Paediatrics - Dermatology, Allergy and Infectious disease Flashcards

1
Q

A child presents with a non-blanching purple rash after having fever and lethargy. What is the diagnosis?

What causes the purpura

A

Meningococcal septicaemia refers to the meningococcus bacterial infection in the bloodstream. Meningococcal septicaemia is the cause of the classic “non-blanching rash” that everybody worries about. This rash indicates the infection has caused disseminated intravascular coagulopathy (DIC) and subcutaneous haemorrhages.

Neisseria meningitidis is a gram-negative diplococcus bacteria. They are circular bacteria (cocci) that occur in pairs (diplo-). It is commonly known as meningococcus.

IT IS NOT THE SAME AS MENINGOCOCCAL MENINGITIS - they can be co-morbid or patients can simply have either (can have menigogococcal mengitis with the rash).

Meningococcal meningitis is when the bacteria is infecting the meninges and the cerebrospinal fluid around the brain and spinal cord.

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2
Q

What are the two most common causes of bacterial meningitis?

In neonates?

A

The most common causes of bacterial meningitis in children and adults are Neisseria meningitidis (meningococcus) and Streptococcus pneumoniae (pneumococcus).

In neonates the most common cause is group B strep (GBS). GBS is usually contracted during birth from GBS bacteria that live harmlessly in the mother’s vagina.

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3
Q

Presentation of meningitis:
- symptoms?
- Sx and Ix in infants?
- Special tests?

A

Sx:
- fever
- neck stiffness
- vomiting
- headache
- photophobia
- altered conciousness and seizures

Me - fever with neffstickness and headache is key, neck stiffness isnt seen in migraine or febrile convulsions (6 mths - 5y/o)

Neonates and babies can present with very non-specific signs and symptoms, such as hypotonia, poor feeding, lethargy, hypothermia and a bulging fontanelle.

NICE recommend a lumbar puncture as part of the investigations for all children:

Under 1 month presenting with fever
1 to 3 months with fever and are unwell
Under 1 year with unexplained fever and other features of serious illness

There are two special tests you can perform to look for meningeal irritation:

Kernig’s test
Brudzinski’s test

Kernig’s test involves lying the patient on their back, flexing one hip and knee to 90 degrees and then slowly straightening the knee whilst keeping the hip flexed at 90 degrees. This creates a slight stretch in the meninges. Where there is meningitis it will produce spinal pain or resistance to movement.

Brudzinski’s test involves lying the patient flat on their back and gently using your hands to lift their head and neck off the bed and flex their chin to their chest. In a positive test this causes the patient to involuntarily flex their hips and knees.

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4
Q

Management of bacterial meningitis in children:

Ix?
Rx?
Post exposure prophalaxis?

A

Meningococcal septicaemia and bacterial meningitis are medical emergencies and should be treated immediately.

Ix:
- blood culture
- lumbar punture
- Blood test for meningococcal PCR

Rx:
- Under 3 months – cefotaxime plus amoxicillin (the amoxicillin is to cover listeria contracted during pregnancy)
- Above 3 months – ceftriaxone plus dexamethsone (prevent hearing loss and neurological damage)
- notifiable disease

PEP:
Significant exposure to a patient with meningococcal infections such as meningitis or septicaemia puts people at risk of contracting the illness (direct contact through respiratory secretions). This risk is highest for people that have had close prolonged contact within the 7 days prior to the onset of the illness

The usual antibiotic choice for this is a single dose of ciprofloxacin. It should be given as soon as possible and ideally within 24 hours of the initial diagnosis.

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5
Q

Cause of viral meningitis?
Ix?
Rx?

A
  • HSV
  • enterovirus
  • VZV

Ix - same as above to rule out bacteria but the CSF from lumbar puncture should be sent for viral PCR tesitng

Viral meningitis tends to be milder than bacterial and often only requires supportive treatment. Aciclovir can be used to treat suspected or confirmed HSV or VZV infection.

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6
Q

Interpretation of CSF results in meningitis

A lumbar puncture involves inserting a needle into the lower back to collect a sample of cerebrospinal fluid (CSF). The spinal cord ends at the L1 – L2 vertebral level, so the needle is usually inserted into the L3 – L4 intervertebral space. Samples are sent for bacterial culture, viral PCR, cell count, protein and glucose. A blood glucose sample should be sent at the same time so that it can be compared to the CSF sample. The samples need to be sent immediately.

Bacterial vs Viral?

A

TOM TIP: Interpreting lumbar puncture results is a common exam question. It is easier to think about what will happen to the CSF with bacteria or viruses living in it rather than trying to rote learn the results. It makes sense that bacteria swimming in the CSF will release proteins and use up the glucose. Viruses don’t use glucose but may release a small amount of protein. The immune system releases neutrophils in response to bacteria and lymphocytes in response to viruses.

Bacterial:
- cloudy
- high protein
- low glucose
- high neutrophils
- positive culture

Viral:
- clear
- normal or mildly raised protein
- normal glucose
- high lyphocyte count
- culture negative

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7
Q

complications of meningitis - 1 key one

A

Hearing loss is a key complication
Seizures and epilepsy
Cognitive impairment and learning disability
Memory loss
Cerebral palsy, with focal neurological deficits such as limb weakness or spasticity - i think only for infants?

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8
Q

Presentation of encephalitis?
Most common cause of encephalitis? Others?

A

Presentation
- altered conciousness
- altered behavoir and impaired cognition
- acute onset of focal neurological symptoms
- acute onset of focal seizures
- fever

Unlike meningitis with headache, photophobia, neck stiffness, vomiting, fever

Cause
Encephalitis means inflammation of the brain. This can be the result of infective or non-infective causes. Non-infective causes are autoimmune, meaning antibodies are created that target brain tissue.

