DCH Paper I
1 a) Briefly
describe hearing tests recommended to screen for hearing loss in young babies.
What questions would you ask the caregiver (parent) of a 9-month-old baby if
you were screening for hearing loss?
b)
Describe briefly the clinical
features and management of giardiasis in children?
c)
How would you manage a child
who presents with paraffin ingestion?
d)
Describe common clinical
complications seen in a child who has spastic quadriplegia?
a.
The hearing test recommended to screen for hearing loss in newborn babies is
called the Otoacoustic
emissions (OAE’s) – otoacoustic
emissions (cochlear echo) are the sounds a normal cochlea produces in response
to receiving an external sound. The absence of an echo can indicate a loss of
hearing. It is non-invasive, does not
require co-operation and can be used to screen newborn babies with a family
history of hearing loss or those exposed to factors that may predispose them to
hearing loss or deafness (Jeffrey 1995). Distraction
tests are still done in infants from the age of 6 – months but have not been
found to be reliable.
It
is commonly recommended that screening be done by asking the parent or
caregiver questions which will identify the baby at risk or will lead to
suspicions that the infant has a hearing loss. An audiologist should formally
assess such infants.
Recommended
questions to the caregiver (parent) of a 9 month old baby if you were screening
for hearing loss are:
·
Is
there a family history of deafness?
·
Was
the infant born prematurely?
·
Did
the infant require ventilation for 5 days or longer?
·
Did
the infant have a low Apgar score? (0-4 at 1 minutes
or 0-6 at 5 minutes)
·
Was
the infant significantly jaundiced?
·
Is
there a history of intra - uterine infections?
·
Does
the infant have craniofacial abnormalities?
·
Was
the infant admitted to ICU?
·
Has
the infant been treated with amino glycosides?
·
Has
the infant had bacterial meningitis?
·
Does
the infant vocalize?
·
Does
the infant respond to sounds?
Giardiasis
is transmitted via contaminated water or direct contact. Prevention of the
infection is therefore through ensuring a clean water supply and the washing of
hands before eating or the preparation of food.
Acute
giardiasis may present with explosive watery diarrhoea, abdominal discomfort, distension, nausea and
anorexia. The condition can resolve with or without the patient developing into
a carrier. Some children develop low-grade chronic or recurrent diarrhoea with weight loss and debility. The stools are
pale, bulky, and offensive and float in the toilet due to the high fat content
as is typical of a malabsorbtion syndrome.
The condition is usually treated with Flagyl (Metranidazole) 25-50 mg
Kg per day in three divided doses for 5 days.
c.
How would you manage a child who presents with paraffin poisoning? (5)
The
main most common problem with Paraffin poisoning is the volatiles, which are
released from the paraffin and cause a chemical pneumonitis
resulting in hypoxia. The pneumonitis may not be
present immediately and children should be admitted for at least 6 hours for
observation. Oxygen therapy is essential in the child that is symptomatic.
Fluids
should be limited to twice the insensible loss as over hydration will result in
pulmonary oedema.
Pyrexia
is a common finding and does not indicate a bacterial infection. Paracetamol can be used to control the pyrexia. Antibiotics
are not always necessary.
Emetics
are absolutely contra indicated.
d.
Describe the common clinical complications seen in a child with spastic
quadriplegia?
(5)
Spastic
quadriplegia is a form of cerebral palsy, which is usually associated with
severe brain damage involving the cortex.
The common associated findings are therefore cognitive impairment
seen as mental retardation, which is usually moderate or severe. These
children are also usually microcephalic. They
commonly have epilepsy.
The
damage to the motor cortex of the brain causes an imbalance between the flexor
and the extensor muscles with increased flexor tone. This results in the
development of contractures across the joints.
Although
there is increases tone in the limbs these children frequently have poor head
and trunk control resulting in poor posture and a secondary scoliosis.
The
lack of movement and secondary deformities predispose these children to
pneumonia, constipation and bedsores.
The
muscles of mastication and swallowing are frequently involved resulting in feeding
difficulties and failure to thrive. They are also at risk for aspiration
due to poor swallowing or gastro oesophageal reflux.
Poor swallowing and prolonged bottle feeding puts these children at an
increased risk for dental caries.
These
children frequently have language delays which may be very severe not
only because of the poor control of the muscles required for speech but also
due to the cognitive problems. There is also a higher incidence of deafness in
these children.
Because
of the diffuse nature of the brain damage the occipital cortex and /or the
optic nerves may be involved resulting in various degrees of visual
impairment.
2 a) Discuss
the practical and prognostic advantages and disadvantages of the Wellcome classification of nutritional state.
b)
Discuss the main causes for,
and interventions to reduce infant mortality.
c)
Discuss how to counsel a
mother wanting to stop breastfeeding her 3-month-old child because of
insufficient breast milk.
d)
Describe the three main
components of the Integrated Management of Childhood Illness strategy.
a)
Simple in that only requires
measurement of weight and presence / absence of oedema.
Therefore has scope for use by wide range of health staff with varying skills.
i.
But
only relates to identification of severe malnutrition i.e. does not pick up on
more subtle signs of malnutrition
ii.
Highlights
marasmus (<60%EWA) as an entity and not just kwash as a sign of severe malnutrition (though kwash is more dramatic)
iii.
