2003
DOI: 10.1016/s0266-6138(03)00020-2
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A randomised controlled trial of admission electronic fetal monitoring in normal labour

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Cited by 28 publications
(33 citation statements)
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“…In a previous study, midwives excluded 13% of the eligible population as they were subjectively judged to be too far advanced in labour or too distressed to give informed consent. 35 Recruitment and randomisation in labour have the advantage of higher yield and clinicians do routinely obtain consent during labour for a wide variety of necessary standard obstetric interventions, such as analgesia and caesarean section. 8,36 In the research setting, the investigator is required to explain the study rationale, risks, benefits and participant rights.…”
Section: Discussionmentioning
confidence: 99%
“…In a previous study, midwives excluded 13% of the eligible population as they were subjectively judged to be too far advanced in labour or too distressed to give informed consent. 35 Recruitment and randomisation in labour have the advantage of higher yield and clinicians do routinely obtain consent during labour for a wide variety of necessary standard obstetric interventions, such as analgesia and caesarean section. 8,36 In the research setting, the investigator is required to explain the study rationale, risks, benefits and participant rights.…”
Section: Discussionmentioning
confidence: 99%
“…Categorisation of monitoring type for data collection purposes was based on the study reported by Cheyne and colleagues in 2003 [26] where continuous CTG was defined as use of the CTG machine for fetal heart monitoring for 75% or more of the labour. For this study, the category, electronic fetal monitoring (EFM), comprised all fetal heart monitoring performed with the CTG machine i.e.…”
Section: Methodsmentioning
confidence: 99%
“…39 We considered women to be eligible for recruitment if they attended a participating maternity unit for assessment of labour and were primiparous, at term, and assessed as low risk on the basis of criteria used in previous intrapartum studies (box). [40][41][42] We used the same eligibility criteria in both experimental and control groups. In order to reduce confounding variables, we excluded multiparous women from the trial.…”
Section: Recruitment and Randomisationmentioning
confidence: 99%