The most common cause is infection with a virus. Bacterial and fungal encephalitis is also possible although much more rare in the UK.

The most common viral cause is herpes simplex virus (HSV). In children the most common cause is herpes simple type 1 (HSV-1) from cold sores. In neonates it is herpes simplex type 2 (HSV-2) from genital herpes, contracted during birth.

Other viral causes include varicella zoster virus (VZV) associated with chickenpox, cytomegalovirus associated with immunodeficiency, Epstein-Barr virus associated with infectious mononucleosis, enterovirus, adenovirus and influenza virus. It is important to ask about vaccinations, as the polio, mumps, rubella and measles viruses can cause encephalitis as well.

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9
Q

Encephalitis

Diagnosis?

Management?

A

Lumbar puncture - CSF for viral PCR testing
CT scan is LP is contraindicated (GCS <9, haemodynamically unstable, active seizsure)
MRI scan after the lumbar puncture to visualise the brain in detail

Others
Swabs of other areas can help establish the causative organism, such as throat and vesicle swabs
HIV testing is recommended in all patients with encephalitis

Management:
- Intravenous antiviral medications are used to treat the suspected or confirmed underlying cause:

Aciclovir treats herpes simplex virus (HSV) and varicella zoster virus (VZV) - usually started empirically until results are available
Ganciclovir treat cytomegalovirus (CMV)

  • Repeat lumbar puncture is usually performed to ensure successful treatment prior to stopping antivirals
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10
Q

What is Kawasaki disease?

key complication?

Presentation?

A

Kawasaki disease is also known as mucocutaneous lymph node syndrome. It is a systemic, medium-sized vessel vasculitis.

It affects young children, typically under 5 years. There is no clear cause or trigger. It is more common in Asian children, particularly Japanese and Korean children. It is also more common in boys.

A key complication is coronary artery aneurysm.

Presentation:
A key feature that should make you consider Kawasaki disease is a persistent high fever (above 39ºC) for more than 5 days. Children will be unhappy and unwell. The key skin findings are a widespread erythematous maculopapular rash and desquamation (skin peeling) on the palms and soles of the feet.

Other features include:

Strawberry tongue (red tongue with large papillae)
Cracked lips
Cervical lymphadenopathy
Bilateral conjunctivitis
TOM TIP: If you come across a child with a fever persisting for more than 5 days, think of Kawasaki disease! A rash, strawberry tongue, lymphadenopathy and conjunctivitis will seal the diagnosis in your exams.

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11
Q

Investigations in kawasaki disease

A

There are several investigations that can be helpful in Kawasaki disease:

Full blood count can show anaemia, leukocytosis and thrombocytosis
Liver function tests can show hypoalbuminemia and elevated liver enzymes
Inflammatory markers (particularly ESR) are raised
Urinalysis can show raised white blood cells without infection
Echocardiogram can demonstrate coronary artery pathology

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12
Q

Disease course of kawasaki disease?

management?

further investigation that is indicated?

A

Disease Course

There are three phases to Kawasaki disease:

Acute phase: The child is most unwell with the fever, rash and lymphadenopathy. This lasts 1 – 2 weeks.
Subacute phase: The acute symptoms settle, the desquamation and arthralgia occur and there is a risk of coronary artery aneurysms forming. This lasts 2 – 4 weeks.
Convalescent stage: The remaining symptoms settle, the blood tests slowly return to normal and the coronary aneurysms may regress. This last 2 – 4 weeks.

Management

There are two first line medical treatments given to patients with Kawasaki disease:

High dose aspirin to reduce the risk of thrombosis
IV immunoglobulins to reduce the risk of coronary artery aneurysms
Patients will need close follow up with echocardiograms to monitor for evidence of coronary artery aneurysms.

TOM TIP: Kawasaki disease is one of the few scenarios where aspirin is used in children. Aspirin is usually avoided due to the risk of Reye’s syndrome. This is a unique fact that examiners like to test.

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13
Q

A child presents with:
- a red-pink, blotchy, macular rash with rough “sandpaper” skin that starts on the trunk and spreads outwards
- fever
- flushed cheeks
- sore throat
- strawberry tongue
- cervical lymphadenopathy?

Diagnosis?
Management?

A

Scarlet fever is associated with group A streptococcus infection, usually tonsillitis. It is not caused by a virus.

Treatment is with antibiotics for the underlying streptococcal bacterial infection. This is with phenoxymethylpenicillin (penicillin V) for 10 days. Scarlet fever is a notifiable disease and all cases need to be reported to public health. Children should be kept off school until 24 hours after starting antibiotics.

Patients can have other conditions associated with group A strep infection:

Post-streptococcal glomerulonephritis
Acute rheumatic fever

The other disease causing strawberry tongue and cervical lyphadenopathy is kawasaki disease, but here the fever is likely to last more than five days are there is often desquamatisation of the palms and soles of feet.

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14
Q

A child presents with:
- fever
- coryzal symptoms
- conjuctivitis
- 3-5 days later a macular (flat) rash appears on the face, behind the ears and then spreads to the rest of the body

Diagnosis?
pathognomonic sign?
management?
complications?

A

Measles is caused by the measles virus. It is highly contagious via respiratory droplets. Symptoms start 10 – 12 days after exposure, with fever, coryzal symptoms and conjunctivitis.