Oedema is used as a surrogate for other signs of severe malnutrition e.g. dermatosis
iv.
The
presence or absence of oedema is regarded as a key
differentiating sign with prognostic implications
v.
Relates
findings to age
vi.
Does
not take into account length/height
vii.
This
has the advantage of avoiding the difficulty of accurate length/height
measurements but limits the interpretation
viii.
Classification
is limited because weight will be influenced by presence of oedema
ix.
Can
be adjusted for by using minimum weight after loss of oedema
x.
Cannot
distinguish between acute and chronic malnutrition
xi.
Allows
comparison of types of severe malnutrition in different places e.g. clinic vs.
hospital or by country or to examine social or environmental differences
between marasmus and kwash
b)
i.
Over
10m children die per year
ii.
Most
occur in sub-Saharan
iii.
Cause
of deaths are often the result of more than one process e.g. measles followed
by pneumonia or diarrhea; HIV and pneumonia or diarrhea.
iv.
Cause
should be classified as combination as demonstrating co-mobidities
has important public health implications
v.
Neonatal
disorders still accounts for 20-40% of all infant deaths
vi.
Factors
placing infants at increase risk of death include
·
Unhygienic
conditions
·
Unsafe
conditions
·
Poor
birth spacing
·
Non-breastfeeding
·
Non
exclusive breastfeeding
vii.
Underlying
causes of death
·
Measles
·
Underweight
·
AIDS
(accounts for
·
Vitamin
A deficiency
·
Prematurity
viii.
Main
clinical causes of death in sub-Saharan
·
Malaria
(~22%)
·
Diarrhoea (~20%)
·
Pneumonia
(~21%)
·
Neonatal
disorders (~25%)
·
AIDS
(~8%) – this might be as high as 30% in
ix.
Interventions
can be divided into Preventive and Treatment
x.
Preventive
interventions with established evidence-base would include:
·
Breastfeeding
·
Insecticide-treated
materials e.g. bednets
·
Good
complementary feeding practices
·
Good
water supply
·
Immunisations
·
Zinc
supplements
·
Vitamin
A supplements
xi.
Treatment
interventions with established evidence-base would include:
·
Oral
rehydration therapy
·
Antimalarials
·
Appropriate
and timely antibiotics for pneumonia, sepsis, dysentery
·
Zinc
and vitamin A supplementations
·
Neonatal
resuscitation including management of hypoglycaemia,
hypothermia, asphyxia
xii.
The
Integrated Management of Childhood Illness strategy is founded on these
principles
c)
i.
Listen
to mother i.e. counsel vs. advise
ii.
Explore
if there are other reasons for her saying that she intends to stop
breastfeeding e.g. returning to school, tired of breastfeeding
iii.
Evaluate
feeding practices so far – technique (attachment and positioning), difficulties
encountered, family expectations, number of wet nappies per day as indication
of adequate intake
iv.
Check
Road to Health Card for child’s weight
v.
Check
knowledge of physiology of breastfeeding i.e. more suckling = more milk
vi.
Discuss
the benefits of continued breastfeeding especially exclusive breastfeeding
vii.
Explain
about growth spurts and increase requirements
viii.
Explain
about non-nutritive suckling
ix.
Explore
HIV status of mother and child
x.
Discuss
early +- rapid cessation of breastfeeding if relevant (HIV-infected mother and
uninfected child)
xi.
Guide
mother to optimal breastfeeding technique if she decides to revert to BF
xii.
Ensure
that she understands about hygienic and adequate preparation of formula feeds
if she chooses to introduce formula
xiii.
Identify
ways in which family can better support
d)
IMCI
supercedes previous WHO programmes e.g. CDD or ARI.
Consists of three components i.e.
A.
Standard treatment guidelines (STGs)
i.
Aims
to reduce the rate of 5 main causes of childhood mortality globally – ARI, Diarrhoea, Measles, Malaria, Malnutrition
ii.
In
iii.
STGs
underwent a local adaptation process both nationally and provincially
iv.
First
step is a triage process i.e. looking for General Danger Signs
v.
Common
approach – Ask, Check, Classify
vi.
Treatment
based on classification rather than diagnoses
vii.
Colour-coded algorithms
viii.
Includes
guidance on follow-up + counseling for prevention
ix.
Generally
needs 60% staff in any given facility to be trained in order for it to become
routine practice
x.
Training
followed by supervision on site
B.
Household and Community Component
i.
Aims
to establish 15 key family practices
ii.
These
cover issues such as breastfeeding, immunizations, disease prevention, early
and appropriate treatment of common conditions e.g. use of ORS, improved
health-care seeking practices
iii.
Also
aims to improve the relationship and communication between primary health care
facilities and local community
iv.
No
single approach but includes identifying local resources and potential
community partners
v.
Multisectoral approach – should include participation of other
non-health sectors e.g. water and sanitation, social welfare, transport – to
increase feasibility of achieving key family practices
C.
Health Systems Review
i.
Aims
to improve the infrastructure of health systems so as to enable primary care
practitioners to effectively conduct their work
ii.
Includes
national, provincial and local activities
iii.
