OBJECTIVE: We aimed to assess the risk for intrapartum cesarean delivery (CD) in pregnancies complicated by small for gestational age (SGA). STUDY DESIGN: A retrospective cohort study of all women who underwent a trial of labor in a University-affiliated tertiary hospital (2010-2016). Cases of SGA (neonatal birthweight<10 th centile according to local customized growth curves) were compared to non-SGA controls. Additionally, risk factors for intrapartum CD were explored in women with SGA infants. Exclusion criteria included women who underwent CD without a trial of labor, multiple gestation, stillbirths or delivery <24 weeks of gestation. RESULTS: 1. Overall, 55,089 women underwent a trial of labor during the study period. Of them 2,501 (4.5%) were complicated by SGA infants. 2. Mean maternal age was similar in both groups. Compared to the non-SGA group, women in the SGA group were more often nulliparous (65.2 vs. 44.0%, p<0.001) had higher rate of hypertensive disorders (6.7 vs. 3.7%, p<0.001)) and higher rates of preterm deliveries <37 weeks (PTD37) (7.8 vs. 4.5%, p<0.001). 3. In multivariate logistic regression, after controlling for potential confounders, SGA was associated with an increased risk for intrapartum CD (OR, 95%CI) (1.51, 1.29-1.76). 4. Of all the SGA group (n¼2,501), the mean gestational age at delivery was 38.6AE2.2 weeks with mean birthweight (BW) of 2,430AE352g and mean BW centile was 5.9AE2.9. An inverse relation was observed between BW-centile and the rate of CD as well as the CD due to fetal distress when stratifying the SGA group according to BW-centiles (Figure). 6. In multivariate logistic regression, after controlling for maternal age, parity, hypertensive disorders, diabetes, induction of labor, epidural analgesia, meconium and gestational age at delivery, factors that were significantly associated with increased risk for CD were nulliparity (2.02, 1.41-2.99), PTD37 (3.32, 2.12-5.19), induction of labor (11.76, 8.27-16.72) and meconium (2.05, 1.49-2.83) (Table). CONCLUSION: Deliveries of SGA infants are associated with an increased risk for intrapartum CD compared to those of non-SGA mainly due to fetal distress. Moreover, in deliveries with SGA the risk for CD is inversely related to BW-centile. Factors such as nulliparity, prematurity, induction of labor and meconium further increase the risk for CD.