Koplik spots are greyish white spots on the buccal mucosa. They appear 2 days after the fever. They are pathognomonic for measles, meaning if a patient has Koplik spots, you can diagnose measles.

The rash starts on the face, classically behind the ears, 3 – 5 days after the fever. It then spreads to the rest of the body. The rash is an erythematous, macular rash with flat lesions.

Measles is self resolving after 7 – 10 days of symptoms. Children should be isolated until 4 days after their symptoms resolve. Measles is a notifiable disease and all cases need to be reported to public health. 30% of patients with measles develop a complication.

Complications include:

Pneumonia
Diarrhoea
Dehydration
Encephalitis
Meningitis
Hearing loss
Vision loss
Death

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15
Q

What causes slapped cheek syndrome/erythema infectiosum?

Presentation?

Management?

Complications?

A

Parovirus B19

Parvovirus infection starts with mild fever, coryza and non-specific viral symptoms such as muscle aches and lethargy. After 2 – 5 days the rash appears quite rapidly as a diffuse bright red rash on both cheeks, as though they have “slapped cheeks”. A few days later a reticular mildly erythematous rash affecting the trunk and limbs appears that can be raised and itchy. Reticular means net-like.

The illness is self limiting and the rash and symptoms usually fade over 1 – 2 weeks. Healthy children and adults have a low risk of any complications and are managed supportively with plenty of fluids and simple analgesia. It is infectious prior to the rash forming, but once the rash has formed they are no longer infectious and do not need to stay off school.

Patients that are at risk of complications include immunocompromised patients, pregnant women and patients with haematological conditions.such as sickle cell anaemia, thalassaemia, hereditary spherocytosis and haemolytic anaemia. These patients require serology testing for parvovirus to confirm the diagnosis and checking of the full blood count and reticulocyte count for aplastic anaemia. People that would be at risk of complications that have come in contact with someone with parvovirus prior to the rash forming, should be informed and may need investigations.

Complications:

**Aplastic anaemia
**Encephalitis or meningitis
Pregnancy complications including fetal death
Rarely hepatitis, myocarditis or nephritis

Key differential is scarlet fever because of the fever and flushed flushed cheeks. However scarlet fever caused by GA strept has a sandpaper rash, cervical lyphadenopathy, and strawberry tongue.

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16
Q

What is an exanthem and list causes of them

A

An “exanthem” is an eruptive widespread rash

  • measels
  • scarlet fever
  • slapped cheeks syndrome
  • rubella
  • roseola infantum
  • kawasaki disease
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17
Q

What is rubella?

Management?

Complications?

Risk in pregnancy?

A

A GENERALLY MILD DISEASE!

Rubella is caused by the rubella virus. It is highly contagious and spread by respiratory droplets. Symptoms start 2 weeks after exposure.

It presents with a milder erythematous macular rash compared with measles. The rash starts on the face and spreads to the rest of the body. The rash classically lasts 3 days. It can be associated with a mild fever, joint pain and a sore throat. Patients often have enlarged lymph nodes (lymphadenopathy) behind the ears and at the back of the neck.

Management is supportive and the condition is self limiting. Rubella is a notifiable disease and all cases need to be reported to public health. Children should stay off school for at least 5 days after the rash appears. Children should avoid pregnant women.

Complications are rare but include thrombocytopenia and encephalitis. Rubella is dangerous in pregnancy and can lead to congenital rubella syndrome, which is a triad of deafness, blindness and congenital heart disease

///

I think basically its mild, focus of the pathognomnic things in the other exanthems - kawasiki 5 day fever, scalded palms and feet, cervical lyphadenopathy, conjunctivitis, strawberry tongue

scarlet fever - strawberry tongue, cervical lyphadenopathy, sandpaper rash

measels - conjunctivitis and koplik spots. Rash behind ears.

18
Q

Roseola Infantum is common viral illness that affects infants and toddlers. It presents with a high fever (up to 40ºC) that comes on suddenly, lasts for 3 – 5 days and then disappears suddenly. There may be coryzal symptoms, sore throat and swollen lymph nodes during the illness. When the fever settles, the rash appears for 1 – 2 days. The rash consists of a mild erythematous macular rash across the arms, legs, trunk and face and is not itchy.

Children make a full recovery within a week and do not generally need to be kept off nursery if they are well enough to attend.

- Which virus causes roseola infantum?
- One main complication of roseola?

A

Roseola is caused by human herpesvirus 6 (HHV-6) and less frequently by human herpesvirus 7 (HHV-7).

The main complication to be aware of is febrile convulsions due to high temperature. Immunocompromised patients may be at risk of rare complications such as myocarditis, thrombocytopenia and Guillain-Barre syndrome.

19
Q

Eczema:
- presentation - when and where on the body?
- Pathophysiology?
- Management - maintenance vs flares
- steroid ladder
- Two main complications of eczema and their management

A

flexor surfaces are the ones that overlay the flexor muscles - pits of elbows and knees

Eczema usually presents in infancy with dry, red, itchy and sore patches of skin over the flexor surfaces (the inside of elbows and knees) and on the face and neck. Patients with eczema experience periods where the condition is well controlled and periods where the eczema is more problematic, known as flares.

The simplified pathophysiology is that eczema is caused by defects in the barrier that the skin provides. Tiny gaps in the skin barrier provide an entrance for irritants, microbes and allergens that create an immune response, resulting in inflammation and the associated symptoms.

Management

Maintenace - emollients and avoiding perfumes or harsh soaps
Ointments are thicker and greasier than creams.
Flares - topical steroids and thicker emollients

Other specialist treatments in severe eczema include zinc impregnated bandages, topical tacrolimus, phototherapy and systemic immunosuppressants, such as oral corticosteroids, methotrexate and azathioprine.

