Commentary on 'How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?' by Grosse and Van Vliet, Hormone Research, 2007;67:284-291.

نویسنده

  • Kelly R Leight
چکیده

– It is difficult to calculate how many deaths could have been prevented by newborn screening for CAH unless there is a 100% autopsy rate for infant deaths. Due to the sudden onset of adrenal crisis, generally within the first 2 weeks of life, and various obstacles to obtaining a rapid diagnosis, undetected CAH-affected children who die are often classified as having died for some reason unrelated to CAH. Without performing an autopsy on every child that dies, we cannot know the true rate of death attributable to CAH. – The symptoms of adrenal crisis easily can be mistaken as signs of complications of prematurity, gastrological or renal difficulties, failure to thrive and any number of other conditions. Babies are misdiagnosed, therefore inappropriately treated, and may die without CAH ever having been identified as the true cause of death. – National Newborn Screening and Genetics Resource Center records for 2006 estimate 3.3 million babies had access to mandated CAH newborn screening last year. Genetic studies have shown that classical CAH occurs I strongly encourage further consideration of the conclusions made by Grosse and Van Vliet [1], published in the last issue of Hormone Research . While these researchers should be commended for examining the effectiveness of congenital adrenal hyperplasia (CAH) infant testing, their conclusion that infant death due to adrenal crisis in salt-wasting CAH in firstworld countries would be 4% or less without screening for CAH is highly questionable as well as dangerously narrow in its scope. CARES Foundation, Inc. is a non-profit organization that provides support to individuals and families affected by CAH, and I serve as its Executive Director. I am also the parent of a child with a form of CAH. I have seen the devastation that can occur when we fail to screen and families suffer unnecessary loss due to a lack of proper diagnosis. Grosse and Van Vliet’s conclusions fail to consider autopsy rates and misdiagnoses as well as ignore the plight of children living in economies that are neither ‘contemporary’ nor ‘advanced’. Any analysis must take into account the following: Received: February 27, 2007 Accepted: March 1, 2007 Published online: March 28, 2007 HORMONE RESEARCH

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

How many deaths can be prevented by newborn screening for congenital adrenal hyperplasia?

BACKGROUND/AIMS Congenital adrenal hyperplasia (CAH) is increasingly being included in newborn screening programs. Screening can prevent neonatal mortality in children with salt-wasting CAH, but the number of deaths prevented is not known. Cost-effectiveness analyses of screening require estimates of the probability of mortality in CAH. METHODS We reviewed the literature to identify cohort st...

متن کامل

The case for newborn screening for congenital adrenal hyperplasia in Australia.

TO THE EDITOR: We write to encourage policy debate over newborn screening for congenital adrenal hyperplasia (CAH). Classical CAH is a severe, life-threatening disease affecting about one in 15 000 liveborn infants in Australia.1 An inexpensive screening test for newborns is available, but this test is not included in the current newborn screening program in Australia. Three-quarters of childre...

متن کامل

Early Diagnosis of Children with Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency by Newborn Screening

Congenital adrenal hyperplasia (CAH) comprises a group of rare autosomal recessively inherited disorders of cortisol biosynthesis in the adrenal cortex. More than 95% are based on a defect in the CYP21A2 gene causing 21-hydroxylase deficiency. Newborn screening (NBS) for CAH by means of 17-hydroxy-progesterone (17-OHP) determination in dried whole blood on filter paper has been introduced as pa...

متن کامل

Growth Pattern of Untreated Boys with Simple Virilizing Congenital Adrenal Hyperplasia Indicates Relative Androgen Insensitivity during the First Six Months of Life

Context: Mild forms of simple virilizing congenital adrenal hyperplasia (CAH) may be missed in newborn screening. In the pre-newborn-screening era, missed diagnosis of simple virilizing CAH was not infrequent in boys. Elevated adrenal androgens lead to accelerated growth and bone maturation. Traditional treatment of CAH consists of the suppression of ACTH through glucocorticoid replacement, in ...

متن کامل

Growth pattern of untreated boys with simple virilizing congenital adrenal hyperplasia indicates relative androgen insensitivity during the first six months of life.

CONTEXT Mild forms of simple virilizing congenital adrenal hyperplasia (CAH) may be missed in newborn screening. In the pre-newborn-screening era, missed diagnosis of simple virilizing CAH was not infrequent in boys. Elevated adrenal androgens lead to accelerated growth and bone maturation. Traditional treatment of CAH consists of the suppression of ACTH through glucocorticoid replacement, in a...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Hormone research

دوره 68 4  شماره 

صفحات  -

تاریخ انتشار 2007