Links
with Essential Drugs List re. availability and dispensing of drugs
3 a) Discuss
the initial management of a newborn born to a mother with meconium
stained liquor.
b)
Describe the management of hypercyanotic
spells in a child with Fallot’s tetralogy.
c)
Describe briefly the acute and chronic complications of otitis media.
d)
List valid contraindications to administering the routine expanded
programme of immunisation (EPI) vaccines.
a) Passage of meconium in utero can occur as a result of fetal stress caused by
hypoxia & acidosis.
Meconium effects --- toxic to lungs causing mechanical obstruction,
chemical pneumonitis, pulmonary vasoconstriction and
inactivation of surfactant.
Thin or thick meconium can lead to MAS in new born
Intrauterine aspiration : 1) Vigorous baby—routine care = keep warm, suction
mouth + nasopharynx, stimulation, ± oxygen
2) Depressed baby---keep
warm, free flow oxygen, no stimulation, direct laryngoscopy
& suctioning of mouth & hypopharynx followed
by intubation and direct suction through the ET tube
as tube is withdrawn. Repeat procedure until little meconiun
is recovered.
Nasogastric tube can be inserted through ET tube for suctioning
while giving IPPV.
Transfer baby to neonatal ICU
or high care.
Intravenous fluids &
antibiotics--- gram + & gram – cover.
Severe distress—ventilation
and surfactant can be given.
b)
A) Precipitating factors—iron
defiency anaemia,
pneumonia, dehydration, excessive crying, hot baths.
B) Acute management
2) Administer 100% oxygen , ↑ blood flow to R side of heart → bend
legs at the hips and knees ( squatting) and give fluids 20ml/ kg Ringers
lactate or normal saline. Ensure adequate hydration.
3) Monitor saturation, heart
& respiratory rates and acid – base status if possible.
4) Sodium bicarbonate IVI
8.5% diluted to 4.2% -- 2ml/ kg or use formula to calculate amount needed if blood gas can be
done.
5) Propanolol—IV
0.1mg/kg over 3 minutes or oral prapanolol followed
by maintenance dose of propanolol 1-5mg/kg in 3 doses
6) Morphine if poor response
to above—0.1-0.2 mg/ kg .
C) Prophylaxis
1) Iron treatment to all infants with cyanotic
heart disease
2) Propanolol
1-3mg/kg
1) Hearing loss—common.
Acute hearing loss caused by ear effusions, ↑ tension and stiffness of
the round window membrane—usually reversible.
Chronic
hearing loss due to adhesive otitis, tympanosclerosis or ossicular
discontinuity.
2) Perforation—rupture of the eardrum --- chronic suppurative
otitis media with mastoiditis.
3) Aquired
cholesteatoma—saclike structure formed by
desquamating epithelial cells . Causes foul smelling
discharge. Can invade and destroy other structure of the temporal bone.
Intracranial spread can also occur.
4.) Mastoiditis—inflamed mastoid cells. Causes peri-auricular swelling & tenderness.
Pinna is displaced
inferiorly and anterioly.
5) Tympanosclerosis—deposits
on tympanic membrane causing hearing loss.
6) Facial nerve paralysis—exposure of facial in the bony canal.
7) Suppurative
labyrinthitis—direct
invasion of bacteria to the inner ear canal. Signs—vertigo, nystagmus, tinnitus, hearing loss, nausea and vomiting.
8) Ossicular
discontinuity—disruption of ear ossicles
9) Petrositis—temporal bone infection.
10) Intracranial
complication—meningitis, focal
encephalitis, brain abscess, sinus thrombophlebitis, extradural & intradural
abscess.
d)
1) Inactivated vaccines
absolute contraindications
Ř
Severe
febrile illness
Ř
Severe
inter –current infection
Ř
Allergy
to egg protein— vaccines grown in egg yolk
Ř
Pertussis
vaccine--Fits and unstable brain damage, progressive brain disease, previous severe
reaction—shock, collapse, screaming for hours post vaccination, convulsions and
encephalopathy.
2) Live attenuated virus
vaccines .
Ř
Pregnancy
Ř
Allergy
to egg protein
Ř
Children
with malignant disease on high dose cytotoxic drigs, irradiation
Ř
Large
doses of steroids or other immunosuppressive treatments—post organ transplant
Ř
Within
3 weeks of another live vaccine
Ř
Within
3 weeks or 3 months of a dose of normal immunoglobulin
Ř
BCG—NOT
to be given to symptomatic AIDS children or a child with a positive tuberculin
skin test, generalized skin conditions like extensive eczema—give only in a site with normal skin.
4 a) Describe
night terrors and how you would manage them.
b)
Describe your management of
a 5-year-old child with the recent onset of faecal
soiling.
c)
Discuss pain management
during investigations involving skin puncture in children.
d)
Write short notes on the
formulations of oral rehydration fluid in diarrhoeal disease in children. What advice would you give
to the mother of a child with diarrhoeal disease on
the use of oral rehydration fluid?
a) Describe night terrors and how you
would manage them
Night
terrors occur most commonly in children aged 5 and 7 yrs, and more commonly in
boys. The child suddenly wakes up
screaming and appears very frightened, but says little or nothing. He cannot be
consoled, and is unaware of his parents or surroundings. Within a few minutes the
child settles and goes back to sleep, with no memory of the episode the next
morning. Parents should be re-assured that night terrors are a fairly common
occurrence in children, and usually short-lived. In children with persistent
and prolonged night terrors, an underlying emotional disorder should be
considered, and a short course of diazepam or imipramine
may be considered while the family dynamics are being explored.
b) Describe your management of a
five-year old child with the recent onset of faecal
soiling.
