全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Randomized Comparison of Isosorbide Mononitrate and PGE2 Gel for Cervical Ripening at Term including High Risk Pregnancy

DOI: 10.1155/2014/147274

Full-Text   Cite this paper   Add to My Lib

Abstract:

Aims. Prostaglandin E2 is the most commonly used drug for cervical ripening prior to labour induction. However, there are concerns regarding uterine tachysystole and nonreassuring fetal heart (N-RFH). Isosorbide mononitrate (IMN) has been used successfully for cervical ripening. The present study was conducted to compare the two drugs for cervical ripening at term in hospital. Methods. Two hundred women with term pregnancies referred for induction of labour with Bishop score less than 6 were randomly allocated to receive either 40?mg IMN tablet vaginally ( ) or 0.5?mg PGE2 gel intracervically ( ). Adverse effects, progress, and outcomes of labour were assessed. Results. PGE2 group had significantly higher postripening mean Bishop score, shorter time from start of medication to vaginal delivery (13.37 ± 10.67 hours versus 30.78 ± 17.29 hours), and shorter labour-delivery interval compared to IMN group (4.53 ± 3.97 hours versus 7.34 ± 5.51 hours). However, PGE2 group also had significantly higher incidence of uterine tachysystole (15%) and N-RFH (11%) compared to none in IMN group, as well as higher caesarean section rate (27% versus 17%). Conclusions. Cervical ripening with IMN was less effective than PGE2 but resulted in fewer adverse effects and was safer especially in high risk pregnancies. 1. Introduction Labour induction in unfavourable cervix is tedious and prolonged resulting in high incidence of failed induction and hence operative deliveries. Therefore, prostaglandin E2 (PGE2, dinoprostone gel) and PGE1 (misoprostol) are commonly used for success of labour induction and to reduce rate of caesarean section [1]. Prostaglandins are quite effective for cervical ripening [2] but have a high incidence of hyperstimulation and tachysystole which may compromise the fetus [3, 4]. An ideal cervical ripening agent should ripen cervix without stimulating uterine activity. Nitric oxide (NO) donors such as isosorbide mononitrate (IMN) and glyceryl trinitrate (GTN) effectively induce cervical ripening without causing uterine contractions by rearranging cervical collagen and ground substance which softens the cervix [5–8]. The efficacy and safety of NO donors have been established in various studies [9–12] but there has been no Indian study to compare IMN with PGE2 gel for preinduction cervical ripening in term high risk pregnancies. With this background in mind, the present study was planned to compare the efficacy and safety of IMN with PGE2 gel for cervical ripening in term pregnancy in Indian population. 2. Methods A prospective, randomized study was