The steroid ladder from weakest to most potent - spells HEBD
Mild: Hydrocortisone 0.5%, 1% and 2.5%
Moderate: Eumovate (clobetasone butyrate 0.05%)
Potent: Betnovate (betamethasone 0.1%)
Very potent: Dermovate (clobetasol propionate 0.05%)

Complication
- opportunistic bacterial infection of the skin with staphylococcus aureus - impetigo. Rx w/ Flucloxaccilin
- eczema herpeticum - HSV or VZV infection of the skin. Can make patients very unwell - widepread rash with fever. Rx w/ Aciclovir.

THESE COMPLICATIONS ARE KEY I THINK

20
Q

What is stephen-johnson syndrome?

SJS vs TEN?

causes? - just generally

presentation?

A

Steven-johnson syndrome is a rare but serious over-reaction of the immune system to a drug or a mild infection. Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are a spectrum of the same pathology, where a disproportional immune response causes epidermal necrosis, resulting in blistering and shedding of the top layer of skin. Generally, SJS affects less that 10% of body surface area whereas TEN affects more than 10% of body surface area.

Causes

Medications:
Anti-epileptics
Antibiotics
Allopurinol
NSAIDs

Infections:
Herpes simplex
Mycoplasma pneumonia
Cytomegalovirus
HIV

Presentation

The condition has a spectrum of severity. Some cases are mild whilst others are very severe and can potentially be fatal.

Patients usually start with non-specific symptoms of fever, cough, sore throat, sore mouth, sore eyes and itchy skin. They then develop a purple or red rash that spreads across the skin and starts to blister.

A few days after the blistering starts, the skin starts to break away and shed leaving the raw tissue underneath. Pain, erythema, blistering and shedding can also happen to the lips and mucous membranes. Eyes can become inflamed and ulcerated. It can also affect the urinary tract, lungs and internal organs.

LOOK UP A PICTURE REALLY QUICK IT’LL HELP WITH YOUR MEMORY.

21
Q

Stephen-Johnson Syndrome 2

Management?

Complications? 3

A

Management:
- emergency admission to dermatology
- steroids, immunoglobulins and immunosuppressants guided by a specialist

Complications

  • Secondary infection: The breaks in the skin can lead to secondary bacterial infection, cellulitis and sepsis.
  • Permanent skin damage: Skin involvement can lead to scarring and damage to skin, hair, nails, lungs and genitals.
  • Visual complications: Depending on the severity, eye involvement can range from sore eyes to severe scarring and blindness.
22
Q

What is urticaria?

Causes - acute and chronic?

Management?

A

LOOK UP A PICTURE OF HIVES

Urticaria are also known as hives. They are small itchy lumps that appear on the skin. They may be associated with a patchy erythematous rash. This can be localised to a specific area or widespread. They may be associated with angioedema and flushing of the skin. Urticaria can be classified as acute urticaria or chronic urticaria.

Urticaria are caused the release of histamine and other pro-inflammatory chemicals by mast cells in the skin. This may be part of an allergic reaction in acute urticaria or an autoimmune reaction in chronic idiopathic urticaria.

Causes:
Acute
- Allergies to food, medications or animals
- Contact with chemicals, latex or stinging nettles
- Medications
- Viral infections
- Insect bites

Chronic Urticaria
- An autoimmune condition where autoantibodies target mast cells and trigger them to release histamines and other chemicals

Management:
- Antihistamines
- Fexofenadine is the antihistamine of choice for chronic urticaria
- Oral steroids may be given for flare ups
- Severe cases: Montelukast or Omalizumab which targets IgE

23
Q

A Toddler presents with tiredness, sore throat, dry cough and raised temperature. After 1 – 2 days small mouth ulcers appear, followed by blistering red spots across the body, particularly on the hands, feet and around the mouth.

Diagnosis?

What is the causative organism?

Management?

A

Hand, foot and mouth disease - **Coxsackie A virus infection **

^^this is the only examinable fact i think.

Me - Similar presentation to chickenpox but the blisters are more localised to the hands, feet and mouth in coxsackie disease. Also the mouth ulcers are sore vs chickenpox blisters are just itchy and not in the moth.

Diagnosis is made based on the clinical appearance of the rash.

There is no treatment for hand, foot and mouth disease. Management is supportive, with adequate fluid intake and simple analgesia such as paracetamol if required. The rash and illness resolve spontaneously without treatment after a week to 10 days

Rarely it can cause complications:

Dehydration
Bacterial superinfection
Encephalitis

wouldn’t even bother testing on these, just be aware

24
Q

Allergic Rhinitis
Pathophysiology? - key

Sx?

Ix?

Triggers?

Management?

A

Allergic rhinitis is a condition caused by an IgE-mediated type 1 hypersensitivity reaction. Environmental allergens cause an allergic inflammatory response in the nasal mucosa.

Allergic rhinitis typically causes:

Runny, blocked and itchy nose
Sneezing
Itchy, red and swollen eyes
Allergic rhinitis is associated with a personal or family history of other allergic conditions (atopy).

