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Screening Protocols

INITIAL VISIT

 

 
NOTES
STOOL
Ova and parasites
3 early-morning stools separated by 24 hours
Giardia-specific antigen
1 early-morning stool; note: if child has bloody diarrhea, consider Shigella, Salmonella, E. coli 0157 and Campylobacter stool studies.
 
Recheck stool 2-3 weeks after completion of treatment
URINE
Clean catch or bag urine for urinalysis
Urinalysis is a simple screen for renal and systemic disease. Schistosoma haematobium should be considered in the older IA who has asymptomatic hematuria if the country of origin is located in West Africa (where prevalence rates of S. haematobium can exceed 90%)
BLOOD
Hemogram
Include red blood cell indices and white blood cell differential
Iron studies
 Ferritin, serum iron, iron saturation, CRP
Vitamin D, Ca, Phos
25 OH total vitamin D
Hb Electrophoresis
Consider initially or at 6 mo follow-up if there is unexplained anemia
Thyroid stimulating hormone, free thyroxine
 
G6PD
Areas where G6PD is common or if prescribing primaquine
Hepatitis A total
If positive, then hepatitis A core IgM antibody
Hepatitis B surface antigen
 
Hepatitis B core antibody
 
Hepatitis B surface antibody
 
Hepatitis C antibody
If positive, then hepatitis C RNA by PCR
HIV types 1 and 2 antibodies
 
RPR, VDRL or Anti-treponemal EIA
 
Newborn metabolic screen
For infants (0 to 12 months)
Malaria PCR
Endemic areas, known malarial illness in family1
Lead
 
Diphtheria anti-toxoid antibody2
 
Tetanus anti-toxoid antibody2
 
Poliovirus types I, II and III neutralizing antibody2
 
Varicella
For children >12 years old or w/ history of infection
Measles, mumps and rubella antibodies
If MMR documented
TST
Tuberculin skin test
 All children, regardless of BCG history
GrowthIGF1 and IGF BP-3If height is far below the 3rd percentile on presentation, or if catch-up growth is inadequate
 
6 MONTHS POST INITIAL VISIT
BLOOD
Hepatitis B panel
Only if child did not have immunity at initial visit
Hepatitis C antibody
 
HIV types 1 and 2 antibody
 
Iron studies
 
Vitamin D, Ca, PhosIf initial screen was abnormal and follow-up has not been done by primary care
TST
Tuberculin skin test
Only if first test was negative
 GrowthIGF1 and IGF BP-3If inadequate catch-up growth between first and second time periods
1 Send to Mayo; will do malarial smear if positive
2 All children over 9 mo old, with or without documentation of vaccination, should be tested for antibodies. Most children received the primary series of DPT, OPV and measles. Pertussis antibody titers do not correlate with immunity.
 

 


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