Faecal
soiling, the involuntary passage of faeces into the
clothing or bedclothes, must be distinguished from the voluntary passage of faeces in places that are inappropriate for the social and
cultural background of the child.
For
faecal soiling, exclude neurologic
deficits on examination. In their absence, faecal
loading, with consequent stool liquefaction and “overflow” incontinence is most
likely. The diagnosis may be confirmed by palpating hard faeces
in the abdomen or on rectal examination, although an abdominal x-ray may be
necessary to confirm the loading of the colon with faeces.
The faecal
loading should be cleared. Fleet or Microlax enemas
for three days may be effective,
but large
volumes of a balanced electrolyte polyethylene glycol solution (given orally)
may be
necessary.
After clearance, daily complete evacuation of the bowel must be re-established.
This
will take
several months. Careful explanation of the objectives of treatment is
necessary, and both
child and
parents should be involved in the management. Follow-up and support is
essential.
Encourage regular daily bowel habits and a
fibre-rich diet. A laxative is usually necessary for
several months,
starting with a bulk laxative, although a stool softener (e.g. lactulose) or a
stimulant (e.g. senna) may be necessary.
c) Discuss pain management during
investigations involving skin puncture in children.
Children, including newborns,
feel and remember pain. Anxiety aggravates pain. Prevent pain when predictable,
and always allay anxiety. Discuss the planned procedure with the child (if
appropriate) and parents. Help the parents to allay the child’s anxiety.
The management of the pain
depends on the individual child, the type of procedure, how long and how
painful the procedure will be, how still the child needs to lie and the child’s
airway and physical status. For skin puncture use topical local anaesthetic, if available, allowing sufficient time before
the procedure for the medication to work. In young infants, non-nutritive
sucking, sucrose solution and breastfeeding are helpful. For more invasive
investigations, such as lumbar puncture, topical application of local anaesthetic, if available, and skin infiltration may be
necessary. If the child is anxious, an anxiolytic such
as hydroxyzine, midazolam
or other benzodiazapine may be needed.
If
systemic analgesics are used, a combination of analgesics, such as paracetamol, codeine and a non-steroidal anti-inflammatory optimises analgesia and minimises
the side-effects of any one drug.
d) Write short notes on the
formulations of oral rehydration solutions in diarrhoeal disease in children. What advice would you give
to the mother of a child with diarrhoeal disease on
the use of oral rehydration fluid?
Oral
rehydration solutions may either be mixed at home
using sugar and salt, or reconstituted from specially prepared sachets.
The oral rehydration solution (ORS), mixed from sachets in a litre
of water, contain sodium,
glucose (2%),
potassium (20mmol/l) and base (30mmol/l). The World Health Organization
previously
recommended a sodium content of 90mmol/l, but a sodium content of approximately
60mmol/l,
similar to the concentration used in
is preferable in
areas without a high prevalence of cholera.
The use of home mixed salt
and sugar solution (SSS) is probably a more sustainable strategy than sachets,
and promotes a greater degree of self-reliance in caregivers. It is
particularly useful in preventing dehydration. However mixing may be less
accurate, and home-mixed solutions do not contain potassium or base. The usual
recommendation in
Teach the mother how to mix
and give the oral rehydration solution. Give frequent
small sips from a cup, or cup and spoon. Give as much as the
child wants, offering 15-30ml/kg/hour. If the child vomits, wait 10
minutes, then continue, but more slowly. Continue giving extra fluid until the diarrhoea stops.
5 a) A 6-month-old, previously
healthy boy, presents with respiratory distress.
His mother has been suffering from a cold for a week. On examination his
temperature is 38oC. Hyperinflation and wheezing are the most
prominent clinical findings. Laboratory investigations show a normal white
blood cell count and a normal CRP.
i)
What is the most likely
diagnosis?
ii)
Which organism(s) is/are the
most likely cause of his illness?
iii)
Briefly describe your
treatment of this patient.
b)
A neonate presents to you
within 24-hours after birth with a swelling on his head. Tabulate the possible
causes for the swelling and the distinguishing features for each cause.
c)
Briefly describe the
diagnosis, prevention and complications of hepatitis A virus infection in
children.
d)
Discuss the indications for
passive immunisation in children.
a.
·
What is the most likely diagnosis?
§
Acute viral bronchiolitis
§
Acute viral bronchopneumonia (mixed picture)
·
Which organism(s) is/are the most likely cause of his
illness?
§
RSV
§
Adenovirus
§
Parainfluenza virus
§
Influenza virus
·
Briefly describe your treatment of this case.
§
Oxygen to prevent hypoxia
§
Fluids per mouth or NG tube, IV restricted to 60ml/kg
§
Trial of adrenaline or
§
Trial of Beta 2 agonists or Ipratropium
bromide
§
Steroids generally not helpful
§
Antibiotics not indicated unless:
·
WBC > 15.0 x 109/l
·
Temp > 38,5oC
·
Patchy opacification on CXR
§
Ventilatory support if necessary
b.
