May 2021 Flashcards
(222 cards)
"Cause of morbidity and mortality in Paracetamol ingestion - A. Metabolic Acidosis B. Hypoxemia C. Gastric bleeding D. Hepatic failure "
D
"A 3 year old male, son of a farmer, was comatose, with weakness, excessive salivation, bradycardia and constricted pupils. These findings are most likely seen in: A. Phenobarbital B. Hydrocarbons C. Mercury D. Organophosphate "
D
“Organophosphate (SLUDGE BBB) - salivation, lacrimation, urination, defacation, gastric emptying, bradycardia, bronchorrhea, bronchospasm
Phenobarbital - difficulty thinking, decreased level of consciousness, bradycardia or rapid and weak pulse, poor coordination, vertigo, nausea, muscle weakness, thirst, oliguria, decreased temperature, and dilated or contracted pupils; coma hypotension, respiratory depression
Hydrocarbon - type of hydrocarbon and the route and amount of hydrocarbon exposure determine the severity and type of clinical toxicity
Mercury - [acute exposure to air concentrations 100-1000mcg/m3] cough, dyspnea and chest pain; stomatitis, inflammation of the gums, and excessive salivation; severe nausea, vomiting, diarrhea (which can lead to shock); conjunctivitis and dermatitis– [>1000mcg/m3] fatal interstitial pneumonitis
“
"Which primitive reflex that persists throughout life? A. Tonic Neck reflex B. Galant reflex C. Parachute reflex D. Grasp reflex "
C
"Paraparesis with autonomic and sensory manifestations suggests affectation of: A. Pons B. Cerebellum C. Spinal cord D. Cortex "
D
"What is the difference between urticaria and angioedema? A. IgE activation B. Depth of involvement C. Duration of lesion D. Response to antihistamine "
B
”- Acute urticaria and angioedema are often caused by an allergic IgE- mediated reaction (21st Nelson page 1222)- so A is wrong
- Angioedema involves the deeper subcutaneous tissues… (21st Nelson page 1225)
- Urticaria occurs more commonly and is less severe than angioedema as it only affects the skin layers whereas angioedema affects the tissues beneath the skin (subcutaneous tissue).https://dermnetnz.org/topics/angioedema
“
"Which of the following is the best screening test for complement deficiency? a. C3 b. CH50 c. Flow cytometry d. C4 "
B
Nelsons 21st ed Chapter 160.1 Testing for total hemolytic complement activity (CH50) effectively screens for the most common diseases of the complement system
". Fulminant hepatitis is frequently seen with: A. B B. A C. C D. E "
A
Nelson 21st table 385.1: fulminant hep common in hep B and D
"A 10-year old female had high-grade on and off fever with good activity for 3 days. 1 day prior to consultation, a maculopapular rash on the trunk appeared. What is the diagnosis? A. Erythema infectiosum B. Scarlet fever C. Erythema subitum D. Rubella "
C
Nelsons 21st ed p1724: a history of 3 days of high fever in an otherwise nontoxic 10 mo old infant with a blanching maculopapular rash on the trunk suggests a diagnosis of roseola
"Inheritance of Duchenne muscular dystrophy? A. Autosomal Dominant B. Autosomal Recessive C. X-linked dominant D. X-linked recessive "
D
Nelsons 21st ed p3281. DMD is the most common hereditary neuromuscular disease affecting all races and ethnic groups…clinical features are progressive weakness, intellectual impairment, and hypertrophy of the calves, with proliferation of connective tissue and progressive fibrosis in muscle. Incidence is 1 in 3,600 liveborn infant boys. This disease is inherited as an X-linked recessive trait
"Most common CHD causing brain abscess? A. VSD B. COA C. TGA D. TOF "
D
"In what diagnostics is heterophile antibody present? A. CMV B. Rabies C. Infectious Mononucleosis D. Behcet’s "
C
Nelsons 21st ed p1717. Heterophile antibodies are cross-reactive immunoglobulin M antibodies that agglutinate mammalian erythrocytes but are not EBV-specific. Heterophile antibody tests such as the monospot test are positive in 90% of cases of EBV-associated infectious mononucleosis in adolescents and adults during the 2nd week of illness but in only up to 50% of cases in children younger than 4 yr of age.