Ix - diagnosis is based on history but Skin prick testing for allergy to pollen, animals and house dust mite can be useful

Triggers
- Tree pollen or grass allergy leads to seasonal symptoms (hay fever)
- House dust mites and pets can lead to year round symptoms, often worse in dusty rooms at night. Pillows can be full of house dust mites.
- Pets can lead to persistent symptoms when the pet or their hair, skin or saliva is present
- Other allergens lead to symptoms after exposure (e.g. mould)

Management:
- avoidance of the trigger
- Oral antihistamines are taken prior to exposure to reduce allergic - cetirizine, loratadine and fexofenadine, chlorphenamine (Piriton - sedating)

Nasal corticosteroid sprays such as fluticasone and mometasone can be taken regularly to suppress local allergic symptoms. (Trying to coat the nose, not inhale)

Nasal antihistamines may be a good option for rapid onset symptoms in response to a trigger.

25
Q

What is nappy rash?

What areas of skin are affected?

Signs of candida infection?

Management?

A

Nappy rash is contact dermatitis in the nappy area. It is usually caused by friction between the skin and nappy and contact with urine and faeces in a dirty nappy. Most babies will get nappy rash at some point, and it is most common between 9 and 12 months of age.

Nappy rash present with sore, red, inflamed skin in the nappy area. The rash appears in individual patches on exposure areas of the skin that come in contact with the nappy. It tends to spare the skin creases, meaning the creases in the groin are healthy. There may be a few red papules beside the affected areas of skin. Nappy rash is uncomfortable, may be itchy and the infant may be distressed. Severe and longstanding nappy rash can lead to erosions and ulceration.

Additionally, the breakdown in skin and the warm moist environment in the nappy can lead to added infection with candida (fungus) or bacteria, usually staphylococcus or streptococcus. Candida in the nappy area (thrush) is a common finding. Signs that would point to a candidal infection rather than simple nappy rash are:

Key
- Rash extending into the skin fold
- Satellite lesions, which are small similar patches of rash or pustules near the main rash
- Oral thursh
others:
Larger red macules
Well demarcated scaly border
Circular pattern to the rash spreading outwards, similar to ringworm

Management
Simple measures can be taken to improve skin health and treat nappy rash within a few days:

Switching to highly absorbent nappies (disposable gel matrix nappies)
Change the nappy and clean the skin as soon as possible after wetting or soiling
Use water or gentle alcohol free products for cleaning the nappy area
Ensure the nappy area is dry before replacing the nappy
Maximise time not wearing a nappy

**Infection with candida or bacteria warrants treatment with an anti-fungal cream (clotrimazole or miconazole) or antibiotic (fusidic acid cream or oral flucloxacillin).
**

26
Q

Differential diagnosis for non-blanching rashes?

A

Non-blanching rashes are caused by bleeding under the skin. Petechiae are small (< 3mm), non blanching, red spots on the skin caused by burst capillaries. Purpura are larger (3 – 10mm) non-blanching, red-purple, macules or papules created by leaking of blood from vessels under the skin.

Any child presenting with a non-blanching rash needs immediate investigation for the underlying cause.

Meningococcal septicaemia or other bacterial sepsis: Often - rash + fever + lethargy. Any features of meningococcal septicaemia indicate emergency management with immediate antibiotics. This can lead to significant morbidity and mortality if treatment is delayed. ME - fever is key here

Henoch-Schonlein purpura (HSP): This typically presents as a purpuric rash on the legs and buttocks and may have associated abdominal or joint pain.

Idiopathic thrombocytopenic purpura (ITP): This develops over several days in an otherwise well child.

Acute leukaemias: This presents with a gradual development of petechiae, potentially with other signs such as anaemia, lymphadenopathy and hepatosplenomegaly.

Haemolytic uraemic syndrome (HUS): This is associated with oliguria (very low urine output) and signs of anaemia. This often presents in a child with recent diarrhoea.

Mechanical: Strong coughing, vomiting or breath holding can produce petechiae in a “superior vena cava distribution”, above the neck and most prominently around the eyes.

Traumatic: Tight pressure on the skin, for example in non-accidental injury, or occlusion of blood in an area of skin can lead to traumatic petechiae.

Viral illness: This is often the explanation when other causes and serious illness are excluded. Typical causes are influenza and enterovirus.

Useful investigations:
- FBC
- U&Es
- CRP
- ESR
- Coag screen
- blood culture
- lumbar puncture
- miningococcal PCR
- Urine dipstick

27
Q

Anaphalaxis:
- type of hypersensativity reaction? - process
- anaphalaxis vs allergic reaction?

Management?

Ix to confirm after the event?

A

Anaphylaxis is a life-threatening medical emergency. It is caused by a severe type 1 hypersensitivity reaction. Immunoglobulin E (IgE) stimulates mast cells to rapidly release histamine and other pro-inflammatory chemicals. This is called mast cell degranulation. This causes a rapid onset of symptoms, with airway, breathing and/or circulation compromise.

The key feature that differentiates anaphylaxis from a non-anaphylactic allergic reaction is compromise of the airway, breathing or circulation.

Allergic symptoms:
- urticaria
- angio-oedema
- abdominal pain

Anphalaxis symptoms:
- SOB
- wheeze
- stridor
- tachycardia
- syncope

Management:
ABCDE approach to diagnose
- lie flat and remove trigger
- IV fluid bolus
- IM adrenaline repeated after five minutes if needed (adult dose is 500micrograms (0.5ml of 1:1000)
- establish airway and give high flow oxygen

Ix:
- children should be monitored in case of biphasic reaction
- Anaphylaxis can be confirmed by measuring the serum mast cell tryptase within 6 hours of the event. Tryptase is released during mast cell degranulation and stays in the blood for 6 hours before gradually disappearing.

All children and adolescnece are given an adrenaline auto-injector after an episode of anaphalaxis

28
Q

A child presents w/ a history of fever and general malaise. 2 days later they break out with widespread, erythematous, raised, vesicular blistering lesions. The rash starts on the trunk or face and spreads outwards affecting the whole body over 2 – 5 days.