A neonate presents to you within 24 hours after birth with a
swelling on his head. Tabulate the possible causes for the swelling and the
distinguishing features for each cause.
|
Sub-aponeurotic
haemorrhage |
Diffuse, underneath aponeurosis, sometimes after vacuum or forceps delivery,
may be present at birth, increases during first 48 hours, crosses suture lines,
bluish discoloration of upper eyelids, severe anaemia,
shock, jaundice, treated with vitamin K or urgent blood transfusion |
|
Sub periosteal
haemorrhage/ cephalhaematoma |
Localized, usually parietal, under
periosteum, presentation sometimes only after 4-6
hours, larger over next 48hours, persist 6 – 8 weeks, centre may fluctuate, anaemia, jaundice, rarely underlying fracture,
observation only |
|
Caput succedaneum |
Diffuse over presenting part,
present at birth, petechiae over swelling,
disappears within 48 hours, no complications or treatment |
|
Vacuum extraction haematoma |
Localized swelling of skin and
subcutaneous tissue, present at birth, localized abrasions at periphery of
swelling, skin may be purple, subsides in 5 – 7 days, may become infected,
treat complications |
|
Encephalocoele/meningocoele |
Midline fluctuating, may be open
with brain tissue protruding |
c.
Briefly describe the diagnosis, prevention and complications
of hepatitis A virus infection in children.
i.
Contact history
ii.
Clinical picture
§
Usually mild
§
Often anicteric or asymptomatic
§
Prodromal symptoms
·
Nausea, vomiting, diarrhoea,
fever, malaise, abdominal pain
§
Jaundice
§
Tender hepatomegaly
§
Urine dark, stools pale
§
Resolves within 2 week- 4 weeks
iii.
Serology
i.
IgM antibody to HAV
ii.
Increased transaminases
i.
Adquate sanitation
ii.
Safe drinking water
iii.
Good personal hygiene
iv.
Isolation (not to school)
v.
Nomal immunoglobulin/Vaccine for post
exposure prophylaxis
vi.
Vaccine
i.
Fulminating hepatitis
ii.
Aplastic anaemia
(very rare)
d.
Discuss the indications for passive immunisation
in children.
·
Hepatitis A, Household or day-care centre contacts given
immunoglobulin within 2 weeks of exposure
·
Rabies, Rabies immunoglobulin post exposure
·
Hepatitis B, HBIG given o newborns of mothers with acute or
chronic hepatitis within 12 hours of delivery
·
Varicella, VZIG within 96 hours for
susceptible children, newborns of moms who contracted chickenpox between 5 days
before to 2 days after delivery
·
Measles, Exposed susceptible children, Immunoglobulin within
6 days of exposure
·
Tetanus, TIG For treatment in newborns and older children, Prophylactically in severe wounds in incompletely immunized
children
DCH
Paper II March
2005
1 A 10-year-old boy presents to your hospital with petechiae, headache and a fever that started a few hours
before he came to the hospital. He mentions that one of his classmates was
admitted to hospital in the previous week with meningitis.
a) Which organism is most
likely to be responsible for his illness? (2)
b)
Discuss the clinical features of infection
with this organism. (10)
c)
Motivate special investigations that you
will do in his case. (6)
d)
Describe your treatment of this patient. (12)
e)
Discuss primary and secondary prevention of
this disease. (10)
a.
Which organism is most likely
to be responsible for his illness? (2)
b.
Discuss the clinical features
of infection with this organism.
(10)
15%
Septicaemia
50% Both
Fever,chills and
prostration.
May be hypothermic
Rash
typically petechial or purperic,
evolves rapidly, involves mucosa
Occasionally
maculo-papular rash
Irritability,
lethargy
Signs of
meningitis
Menigeal irritation
Positive
Kernig and Brudzinski
Headache,
vomiting, , stupor, coma
Extensive purpura, DIC, Shock
Seizures,
not as common as in pneumococcus or H. influenzae
Other:
Pneumonia, myocarditis, pericarditis,
septic arthritis (rare)
Case
fatality 8 – 25%
Poor
predictive factors
Rapid onset
Shock
Coma
Acidosis
Seizures
DIC
Absence
of meningitis
Adrenal
haemorrhage (Waterhouse Friderichsen syndrome
Chronic
meningococcemia
c.
Motivate special
investigations that you will do in his case.
(6)
FBC with
differential count
Acute phase
reactants
LP not done
when fears of raise intracranial pressure/ some authors - never in suspected N.meningitides meningitis
Lumbar
puncture
Microscopy
Culture
Biochemistry
Cell count
Capsular
antibodies in CSF or urine
Skin
scrapings for microscopy and culture or biopsy
Buffy coat
microscopy
Electrolytes
if adrenal haemorrhage or SIADH
d.
Describe your treatment of
this
case.
(12)
Emergency
First dose
of antibiotics
Parental
Penicillin or third generation cephalosporin,
Penicillin
resistant strains described
Chloramphenicol
for Beta-lactam allergic patients
Continue 5 –
7 days
If treated
with penicillin – chemoprophylaxis before discharge
Treat
seizures if present
Treat raised
ICP
Fluid restriction
Mannitol
Supportive
treatment
Treat
septicaemia and shock
Oxygen
Ventilation if necessary
Volume expansion with Ringers or Saline
Inotropes
DIC
FFP
Heparin?
