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Disusun oleh :
Alif Luqman Hakim 22010116210043
Bellakusuma N 22010116210023
Sherly Mediana 22010116210128
Risky Maulida Hasanah 22010116210146
Radityo Utomo 22010116210113
Azizatul Yaumul Adha 22010116210006
Aulia Izzati 22010116210082
Stefanie Pramudita Jaya 22010116210091
Pembimbing :
dr. Arufiadi Anityo, MSi.Med, Sp.OG (K)
C (COMPARISON)
There is no comparison in this study.
O (OUTCOME of interest)
Intrauterine balloon tamponade was attempted in 226 women: 171 after vaginal de-
livery (VD) (75.7%) and 55 during or after caesarean delivery (CD) (24.3%). The
global success rate was 83.2% (188/226) and was significantly higher after VD
(152/171,88.9%) than CD (36/55, 65.5%, P < 0.01).
Caesarean Delivery, estimated blood loss before IUBT and coagulopathy were pre-
dictive of IUBT failure.
Is the results of research VALID ?
The result of this study cannot be said as valid, because there is no randomization
and blinding in sampling so it can not be representative of the intended research
population. This study also lack of control group which probably induces overesti-
mation of the IUBT efficacy. The inclusion criteria for being a research sample are
clearly stated that is women with severe post partum hemorrhage unresponsive to
first line therapy and treted with IUBT. The design in this study is appropriate,
which using prospective cohort study method that follows over time a group of
similar individuals who differ with respect to certain factors under study, to deter-
mine how these factors affect rates of a certain outcome.
This study can be applied to the population and in Indonesia but requires further
research.
Mengetahui
Penilai,