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8/18/2019 OSPE Paeds Medicine Set 3 http://slidepdf.com/reader/full/ospe-paeds-medicine-set-3 1/25 OSPE Peads Medicine Set 3 SurgicoMed.com OSPE PEADS MEDICINE SET 3 Case 1 1. What is the abnormal findings in this eye? 1 2. Which vitamin deficiency cause this condition? 2 3. What is the WHO classification and recommendation to treat this condition? 3 Key 1.  Bitot spots 2. Vitamin A deficiency 3. Classification Primary Signs X1A Conjunctival xerosis X1B Bitot spots with conjunctival xerosis X2 Corneal xerosis X3A Corneal ulceration with xerosis X3B Keratomalacia XN Night blindness XF Xerophthalmic fundus XS Corneal scars XB Bitot spots Vitamin A: 200,000 IU (100,000 in < 1 year of age) on day 1, 3 and 14.

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OSPE PEADS MEDICINE SET 3

Case 1

1.  What is the abnormal findings in this eye? 1

2. 

Which vitamin deficiency cause this condition? 2

3.  What is the WHO classification and recommendation to treat this condition? 3

Key

1. 

Bitot spots2.  Vitamin A deficiency

3. 

Classification Primary Signs

X1A Conjunctival xerosis

X1B Bitot spots with conjunctival xerosis

X2 Corneal xerosis

X3A Corneal ulceration with xerosis

X3B Keratomalacia

XN Night blindness

XF Xerophthalmic fundus

XS Corneal scars

XB Bitot spots

Vitamin A: 200,000 IU (100,000 in < 1 year of age) on day 1, 3 and 14.

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Case 2

(Nutrition)

1. 

What are the complications of bottle feeding? 3

2. 

Enumerate benefits of breast feeding? 2

3. 

Write two absolute contra-indications of breast feeding?

Key

1.  Complication:

 

Repeated GIT infections 

Repeated respiratory infections

 

Expensive

 

Difficult to maintain hygiene

2.  Benefits:

 

Inexpensive

  Available all the time

 

Composition is ideal for the infant growth

 

Emotionally satisfactory

 

Bifidus factor which promote the growth of lactobacillus

 

Promote involution of the uterus

  Natural contraception

 

Decreased incidence of breast cancer

 

Lactofarin

 

Species specific, no allergy

 

Decreased incidence of infection

3. 

Absolute contraindications:

 

Galactosemia

 

Phenylketonuria

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Case 3

1. 

What is the sign shown in the photograph? 1

2. 

Write down 4 other signs of this condition? 2

3. 

Write down the management steps of this condition according to WHO protocol? 2

Key

1. 

To check skin turgor in dehydration2.

 

Other signs:

 

Lethargic or unconscious

 

Sunken eyes

 

Not able to drink or drinking properly

  Pulse weak or absent

3. 

ORS / Homemade remedies

Age First give 30 ml/kg in Then give 70 ml/kgInfants (< 12 months) 1 hour 5 hours

Children (12 M up to 5 Years) 30 min 1 ½ hours

Type of fluid is Linger lactate or normal saline

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Case 4

A 12 hours old full term baby having 1.5 kg weight presented with focal fits. His investigations

are: Blood sugar 28 mg/dl, S/Ca2+ 8.5 mg/dl and Na+ 128 mg/dl.

1. 

Name the diagnosis and its complications in this case? 1

2. 

Enumerate four common causes of SGA? 2

3. 

Enumerate eight common complication of SGA? 2

Key

1. 

SGA (small for gestational age) with hypoglycemic fits

2. 

a. 

Maternal Causes: 

Chronic illness like essential HTN, PIH, CRF, Diabetes

  Young maternal age < 18 years

 

Poor maternal weight gain

 

Short stature (maternal malnutrition)

 

Anemia

 

Smoking in mother

b. 

Fetal Causes: 

Chromosomal disorders

  Congenital infections

c. 

Placental Causes:

 

Decreases placental weight

 

Placental separation

 

Twin twin transfer syndrome

3. 

Complications:

  Hypoglycemia

  Hypothermia

  Hypocalcaemia

  Polycythemia

  Infections

  Perinatal asphyxia

  Meconium aspiration

  Congenital malformation

  Pulmonary haemorrhage

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Case 5

(Nutrition)

1. 

Name the final step in the formation of vitamin D? 2

2.  Name 6 common causes of rickets? 1.5

3. 

Name 6 common clinical features of rickets? 1.5

Key

1. 

Renal activation of 25-hydroxycholecalciferol

With the help of 1 α-hydroxylase to form 1, 25-hydroxycholecalfiferol

2. 