Platelets
Steroids
controversial – may help in ARDS
Adrenal
haemorrhage (Waterhouse Friderichsen syndrome)
Salt and fluid replacement
Glucose
Hydrocortisone
Notify
disease!
e.
Discuss primary and secondary
prevention of this
disease.
(10)
Casular
polysaccharide vaccines available against group A,C,Y
and W135
Poorly
immunogenic against group B
Indicated to
control outbreaks, travellers to endemic areas and household contacts
Group B
vaccine being developed
Chemoprophylaxis
in
Infants
Household
contacts
Epidemic
Health
care workers – e.g. mouth to mouth
Patient,
after treatment with Penicillin
Rifampicin
Ceftriaxone
Ciprofloxacin
Minocycline
2 A 6-year-old
boy presents with a two-day history of swollen legs, having been previously
well. His urine is a dark brown colour. He has an
inflamed pharynx and healing impetigo on his legs. Urine dipstix
reveals blood (4+) and protein (2+). Clinical examination is otherwise normal.
a) What is the most likely diagnosis? (3)
b) What is the most likely underlying cause
of the condition? (2)
c) List three common complications of the
condition. (6)
d) What investigations
would you perform? Provide the reason for each investigation.
(9)
e) Describe your management of this child.
(20)
What is the most likely diagnosis? (3)
Acute post-streptococcal glomerulonephritis
What is the most likely underlying cause of the
condition? (2)
Streptococcal infection (impetigo)
List three common complications of the condition. (3)
Hypertension
Pulmonary oedema/cardiac
failure
Acute renal failure
What investigations would you perform? Provide the
reason for each investigation. (9)
AntiDNaseB antibodies give an indication of recent Streptococcal
infection. Anti-streptolysin O titre
is less sensitive for skin infections, the usual form of infection causing glomerulonephritis (one mark for ASOT). The presence of
healing impetigo and a typical clinical picture in this case means that the
serological test may add little additional information.
Urea and creatinine provide
information about the adequacy of renal function that is not ascertainable
clinically.
Potassium and sodium. Hyperkalaemia is an
important complication of renal failure, and cannot be detected clinically.
Chest x-ray, to detect pulmonary
congestion or cardiomegaly in this child before overt
cardiac failure.
Complement. A low C3 is characteristic, but the
finding provides little useful additional information in this case, where
post-Streptococcal acute glomerulonephritis appears
highly likely.
Urine microscopy. Red cell casts would confirm the diagnosis,
but are seldom seen in routinely processed specimens, and the diagnosis of glomerular disease is very likely.
Urine culture. To exclude a urinary tract
infection.
Skin or throat culture – organisms may no longer be
present on the impetigo, which appears the more likely cause than the current
inflamed pharynx.
[Award marks for reasons given for not doing a test]
Describe your management of this child. (20)
Penicillin orally for 10 days, or benzathine
penicillin intramuscularly
Monitoring
Daily fluid intake/output
Daily weight
Daily urine dipstix,
specific gravity, colour
3-hrly blood pressure
Fluid restriction (formula)
Restrict to 20ml/kg/day plus previous day’s urine
output (less if already fluid overloaded)
Food
High carbohydrate diet
Low potassium, low sodium
Low protein diet if urea > 20 mmol/l
Avoid drugs excreted by kidney (NB digoxin)
If hypertension were to develop
Frusemide 1-2mg/kg/dose orally 1-3 times daily
Treat hypertensive episodes with nifedipine
or hydralazine
If circulatory congestion and pulmonary oedema were to develop
Oxygen
Morphine
Frusemide IVI
Rotating tourniquets
Venesection
Peritoneal dialysis
Artificial ventilation
If seizures
Diazepam
3 You are
called to casualty to see a teenage girl who was found wandering around the streets
confused and smelling of alcohol. She has torn clothing, a laceration on her
scalp and blood stained panties. The accompanying policeman suspects that she
has been assaulted and possibly raped.
a) You need to
consider consent to proceed with an examination. What consent do you consider
necessary? In the absence of any parent what options are available to you?
(4)
b)
Discuss three possible
causes for her confusion and describe how you would manage each of these. (6)
Your
examination reveals a young girl with confusion but no depressed level of
consciousness or neurological deficit. She has stage 4 pubarche,
stage 4 thelarche and findings suggestive of rape as
you find semen on her thighs and signs of acute genital trauma.
c)
What investigations will you
undertake and what treatment will you prescribe? (8)
d)
Do you require consent for
any of the above investigations or treatment, and if so what would you do in
this instance? (3)
Although
her initial HIV Elisa test was negative, a follow up test 3 months later is
positive.
e)
In the South African public
health sector what are the criteria for prescribing antiretroviral therapy? (8)
f)
If she does not meet these
criteria how would you care for her?
(8)
g)
When and how would you
reassess her eligibility for antiretroviral therapy?
(3)
Consent
from the child.
AND
Consent
from the parent or guardian.
If, in a
case of suspected child abuse, this is refused consent should be obtained from
the police – SAP 308 which is consent to examine a person in the event of a suspected
criminal offence.
In the
absence of a parent proceed with police consent – SAP 308.
Intoxication:
Rehydrate.
Monitor blood glucose.
Observe and give it time.
