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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
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Nutritional assessment during routine care at a cystic fibrosis center

Nutritional assessment during routine care at a cystic fibrosis center
  At diagnosis Every 3 months,
from birth to 24 months
Every 3 months Annually
Head circumference X* X    
Weight (to 0.1 kg) X X X  
Length (to 0.1 cm) X* X    
Height (to 0.1 cm) X   X  
Weight for length (birth to 24 months) X* X    
BMI percentile (24 months to adult) X   X  
Biologic parents' height X      
Pubertal status, femaleΔ       X
Pubertal status, male       X
24-hour diet recall     X  
Nutritional supplement intake§     X  
Anticipatory dietary and feeding behavior guidance¥   X X  
This table describes recommended office procedures for nutritional monitoring of children with cystic fibrosis. For recommendations for laboratory tests, refer to UpToDate topic and table on monitoring nutritional status for children with cystic fibrosis.

BMI: body mass index.

* If less than 24 months of age at diagnosis.

¶ Record in cm and sex-specific height percentile; note patient's target height percentile on all growth charts.

Δ Starting at age 9 years, use annual pubertal self-assessment form (patient, or parent and patient) or perform a clinician examination for breast and pubic hair and Tanner stage determination; note menarcheal status. Record month and year of menarche on all growth charts.

◊ Starting at age 10 years, use annual pubertal self-assessment form (patient, or parent and patient) or perform a clinician examination for genital development and pubic hair and Tanner stage determination.

§ A review of enzymes, vitamins, minerals, oral or enteral formulas, as well as herbal, botanical, and other complementary and alternative medicine products.

¥ Other team members may perform informal routine surveillance, but the center dietitian should perform the annual assessment and monitoring visits (every 3 months) in the first 2 years of life and for patients at nutritional risk.
Modified with permission from: Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 2002; 35:246. Copyright © 2002 Lippincott Williams & Wilkins.
Graphic 76676 Version 18.0

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