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Table 3 Self-reported practices of primary-care pediatricians on the management of celiac disease (CD) in children

From: A survey of primary-care pediatricians regarding the management of Helicobacter pylori infection and celiac disease

 

Number/ Total (percent)

Weighted percent*

Comment [6]

Reasons for testing for CD

  

Patients with CD may present with a wide range of symptoms and signs or be asymptomatic

 Chronic/intermittent diarrhea

100/108 (93%)

92%

 

 Growth impairment

105/108 (97%)

98%

 

 IDA

102/108 (94%)

95%

 

 Abdominal pain

92/108 (85%)

86%

 

Reasons for screening for CD

  

First-degree relatives with CD, type 1 diabetes, Down syndrome, Turner syndrome autoimmune thyroid disease, Williams syndrome, IgA deficiency and autoimmune liver disease.

 Autoimmune diseases, e.g., type 1 diabetes

99/108 (92%)

91%

 

 Down syndrome

66/108 (61%)

62%

 

 First-degree relatives of CD patients

106/108 (98%)

98%

 

Referral for diagnosis in suspected cases of CD**

 Specialist in gastroenterology

17/108 (16%)

16%

 

 Serological assays

108/108 (100%)

100%

Recommended as the first tool to identify patients with symptoms and signs suggestive of CD for further diagnostic workup

 In cases of positive serological test; referral to specialist in gastroenterology for final diagnosis.

96/108 (89%)

90%

If anti-TG2 antibody testing is positive, then patients should be referred to a pediatric gastroenterologist for further diagnostic workup

 Final decision of intestinal biopsy by specialist in gastroenterology

106/108 (98%)

98%

 

Treatment and follow-up**

 Recommend on gluten free diet only after diagnosis of CD

107/107 (100%)

100%

 

 Recommend yearly follow-up for physical growth

106/108 (98%)

98%

 

 Recommend follow-up by specialist in gastroenterology

69/108 (64%)

65%

 
  1. *Inverse probability weighting; **Physicians who answered “always” or “usually”. CD Celiac disease, IDA Iron deficiency anemia, IgA Immunoglobulin A