References

[1]  M. J. N. C. Keirse and H. J. De Koning Gans, “Randomized comparison of the effects of endocervical and vaginal prostaglandin E 2 gel in women with various degrees of cervical ripeness,” The American Journal of Obstetrics and Gynecology, vol. 173, no. 6, pp. 1859–1864, 1995.
[2]  M. J. N. C. Keirse, “Prostaglandins in preinduction cervical ripening: meta-analysis of worldwide clinical experience,” Journal of Reproductive Medicine for the Obstetrician and Gynecologist, vol. 38, supplement 1, pp. 89–100, 1993.
[3]  Y. Herabutya, P. O-Prasertsawat, and J. Pokpirom, “A comparison of intravaginal misoprostol and intracervical prostaglandin E2 gel for ripening of unfavorable cervix and labor induction,” Journal of Obstetrics and Gynaecology Research, vol. 23, no. 4, pp. 369–374, 1997.
[4]  D. A. Wing, M. M. Jones, A. Rahall, T. M. Goodwin, and R. H. Paul, “A comparison of misoprostol and prostaglandin E2 gel for preinduction cervical ripening and labor induction,” The American Journal of Obstetrics and Gynecology, vol. 172, no. 6, pp. 1804–1810, 1995.
[5]  W. Tschugguel, C. Schneeberger, H. Lass et al., “Human cervical ripening is associated with an increase in cervical inducible nitric oxide synthase expression,” Biology of Reproduction, vol. 60, no. 6, pp. 1367–1372, 1999.
[6]  M. A. Ledingham, A. J. Thomson, A. Young, L. M. Macara, I. A. Greer, and J. E. Norman, “Changes in the expression of nitric oxide synthase in the human uterine cervix during pregnancy and parturition,” Molecular Human Reproduction, vol. 6, no. 11, pp. 1041–1048, 2000.
[7]  M. V?is?nen-Tommiska, M. Nuutila, K. Aittom?ki, V. Hiilesmaa, and O. Ylikorkala, “Nitric oxide metabolites in cervical fluid during pregnancy: further evidence for the role of cervical nitric oxide in cervical ripening,” The American Journal of Obstetrics and Gynecology, vol. 188, no. 3, pp. 779–785, 2003.
[8]  K. Chwalisz, S. Shao-Qing, R. E. Garfield, and H. M. Beier, “Cervical ripening in guinea-pigs after a local application of nitric oxide,” Human Reproduction, vol. 12, no. 10, pp. 2093–2101, 1997.
[9]  B. Chanrachakul, Y. Herabutya, and P. Punyavachira, “Potential efficacy of nitric oxide for cervical ripening in pregnancy at term,” International Journal of Gynecology and Obstetrics, vol. 71, no. 3, pp. 217–219, 2000.
[10]  B. Chanrachakul, Y. Herabutya, and P. Punyavachira, “Randomized comparison of glyceryl trinitrate and prostaglandin E2 for cervical ripening at term,” Obstetrics and Gynecology, vol. 96, no. 4, pp. 549–553, 2000.
[11]  B. Chanrachakul, Y. Herabutya, and P. Punyavachira, “Randomized trial of isosorbide mononitrate versus misoprostol for cervical ripening at term,” International Journal of Gynecology and Obstetrics, vol. 78, no. 2, pp. 139–145, 2002.
[12]  Y. Sharma, S. Kumar, S. Mittal, R. Misra, and V. Dadhwal, “Evaluation of glyceryl trinitrate, misoprostol, and prostaglandin E 2 gel for preinduction cervical ripening in term pregnancy,” Journal of Obstetrics and Gynaecology Research, vol. 31, no. 3, pp. 210–215, 2005.
[13]  I. Osman, F. MacKenzie, J. Norrie, H. M. Murray, I. A. Greer, and J. E. Norman, “The “PRIM” study: a randomized comparison of prostaglandin E2 gel with the nitric oxide donor isosorbide mononitrate for cervical ripening before the induction of labor at term,” American Journal of Obstetrics & Gynecology, vol. 194, no. 4, pp. 1012–1021, 2006.
[14]  C. D. Bates, A. E. Nicoll, A. B. Mullen, F. Mackenzie, A. J. Thomson, and J. E. Norman, “Serum profile of isosorbide mononitrate after vaginal administration in the third trimester,” BJOG, vol. 110, no. 1, pp. 64–67, 2003.
[15]  Dorland's Medical Dictionary for Health Consumers, 2007.
[16]  S. S. Bollapragada, F. MacKenzie, J. D. Norrie et al., “Randomised placebo-controlled trial of outpatient (at home) cervical ripening with isosorbide mononitrate (IMN) prior to induction of labour—clinical trial with analyses of efficacy and acceptability. The IMOP Study,” BJOG, vol. 116, no. 9, pp. 1185–1195, 2009.
[17]  M. Bullarbo, M. E. Orrskog, B. Andersch, L. Granstr?m, A. Norstr?m, and E. Ekerhovd, “Outpatient vaginal administration of the nitric oxide donor isosorbide mononitrate for cervical ripening and labor induction postterm: a randomized controlled study,” American Journal of Obstetrics and Gynecology, vol. 196, no. 1, pp. 50.e1–50.e5, 2007.
[18]  S. M. Habib, S. S. Emam, and A. S. Saber, “Outpatient cervical ripening with nitric oxide donor isosorbide mononitrate prior to induction of labor,” International Journal of Gynecology and Obstetrics, vol. 101, no. 1, pp. 57–61, 2008.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133