| Literature DB >> 21879334 |
Hinke de Lau1, Hendrik Gremmels, Nico W Schuitemaker, Anneke Kwee.
Abstract
PURPOSE: To determine the risk of uterine rupture for women undergoing trial of labour (TOL) with both a prior caesarean section (CS) and a vaginal delivery.Entities:
Mesh:
Year: 2011 PMID: 21879334 PMCID: PMC3190082 DOI: 10.1007/s00404-011-2048-x
Source DB: PubMed Journal: Arch Gynecol Obstet ISSN: 0932-0067 Impact factor: 2.344
Search strategy
| Patients | Outcome | |
|---|---|---|
| Caesarean | Uterine | Separation |
| Caesarean | Uterus | Rupture |
| Section | Scar | Dehiscence |
| Scar | ||
| VBAC | ||
| Search syntax | ||
(caesarean[TIAB] OR caesarean[TIAB] OR section[TIAB] OR scar[TIAB] OR VBAC[TIAB]) AND (uterine[TIAB] OR uterus[TIAB] OR scar[TIAB]) AND (seperation[TIAB] OR rupture[TIAB] OR dehiscence[TIAB]) | ||
Critical appraisal overview
| Study | Relevance | Validity | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Patientsa | Predictorb | Outcomec | Overall relevance | Study designd | Control groupe | Blinding for PVD statusf | Selection biasg | Population sizeh | Subset analysisi | Prediction rulesj | Outcome measuresk | Level of evidencel | Overall validity | |
| Bedoya et al. [ | + | +/− | +/− | 2 | +/− | + | – | +/− | – | +/− | +/− | – | 2− | 3 |
| Shimonovitz et al. [ | + | – | +/− | 1.5 | – | + | – | +/− | +/− | + | +/− | – | 2− | 3.5 |
| Zelop et al. [ | + | +/− | + | 2.5 | +/− | + | – | + | +/− | + | +/− | +/− | 2+ | 5 |
| Hendler and Bujold [ | + | + | +/− | 2.5 | +/− | + | – | + | +/− | + | +/− | +/− | 2+ | 5 |
| Smith et al. [ | + | +/− | +/− | 2 | +/− | + | – | +/− | + | +/− | +/− | +/− | 2+ | 4.5 |
| Macones et al. [ | +/− | +/− | +/− | 1.5 | – | + | – | +/− | + | +/− | +/− | + | 2+ | 4.5 |
| Grobman et al. [ | + | +/− | +/− | 2 | + | + | – | + | + | + | +/− | + | 2+ | 6.5 |
| Kwee et al. [ | +/− | +/− | + | 2 | + | + | – | +/− | +/− | + | +/− | +/− | 2++ | 5 |
| Grobman et al. [ | + | +/− | +/− | 2 | + | + | – | + | + | +/− | + | + | 2+ | 6.5 |
| Mercer et al. [ | +/− | – | +/− | 1 | + | + | – | + | + | + | +/− | + | 2++ | 6.5 |
a+, one caesarean section; +/−, one or more caesarean sections; +/−, both a caesarean section and induction of labour
b+, one prior vaginal birth; +/−, one or more vaginal deliveries; +/−, subset; −, VBAC
c+, absolute and relative risk of uterine rupture; +/−, only relative or absolute risk
d+, prospective; +/−, retrospective cohort study; −, case–control study; −, other
e+, no prior vaginal birth; −, no control group
f+, present; −, no blinding or not described
g+, unlikely; +/−, unclear; −, likely
h+, >10,000; +/−, 1,500–10,000; −, <1,500
i+, vaginal delivery before or after caesarean section; +, >1 vaginal births; +, >1 caesareans; +, scar type; +, induction of labour; +/−, none
j+, prediction model; +/−, no prediction model
k+, externally validated clinically manifest uterus rupture; +/−, clinically manifest uterus rupture; −, not clearly described
lAccording to the criteria of Harbour and Miller [14]
Fig. 1Flowchart of the study selection process
Fig. 2Forest plot of the analyzed studies
Results of analyzed studies
| Study | Study design | Population size | AR without vaginal delivery (%) | AR with vaginal delivery (%) | Odds ratio | 95% Confidence interval |
|---|---|---|---|---|---|---|
| Hendler and Bujold [ | Retrospective cohort | 2,204 |
|
|
|
|
| Smith et al. [ | Retrospective cohort | 35,854 |
|
|
|
|
| Zelop et al. [ | Retrospective cohort | 3,783 | 1.1 | 0.20 | OR 0.18 | 0.04–0.74 |
| Kwee et al. [ | Prospective cohort | 3,273 |
|
|
|
|
| Grobman et al. [ | Prospective cohort | 11,778 |
|
|
|
|
| Grobman et al. [ | Prospective cohort | 11,816 | 0.95 | 0.43 | OR 0.44 | 0.27–0.71 |
Calculated data have been italicized
* Not statistically significant
aNot used in the final analysis