Pediatric Shelf: Quick Hits Flashcards

(42 cards)

0
Q

Acetaminophen OD

A

Nausea, vomiting, asx until 24 hours ingestion

No acute hematemesis

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1
Q

Iron toxicity

A

Abdominal pain, vomiting, HEMATEMESIS, diarrhea, hypotensive shock, metabolic acidosis; hepatic necrosis, pyloric stenosis

  • Dx*: anion gap metabolic acidosis, RADIOPAQUE
  • Tx*: whole bowel irrigation, deferoxamine, supportive care
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2
Q

Aspirin OD

A

Tinnitus, fever, hyperpnea, metabolic acidosis; not radiopaque and would not appear on abdominal Xray

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3
Q

Lead OD

A

Abdominal pain, vomiting, anemia, behavioral problems; radiopaque on X-ray; not corrosive to gastric mucosa

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4
Q

Vitamin A OD

A

nausea, vomiting, bury vision

pseudotumor cerebri; no hematemesis

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5
Q

Vitamin B12 OD

A

Water soluble, large amounts unlikely to cause toxicity

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6
Q

Vitamin D OD

A

Nausea, vomiting, confusion, polyuria, polydipsia, does not erode gastric mucosa or cause hematemesis

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7
Q

Vitamin K OD

A

Hemolytic anemia and hyperbilirubinemia

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8
Q

Causes of aplastic anemia

A

Drugs, toxic chemicals, idiopathic, viral infecitons, immune disorders, thymoma

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9
Q

Fanconi anemia

A

MC congenital cause of aplastic anemia

  • Autosomal recessive or X linked, cancer predisposition*
  • Pt*: Bone marrow failure, short stature, abnormal thumbs, hypogonadism, hypo/hyperpigmented areas, cafe au late, strabismus, low set ears, middle ear abnormalities
  • Dx*: chromosomal breaks on genetic analysis
  • Tx*: hematopoietic stem cell transplant
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10
Q

G6PD deficiency

A

RBC enzyme deficiency, oxidant drugs and infection cause hemolysis

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11
Q

Benzene

A

Chemical that causes aplastic anemia

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12
Q

Thymic tumors

A

MC in older women, pure red cell aplasia (ISOLATED)

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13
Q

Autoimmune pernicious anemia

A

Anti intrinsic factor autoantibodies= cobalamin deficiency

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14
Q

Sun protection

A

Apply sunscreen 30 minutes before sun exposure
Remain indoors from 10 to 4
Wear protective clothing
Avoid tanning beds

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15
Q

Breastfeeding failure jaundice

A

First week of life
Lactation resultin gin: decreased bilirubin elimination, increased enterohepatic circulation, unconjugated hyperbilirubimemia
CM: suboptimal breastfeeding, signs of dehydration

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16
Q

Breast milk jaundice

A

3-5 days, peaks at 2 weeks
High level of beta glucuronidase in breast milk deconjugate intestinal bilirubin and increase enterohepatic circulation
CM: adequate breast feeding, normal examination, no signs of dehydration

17
Q

Alloimune hemolytic disease

A

Hemolysis of RBCs due to ABO or Rh incompatibility

18
Q

Biliary atresia

A

Conjugated hyperbilirubinemia, in first 2 months of life

Clay colored stools, dark urine, enlarged liver

19
Q

Dubin Johnson

A

Autosomal recessive, conjugated hyperbilirubinemia, asx except scleral icterus

20
Q

Galactosemia

A

Conjgated hyperbilirubinemia, Galactose 1 phosphade uridyl transferase deficiecny, vomiting, growth failure, inability to digest breast milk

21
Q

Treatment for breastfeeding failure jaundice

A

Increase the number of feeds; breastfeed every 15 minutes per side every 2-3 hours

22
Q

Soy formula

A

Tx for jaundice cause by galactosemia

23
Q

B1 deficiency; thiamine

A

Beriberi (peripheral neuropathy)

Wernicke Korsakoff

24
B2 deficiency; riboflavin
Angular cheilosis, stomatitis, glossitis Normocytic anemia Seborrheaic dermatitis *No toxic effects because water soluble and excreted in urine
25
B3 deficiency; niacin
Pellagra (dermatitis, diarrhea, delusions, dementia)
26
B6 deficiency; pyridoxine
Cheilosis, stomatitis, glossitis | Irritability, confusion, depression
27
B9 deficiency; folate
Megaloblastic anemia | Neural tube defects
28
B12 deficiency; cobalamin
Megaloblastic anemia | Neurologic deifits
29
C deficiency; ascorbic acid
Scurvy
30
K deficiency
Impaired coagulation; can be in patients with long term abx
31
ADHD
Inattention, impulsivity, hyperactivity in 2 or more settings; academic difficulty, impaired family and peer relationships
32
Myotonic muscular dystrophy
Autosomal dominant Grip myotonia (delayed muscle relaxation), muscle weakness, facial weakness, foot drop, dysphagia, cardiac conduction anomalies, cataracts, testicular atrophy, baldness *Chromosome 19, CTG trinucleotide repeat* Death from respiratory failure
33
Duchenne dystrophy
X linked recessive (deletion of dystrophin on chromosome 21) Onset age 2-3 Gower, pseudohypertrophy, progressive weakness Wheelchair dependence Death by 20-30
34
Becker dystrophy
X linked recessive (deletion of dystrophin on chromosome 21) Onset 5-15y Death by 40-50 from heart failure
35
Fragile X syndrome
X linked dominant; *macroorchidism*, low muscle tone, facial weakness
36
Cri du Chat
Deletion of 5p | Moonlike facies, hypertelorism, bilateral epicanthal folds, high arched palate, wide flat nasal bridge, cat like cry
37
Wolf Hirschorn sndorme
Deletion of 4p | Microcephaly, bilateral epicanthal folds, Greek helmet facies, beaked nose, cardiac malformations
38
13q deletion
Microcephaly, flat wide nasal bridge, LBW, failure to thrive, ocular malformations, syndactyly
39
18q deletion
Hypotonia, froglike legs, depressed midface, protruded mandible, deep set eyes, short upper lip, everted lower lip, prominent anti helix of ears, mental retardation, belligerent personality
40
21q deletion
Hypertonia, downward slanting palpebral fissures, high palate, prominent nasal bridge, large low set ears, micrognathia, mental retardation
41
Interosseous lines
Place when emergency access necessary and peripheral access cannot be obtained