Robertson Charlene M T, Watt Man-Joe, Yasui Yutaka
Section of Neurosciences, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
JAMA. 2007 Jun 27;297(24):2733-40. doi: 10.1001/jama.297.24.2733.
Although cerebral palsy (CP) among extremely premature infants has been reported as a major morbidity outcome, there are difficulties comparing published CP rates from many sites over various birth years.
To assess the changes in population-based, gestational age-specific prevalence rates of CP among extremely premature infants over 30 years.
Prospective population-based longitudinal outcome study.
In Northern Alberta, 2318 infants 20 to 27 weeks' gestational age with birth weights of 500 to 1249 g were liveborn from 1974 through 2003. By 2 years of age, 1437 (62%) had died, 23 (1%) were lost to follow-up, and 858 (37%) had received multidisciplinary neurodevelopmental assessment.
Population-based prevalence rates of CP were determined. Logistic regression with linear spline was used to assess changes in CP prevalence over time.
At age 2 years, 122 (14.2%) of 858 survivors had CP. This diagnosis was confirmed for each child by age 3 years or older. Among those whose gestational age was 20 to 25 weeks, population-based survival increased from 4% to 31% (P<.001), while CP prevalence per 1000 live births increased monotonically from 0 to 110 until the years 1992-1994 (P<.001) and decreased thereafter to 22 in the years 2001-2003 (P<.001). Among those whose gestational age was 26 to 27 weeks, population-based survival increased from 23% to between 75% and 80% (P<.001), while CP prevalence per 1000 live births increased monotonically from 15 to 155 until the years 1992-1994 (P<.001) and then decreased to 16 in the years 2001-2003 (P<.001). For all survivors born in the years 2001-2003, CP prevalence was 19 per 1000 live births.
Population-based CP prevalence rates for children whose gestational age was 20 to 27 weeks and whose birth weight ranged from 500 to 1249 g show steady reductions in the last decade with stable or reducing mortality, reversing trends prior to 1992-1994.
尽管已有报道称极早产儿患脑瘫(CP)是主要的发病结局,但比较不同出生年份多个地点公布的脑瘫发病率存在困难。
评估30年间极早产儿中基于人群、按胎龄划分的脑瘫患病率变化。
基于人群的前瞻性纵向结局研究。
在阿尔伯塔省北部,1974年至2003年期间,有2318名孕20至27周、出生体重500至1249克的婴儿存活出生。到2岁时,1437名(62%)婴儿死亡,23名(1%)失访,858名(37%)接受了多学科神经发育评估。
确定基于人群的脑瘫患病率。采用带线性样条的逻辑回归评估脑瘫患病率随时间的变化。
在858名存活者中,122名(14.2%)在2岁时患脑瘫。每个儿童在3岁及以上时确诊该诊断。在孕20至25周的婴儿中,基于人群的存活率从4%增至31%(P<0.001),而每1000例活产中的脑瘫患病率在1992 - 1994年之前从0单调增至110(P<0.001),此后在2001 - 2003年降至22(P<0.001)。在孕26至27周的婴儿中,基于人群的存活率从23%增至75%至80%之间(P<0.001),而每1000例活产中的脑瘫患病率在1992 - 1994年之前从15单调增至155(P<0.001),然后在2001 - 2003年降至16(P<0.001)。对于2001 - 2003年出生的所有存活者,每1000例活产中的脑瘫患病率为19。
孕20至27周、出生体重500至1249克儿童的基于人群的脑瘫患病率在过去十年稳步下降,死亡率稳定或降低,扭转了1992 - 1994年之前的趋势。