Font Luis, Lew Lily Q, Kupferman Fernanda, Rapaport Susana
Department of Pediatrics, Flushing Hospital Medical Center, Flushing, New York, USA.
Bol Asoc Med P R. 2007 Jan-Mar;99(1):13-7.
Newborn screening (NBS) program is a simple and inexpensive method for early detection and treatment of over forty conditions as of 2005. Most cases of congenital hypothyroidism (CH) are sporadic and occurs in 1 in 3500 live births. Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders that occurs in 1 in 1600 live births. The detection of CH is determined by either low T4 and/or elevated TSH and the detection of CAH is determined by elevated 17OH progesterone on Guthrie filter paper. Infants who meet the above criteria on NBS for either condition must undergo confirmatory testing.
Is the incidence of CH and CAH at FHMC, a community hospital in northern Queens, New York serving a multiethnic population different from theincidence of CH and CAH in New York State (NYS)?
DESIGN/METHODS: We reviewed records of the infants recalled and confirmed to have CH and CAH for 2000, 2001 and 2004 and compared with reported incidence of the same conditions in NYS.
The total number of live births in NYS was 760,112 and in FHMC 6348 for the three years studied, accounting for 0.7 to 0.8% of total NYS live births. The population served by FHMC included 43% White, 35% Asian, 16% Hispanic, 3% Afro-American and 3% other. A total of 5 patients were identified to have CH in the three years studied, accounting for an incidence of 0.12 (p > 0.05). Three patients were identified to have CAH in 2004 or an incidence of 1.4 (p < 0.05). [Table 1].
The incidence rate of CH was similar to that of NYS. However, the incidence rate of CAH at FHMC was greater than that reported by NYS. This difference in incidence rate for CAH may be related to the ethnic composition of the population that FHMC serves. Pediatricians and pediatric endocrinologists must be cognizant of the signs and symptoms of CAH in certain populations known to have higher incidence for this condition. Further follow up of incidence rate for CAH at FHMC is indicated since CAH was added to the NBS in 2003.
截至2005年,新生儿筛查(NBS)项目是一种用于早期检测和治疗四十多种疾病的简单且经济的方法。大多数先天性甲状腺功能减退症(CH)病例为散发性,在每3500例活产中出现1例。先天性肾上腺皮质增生症(CAH)是一组常染色体隐性疾病,在每1600例活产中出现1例。CH的检测通过低T4和/或高促甲状腺激素来确定,CAH的检测通过Guthrie滤纸上17-羟孕酮升高来确定。在NBS中符合上述任何一种疾病标准的婴儿必须接受确诊检测。
纽约皇后区北部一家为多民族人群服务的社区医院——FHMC的CH和CAH发病率与纽约州(NYS)的CH和CAH发病率是否不同?
设计/方法:我们回顾了2000年、2001年和2004年被召回并确诊患有CH和CAH的婴儿记录,并与NYS报告的相同疾病发病率进行比较。
在研究的三年中,NYS的活产总数为760,112例,FHMC为6348例,占NYS活产总数的0.7%至0.8%。FHMC服务的人群包括43%白人、35%亚洲人、16%西班牙裔、3%非裔美国人和3%其他种族。在研究的三年中,共确定5例患有CH,发病率为0.12(p>0.05)。2004年确定3例患有CAH,发病率为1.4(p<0.05)。[表1]
CH的发病率与NYS相似。然而,FHMC的CAH发病率高于NYS报告的发病率。CAH发病率的这种差异可能与FHMC服务人群的种族构成有关。儿科医生和儿科内分泌学家必须认识到在已知CAH发病率较高的特定人群中CAH的体征和症状。由于CAH于2003年被纳入NBS,因此有必要对FHMC的CAH发病率进行进一步随访。