diagnoses
and plans of management. All patients seen by them will be
reviewed by a paediatric resident.
They will be expected to research each assigned patient's
disease by the use of appropriate texts and journals..
Appendix A: Guide for the Student Evaluation
Evaluation is done based on the daily performance
during the clinical posting (8 marks), submitted 12
history cases (5 marks) and the unit examination of
the theory classes (7 marks) by the individual
teachers. These marks will be combined and will be
for the internal assessment mark.
Criteria for clinical Skill
This is not for neonatal examination. Headings
might differ according to the situation.
STUDENT’S Name and roll no:____________________________
Initial Encounter:
o Introduce self
o Wash hands
o Observe general appearance, including nutritional status,
hygiene & comfort level
o POSITION CHANGE:

24
Appendix B: Guide for the Student Evaluation
Criteria for History taking Skill
This is not for neonatal history taking.
Headings might differ according to the
situation.
° Introduces himself to the parent.
° Talks with the child
° Takes consent from the parent.
° Speaks politely, clearly using simple language.
° Uses open ended questions.
° Asks relevant questions to the presenting complaints.
° Asks for associated conditions relating to the presenting
problems.
° Asks for the signs that could have been observed by the
parent
° Asks child if can narrate.
° Formulates questions that will probably gives back good
information to make diagnosis.
° Finds calorie intake of the child during the illness and
previous to illness.

25
° Finds risk factors for respiratory and diarrhoeal disease,
immunizations status, and deworming status.
° Narrates summary to the parent and asks if he has
missed any information which they want to tell.
Signs seen during the MBBS paediatric posting.
Please give one star ( * )every time you see a sign.
Please show this to your teacher every week.
Name of the student:………………………. Paediatric posting date:………………..
Pallor Cyanosis Jaundice Clubbing Odema Stunting
Wasting Tachypnoea Macular rash Pustules Purpuric
rash
Echymosis
Wheeze Stridor Ronchi Vesicular
Breath
sounds
Bronchial
Breath
sounds
Chest indrawing
Propped up
position
Raised JVP Systolic and
diastolic murmurs
Dull
percussion
node
Reduced air
entry
Crackles
Flaring alae
nasi
Grunting Capillary refill time Bulged
fontanalle
Convulsion Unconsciousness
Spleenomegaly Hepatomegaly Lymphadenopathy Ascitis Prote
(froat
Abnormal
movement
Macrocephaly Hypotonia Slow skin
pinch
Eage
dri
Microcephaly
Cranial nerve
palsy
Paresis/paralysis Exaggerated
jerk
Ne
rigi
Exudative fluid
Transudative
fluid
Straw colour fluid Chylous fluid
PRESENTATION GUIDELINES FOR RESIDENTS, HOUSE OFFICERS AND
STUDENTS.
At the Bedside clinical round or the clinical case discussion seminars.
Before presentation follow the following rules
1. Never present the case if you have not taken the history and
examined the patient.
2. Always stand on the right side of the patient and towards the head
end of the bed.
3. Stand in front of consultant/senior faculty.
4. Hold the case notes in the right hand.
5. Never keep another hand in pocket, do not lean in the bed.

26
6. Keep smiling.
7. During presentation never become quiet for more than 30 seconds.
8. Speak softly but loud enough to be heard from the foot end of the
bed.
Make an effort to present cases without the aid of the chart, without
reading the chart notes verbatim. If there are three or fewer
admissions to be presented, then an extemporaneous oral
presentation is a reasonable expectation of an intern or resident. A
physician should and must have the intellectual capacity to present
a case from memory.
9. Follow the following order for presentation:
Start as: My patient is Pushpa Raj Sharma, aged 8 months from
Palpa presented to this hospital three days back with the presenting
complaints of fever for 10 days and convulsion for 10 minutes one
days back. Pushpa was alright 10 days back when his mother
noticed ………………………….
………………
• Presentation
History:
o Gender(it may be awkward if the child is old enough to
understand his/her sex), age, race, place of residence,
presenting complaint (in the chronological order), and relevant
HPI (include systemic review), PMH, medications, birth and
development history, immunization history, nutritional history
(always refer to the calorie: required and received by the child),
personal history (school), social history, family history (include
contact and consanguinity).
o Do not meander randomly from one problem to another in your
presentation. If a patient has more than one problem to be
included in the present illness, give a full report on just one
problem at a time. Do not repeat information that was already
included in the HPI in PMH.
Physical exam:
Do start with a general description of the patient's appearance and
the degree of distress, if present.
o Present vitals, (in an unconscious patient mention the Glasgow
coma scale) anthropometric findings (always relate to the
percentiles), and physical exam findings (some times negative
findings are equally important).
Do give a particularly detailed, precise, and complete report
of the examination of the organ that is involved in the present
illness (e.g., Do not state simply that lungs are "clear" in patient
admitted for pneumonia; rather specify the quality of breath
sounds, and specify the presence or absence of wheeze,
crepitations, percussion nodes).
o Do not take time to state your interpretation of physical
findings while reporting the physical exam. When you are
reporting the physical exam, just state the facts. When you are
stating your assessment of the patient's problems, then you
can give your interpretation of the facts.
• Lab tests and Imaging
o What was done for the patient upon presentation?
o Relevant past blood labs and chemistries and images
• Clinical Diagnosis
• Differential diagnosis
o What (at least) three things may this patient most likely have?
o What diagnosis can you not miss!
o Use the presentation, history, labs and images to argue for and
against the differential
• Hospital course
o How was the patient managed for their hospital course?
o Were there crucial turning points?
• Treatment
o Medical , referral, psychosocial or behavioral management
o Follow-up
• Discussion
o Comment on all aspects on the patient care, paying special
attention to areas where there might have been alternative
methods of care. You may also engage some of your faculty to
comment as to how they might have managed this patient.

