Value of fetal fibronectin as a predictor of preterm delivery for a low-risk population

被引:32
作者
Greenhagen, JB [1 ]
VanWagoner, J [1 ]
Dudley, D [1 ]
Hunter, C [1 ]
Mitchell, M [1 ]
Logsdon, V [1 ]
Casal, D [1 ]
Varner, M [1 ]
机构
[1] ADEZA BIOMED,SUNNYVALE,CA
关键词
fetal fibronectin; preterm birth; population screening;
D O I
10.1016/S0002-9378(96)80052-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: We examined clinical value of cervical fetal fibronectin detection by a quantitative enzyme-linked immunosorbent assay as a predictor of preterm delivery in a population (n = 111) of middle-class pregnant women considered to be at low risk for preterm delivery. STUDY DES[GN: In this prospective study, fetal fibronectin samples from cervicovaginal secretions were obtained biweekly from 24 to 34 weeks' gestation. RESULTS: Twenty-two (20%) patients had at least one positive fetal fibronectin test result. Eleven women (10%) were delivered spontaneously at <37 weeks; seven of these had at [east: one positive fetal fibronectin lest result (positive predictive value = 31.8%, sensitivity = 63.6). An additional three women were delivered prematurely because of other obstetric indications, and all had negative fetal fibronectin test results. The remaining 15 patients with at least one positive fetal fibronectin test result were delivered at term (greater than or equal to 37 weeks). Of the seven women with positive fetal fibronectin results who were delivered prematurely, five were delivered within 2 weeks of obtaining a positive result. However, there were no obvious clinical discriminators between true-positive and false-positive: fetal fibronectin results. Eighty-nine women tested negative, and 85 of these women were delivered at term (specificity = 82.0%). The negative predictive value of fetal fibronectin as a predictor of term delivery in this low-risk population is 96.6%, with odds ratio = 8.8 (95% confidence interval 1.9 to 40.3), relative risk = 6.9 (95% confidence interval 1.8 to 26.6), and Fisher Exact Test p = 0.007. CONCLUSIONS: Although negative biweekly fetal fibronectin determinations for prediction of preterm delivery in this low-risk obstetric population correlate well with the absence of preterm delivery, they are of limited clinical value for the prediction of preterm birth.
引用
收藏
页码:1054 / 1056
页数:3
相关论文
共 16 条
[1]   PHARMACOLOGIC INHIBITION OF PRETERM LABOR [J].
CARITIS, SN ;
EDELSTONE, DI ;
MUELLERHEUBACH, E .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1979, 133 (05) :557-578
[2]   PREVENTING PRETERM BIRTH [J].
CREASY, RK .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (10) :727-729
[3]   PRETERM BIRTH PREVENTION - WHERE ARE WE [J].
CREASY, RK .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 168 (04) :1223-1230
[4]  
Goldenberg R., 1995, American Journal of Obstetrics and Gynecology, V172, P254
[5]   FETAL FIBRONECTIN DETECTION FOR PREDICTION OF PRETERM BIRTH IN LOW-RISK WOMEN [J].
HELLEMANS, P ;
GERRIS, J ;
VERDONK, P .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1995, 102 (03) :207-212
[6]   DO TOCOLYTIC AGENTS STOP PRETERM LABOR - A CRITICAL AND COMPREHENSIVE REVIEW OF EFFICACY AND SAFETY [J].
HIGBY, K ;
XENAKIS, EMJ ;
PAUERSTEIN, CJ ;
HARBERT, GM ;
JONES, H ;
MERKATZ, IR ;
CREASY ;
WOODS, J ;
CEFALO, RC ;
GIBBS, RS ;
SCOTT, S ;
QUEENAN, JT ;
KIRSCHBAUM ;
NELSON, K .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 168 (04) :1247-1259
[7]   THE EFFECTIVENESS OF PRETERM-BIRTH PREVENTION EDUCATIONAL-PROGRAMS FOR HIGH-RISK WOMEN - A METAANALYSIS [J].
HUESTON, WJ ;
KNOX, MA ;
EILERS, G ;
PAUWELS, J ;
LONSDORF, D .
OBSTETRICS AND GYNECOLOGY, 1995, 86 (04) :705-712
[8]  
IRON O, 1994, AM J OBSTET GYNECOL, V170, P384
[9]   THE PRESENCE OF CERVICAL AND VAGINAL FETAL FIBRONECTIN PREDICTS PRETERM DELIVERY IN AN INNER-CITY OBSTETRIC POPULATION [J].
LOCKWOOD, CJ ;
WEIN, R ;
LAPINSKI, R ;
CASAL, D ;
BERKOWITZ, G ;
ALVAREZ, M ;
BERKOWITZ, RL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 169 (04) :798-804
[10]   FETAL FIBRONECTIN IN CERVICAL AND VAGINAL SECRETIONS AS A PREDICTOR OF PRETERM DELIVERY [J].
LOCKWOOD, CJ ;
SENYEI, AE ;
DISCHE, MR ;
CASAL, D ;
SHAH, KD ;
THUNG, SN ;
JONES, L ;
DELIGDISCH, L ;
GARITE, TJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (10) :669-674