Head
injury:
Neurologic examination.
Focal
signs or depressed level of consciousness – CT scan head.
Neurological
observations.
Appropriate
management for cerebral oedema if indicated.
Post
traumatic stress disorder:
Debriefing.
Review in 1 – 2weeks and consider
ongoing counselling.
Your
examination reveals a young girl with confusion but no depressed level of
consciousness or neurological deficit. She has stage 4 pubarche,
stage 4 thelarche and findings suggestive of rape as
you find semen on her thighs and signs of acute genital trauma.
Investigations:
WR, Hepatitis B, HIV & pregnancy
test.
If HIV test is negative also
requires FBC, U&E & LFTs.
STI prophylaxis:
Rocephin – 250 mg IMI stat
Erythromycin 250 mg qid for 14 days
Flagyl 200 mg tds
for 10 days
Pregnancy prophylaxis –
Ovral 28 two tablets stat 7 two in 12
hours
Maxalon 10 mg po
tds prn for 24 hours
If HIV test
–ve: AZT & 3TC according to weight & surface
area size for
4 weeks.
Consent
required for HIV test.
Consent
required for off label use of ART in PEP of HIV exposure.
As this is a potentially life threatening situation, possible exposure
to HIV, and parents are not available to give consent use commissioner’s or
medical superintendent’s consent.
Although
her initial HIV Elisa test was negative, a follow up test 3 months later is
positive.
South African birth certificate.
One
identified caregiver.
Demonstrated reliability.
Supportive social environment.
Clinical
eligibility
2 or more admissions or 1 prolonged
admission for HIV related
problem in previous year.
CD4 of <20% if under 18 months
old and <15% if over 18 months old.
WHO stage 2 or 3 disease.
Holistic approach to HIV infected child and her family,
ideally in a multidisciplinary setting.
Education and ongoing counselling.
Nutritional support with both macro
& micronutrient supplements, especially Vit A
supplements (200 000 IU every 6 months)
Deworm if appropriate.
Ensure immunisations
covered and consider annual ‘flu vaccine.
Promote good hygiene practices –
environmental, food preparation, dental & personal hygiene.
Positive living – balance exercise
& rest, avoid toxins (especially alcohol & nicotine), reduce stress.
Prophylactic cotrimoxazole
when symptomatic or CD4 count down.
Treat inter current illnesses early and appropriately,
preferably on an outpatient basis.
Correct
social circumstances to ensure these meet the requirements.
Reassess
clinical status on an ongoing basis and formally every 6 months
Review CD4
count every 6 months.
4 Sibusisu
Mgwali is a 3-year-old boy with a two-week history of
increasing dullness and listlessness. He has neck stiffness. He is able to
respond appropriately to simple verbal commands. There are no focal
neurological signs or papilloedema.
Cells
– Red Cells 15 cells/mm3
Lymphocytes 270
cells/mm3
Polymorphs 120
cells/mm3
Chem - Protein 1.1
g/l (N 0.2-0.4)
Pandy test for Globulin + ve
Glucose 1
mmol/l (N ~3-5 [~ ⅔Blood level])
Chloride 102 mmol/l (N 116-130)
a) What are valid
contraindications to doing a lumbar puncture in a child?
(4)
b)
TB Meningitis is a possible
diagnosis. Postulate two other possible diagnoses and describe two clinical
signs or special investigations that you could use to confirm or refute each of
these alternate diagnoses.
(6)
c)
You confirm that Sibusisu has TB Meningitis. Describe your initial
therapeutic approach. (10)
d)
List three complications of
TB Meningitis, and explain the pathophysiological
mechanism for each. (9)
e)
Considering his clinical
condition, what would you estimate Sibusiso’s chances
of full neurological and cognitive recovery to be? (2)
f)
What is the likely route
whereby the tuberculous bacillus gained entry into
the CSF? How was the infection likely to have been acquired? (5)
g)
What strategy(ies) could you propose to
i) Prevent children developing TB Meningitis. (2)
ii) Detect it before
neurological findings are irreversible.
(2)
1 Complications that might be expected
a. Hydrocephalus (1)
(Communicating) Obstruction of drainage by arachnoid villi due to high protein / inflammatory response
(Non-communicating) Obstruction of drainage from 4th ventricle by local inflammatory response and coagulation in CSF of this area.
b. Inappropriate ADH secretion (1)
Inflammatory response direct effect leading to increased ADH secretion or increased renal sensitivity to ADH.
c. Cerebral vessel vasculitis (1)
Perivascular inflammation leading to vasculitis and obstruction to blood flow
d. Seizure (1)
Local inflammation, tissue damage from hypoxia, peri tuberculoma inflammation, sodium abnormalities, hypoglycaemia from starvation, cerebral oedema.
e. Cerebral salt / water wasting (1)
Unsure ? Increased Atrial Natriuretic Peptide secretion, ? direct neural effect on renal function
f. Later mental retardation or focal neurological fall out (1)
Local cerebral tissue damage from any or all of the above
Any 3 of the above plus a reasonable explanation (2marks each) where known for the
complication.