27
• Preventive measures
o Present known screening and preventive methods
o This is one of the key sections in this Case Presentation. Use
research publications, and references to illustrate your point.
o Please offer (at least) three suggestions for improving medical
care for minorities.
GUIDELINES FOR THE DISCHARGE SUMMARY
The following guidelines are directed towards improving the quality of the
contents of the discharge summary.
"DIAGNOSIS"
1. Do list final diagnosis. Symptoms, physical signs, and abnormal
laboratory values, which should be included among problems on your
problem list, are not necessarily diagnoses. For example, anemia is not
a diagnosis. Nutritional iron deficiency anemia is a specific diagnosis. If
a patient has an anemia that has eluded explanation, then an
appropriate discharge diagnosis is "normocytic anemia of unknown
etiology" rather than just "anemia".
2. Do list all active problems. For example, if an electrolyte imbalance is
resolved during the course of the hospitalization, or is present only
transiently, then do not list it as a final diagnosis.
3. Do not use abbreviations in the list of final diagnosis. The list of
diagnosis is read and codified by non-medical personnel in the medical
records department. Although some abbreviations are readily
recognizable, it is easier for everyone if abbreviations are not used for
diagnosis. (In general, the use of abbreviations anywhere in the chart
should be minimized.)
"SUMMARY"
1. Do write a very brief, cogent history and physical exam. There is, after
all, a full admission work-up in the chart, and there is no need to rewrite
the history and physical exam in the discharge summary. Often, it is
appropriate to just list the relevant findings within the discussion of
specific problems, instead of writing a separate abstract of the history
and physical exam.
2. Do write the summary like a progress note. List each problem
separately and write a separate paragraph to describe the hospital
course of each problem.
N.B. It is appropriate to include within the text of the written summary discussion
of both :final diagnosis" and other significant problems. For example, a patient
was admitted for pneumonia, and during the course of his illness developed
convulsion that required anticonvulsant therapy for two days, but that resolved
by the time of discharge. The final diagnosis should include pneumonia, but not
seizure disorder. However, the written summary should indicate that the
hospitalization was complicated by the need for anticonvulsant therapy (how
much, what type of anticonvulsant, etc.) for two days (indicating the presence of
hypoxia, for future reference).
3. Do list all pertinent tests and their results. Also, list what results, if any,
are pending.
4. Do specify whether a problem improved, resolved or continued
unchanged.
5. Do specify the justification for the final diagnosis, unless it is
immediately obvious.
6. Do list all medications that the patient is being told to take upon
discharge.
7. Do mention what, if any, follow-up in clinic -- and which clinic-- has been
arranged.
8. Do make a special effort to be legible and neat!!! The discharge
summary should clearly and easily communicate information. It should
not obfuscate information. Remember other hospitals can imagine your
knowledge and your hospitals efficiency.
Remember: the discharge summary for is extremely important. A good summary
provides concise and accurate information and ensures a degree of continuity of
care for the patient. A haphazard or nonchalant summary is an unnecessary
obstacle. A bad summary forces the reader to take the time to go through the
interrogation with the parent and parents may not know the hospital medical
events.
A discharge summary should be accomplished before the morning
of discharge. It should be a written summary on a specially
prepared summary sheet and must be signed by the third year MD

