Patient satisfaction with the cervical ripening balloon as a method for induction of labour: a randomised controlled trial
| Autor: | Shephali Tagore, Ng Gyh, Tan Tl, Kyaw Eep, Lim Se, Yeo Gsh |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Adult
medicine.medical_specialty genetic structures medicine.medical_treatment Cervix Uteri law.invention Young Adult 03 medical and health sciences 0302 clinical medicine Patient satisfaction Randomized controlled trial Pregnancy law Oxytocics Patient experience Humans Pain Management Medicine Caesarean section Labor Induced Prospective Studies 030212 general & internal medicine Prospective cohort study 030219 obstetrics & reproductive medicine Cesarean Section business.industry Obstetrics Vaginal delivery Balloon catheter General Medicine Balloon Occlusion Delivery Obstetric medicine.disease eye diseases Patient Satisfaction Original Article Female business Cervical Ripening |
| Zdroj: | Singapore Medical Journal. 59:419-424 |
| ISSN: | 0037-5675 |
| Popis: | INTRODUCTION Evidence has shown that balloon catheters are as effective as prostaglandins (PGE) in achieving vaginal delivery within 24 hours of the start of induction of labour (IOL), with lower rates of uterine hyperstimulation, and similar Caesarean section and infection rates. International guidelines recommend mechanical methods as a method of IOL. We designed a prospective randomised controlled study to evaluate patient acceptance of the cervical ripening balloon (CRB) for IOL. METHODS Suitable women with a singleton term pregnancy without major fetal anomaly suitable for vaginal delivery were recruited and randomised to receive the CRB or PGE on the day of IOL. Characteristics of the women, labour and birth outcomes were obtained from case notes. Pain and satisfaction scores were obtained by interviewing the women at IOL and after delivery. The main outcome measures were participant characteristics, labour and birth outcomes, pain score, satisfaction scores, and whether the participant would recommend the mode of IOL. RESULTS There was no difference in the pain score between the two groups at the start of IOL, but thereafter, pain scores were lower in the CRB group compared to the PGE group (4.5 ± 2.3 vs. 5.6 ± 2.4, p = 0.044). Women were equally satisfied with both methods and equally likely to recommend their method for IOL. CONCLUSION Patient experience of IOL with CRB or PGE was equally satisfactory, although pain during induction was lower in the CRB group. We found that both methods of IOL are acceptable to women and should be made available to provide more options. |
| Databáze: | OpenAIRE |
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