Most likely Dx?
Causative organism?
Transmission?
Complications? - CAME UP
Reactivation of the virus leads to?
Management in children?

A

Chickenpox is caused by the varicella zoster virus (VZV). It causes a highly contagious, generalised vesicular rash. It is common in children. Once a child has had an episode of chickenpox, they develop immunity to the VZV virus and will not be affected again.

Chickenpox is highly contagious and spread through direct contact with the lesions or through infected droplets from a cough or sneeze. Patients become symptomatic 10 days to 3 weeks after exposure. The stop being contagious after all the lesions have crusted over.

Complications:

Bacterial superinfection
Dehydration
Conjunctival lesions
Pneumonia
Encephalitis (presenting as ataxia) - THIS CAME UP

After the infection the virus can lie dormant in the sensory dorsal root ganglion cells and cranial nerves reactivate later in life as shingles or Ramsay Hunt syndrome.

/////

Management

Chickenpox is usually a mild self limiting condition that does not require treatment in otherwise healthy children.

Aciclovir may be considered in immunocompromised patients or neonates

Complications such as encephalitis require admission for inpatient management.

Symptoms of itching can be treated with calamine lotion and chlorphenamine (antihistamine). Me Calamine is the wierd pink cream people with chickenpox wear

Patients should be kept off school and avoid pregnant women and immunocompromised patients until all the lesions are dry and crusted over. This is usually around 5 days after the rash appears.

29
Q

Chickenpox : Risk in pregnancy? Management of exposure and infection?

A

Antenatal and Neonatal Chickenpox
Pregnant women that are known to be immune to chickenpox are not at risk when in contact with chickenpox. When they are not immune, varicella zoster immunoglobulins can be given to protect them against the virus after exposure. Aciclovir is used to treat women who develop chicken pox in pregnancy.

Chickenpox in pregnancy, before 28 weeks gestation, can cause developmental problems in the fetus in a small portion of patients. This is known as congenital varicella syndrome - microcephaly, limb hypoplasia, chorioretinitis.

Chickenpox in the mother around the time of delivery can lead to life threatening neonatal infection - as above mother is treated with aciclovir

30
Q

Diptheria Main sx?

Mx?

A

Pseodomembrane formation in the upper respiratory tract (Key Sx is greyish tonsils).
Croup used to be caused by diphtheria. Croup caused by diphtheria leads to epiglottitis (Croup is usually a laryngitis caused by parainfluenza) and has a **high mortality. **

systemically it also causes myocarditis and neurological symptoms.

Vaccination mean that this is very rare in developed countries.

Anti-toxin (very virulent toxin) and erythromycin are the treatments

31
Q

A child presents with a history of generalised patches of erythema on the skin, the skin looks thin and wrinkled. This was followed by the formation of fluid filled blisters called bullae, which burst and leave very sore, erythematous skin below. Systemically the child also has a fever and general malaise

Most likely diagnosis?
Infectious organism? And toxin produced?
what is Nikolsky sign?
Management?

A

The skin has a very similar appearance to being burnt -> Staphylococcal scalded skin syndrome (SSSS)

A condition caused by a type of staphylococcus aureus bacteria that produces epidermolytic toxins. These toxins are protease enzymes that break down the proteins that hold skin cells together. When a skin infection occurs and these toxins are produced, the skin is damaged and breaks down. This condition usually affects children under 5 years. Older children and adults have usually developed immunity to the epidermolytic toxins.

Nikolsky sign is where very gentle rubbing of the skin causes it to peel away. This is positive in SSSS.

Management
If untreated it can lead to sepsis and potentially death.
Most patients will require admission and treatment with IV antibiotics (Flucloxaccilin). Fluid and electrolyte balance is key to management as patients are prone to dehydration.

32
Q

Impetigo:
- two causative organisms?
- characteristic feature?
- two types of impetigo?
- Management for each type

A

Impetigo is a superficial bacterial skin infection, usually caused by the staphylococcus aureus bacteria. A “golden crust” is characteristic of a staphylococcus skin infection. It is also less commonly caused by the streptococcus pyogenes bacteria (GA strept). Impetigo is contagious and children should be kept off school during the infection.

Impetigo occurs when bacteria enter via a break in the skin - lol never knew this. This may be in otherwise healthy skin or may be related to eczema or dermatitis.

Impetigo can be classified as non-bullous or bullous.

Non-Bullous
Non-bullous impetigo typically occurs around the nose or mouth. The exudate from the lesions dries to form a “golden crust”. They are often unsightly but do not usually cause systemic symptoms or make the person unwell.

Management
- localised - **antiseptic cream (hydrogen peroxide 1% cream) **
- Widespread - Topical fusidic acid
- Oral flucloxacillin - systemic symptoms

Bullous
Bullous impetigo is always caused by the staphylococcus aureus bacteria. These bacteria can produce epidermolytic toxins that break down the proteins that hold skin cells together. This causes 1 – 2 cm fluid filled vesicles to form on the skin. These vesicles grow in size and then burst, forming a “golden crust”. Eventually they heal without scarring. These lesions can be painful and itchy.

This type of impetigo is more common in neonates and children under 2 years, however it can occur in older children and adults. It is more common for patients to have systemic symptoms. They may be feverish and generally unwell. In severe infections when the lesions are widespread, it is called staphylococcus scalded skin syndrome.