28
resident. If the patient has been hospitalized for more than three
days, the summary must be dictated. All summaries must contain:
a. Chief complaint
b. Relevant HPI, PMH, Developmental, medications,
birth and development history, immunization history
(in brief)
c. Relevant admission physical exam (in brief)
d. Pertinent laboratory data
e. Diagnostic impressions
f. Hospital course
g. Condition on discharge
h. Medications, diet, disposition and allergic reactions
i. Discharge follow-up including the DATE OF THE
NEXT FOLLOW-UP CLINIC
j. Final diagnoses in order of importance to the patient's
hospitalization
GUIDELINES FOR CONDUCT AT BEDSIDE
ROUNDS FOR FACULTY
Bedside rounds, whether during daily morning rounds, ward attending rounds, or
consultation rounds, are an integral part of any training program. Bedside rounds,
in contrast to sit-down conferences, require particular attention to a code of
behavior that can best be labeled "Professionalism". The following guidelines
are meant to emphasize certain points of professional behavior for all participants
of bedside rounds.
1. Do not laugh, side chat or discuss other things at the bedside. This is
simply "unprofessional" and should never be done.
2. Do greet the patients guardian and say “hello to a child”. However the
child is small show some gesture so that parent think you are really
there to care his/her child. It is very bad form to go to a patient's bed
and talk about him or her, but not to him or her. It is inexcusable to not
even say, "Namaste".
3. Never refer to any patient in disparaging terms in public! What is said in
private is a matter of personal conscience, but what is said in public is a
matter of professional ethics.
4. Assume that the parent of unresponsive patient, or the patient with an
altered mental status could possibly understand what is said at the
bedside, and maintain professional decorum in front of all parents.
5. Do talk with the older children about their illness. Describe what is
his/her illness.
6. Do maintain the patient's personal privacy and dignity as much as
possible.
7. Do not argue at the bedside. If an earnest difference of opinion
becomes apparent, continue the discussion outside the room.
8. Do use appropriate language at the bedside. Know what to say and
what not to say at the bedside. For example, never say "cancer" or
"tumor" or “bad prognosis” in front of a patient who has not yet been
diagnosed and told of having cancer.
9. Do talk to the patient. Before leaving the bedside, translate the medical
discussion into an appropriate explanation for the parent.
Remember: even if the patient being discussed is not physically present, other
patients in the room will hear the discussion and will more than likely talk among
themselves, talk to the patient in question, spread rumors, etc. If any patient is
within earshot, all the rules of professional behavior apply.
Department of Child Health
Student Evaluation
Date Evaluated:
You may or may not write your name.
For all of the questions below please insert the appropriate number hat best fits
your response:
0 = terrible, unacceptable, definitely no
1 = poor, marginal

29
2 = average, acceptable
3 = good, very satisfactory
4 = superior or excellent, definitely yes
1. Rate the overall quality of this posting:
2. List and evaluate your Faculty:
a. Dr.
a. teaching ability
b. availability
c. enthusiasm
b. Dr.
a. teaching ability
b. availability
c. enthusiasm
c. Dr.
a. teaching ability
b. availability
c. enthusiasm
3. List and evaluate the MD Resident/House Staff with whom you had
closest contact:
a. Dr.
a. teaching ability
b. availability
c. enthusiasm
b. Dr.
a. teaching ability
b. availability
c. enthusiasm
b. Dr.
a. teaching ability
b. availability
c. enthusiasm
4. Rate the MD Resident/house Staff in general
regarding:
a. teaching ability
b. availability
c. enthusiasm
5. Rate your interaction with Full-Time Faculty. Explain:
6. Rate the degree of direct supervision regarding review of your history
and physical findings, progress notes, etc.
Who usually did this?
7. Please rate the following:
• Orientation
• Patient Load
• Ambulatory Experience
• Teaching Rounds
• Teaching Conferences
• Degree of cooperation from Full-Time Staff
8. Rate your interest in this field:
a. before taking this paediatric posting
b. after taking this paediatric posting
9. Rate the organization of this paediatric posting:
10. Was the method of evaluating your performance explained to you at the
beginning of this paediatric posting?
Did you receive adequate feedback on your performance during the course of
this posting?
11. What do you consider to be the appropriate length of time for this
posting?
12. What did you like least about this posting?

30
13. What did you like best about this posting?
14. Comment on the lecture series at your hospital site:
15. Do you have any comments or suggestions?
Please return this evaluation to: Prof. Pushpa Raj Sharma, Department of
Paediatrics, HLMC.
Examples for the Paediatric Cases:
A. Problems:
1.
A 6 year old girl developed swelling of the left knee. She had been
well that morning at home, but then complained of pain in her left
knee, which subsequently became swollen.
There was no history of trauma. There had been no recent illness,
her appetite was good and she did not suffer from dysentery. She
was admitted 5 months back in Kanti Children`s Hospital for
respiratory problems.
She was born by lower caesarean section as the mother had
as the mother had two previous LCS. The neonatal period was
normal. Her developmental mile stones were normal. The two other
siblings were healthy. She is fully immunized.
Examination:
Height 118 cm.
Weight 20 kg.
Not clinically anaemic.
Pyrexial 37oC axillary.
Pulse 92/min; B.P. 95/60 mm of Hg.
Breath sounds normal.
Abdomen non tender. No hepatosplenomegaly.
Tonsils enlarged not infected.
No rash.
Left knee: swollen, inflamed, tender, with restricted movement.
Investigations:
Hb 9.2 G%
WBC 10,000/cmm; N 73%, L 24%, E 3%,
Platelet adequate.
X-ray left knee soft tissue swelling.
Questions:
1. What is your most probable diagnosis?
2. Mention two other differential diagnosis.
3. What other investigations you will ask for?
4. Will you admit this patient in a hospital?
5. What drug will you prescribe before getting further
investigation reports?
Answers to problem no 1.
1. Stills disease.
2. Septic arthritis, rheumatic arthritis,
3. ESR; rheumatoid factor; antinuclear factor; ASO titre;
4. This patient can be treated from OPD.
5. Acetylsalicylic acid; 450 mg every six hourly.Ô
0*0*0*
2.
A eight year old girl was admitted from OPD. She had a dry cough
for three weeks, starting with a mild pyrexia, sore