Causes:

  Nutritional rickets

 

Vitamin D dependent rickets

 

Vitamin D resistant rickets

 

Rickets due to malabsorption

 

Rickets due to chronic anti-convulsant therapy

 

Hepatic

 

Renal

  Hypophosphatemia rickets

3. 

Clinical features:

 

Head large with frontal bossing

 

Delayed eruption of teeth with defective enamel

  Thorax (Rachitic rosary, Harrison’s sulcus, Pigeon chest deformity) 

 

Spine (Kyphosis, scoliosis, lordosis)

 

Pelvis (contracted pelvis)

  Extremities (Widening of head of long bones, genu valgum or genu varus

deformity )

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Case 6

(Nutrition)

1. 

What is the findings in this photograph? 1.5

2. 

What is the most likely diagnosis? 1.0

3. 

What is the treatment? 1.5

Key

1.  Widening, cupping and fraying of ends

2. 

Rickets

3.  Treatment:

 

Vitamin D3 (either oral or IM injection) 

Calcium supplements

 

Vitamin D dependent rickets 1, 25 (OH)2-D3 

 

Diet high in calcium and vitamin D

 

Exposure to sunlight

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Case 7

(Infectious Diseases)

1. 

What is the abnormal finding? 1

2. 

What is the diagnosis and complications? 2

3. 

What is the treatment? 2

Key

1. 

Bilateral greyish membrane on tonsils with surrounding hyperemia

2. 

Pharyngeal diphtheria

Complications:

  Myocarditis

  Polyneuritis

  Bronchopneumonia

 

Miscellaneous (Hepatitis, nephritis, adrenal hemorrhage, gastritis)

3. 

Treatment:

 

Diphtheria antitoxin

  Antibiotics (Penicillin, Erythromycin)

  Suppurative intervention directed at complications

  Strict isolation

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Case 8

(Infectious Diseases)

1. 

What are the different methods to prevent neonatal tetanus? 2

2. 

Write down the management steps of neonatal tetanus? 3

Key

1. 

Prevention:

  Conduct the delivery in the hospital

 

Strict aseptic techniques as washing of hands, sterilized instruments and Lenin

 

First dose immunization schedule

2. 

Management:

 

Sedation

  Feeding

 

Nursing care

  Antitoxin

 

Antibiotics (Benzyl penicillin to kill vegetative Clostridium tetani)

  Counselling

 

Follow up

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Case 9

(Infectious Diseases)

1.  What is the abnormal findings in this baby? 2

2. 

What is the diagnosis? 1

3. 

What are the management steps of this condition? 2

Key

1. 

Findings:

 

Risus sardonicus / Lockjaw

 

Generalized spasm

2. 

Tetanus neonatorum

3. 

Management:

  Sedation

 

Feeding

  Nursing care

  Antitoxin (ATS, TIG)

  Antibiotics (Benzyl penicillin to kill vegetative C. tetani)

  Counselling

  Follow up

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Case 1

1.  Which is the abnormal findings and diagnosis? 1

2. 

What are the steps of management? 2

3.  How can you eliminate this disease in the neonate? 2

Key

1. 

Risus sardonicus / Lockjaw & tetanus neonatorum

2. 

Management:

 

Sedation

 

Feeding

  Nursing care

 

Antitoxin (ATS, TIG)

 

Antibiotics (Benzyl penicillin to kill vegetative C. tetani)

 

Counselling

 

Follow up3.

 

Elimination of disease:

 

5 dose schedule of TT (tetanus toxoid) to mother

 

5 Cs (clean delivery, clean cutting, clean umbilicus, clean tying, clean…..)

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Case 11

(Infectious Diseases)

1. 

What is the type of rash and what is the diagnosis?

2.  Write 6 conditions which produce such type of skin irruption?

3. 

What are 8 complications of most likely diagnosis?

Key

1. 

Maculopapular rash in Measles

2. 

Conditions

  Measles

  Rubella

  Scarlet fever

  Typhoid fever

  Roseola infectiosum

3. 

Complications:

  Otitis media

  Pneumonia

 

Encephalitis

  Hemorrhage measles

  Gastroenteritis

  Myocarditis

  Immune suppression

  SSPE (subacute sclerosing pain encephalitis)

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Case 12

(Infectious Disease)

1. 

What is the diagnosis of this vaccine preventable infectious disease? 1

2. 

How can you prevent this condition by immunization? 2

3. 

Write 8 complications of this disease? 2

Key

1. 

Mumps

2. 