". Which one is not affected in congenital varicella? A. Heart B. Skin C. Eyes D. Extremities "
A
Chapter 280, page 1711 Nelson’s: The congenital varicella syndrome is characterized by cicatricial skin scarring in a zoster-like distribution; limb hypoplasia; and abnormalities of the neurologic system (e.g., microcephaly, cortical atrophy, seizures, and mental retardation), eye (e.g., chorioretinitis, microphthalmia, and cataracts), renal system (e.g., hydroureter and hydronephrosis), and autonomic nervous system (e.g., neurogenic bladder, swallowing dysfunction, and aspiration pneumonia).
"Recommended dose of VItamin A for patients 6 months of age? A. 100,000 IU Single dose B. 200,000 IU Single dose C. 100k IU every 6 mos D. 200k IU every 6 mos "
A
“Prev Ped 2018
Vitamin A supplementation as recommended by the DOH
Infants 6 - 11 months: 100,000 I.U. 1 dose only (one capsule is given anytime between 6-11 months but usually given at 9 months of age during the measles immunization.
Children 12-59 months: 200,000 I.U. 1 capsule every 6 months.
The World Health Organization (WHO) recommends administration of an oral dose of 200,000 IU (or 100,000 IU in infants) of vitamin A per day for two days to children with measles in areas where vitamin A deficiency may be present.
50,000 I.U. if less than 6mos.
Answer: A. Checked with WHO website and PPS handbook 2018, for PPS usually given at 9 months of age with the Measles vaccine, 100k IU for 6 months to 11 mos. for 12 mos to 59 months we give 200k iu every 4- 6 mos
“
"West Syndrome consists of the triad of infantile spasm, mental retardation and A. Pulmonary hypoplasia B. Hypsarrhythmia C. Hemiparesis D. Encephalopathy "
B
Nelson’s 21st ed p 3098. West syndrome starts between the ages of 2 and 12months and consists of a triad of infantile epileptic spasms that usually occur in clusters (particularly in drowsiness or upon arousal), developmental regression and a typical EEG picture called hypsarrhythmia ( a high voltage, slow, chaotic background with multifocal spikes).
"A negative allergy skin test is most useful and clinically significant in: A. Food Allergy B. Atopic Dermatitis C. Allergic Rhinitis D. Asthma "
C
"SELECT ONE: A. Tuberculosis B. Asthma C. Allergy D. Bronchiectasis "
A
?????
“A 2 yo female diagnosed with PTB. No history of exposure. All household members chest xrays were negative. She plays daily with his 20month old cousin who lives next door. What is the intervention for his cousin?
A. Start preventive H therapy
B. Do TST
C. No necessary intervention at this time
D. Request for CXR
“
B
“MOP 6th ed. If bacteriologic confirmed, treat. If clinically diagnosed, do TST first.
P68. The following eligible groups do not require TST. They may be offered TPT once active TB is ruled out:
a. PLHIV aged 1 year or older;
b. children less than 5 years old who are household contacts of bacteriologically
confirmed PTB; and
c. individuals aged 5 years and older with other TB risk factors (i.e. PLHIV, diabetes,
smoking, those with immune-suppressive medical conditions, malnourished, with multiple TB cases in the same household) and who are household contacts of bacteriologically confirmed PTB.
“
"A 4 year old presented with massive pneumothorax on the right. What is the MOST appropriate intervention? A. observe B. CTT C. Serial needling D. O2 100% "
B
“Nelsons 21st ed p2320. A small or even moderate-sized pneumothorax in an otherwise normal child may resolve without specific treatment, usually within one week..administering 100% O2 may hasten resolution but patients with chronic hypoxemia should be monitored closely during administration of O2. Needle aspiration into the second ICS in the MCL may be required on an emergency basis for tension pneumothorax..if the pneumothorax is recurrent, secondary, or under tension, or there is more than a small collapse, chest tube drainage may be necessary
Addendum: Stable patient small to moderate <30%- Supportive may resolve spontaneously.