31
throat and headache. She was being treated from OPD with
ampicillin, cephalosporin and chloramphenicol with out any
improvement. Since two days she has developed mild macular
erythematous rashes over the trunk. She had become anorexic
and lost 1.5 kg in weight.
Her previous health was good. There are four siblings and all were
in good health. Her father had recently a chest
infection treated with antibiotics but is now well. Her mother had
tuberculosis at the age of 23 years. She was fully treated and is
off the medicines since last six years.
This child is fully immunized.
Examination:
Height 1.44 m.
Weight 27.1 kg.
Temperature 37.2oC axillary.
Pulse 92/min. Respiratory rate 58/min. B.P. 110/60 mm of Hg.
No cyanosis.
Heart sounds normal.
Crepitations at right base. Percussion dull at right base.
Fauces congested. Tympanic membrane mild congestion.
Small mobile non tender tonsillar lymph nodes.
Investigations:
Hb 11 g%, WBC 6400/cmm, N 64%, E 2%, L 30%, M 4%.
Chest X-ray nodular opacities at the right lower zone with
small right pleural effusion.
Mantoux test negative.
Pleural fluid clear, 2 wbc/cmm, culture no growth.
Urine analysis normal.
Stool ova of ascariasis.
3.
A 3 week old neonate was admitted from the emergency room of Kanti
Children Hospital with the history of vomiting. He had been well
until one week before admission when he had begun to vomit 4-5
times daily. The vomiting was not related to feeding and was not
projectile. The vomitus contained neither blood nor bile and there
was no accompanying diarrhoea. The child was breast fed
exclusively. Her pregnancy was normal and terminated spontaneously.
Birth weight was 3.462 kg. There were no neonatal problems. This
was the first child of parent.
Examination: Weight 3.003 kg; Rectal temperature 37.3oC.
Clinically dehydrated mild
Pulse 164/min; regular. Respiratory rate 42/min.
Normal chest sounds.
Abdomen not distended. Liver one cm and spleen not palpable.
Bowel sounds normal.
Normal male genitalia with both testis descended.
Reflexes normal.Ô
0*0*0*
Investigations:
A test meal did not reveal any visible peristalsis.
Hb: 12.9g%; WBC 4300/cmm. Differential count normal.
Sodium (serum) 125 mmol/l. Potassium 7.1 mmol/l.
Urea 12.3 mmol/l. Urinary 17 oxosteroids 0.8 mmol/l
( 4-24 mmol/l

32
4.
A 8 year male child was seen in the OPD of Kanti Children Hospital
with the complain of mild pain in the right hip
preceded by a mild fever and common cold of one week duration. He
had similar type of illness three months earlier which subsided
with paracetamol.
His paternal grand father suffered from osteoarthritis and
maternal grand mother suffered from rheumatoid arthritis.
He has two siblings both of them are in good health.
Examination: Height 105 cms. Weight 16 kg.
Pulse 96/min; Blood pressure 100/60 mm Hg.
Heart sounds are normal.
Right hip limitation of active and passive movement.
All other joints are normal.
Gait limp on right leg.
Investigations: Hb 10.5g%; Haematocrit 36%;
WBC 7,800/cmm; P 85%, L 15%;
ESR 20 mm first hour;
X-Ray hips sclerosis and partial collapse of the right femoral
head.
5.
An 18 months old child was seen in the OPD for fever since
3 days associated with a cough and occasional vomiting. She
was treated out side on the second day with oral cephalosporins one
TSF eight hourly.
Examination: Miserable child. Temperature 38oC axillary.
No jaundice. Pulse 124/min. Respiratory rate 40/min.
Fauces were mildly congested. Bilateral wax . Tonsillar nodes
palpable they were less than 1 cm and non tender.
Soft systolic murmur over left parasternal 2 ICS.
Breath sounds were normal.
Investigations:
Hb 8.3g%; WBC 18300/cmm; P 63%, L 31%, M 4%, E 2%;
Urea 5.4 mmol/l; Na 139 mmol/l; K 3.7 mmol/l;
Throat swab culture no growth;
Urine culture no growth; Urine WBC 10/cmm.
Blood culture no growth.
X©ray: consolidation of the right upper lobe.
She was treated with penicillin intramuscularly. Temperature
settled after 24 hours. Thereafter oral amoxycillin was given. She
again became pyrexial next day. Penicillin was restarted again the
temperature settled. She started vomiting off and on. She lookedÔ
0*0*0*
very miserable, withdrawn and anorexic. No new physical signs could
be found on examination.
6. A 2 years old girl was admitted from the emergency room
of KCH with difficulty in moving her right arm and leg. She had a
mild cold during the previous days, and on the day before admission
her mother noticed that she was not moving the right leg. On
waking up the following morning, she had paralysis of the body
which regressed within a few hours.