By MMR vaccine at 15 months and before school entry

3.  Complications:

  Meningoencephalomyelitis

  Epididymo-orchitis

  Pancreatitis

  Deafness

  Oophoritis

  Thyroiditis

  Myocarditis

  Arthritis

  Thrombocytopenia

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Case 13

1. 

What is the abnormal finding? 1.0

2. 

What are three differential diagnosis? 1.5

3.  What are the complications of the most probable diagnosis? 2.5

Key

1. 

Bilateral greyish membrane on tonsils with surrounding hyperemia

2. 

Differential:

 

Diphtheria

 

Acute tonsillitis

  Infectious mononucleosis

3. 

Complications:

  Myocarditis

 

Toxic polyneuritis 

Broncho pneumonia

 

Hepatitis, Gastritis

 

Nephritis, Adrenal hemorrhage

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Case 14

(Infectious Diseases)

1. 

What do the figures show? 1

2.  What are the different modes of transmission of infectious diseases? 2

3.  Write down the treatment of pulmonary tuberculosis? 2

Key

1. 

  Droplet infection

  Right lung involvement in pulmonary tuberculosis

2. 

Modes of Transmission:  Droplet infection

  Sexual route

  Needle pricks

  Fecal-oral route

3.  Treatment:

a.  General Supportive

  Hygienic and nutritional care

  Screening of family

b.  Specific Treatment

  Isoniazid

  Rifampicin

  Pyrazinamide

  Ethambutol / Streptomycin (depending upon the severity of the infection such as Miliary and

disseminated tuberculosis)

c.  Counselling

d.  Follow Up

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Case 15

(Hematology)

1. 

Write two positive findings in the photographs? 1.0

2. 

Write three common differential diagnosis? 1.5

3.  Write the management steps of the most common acquired disorder of the childhood?  2.5

Key

1. 

 

Purpuric rash on the feet

  Subconjunctival hemorrhage

2.  Differentials:

  ITP

  Leukemia

  Aplastic anemia

3. 

a)  Supportive measures

 

Prevention of trauma  Restrict physical activity

  Avoid anti-platelet medication

  Platelet transfusion

b)  Pharmacological Treatment

 

IVIG  Anti Rh-D

  Steroid

c)  Management of chronic ITP

  As above + splenectomy with pneumococcal, meningococcal and H iB vaccination

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Case 16

(Hematology)

 

1.  Write down the positive findings in the photograph? 0.5

2.  Which inherited bleeding disorder causes such swelling and what is the heritance? 1.0

3.  Write down the management steps of this condition? 3.5

Key

1.  Swollen knee joints / Hemarthrosis

2. 

 

Hemophilia  X-linked recessive

3.  Management:

a.  General Supportive Management

  Prevention of trauma

  Avoid aspirin

  Immunization against Hepatitis B

b.  Pharmacological Treatment

  Desmopressin

 

Aminocaproic acid

  Tranexamic acid

  FFP, cryoprecipitate

  Administration of factor VIII concentrate

c.  Counselling

  General counselling to the parents

  Genetic counselling

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Case 17

(CNS)

1.  Which cranial nerve is paralyzed in this photograph? 1

2. 

Enumerate 8 other clinical findings in such a patient? 2

3. 

Name 8 causes of this condition in children? 2

Key

1. 

Facial nerve palsy2.  Clinical findings:

 

Loss of frowning of forehead

 

Loss of closure of eye

  Loss of nasolabial fold

 

Collection of food particles on the

effected side

 

Deviation of angle of mouth to

the opposite side

  Whistling is inappropriate

  Loss of taste of anterior 2/3 of tongue

  Hyperacusis

3. 

Causes:

  Idiopathic (Bell’s palsy) 

 

Acute or chronic otitis media

 

Temporal bone fracture

  Herpes zoster oticus

 

Pyo-meningitis

 

Encephalitis

 

Tuberculous meningitis

 

Brain tumor

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Case 18

(CNS)

1.  What is the abnormality visible in the photograph? 0.5

2.  What is the definition of cerebral palsy? 1.0

3.  What is management steps of cerebral palsy? 3.5

Key 

1. 

  Left lower limb is flexed

  Toe walking

These conditions are present in upper motor neuron type of hemiplegia.

2.  It is static encephalopathy in which there is non-progressive, permanent disorder of posture and

movement due to insult of immature brain.

3. 

a.  Multidisciplinary approach

  Pediatrician (major role)

  Psychotherapist

  Occupation therapist

  Psychiatrist

  Orthopedic surgeon

  Nutritionists

b.  To reduce spasticity

  Diazepam, Baclofen, Dantrolene

  Hearing, vision, learning and mental disorders are managed accordingly

c.  Counselling

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Case 19

(CNS)

1. 

