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A Prospective observational study to assess the efficacy of oral progestogen in patients with first trimester threatened miscarriage

dc.contributor.affiliation#PLACEHOLDER_PARENT_METADATA_VALUE#en_US
dc.contributor.authorMazrin Nur Mohd Alien_US
dc.contributor.supervisorMuna Khaleel Al-Kubaisi, Ph.Den_US
dc.contributor.supervisorFaridah Mohd Yusof, Ph.Den_US
dc.date.accessioned2024-10-09T04:37:43Z
dc.date.available2024-10-09T04:37:43Z
dc.date.issued2021
dc.description.abstractMiscarriage is a common complication of pregnancy occurring in 15-20% of all clinically recognized pregnancies. Threatened miscarriage is characterised by vaginal bleeding associated with or without abdominal pain, where the cervix is closed and the fetus is still viable intrauterine. The aim of this study was to establish the efficacy of oral progestogen (intervention group) compared to conservative management, which was bed rest (control group) in subjects with the first trimester threatened miscarriage. The primary outcome of this study was represented based on the number of miscarriages by 20 weeks of gestation. This prospective observational study was conducted at gynaecology ward and Early Pregnancy Assessment Unit (EPAU) of Hospital Sultanah Nur Zahirah and the Department of Obstetrics and Gynaecology, Sultan Ahmad Shah Medical Centre IIUM for ten months, from June 2019 until March 2020. A total of 217 pregnant women were recruited as the subjects in this study. They were presented with threatened miscarriage of less or equal to 12 weeks of gestation, who fulfilled inclusion criteria and provided informed consent. They were divided into the intervention and control groups. In the intervention group, the subjects were given 40 mg (4 tablets) of dydrogesterone orally at once, then 10 mg (1 tablet) in the interval of every 8 h until the symptoms abate, while the subjects in the control group were advised for bed rest as conservative management. The baseline demographic data in both studied groups were similar and there was no significant (p>0.05) difference in age, BMI, parity, and time interval to pregnancy in both groups. Based on the outcome, there was a smaller number of miscarriages in the intervention group (23, 46%) compared to the control group (27, 54%). However, it was not statistically significant (p>0.05). In conclusion, oral progestogen therapy was an ineffective way to reduce the number of miscarriages in patients with the first trimester threatened miscarriage.en_US
dc.description.callnumbert RG 129 P66 M476P 2021en_US
dc.description.identifierA Prospective observational study to assess the efficacy of oral progestogen in patients with first trimester threatened miscarriageen_US
dc.description.identityt11100436582MazrinNurBintiMohdAlien_US
dc.description.kulliyahKulliyyah of Medicineen_US
dc.description.nationalityMalaysianen_US
dc.description.notesThesis (MOG)--International Islamic University Malaysia, 2021.en_US
dc.description.physicaldescriptionxii, 45 leaves : colour illustrations ; 30cm.en_US
dc.description.programmeMaster of Obstetrics and Gynaecologyen_US
dc.identifier.urihttps://studentrepo.iium.edu.my/handle/123456789/10892
dc.language.isoenen_US
dc.publisherKuantan, Pahang : Kulliyyah of Medicine, International Islamic University Malaysia, 2021en_US
dc.subject.lcshHospital Sultanah Nur Zahirah -- Early Pregnancy Assessment Unit (EPAU) -- Malaysiaen_US
dc.subject.lcshSultan Ahmad Shah Medical Centre -- Department of Obstetrics and Gynaecology -- Malaysiaen_US
dc.subject.lcshProgestational hormones -- Therapeutic use -- Effectivenessen_US
dc.subject.lcshMiscarriage -- Treatment -- Complicationsen_US
dc.subject.lcshPregnancy -- Trimester, Firsten_US
dc.titleA Prospective observational study to assess the efficacy of oral progestogen in patients with first trimester threatened miscarriageen_US
dc.typeMaster Thesisen_US
dspace.entity.typePublication

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