33
Before coming to the ER parents noticed clonic right sided
convulsion with mild drowsiness and recurrence of the right
sided paralysis. She had been full term normal delivery weighing
2.580 kg following a normal pregnancy. She sat at
six months, walked at 12 months spoke baba at 7 months.
She had measles and chicken pox at 9 and 15 months respectively.
Examination: Height 77 cms; Weight 10.9 kg;
Temperature 37.2oC axillary.
Fully conscious.
Sub total flaccid right sided hemiplegia.
Right facial palsy lower part affected mainly.
All other cranial nerves are normal.
Decreased right sided reflex.
Planters: right extensor; left flexor.
Investigations: Hb 11 g%; WBC 6800/cmm; P 56%, L 40%, E 4%;
Platelet 210000/cmm
Prothrombin time normal.
Blood culture no growth.
Lumber puncture cells 386/cmm; L 76%, P 24%,
protein 60 g/l, sugar 80mg%.
7. An eight year old girl from Baglung was referred because
of high temperature of gradual onset since last two weeks.
She was treated with various antibiotics including cephalosporins,
penicillin, amoxycillin. In Baglung urine
culture showed E.coli which was sensitive to Nalidixic acid.
She had 10 days treatment of nalidixic acid.
She did not have any major illness in the past. She was fully
immunized. She has two siblings all are in good health. Over the
last two days she has developed a temperature and been extremely
miserable.
Examination: She was pyrexial and pale. Liver was palpable and
spleen was 1 cm enlarged. All the joints appeared normal. Other
systems were normal.
Investigations: Hb 9g5; WBC 10000/cmm; P 60%, L 40%.
ESR 58 mm in first hour.
Mantoux test was negative.
Blood culture no growth. Urine culture no growth.
Salmonella agglutination test normal.
Chest x ray normal.
Bone marrow reported as normal.Ô
0*0*0*
She was treated with ciprofloxacin for 6 days but the temperature
did not subsided. She was noted to be pale.
A repeat blood count was as follows:
Hb 7 g%; WBC 11000/cmm; P 20%, L 80%.
8.
A 14 month old boy has had a mild upper respiratory tract infection
associated with occasional vomiting for the past
5 days, but for the previous 48 hours has severe colicky
abdominal pain with bloody diarrhoea and lethargy.
He was born at 36 weeks gestation by caesarean section

34
weighing 2.7 kg to a 21 year old mother who now has another 3 month
old baby.
Apart from several upper respiratory tract infections and two
episodes of diarrhoea, the child has been well.
Examination:
Height 72 cms. Weight 9.5 kg.
Pyrexial 37.2 oC (axilla).
Pulse 95/minute. Respiratory rate: 32/minute.
Hearts sounds normal. Chest clear.
Pharynx inflamed. Wax in both ear.
Abdomen diffuse tenderness, no rebound tenderness.
Rectal examination normal.
Irritable and restless.
No meningism. No central nervous system localizing signs.
Investigations:
Hb 7.5g%; WBC 10000/cmm; P 80%, L 15%, M 4%, E 1%;
Platelets 22000/cmm.
Prothrombin time normal.
Urea 12 mmol/l.
Creatinine 150 mmol/l.
Urine : RBC plenty; Protein 2+.
Stool occult blood : positive.
9
A 3 year old boy was admitted from the emergency room in the
medical ward with the history of acute onset of noisy breathing.
This has worsened over three hours. He did not has this type of
episode in the past. He was not eating any thing during this
episode and there was no history of choking .
Examination:
Fever 38.5oC axillary.
Drooling, flushed, centrally cyanosed.
No rash.
Pulse 132/min. Respiratory rate 68/minute.
Inspiratory and expiratory stridor.
Suprasternal, sternal, and subcostal recession.
Restless, but conscious.
Ô
0*0*0*
Questions:
1. Mention three differential diagnosis.
2. In emergency observation ward how will you manage this child?
3. Mention three commonest bacterial pathogens that causes ARI.
4. What further investigation you will ask for?
5. Which antibiotic will you use? What is its dose?
Answers:
1. Acute epiglottitis; retro©pharyngeal abscess; ludwig's angina.
2. a. Oxygen by nasal canula at 2 litres/ minute.
b. Put an i.v line.
c. Hydrocortisone and chloramphenicol i.v.
d. Prepare for tracheostomy if the cyanosis does not relieved.
3. Haem. influenzae; strep. pneumoniae; staph. aureus.
4. Lat x©ray of neck.