What is developmental age of this child?

2. 

What are the different field development?

3. 

Write down the one developmental milestone in each field in a 9 month old infant?

Key

1. 

4 to 8 weeks

2. 

 

Gross motor

 

Fine motor and visions

  Hearing and speech

 

Social behavior

3. 

 

Gross motor (site without support, reach for the toy in front, pull to stand, crawl)

 

Fine motor and visions (watches rolling ball at 10 feet, drops an object and look at fallen

object, uncover the toy)

 

Hearing and speech (localized sound above and below ear level at 3-6 feet, imitates

adult playful sound)

 

Social behavior (holds, bites and chews a biscuit, stranger anxiety, grasps bell by handle

and ring in imitation, follow one step verbal command)

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Case 2

(CVS)

1. 

What are the abnormal findings? 22.  What is the diagnosis? 1

3.  What are the management steps? 2

Key

1. 

 

Cyanosis / cyanotic spells

 

Clubbing of the fingers

2. 

Cyanotic congenital heart disease (TOF)

3. 

a. 

Medical Management

  Nutritional and hygienic care

  Maintain adequate hydration

  Maintain body temperature

  Maintain hematocrit in adequate range

 

Iron supplements

  Prophylaxis of bacterial endocarditis

 

Treat polycythemia

 

Management of cyanotic spells

b. 

Surgical Management

 

Palliative surgery

 

BT shunt, Waterston shunt, Pots shunt

 

Corrective surgery

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Case 21

(CVS)

1.  Write two abnormal findings in this x-ray of cyanotic infant? 1

2.  What is the diagnosis? 1

3.  What are the steps of management? 3

Key

1. 

  Boot shaped heart (with up tilted apex due to RVH)

  Oligemic lung fields (diminished pulmonary vascular markings)

 

Narrow pedicle / base

  Pulmonary artery bay

2. 

Tetralogy of Fallot (TOF)

3. 

a.  Medical Management

 

Nutritional and hygienic care

 

Maintain adequate hydration

  Maintain body temperature

 

Maintain hematocrit in adequate range

  Iron supplements

  Prophylaxis of bacterial endocarditis

  Treat polycythemia

  Management of cyanotic spells

b. 

Surgical Management

 

Palliative surgery

  BT shunt, Waterston shunt, Pots shunt

 

Corrective surgery

 

Closing of VSD and resecting the right ventricular outflow obstruction

c.  Counselling

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Case 22

(CVS)

1.  What is the diagnosis of this condition?

2. 

Name the commonest acquired cause of this condition in Pediatrics?

3.  What clinical findings will be present in this case?

Key

1.  Aortic regurgitation disease

2.  Rheumatic fever / rheumatic valvular heart disease

3.  Clinical findings:

 

High volume bounding pulses

 

Collapsing / Water hammer pulse

 

Bulging of precordium

 

Lateral and downward shifting of apex beat

  Muffled second heart sound

 

Early diagnostic murmur at aortic area

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Case 23

(Musculo-skeletal)

1. 

Identify the sign which is being demonstrated? 1

2. 

What is the diagnosis and its inheritance? 2

3. 

Enumerate 4 investigations with their yield? 2

Key

1. 

Gower’s sign 

2.  Duchene’s muscular dystrophy and it is x-linked recessive disorder

3.  Investigations:

 

CPK

 

EMG

 

Muscle biopsy

 

Gene analysis (DNA) from peripheral blood

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Case 24

(Musculo-skeletal)

1.  Identify the procedure which is being performed in the photograph? 1

2. 

What are the indications of this procedure? 23.  What are the contra-indications of this procedure? 2

Key

1.  Thoracentesis / Pleural tap

2.  Indication:

 

Diagnostic evaluation of pleural effusion

 

Therapeutic drainage of pleural effusion in patients with respiratory compromise

3.  Contra-indications:

 

Local skin infections (e.g. Herpes zoster)

  Bleeding diathesis, anticoagulant therapy

 

Mechanical ventilation

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Case 25(Infectious Diseases)

1.  Identify the pathological pulmonary lesions shown in the photograph? 1.5

2.  What is the clinical diagnosis? 1.0

3.  Enumerate the 10 complications / sites of extra pulmonary involvement

of this infectious disease? 2.5

Key

1.  Primary complex comprised by lymph nodes, lymphatics and ghon focus

2.  Primary tuberculosis

3.  Complications:

  Miliary tuberculosis

 

TBM

 

Pneumonia

 

Pleural effusion

 

Atelectasis

  Pneumothorax

 

Abdominal tuberculosis

  Carries spine

 

Bronchiectasis