2 He is able to respond and has no focalizing or lateralizing signs but has signs of meningeal irritation.
a. His classification would be stage 1 (signs of meningeal irritation: fever; lethargy; conscious; rational; no focal neurological signs; no hydrocephalus)
(1)
The underlined findings are present. Rationality is difficult to assess
at this age. Hydrocephalus has not been excluded – but not overt. Fever is not
mentioned.
b. His chances of full recovery while guarded but reasonably good.
(1)
1 mark for assessing the stage in some
manner, 1 mark for assessing the outcome as reasonable.
3 The likely route of infection would be:
a. Exposure to adult open TB (1)
b. Bacillus inhaled and settles in lung ( ˝ )
c. Local primary TB infection in child’s lung ( ˝ )
d. Spread to pulmonary lymph node ( ˝ )
e. Spread up lymphatics as intermittent bacillaemia into circulating blood ( ˝ )
f. Deposition in brain in parameningeal site ( ˝ )
g. Progression of small local tuberculoma in parameningeal site ( ˝ )
h. Rupture into CSF ( ˝ )
i. Reaction to presence of bacilli in CSF (low bacilli load) ( ˝ )
The above marking or
similar.
4
a. Preventing TBM in children – sensitise health care workers to:
i. Detecting and treating prophylactically children in contact with adults with open TB. In all cases where adults are treated for TB, child contacts should be actively sought and treated. (1)
ii. BCG immunization of all children. (1)
iii. Active exclusion or detection of TB infection in all children where TB is suspected: (history of contact, clinical signs or symptoms, tuberculin testing, CXR and microbiological testing as appropriate) NB. (1)
1. Children with growth faltering, failure or weight loss.
2. Children with chronic cough.
Any 2 of the above or reasonable reference to these
b. Early detection of TBM in children while still successfully treatable – sensitise health care workers to:
i. Sensitivity to behavioural/ neurological presentation as possible presentation of TBM. (1)
ii. Suspicion of TB, and later TBM, in children with growth faltering/failure.
(1)
iii. Early treatment of all cases of likely / possible TBM while the diagnosis is being confirmed. (e.g. in meningitis where the diagnosis is not clear but might include TBM; treat and if later shown not to be TBM treatment may be stopped then) (1)
iv. Lumbar puncture of all children where the diagnosis is reasonably likely and in whom contraindications are not present. (1)
Any 2 of the above or reasonable reference to these
5 You are the medical officer at a district hospital. You are
concerned about the high mortality in low birth weight babies at the hospital.
A colleague suggests that kangaroo mother care may assist in reducing this
toll.
a) What are the key
components of kangaroo mother care? (5)
b)
Under what circumstances is
kangaroo mother care particularly beneficial? (5)
c)
Tabulate the advantages and
disadvantages of kangaroo mother care to the mother, the infant and the
hospital. (15)
d)
Describe how you would
establish a kangaroo mother care unit in your hospital? (15)
a. What are the key
components of kangaroo care?
(5)
The key components of
kangaroo care are that -
b. Under what circumstances
is kangaroo mother care particularly beneficial? (5)
Kangaroo mother care is
particularly beneficial -
c. Tabulate the advantages
and disadvantages of kangaroo mother care to the mother, the infant and the
hospital. (15)
|
|
Advantages |
Disadvantages |
|
Mother |
Promotes bonding |
The siblings may have
nobody to care for them |
|
|
She has time to recover
from the birth without having to take up the responsibility of running a home
as well as caring for the baby. |
Some women need to return
to work for financial reasons. |
|
|
She has an opportunity to
establish breast feeding |
Mother’s who have AIDS may
decide not to breast-feed. |
|
|
Mothers become more
confident in the care of their babies. This allows for earlier discharge. |
|
|
|
The volume of breast milk
has been found to increase with skin-skin contact |
|
|
Baby |
The rate of infection is
reduced by colonization of the infant with the mothers own skin flora. |
|
|
|
Improved cardio respiratory
stability |
|
|
|
Babies grow and develop
faster. |
|
|
|
Decreased mortality rate. |
|
|
Hospital |
Infants can be moved out of
the incubator earlier, these reduce hospital expenses and the load on staff. |
Setting up and staffing
such a unit requires allocation of both staff, money for equipment, time to
train staff and a space. |
|
|
Earlier discharge cuts
patient loads and costs. |
|
|
|
Improved relationships
between mothers and staff. |
|
|
|
Better survival – Third
world |
|
|
|
Better care - First world |
|
|
|
|
|
d. Describe how you would
establish a kangaroo mother care unit in your hospital.
The technique of kangaroo
mother care consists of placing the naked baby on the mother’s chest and
holding it there firmly with a cloth until it is ready for discharge.
The complexity in setting up
KMC is to establish an environment in which this can take place.
Initially the hospital management will need to
be convinced that there is a benefit to both the hospital and the community in
establishing such a unit.
Once the concept has been
adopted and agreed to by the hospital, the hospital then needs to establish a
comprehensive plan involving all stakeholders including the community. The
media can be used to inform the community and antenatal clinics to teach
mothers about the concept at the first visit.
The practical aspect of
establishing the unit will involve finding a suitable area to where the mothers
can stay, nursing staff to run the unit and funding for equipment such as extra
beds, food for the mothers, etc.
The staff working in the unit
will need to be trained. There also needs to be buy in
from all the hospital departments such as obstetrics, ICU and ANC with the
development of protocols, which will allow for the progression of care.