35
5. Chloramphenicol. 50 mg/Kg/day.
10.
A 10 year old boy was seen in the OPD for the complain of
sore throat since 5 days. He also had frontal headache and
posterior neck pain. He was seen by a practitioner earlier
in the week when a diagnosis of URTI was made for which
oral cephalosporin was prescribed. On the day before coming
to OPD he was seen in emergency department in view of his
lack of improvement, and changed to cloxacillin. This boy
was admitted in the medical ward.
Over the next 24 hours he had became progressively distressed with
difficulty in breathing and with neck pain.
Examination:
Temperature: 38.5oC;
Distressed unable to lie down comfortably.
Pulse 100/min, regular with marked diminution in volume
during inspiration.
Heart sounds normal, no added sounds.
Respiratory rate 40/min.
Breath sounds normal, no added sounds.
no other positive signs on examination.
He was observed overnight but the following morning there was no
improvement and he was still complaining pain in
neck. On examination he had shallow rapid breathing and
on auscultation bronchial breathing could be heard in
a small area of the lower anterolateral chest of the right
side. There was also a rough scratching sound in time with the
heart beat heard at the lower left sternal border.
Investigations;
Hb: 10.3g%; WBC 11000/cmm; P 84% L 13%, M 1%;
11. A two and half months old male child presented with the history
of bluish discoloration of lips and fingers since last two months.
Since last one week he has cough on and off with episodes of
excessive crying. He was born by normal vaginal dilivary at term inÔ
0*0*0*
home. There were no perinatal complications. He was breast fed but
had excessive sweating during sucking and could not continue
sucking continuously for more than 5-10 minutes.
Examination:
Weight: 4 Kg. Length: 56 cms. OFC: 36 cms.
Pulse rate: 120/min. R.R: 30/min. Temp: 99.4 o F.
Central cyanosis present.
Apex beat: 6th left intercostal space lateral to the midclavicular
line. No thrill. Heart sounds normal.
No murmur.
Mild hepatomegaly was noted.
Investigations:
Hb: 16.3 G%. WBC: 6700/ cmm. P: 46%; L:54%.
12.
Nine month old male child presented with the history of increasing
abdominal distension since last 20 days. His mother had noticed
abdominal distension since last 6 months for which she was

36
investigated in another hospital but no cause was found. There was
no history of vomiting, jaundice,
pallor , fever, constipation or bleeding from anywhere.
His appetite was normal.
He was born in hospital at term by normal vaginal dilivary with the
weight of 2.5 Kg. There were no perinatal problem.
He was absolutely breast fed till 4 months and then weaned with
lito. He began to smile at 2 months but sat with support a few days
back. He is completely immunized. He has one brother of 3 years
who is healthy.
Examination:
Length: 66 cms. Weight: 6.8 Kg. OFC: 43 cms.
Scalp hair sparse and brittle. Discrete cervical lymphnodes of less
than 2 cms in the right post. triangle of neck.
Pulse: 100/minute. R/R: 24/min. T: 97 o F.
Liver was 9 cms enlarged which was firm, non tender and smooth.
Spleen was 10 cms enlarged firm, non tender and smooth. No free
fluid in the abdomen was noticed clinically.
Investigations:
WBC: 11,560/cmm. N 25%; L 74%; E 1%; Hb 9.6 G%.
PCV 31%; MCHC 31%; MCV 73.8%; Film: Hypochromic, microcytic. Hb F
1%. MP absent.
Ultrosonography: hepato spleno megaly.
Bone marrow: Hypercellular, adequate megakaryocutes, normoblastic
erythropoesis, M:E ratio was 10:1.
No parasite were found. Diagnostic cells (Gaucheres) were present.
Serum acid phosphatase: 46.5 KAU. ( 1.5 -3.5 KAU ).
13.
12 year old male child was admitted from the emergency with the
history of fever since last 8 days, generalized skin rash for 5
days and irritability since one day. There was no history of
vomiting, unconsciousness or convulsion. He did not had any episode
of throat infection, dysentery or other illness in the recent past.
Examination:
Conscious but irritable.
T: 99.8 o F ( axillary ). P: 120/min. R/R: 28/min.Ô
0*0*0*
B.P. 100/70 mm of Hg.
Purpuric rashes were present over the abdominal wall.
Mild hepatosplenomegaly was noted.
No neck stiffness.
Investigations:
WBC: 3800/cmm; P: 55%; L: 45%; HCT 32%, Platelet: 18000/cmm.
CSF: RBC: 330/cmm; WBC: 0; Protein: 16mg%; Sugar: 51mg%;
Creatinine: 4.1mg/100 ml ( 0.9 - 1.4mg/100ml ).
CXR: normal.
Blood culture: Salmonella typhi positive.
Bone marrow: ITP with hypoplastic marrow.
14.
An eight year girl presented in the OPD of Kanti Children's
Hospital with the complain of yellow dark coloured urine, pain in
right upper abdomen and palpitation since two week. She also had
loss of apetite since three weeks.
She also had the history of intermittent joint pain which was
associated with palpitation and dry cough since last four years.
She could not run fast as her friends because of shortness of

