B
irth
route
in
case
of
cesarean
section
in
a
previous
pregnancy
R
ev
A
ssoc
M
ed
B
ras
2015; 61(3):196-202
201
patients compared to trial of labor in terms of effective-
ness and safety.
The study by Landon et al. illustrates the difficulties
presented above because, despite being the most impor-
tant prospective observational longitudinal study con-
ducted to evaluate this outcome, it has biases inherent to
the study design, which are easily identified and compro-
mise the analysis (
B
)
.
7
In this study, despite the fact that
the women included in both groups were mostly obese,
with BMI > 30 Kg/m
2
, there was heterogeneity especially
regarding maternal age, ethnicity, smoking status, obstet-
ric history, factors leading to indication of the first cesar-
ean delivery, obstetric diseases, gestational age, and fetal
weight at birth. The study was multicentric, and thus tri-
al of labor rates varied greatly among different centers
included (ranging from 18 to 63%), with a decrease
throughout the study period (in 1999, there were on av-
erage 48% of patients undergoing trial of labor, falling to
30%, in 2002). Despite that, we have identified a signifi-
cant increase in the number of maternal complications
in cases of pregnant women undergoing trial of labor
(such as need for blood transfusion, diagnosis of endo-
metriosis, and uterine rupture), compared to patients re-
ferred for elective cesarean section, especially in cases
where there was failure to progress. However, due to the
heterogeneity of the groups and the exclusion of patients
who underwent elective cesarean section at the beginning
of labor, the interpretation of these results has limited
range (
B
)
.
7
In 2012, another concurrent observational longitudi-
nal study, aimed at analyzing the outcomes related to type
of delivery on maternal morbidity and mortality (here con-
sidered as a secondary outcome), was published
6
(
B
)
.
Also
multicentric, this study was less questioned in terms of
methodology compared to the first trial shown above, since
the groups were homogeneous regarding intention to treat
(excluding body mass index, socioeconomic status and ob-
stetric indication of first cesarean section). There was no
significant difference between the groups; however, it should
be noted that the outcome of interest (maternal morbidi-
ty and mortality expressed by the occurrence of at least one
serious complication such as death, uterine rupture, post-
operative complications, bleeding, thromboembolism and
infection) was characterized as secondary (
B
)
.
6
Also in 2012, a study (secondary analysis of the co-
hort study by Landon et al.,
7
published in 2004) that ad-
opted a multiple logistic regression model was published.
Using a propensity score with control of presented con-
founding factors (heterogeneity between groups), the
study had the main objective of comparing the progno-
sis by type of delivery in cases with previous cesarean sec-
tion. Even after this analysis, consistent with findings re-
ported in the initial study, it was found that elective
cesarean indication was associated, to the detriment of
trial of labor, to a significant reduction of maternal com-
plications (
B
).
15
F
inal
recommendations
Based on the evidence available at present, trial of labor
(TOL) is a reasonable option for women with a previous
cesarean section (performed through transverse uterine
section).
The available data derived from observational longi-
tudinal studies (concurrent or not) show that both labor
and elective cesarean section in pregnant women (with a
single fetus in cephalic presentation) with one previous
cesarean section are associated with significant risks and
benefits, which differ for the mother and the fetus (risk
of uterine rupture, febrile morbidity, need for blood trans-
fusion and hysterectomy).
Characteristics that are clearly associated with a fa-
vorable progress of trial of labor are: indication of the
first cesarean section (non-recurring reason) and a histo-
ry of vaginal delivery, in the case of multiparous women
with a previous cesarean section.
Since data is not conclusive as to the best type of de-
livery in this context, recognition of the prognostic fac-
tors associated with the failure of the trial of labor should
be helpful, as an attempt to select more properly women
who should effectively undergo such procedure.
R
eferences
1. Marshall NE, Fu R, Guise J-M. Impact of multiple cesarean deliveries onmaternal
morbidity: a systematic review. Am J Obstet Gynecol. 2011; 205:262.e1-8.
2.
Matias JP, Parpinelli MA, Cecatti JG. A prova de trabalho e a via de parto
em primíparas com uma cesárea anterior. Rev Assoc Med Bras. 2007; 53(2):
109-15.
3.
NIH Consensus Development Conference Statement on Vaginal Birth After
Cesarean: new insights 2010; 27(3).
4.
Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJ, Gavaghan DJ,
et al. Assessing the quality of reports of randomized clinical trials: is blinding
necessary? Control Clin Trials. 1996; 17(1):1-12.
5. Wells GA, Shea B, O’Connell D, Peterson J, Welch V, Losos M, et al. The
Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised
studies in meta-analyses. Available at:
www.ohri.ca/programs/clinical_epidemiology/oxford.asp. Acessado: 10 fev 2014.
6. Crowther CA, Dodd JM, Hiller JE, Haslam RR, Robinson JS; Birth After
Caesarean Study Group. Planned vaginal birth or elective repeat caesarean:
patient preference restricted cohort with nested randomised trial. PLoS
Med. 2012; 9(3):e1001192.
7.
Landon MB, Hauth JC, Leveno KJ, Spong CY, Leindecker S, Varner MW, et
al.; National Institute of Child Health and Human Development Maternal-
Fetal Medicine Units Network. Maternal and perinatal outcomes associated
with a trial of labor after prior cesarean delivery. N Engl J Med. 2004;
351(25):2581-9.