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无应激试验反应性与孕周的关系。

Relationship of nonstress test reactivity and gestational age.

作者信息

Lavin J P, Miodovnik M, Barden T P

出版信息

Obstet Gynecol. 1984 Mar;63(3):338-44.

PMID:6700856
Abstract

The relationship between gestational age and reactivity during the nonstress test was evaluated in 297 high-risk patients. When the incidence of nonreactive tests at gestational ages of 28 to 44 weeks was evaluated week-by-week, either on the basis of tests performed or patients tested, there was no statistically significant relationship between reactivity and gestational age (P = .184 tests; P = .222 patients). Four grouped gestational-age intervals were evaluated. Interval A consisted of the period from 28 to 32 weeks' gestation, interval B consisted of the period from 33 to 36 weeks' gestation, interval C consisted of the period from 37 to 41 weeks' gestation, and interval D consisted of the period from 42 to 44 weeks' gestation. The incidences of nonreactive tests were 15.3, 3.9, 2.5, and 5.9% in intervals A, B, C, and D, respectively. The differences in the incidences of nonreactive tests between those performed in intervals A and B and intervals A and C were highly statistically significant (P less than .001). Differences in the incidences between other intervals did not reach statistical significance. The incidences of patients who experienced a nonreactive test were 10.2, 2.4, 2.8, and 4.7% in intervals A, B, C, and D, respectively. The differences in the incidences of patients who experienced a nonreactive test in intervals A and B and intervals A and C were highly statistically significant (P less than .001). Differences in the incidences between other intervals did not reach statistical significance.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对297名高危患者进行了非应激试验期间胎龄与反应性之间关系的评估。当按周评估28至44周胎龄时无反应试验的发生率时,无论是基于所进行的试验还是受检患者,反应性与胎龄之间均无统计学显著关系(试验:P = 0.184;患者:P = 0.222)。评估了四个分组的胎龄区间。A组为妊娠28至32周,B组为妊娠33至36周,C组为妊娠37至41周,D组为妊娠42至44周。A、B、C、D组无反应试验的发生率分别为15.3%、3.9%、2.5%和5.9%。A组与B组以及A组与C组之间无反应试验发生率的差异具有高度统计学显著性(P<0.001)。其他区间之间发生率的差异未达到统计学显著性。A、B、C、D组经历无反应试验的患者发生率分别为10.2%、2.4%、2.8%和4.7%。A组与B组以及A组与C组之间经历无反应试验患者发生率的差异具有高度统计学显著性(P<0.001)。其他区间之间发生率的差异未达到统计学显著性。(摘要截短于250字)

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