37
breath. There was no history of chest pain. She did not have recent
episode of sore throat.
Examination:
Temperature: 102 o F. Pulse: 120/min. regular with fair volume.
B.P.: 84/60 mm of Hg in supine posititon.
Height: 113 cms. Weight: 18 Kg.
Jaundice present. Oedema absent.
Apical impulse in 6th intercostal space in the anterior axillary
line. There was systolic murmur in the mitral area.
There was hepatomegaly of 3 cms below the costal margin in the
midclavicular line. Spleen was not palpable.
Invesatigations:
WBC: 13000/cmm; P: 52%; L: 48%. Hb:9.4 G%.
S.B. 130 mmol/L.
ASO titre: more than 400 U.
Urine and stool examination were normal.
15.
A thirteen year old girl presented in the emergency with the
complain of abdominal pain, occasional vomiting, large joints pain
and rashes over the extremities since last five days. She had sore
throat one week prior to the appearence of these symptoms. There
was no history of fever, cough, bleeding from any sites, altered
sensorium or convulsion.
Her apetitie is good, bowel and bladder habbit were normal.
Examination;
Vital signs were normal.
Skin: Multiple purpuric rashes limited to the buttocks and
extremities.
Other systemic examination were normal.
Investigations:
WBC: 10,000/cmm; P: 67%; L: 32%; E: 1%; Hb: 12.4 G%; ESR: 13mm inÔ
0*0*0*
one hour. Platelet: 1,95,000/cmm.
Urine: Albumin +; RBC 4-8/HPF.
Stool: Cyst of Giardia lamblia.
16.
A six year old girl from Nuwakot presented in the OPD with the
complain of pallor, abdominal pain and occasional passing of black
stool since last 2 months. There was no history of bleeding from
other sites, fever, any medications or joint pain. She was
delivered at home at term. There was no any perinatal or neonatal
problems. She was absolutely breast fed till weaning at six months
but continued to breast fed till one year of age. She was not
immunized. There was no significant past history of any illnesses.
Examination:
Height: 92 cms. Weight: 10.6 Kg. Vital signs were normal except
pulse which was 140 per minute.
Markedly pallor. No sternal tenderness. No oedema.
Systemic examination of respiratory, neurological, musculo©skeletal
and genito©urinary system were normal.
On cardio©vascular examination she had apical impulse at 5th
intercostal space in the mid clavicular line and systolic murmur of
2/4 grade over the mitral area without any radiation.
On examination of gastro©intestinal system: abdomen was distended,
no visible superficial veins, liver was 2 cms. palpable which was

38
smooth and non tender, shifting dullness was not present.
Investigations:
Blood; Hb: 4 gm%, TLC: P 40%, L 54%, E 6%, ESR 66 mm in first hour.
Platelet: 150,000/cmm.
Stool examination: Hook worm ova.
17. An 2500 gm male infant, was delivered vaginally after 38©week
gestation. The apgar score at 1 minute was 6 and 8 at five minutes.
He was immidiatly given to mother. Mother complained of difficulty
breathing and bluish tinge over the face. On examination the
neonate was cyanosed with marked subcostal indrawing during
inspiration. He was immidiaatly kept in headbox with oxygen and
started intravenous penicillin and gentamycin. However his
condition deteriorated and an urgent x©ray was done.
How yould you proceed for the management?
18. A 2900©gm ,40©week gestation neonate covered with "pea soup"
meconium is handed to you in the delivary room. He was allready
cried loudly but now appears well. How you would you proceed?
a. Start antibiotics intramuscularly.
b. Start antibiotics inrravenously.
c. Intubate and aspirate the trachea.
d. Observe for another few hours.
19. A 2900©gm, 42 week gestation neoanate covered with green
coloured fluid, delivered by caeserian section is handed to you. He
has allready cried loudly but now appears depressed on the
ruscitation table. He was given IPPV with bag and mask.
How would you treat this patient?
2051.3.13.
20. Ram Prasad aged 11 months was brought in the OPD of Kanti
Children's Hospital with the chief complaints of cough and fever
of two days duration.
Ram was absolutely normal 2 days back when he developed mild fever.
Since then he was not eating well and was irritable. Mother noticed
mild nasal discharge and cough on that evening. His cough became
worse during feeding and was dry.
He was born by normal vaginal delivery with the birth weight ofÔ
0*0*0*
2.2Kg at term. Mother had attended the ANC clinic and was advised
about the care of breast and advantages of breast feeding. His
neonatal period was uneventful. He was bottle fed from the begining
and used to get choking episode on and off. He is immunized with
BCG, Polio and DPT. Mother and father both are smoker. He is the
only child. Both parents work in a carpet factory.
On examination:
Weight: 7 kg. Temperature: 39.1oC. Respiration rate: 62/minute when
observed from distance. ENT: mildly congested nasal and pharyngeal
mucosa. Ear drum was not visible because of wax in both sides.
There was no subcostal indrawing. Chest: it was difficult to hear
any added sound because the child cried when auscultation was
tried. Other examination could not be performed because of crying.
21. An one year old female child presented with the history of

