2019
DOI: 10.1016/j.ejogrb.2019.01.023
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Cardiotocography alone vs. cardiotocography with ST segment analysis for intrapartum fetal monitoring in women with late-term pregnancy. A randomized controlled trial

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Cited by 7 publications
(15 citation statements)
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“…In the present population study, we did not find that the introduction of STAN had any effect on the occurrence of intrapartum cesarean sections. This is in line with results from previous randomized controlled trials comparing CTG plus STAN with CTG alone 12–15 . However, meta‐analyses of six randomized controlled trials suggested that women randomized to fetal monitoring with STAN plus CTG had a reduced risk of instrumental vaginal delivery compared with women randomized to CTG alone 13–15 …”
Section: Discussionsupporting
confidence: 88%
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“…In the present population study, we did not find that the introduction of STAN had any effect on the occurrence of intrapartum cesarean sections. This is in line with results from previous randomized controlled trials comparing CTG plus STAN with CTG alone 12–15 . However, meta‐analyses of six randomized controlled trials suggested that women randomized to fetal monitoring with STAN plus CTG had a reduced risk of instrumental vaginal delivery compared with women randomized to CTG alone 13–15 …”
Section: Discussionsupporting
confidence: 88%
“…This is in line with results from previous randomized controlled trials comparing CTG plus STAN with CTG alone. [12][13][14][15] However, meta-analyses of six randomized controlled trials suggested that women randomized to fetal monitoring with STAN plus CTG had a reduced risk of instrumental vaginal delivery compared with women randomized to CTG alone. [13][14][15] We found that the introduction of STAN increased the occurrence of Apgar score <7 at 5 min after birth.…”
Section: Discussionmentioning
confidence: 99%
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“…41,42 The median sam ple size was 894 patients (range 100-47 062). Fifteen trials (45%) [25][26][27]31,32,36,39,41,[43][44][45][46]49,51,53 included patients at 36 weeks' ges tation or more, and the remaining included patients at 26-42 weeks' gestation. [28][29][30][33][34][35]38,40,50,52,54,56 Twothirds of trials ( 7 3 % ) i n c l u d e d p a t i e n t s w i t h h i g h r i s k p r e g n a n cies, [25][26][27][28][29][30][31][32][33][34]36,38,39,41,44,47,48,50,51,53,54 3 (9%) included patients with low risk ...…”
Section: Resultsmentioning
confidence: 99%
“…40,42,43,52 Three studies did not report on pregnancy risks. 45,46,49 The inclusion and exclusion criteria of each trial are summarized in Appendix 1, Supplementary Table 1.…”
Section: Resultsmentioning
confidence: 99%