Stable Massive/Large >30% pneumothorax- O2 support
Emergency/Unstable Patient-Needling then CTT
“
"Pulmonary radiologic findings in tuberculosis resolve in how many months? A. 6-24 months B. 6-12 months C. 3-6 months D. 3-9 months "
A
PPS TB Guidelines p. 100: “In the small proportion of children with radiologic evidence of the disease, clearing usually occurs within six months to two years after institution of therapy.”
". A mother came into the clinic with her child noted with yellowish discharge on the post BCG site 4 weeks post vaccination. How do you advise this mother? A. Observe this is normal B. Start topical antibiotics C. Diagnose disseminated TB D. None of the above "
A
“A 72 hours-old neonate came into the clinic due to jaundice. No other manifestations noted. Total bilirubin = 10mg/dL. Both baby’s and mother’s blood type are A+. Hgb = 16. What is the diagnosis?
A. Physiologic jaundice
B. Biliary atresia
C. Hemorrhagic disease of the newborn
D. Hemolytic disease of the newborn
“
A
“Physiologic jaundice (Nelsons 21st, Chapter 123.3) - Icterus Neonatorum. Jaundice that first appears on the 2nd or 3rd day is usually physiologic. Under normal circumstances, the level of indirect bilirubin in umbilical cord serum is 1-3mg/dl and rises at a rate of <5mg/dl/24 hours; thus, jaundice becomes visible on the 2nd or 3rd day, usually peaking between the 2nd and 4th days at 5-6mg/dl and decreasing to <2mg/dl between the 5th and 7th days after birth.
Biliary atresia (Nelsons 21st, Chapter 123.3) - Jaundice persisting for > 2 weeks or associated with alcoholic stools and dark urine suggests biliary atresia.
Hemorrhagic disease of the newborn (Nelsons 21st, Chapter 124.4) - known as Vitamin K deficiency bleeding, results from transient but severe deficiencies in the vitamin K-dependent factors and is characterized by hemorrhage that is most frequently GI, nasal, Mo subgaleal, intracranial, or post-circumcision. (Since the baby had no other s/sx other than jaundice, this is less likely)
Hemolytic disease of the newborn (Nelsons 21st, Chapter 124.2) - also known as erythroblastosis fetalis, is caused by the transplacental passage of maternal antibodies directed against paternally derived RBC antigens causing hemolysis in the infant; associated primarily with incompatibility of ABO blood groups and the RhD antigen. (Since both baby’s and mother’s blood type are A+, this is less likely)
“
"35-year old G1P1 diabetic mother with BT O+ delivered 5 weeks before EDC. Baby limp and gasping, with cyanotic face, pale body, weak pulses and no response to stimulation/suctioning. APGAR score? A. 1 B. 3 C. 4 D. 2 "
D
Gasping is 1
"Who is at risk to develop HMD? A. Diabetic mother B. Hypertensive mother C. Maternal use of opiates D. Prolonged rupture of membrane "
A
The risk factors for development of RDS increases with maternal diabetes, multiple births, CS delivery, precipituous delivery, asphyxia, cold stress, and maternal history of previously infected infants. - (21st Nelson, page 932)
"Which of the following is characterized by intractable neonatal hypoglycemia, ear creases, macroglossia, facial nevus flemens, increased risk for Wilm’s tumor, renal medullary dysplasia…? A. Turner Syndrome B. Pierre-Robin Syndrome C. Pierre-Robin Syndrome D. Beckwith-Wiedemann Syndrome "
D
Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by neonatal hypoglycemia, macrosomia, macroglossia, hemihyperplasia, omphalocele, embryonal tumors (e.g., Wilms tumor, hepatoblastoma, neuroblastoma, and rhabdomyosarcoma), visceromegaly, adrenocortical cytomegaly, renal abnormalities (e.g., medullary dysplasia, nephrocalcinosis, medullary sponge kidney, and nephromegaly), and ear creases/pits. (From Genetics NCBI website)