39
loose motions since last 4 weeks. The frequency of loose motions
varied from 1©5 daily. The stool was loose and small in amount. It
was greenish yellow to dark brown in colour in different occasion.
There was no history of fever, vomiting, abdominal pain, melena,
jaundice or difficulty in micturition.
4 weeks back he had acute onset of watery diarrhoea with the
frequency of 10©14 per day with mild fever and vomiting which
gradually subsided to present condition. Parent consulted a
paediatrician who advised to give soya based milk instead of
lactose containing milk.
On examination:
She was irritable,lethargic and in no distress. Height was 75 cms
and the weight was 7.5 Kg and head circumference 46 cms. He had
excoriation over the angle of mouth. Mouth was moist but there was
loss of elasticity of skin over the abdomen.
Liver was 1 cm palpable bellow the right costal margin in the
midclavicular line. Abdomen was mildly distended but there was no
free fluid.
Laboratory data:
Haemoglobin: 9.0 gm%. Haematocrit: 30%.
WBC: 6500/cmm; P: 44%; L: 46%; E: 10%.
ESR: 36mm in first hour.
22. Deepak Sirohiya aged about 9 years from Janakpur presented with
the history of fever and cough on and off since last one month.
Parents have noticed difficulty in breathing since last two weeks
and had significnant weight loss within this period. There was no
history of contact and was fully immunized. There was no history of
haempoptysis.
He was treated at Janakpur waith oral amoxycillin but without any
improvement. He was brought in Kathmandu where following
investigations were done and started antitubercular therapy.
Blood: TLC: 12000/cmm; P:64%; L:34%; E:2%.
Hb: 9.2g%; ESR:44mm in first hour.
Mantaux test: negetive.
Chest x©ray: Left pleural effusion with shifting of mediastinum to
right.
Inspite of one week of antitubercular therapy his condition wasÔ
0*0*0*
deteriorated. He was seen in OPD of KCH.
On examination:
He was dyspnoeic and looked ill. Respiratory rate was 44/min.
No purpuric rashes were noted.
Axillary temperature was 37.6oC. Pulse: 96/min.
Left supraclavicular lymphnode was enalrged (>1cm),non tender and
mobile. Superficial veins were prominent over the left mammary and
left lower side of neck. Left JVP was raised. Left axillary single
lymphnode was also palpable. Left side of the chest was elevated
and the intercostal spaces were full. Apical impulse was not
palpable. Air entry was diminished and left chest was dull on
percussion. Spleen was enlarged to one cm below the left costal
margin. Liver was not palpable and there was no free fluid.
An urgent diagnostic pleural tap was done and it was haemorrhagic.
180 ml of fluid was removed and all the fluid was haemorrhagic.
The laboratory findings of the fluid was as follows:
Cells:6900/cmm. Immature cells with very little cytoplasm.
Protein: 4.6g%. LDH: 1690.
Suggestive of malgnant pleural effusion.

40
This child was referred to Tata Memorial Hospital Bombay for
further followup.
23. Miss Nisha 13 year old presented with the history of fever
since last one week. Fever was associated with chills. It used to
subside with paracetamol. She used to take one tablet of
paracetamol daily whenever the temperature used to come. She did
not had history of sore throat, pain during micturition, cough or
headache. She has returned from India about one and half month
back.
On examination: She was well looking. Her vitals were normal. The
only positive findings was palpable spleen.
Investigatiaon:
TLC: 6500/cmm; P:60%; L:40%. Hb:10g%
Plasmodium vivax was seen on peripheral smear.
She was given one dose of Pyralfin. She still continued to have
temperature.

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