Swabs of the vesicles can confirm the diagnosis, bacteria and antibiotic sensitivities. Treatment of bullous impetigo is with antibiotics, usually flucloxacillin. This may be given orally or intravenously if they are very unwell or at risk of complications. The condition is very contagious and patients should be isolated where possible.

33
Q

Pathophysiology of toxic shock syndrome?
Common causes?
Presentation?
Management

A

Toxic shock syndrome (TSS) is an exotoxin-mediated illness caused by bacterial infection, most commonly group A streptococcus or Staphylococcus aureus.

Presenting signs and symptoms can be non-specific, but the course of the disease is precipitous and toxicity occurs early, resulting in serious life-threatening disease and multi-organ system failure.

Presentation:
- fever >39
- hypotension
- diffuse erythematous,macular rash
- Multiorgan dysfuntion - mucositis, gastroentiritis, renal impairment, hepatic impairment, clotting disorder.

Usually caused by:
- extended tampon use
- infection of surgical wounds
- post-partum infection in mothers
- skin infection

Management
- intensive care support
- surgical debridement of SSTIs
- Empirical antibiotics - cetriaxone with clindamycin

**Me - this is not septic shock:
**
Toxic Shock Syndrome (TSS):
Primarily caused by toxins produced by certain bacteria, such as Staphylococcus aureus and Streptococcus pyogenes.
Often associated with the use of tampons, contraceptive devices, or skin wounds.
Hence the name Toxic and shock (low BP)

Sepsis:
Caused by the body’s extreme response to an infection, which can be bacterial, viral, fungal, or parasitic.
Can result from any type of infection, such as pneumonia, urinary tract infections, abdominal infections, or bloodstream infections.

34
Q

A patient with a chronic cough and night sweats. Sputum culture grows “acid-fast bacilli” that stain red with “Zeihl-Neelsen staining”

Diagnosis?

Possible disease courses?

Symptoms?

2 Tests before having a BCG?

A

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis

Tuberculosis is mostly spread by inhaling saliva droplets from infected people. Once in the body, there are several possible outcomes:

Immediate clearance of the bacteria (in most cases)
Primary active tuberculosis (active infection after exposure)
Latent tuberculosis (presence of the bacteria without being symptomatic or contagious)
Secondary tuberculosis (reactivation of latent tuberculosis to active infection)

Latent tuberculosis is present when the immune system encapsulates the bacteria and stops the progression of the disease. Patients with latent tuberculosis have no symptoms and cannot spread the bacteria. Most otherwise healthy patients with latent tuberculosis never develop an active infection. When latent tuberculosis reactivates, and an infection develops, usually due to immunosuppression, this is called secondary tuberculosis.

The most common site for TB infection is in the lungs, where it gets plenty of oxygen. Extrapulmonary tuberculosis refers to disease in other areas - literally everywhere

If children have latent TB they will be asymptomatic but will test positive on the mantoux test. Typical signs and symptoms of tuberculosis include:

Cough
Haemoptysis (coughing up blood)
Lethargy
Fever or night sweats
Weight loss
Lymphadenopathy
Erythema nodosum (tender, red nodules on the shins caused by inflammation of the subcutaneous fat)
Spinal pain in spinal tuberculosis (also known as Pott’s disease of the spine)

Patients need a mantoux test and HIV test before recieving the vaccine.

35
Q

TB:
- Investigations -5?and findings
- Management, inluding for latent TB?
- Side effects - one for each drug

A

There are two tests for an immune response to tuberculosis caused by previous infection, latent TB or active TB:

Mantoux test
Interferon‑gamma release assay (IGRA)

In patients where active disease is suspected, investigations to support the diagnosis include:

Chest x-ray
Cultures
In children- NAAT testing - quicker.

CXR shows:
Primary TB - Hilar lymphadeonpathy, patchy consolidation
Disseminated miliary tuberculosis gives a characteristic appearance of “millet seeds” on a chest x-ray, with many small (1-3mm) nodules disseminated throughout the lung fields. This makes it a popular spot diagnosis in exams. It is worth becoming familiar with the appearance.

There are several ways to collect cultures:

Sputum cultures (3 separate sputum samples are collected) - might require bronchocoscopy and bronchoalveolar lavage.
Mycobacterium blood cultures (require special blood culture bottle)
Lymph node aspiration or biopsy

**Treatment
**
Latent tuberculosis is treated with either:

Isoniazid and rifampicin for 3 months
Isoniazid for 6 months

The treatment for active tuberculosis can be remembered with the RIPE mnemonic:

R – Rifampicin for 6 months
I – Isoniazid for 6 months
P – Pyrazinamide for 2 months
E – Ethambutol for 2 months

TOM TIP: Remember that isoniazid causes peripheral neuropathy, and pyridoxine (vitamin B6) is co-prescribed to help prevent this. An exam question might say, “…are started on R, I, P and E. What else should be prescribed?” The answer would be pyridoxine or vitamin B6.

**Side Effects
**
Red-and-orange pissin - red/orange discolouration of secretions, such as urine and tears.

I’m-so-numb-azid - peripheral neuropathy

Pyrazinamide - hyperuricaemia (high uric acid levels), resulting in gout and kidney stones.

Eye-thambutol - can cause colour blindness and reduced visual acuity

36
Q

Paediatric HIV:
Basic Pathophysiology
Route of transmission in children
**Prevention of HIV transmission in Childbirth **
Prevention during breast feeding?

A

HIV is an RNA retrovirus. HIV-1 is most common type. HIV-2 is rare outside West Africa. The virus enters and destroys the CD4 T helper cells. An initial seroconversion flu like illness occurs within a few weeks of infection. The infection is then asymptomatic until it progresses and the patient becomes immunocompromised and beings developing AIDS defining illnesses and opportunistic infections, potentially years later.

Main route of transmission in children - Mother to child at any stage of pregnancy, birth or breastfeeding. This is referred to as vertical transmission.

Prevention:

Mode of delivery will be determined by the mother viral load:

Normal vaginal delivery is recommended for women with a viral load < 50 copies / ml
Caesarean sections are considered in patients with > 50 copies copies / ml and in all women with > 400 copies / ml
IV zidovudine should be given during the caesarean if the viral load is unknown or there are > 1000 copies / ml
Prophylaxis treatment may be given to the baby depending on the mothers viral load:

Low risk babies, where mums viral load is < 50 copies per ml, should be given zidovudine for 4 weeks
High risk babies, where mums viral load is > 50 copies / ml, should be given zidovudine, lamivudine and nevirapine for 4 weeks

Breastfeeding - HIV can be transmitted during breastfeeding, even if the mother’s viral load is undetectable. Breastfeeding is never recommended for mothers with HIV, however if the mum is adamant and the viral load is undetectable, sometimes it is attempted with close monitoring by the HIV team.

37
Q

Peadiatric HIV:
Which tests are used for screening and monitoring?
When should children be tested for HIV? 2
How are babies to HIV Positive parents tested? - key question

Management for children who test positive?

A

Screening: p24 viral antigen and HIV antibody; window period 45 days

Monitoring:
- Viral load - RNA copies
- CD4 count

When to test for HIV

Babies to HIV positive parents
When immunodeficiency is suspected, for example where there are unusual, severe or frequent infections
Young people who are sexually active can be offered testing if there are concerns
Risk factors such as needle stick injuries, sexual abuse or IV drug use

Babies to HIV positive parents are tested twice for HIV:

HIV viral load test at 3 months. If this is negative, the child has not contracted HIV during birth and will not develop HIV unless they have further exposure.

HIV antibody test at 24 months. This is to assess whether they have contracted HIV since their 3 month viral load, for example through breast feeding. If the 3 month test is negative and they are not breastfed, this should be negative.Note that the antibody test can be positive in infants who do not have HIV for up to 18 months of age. This is due to maternal antibodies that have crossed the placenta during pregnancy.

Treatment should be coordinated by a specialist in paediatric HIV. The key principles of medical care are:

Antiretroviral therapy (ART) to suppress the HIV infection
Normal childhood vaccines, avoiding or delaying live vaccines if severely immunosuppressed.
Prophylactic co-trimoxazole (Septrin) for children with low CD4 counts, to protect against pneumocystis jirovecii pneumonia (PCP)
Regular follow up including, weight development and clinical signs of the disease - whole MDT approach

38
Q

What type of hypersensitivity reaction is IgE mediated?

A

Type 1 - allergy, anaphylaxis

2- IgG
3- Immune-complex
4- T cell mediated.

ACID is one mnemonic put i would just focus on allergy being type 1

39
Q

Compare and Contrast congenital Rubella Syndrome with Congenital Varicella

A

The features of congenital rubella syndrome to be aware of are:

Congenital deafness
Congenital cataracts
Congenital heart disease (PDA and pulmonary stenosis)
Learning disability

Congenital varicella syndrome occurs in around 1% of cases of chickenpox in pregnancy. It occurs when infection occurs in the first 28 weeks of gestation. The typical features include:

Fetal growth restriction
Microcephaly, hydrocephalus and learning disability
Scars and significant skin changes located in specific dermatomes
Limb hypoplasia (underdeveloped limbs)
Cataracts and inflammation in the eye (chorioretinitis)

So they are similar but Rubella is heart and ears, and Varicella is limbs

It can also cause severe neonatal infection if infection occours around the time of delivery

40
Q

What does the 6 in 1 vaccine protect against?

Outline the UK vaccination Schedule?

To help:
- When is HPV given
- When is 6-in-1 given
- When is Men B given
- When is rota-virus given
- When is MMR
-

A

8 weeks:
- 6 in 1 vaccine (diphtheria, tetanus, pertussis, polio, haemophilus influenzae type B (Hib) and hepatitis B)
- Meningococcal type B
- Rotavirus (oral vaccine)

12 weeks:
- 6 in 1 vaccine (again)
- Pneumococcal (13 different serotypes)
- Rotavirus (again)

16 weeks:
- 6 in 1 vaccine (again)
- Meningococcal type B (again)

1 year:
- 2 in 1 (haemophilus influenza type B and meningococcal type C)
- Pneumococcal (again)
- MMR vaccine (measles, mumps and rubella)
- Meningococcal type B (again)

Yearly from age 2 – 8:
- Influenza vaccine (nasal vaccine)

3 years 4 months:
- 4 in 1 (diphtheria, tetanus, pertussis and polio)
- MMR vaccine (again)

12 – 13 years:
- Human papillomavirus (HPV) vaccine (2 doses given 6 to 24 months apart)

14 years:
- 3 in 1 (tetanus, diphtheria and polio)
- Meningococcal groups A, C, W and Y

Summary to memorise:

  • 6 in 1 is given int he first 3 visits, every 4 weeks. Then 4 in 1 (no Hs) with MMR at 3 +4mths
  • Rota is in the first 2.
  • MMR isn’t given until 1 years (live) and then again at 3 + 4 mths - 2 doses
  • Men B is given at 8wks, 16wks, 1 year - important to protct against mengitis ASAP
  • HPV is given to 12 years and parents hate it because it implies their kid is a slag
  • 14 year old booster 3 in 1 and Meningitis before they start going out.