TY - JOUR
T1 - Adenocarcinoma in situ or early-stage cervical cancer is a risk factor for preterm delivery after cervical conization
T2 - a multicenter observational study
AU - Kasuga, Yoshifumi
AU - Ikenoue, Satoru
AU - Nishio, Hiroshi
AU - Yamagami, Wataru
AU - Ochiai, Daigo
AU - Tanabe, Kiyoo
AU - Tashima, Yasuhiro
AU - Hirao, Nobumaru
AU - Miyakoshi, Kei
AU - Kasai, Kenji
AU - Suda, Yoshio
AU - Nemoto, Taiko
AU - Shiraishi, Satoru
AU - Yoshida, Hiroyuki
AU - Kurahashi, Takashi
AU - Takamatsu, Kiyoshi
AU - Iwasaki, Shinya
AU - Yamashita, Hiroshi
AU - Akiba, Yasuo
AU - Arase, Toru
AU - Hara, Sumiko
AU - Nakada, Sakura
AU - Tanaka, Mamoru
AU - Aoki, Daisuke
N1 - Funding Information:
This study was supported by JSPS KAKENHI under grant number 20K18173. The authors are grateful to all medical staff in the perinatal units of all institutions that participated in this study for their excellent patient care. We would like to thank Editage (www.editage.jp) for English language editing.
Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Objective: Pregnancy after conization is associated with a high risk of preterm delivery. However, because risk factors for preterm delivery after conization remain unknown, we conducted a multicenter observational study to investigate risk factors associated with preterm delivery. Methods: We selected patients who had previously undergone conization and reviewed medical records from 18 hospitals in cooperation with Keio University School of Medicine between January 2013 and December 2019. Women were classified as nulliparous and primiparous, and a multiple logistic regression analysis was performed to evaluate the relative contributions of the various maternal risk factors for preterm delivery (i.e. delivery before 37 gestational weeks). Results: Among 409 pregnant women after conization, 68 women delivered preterm (17%). The incidence of nulliparity (p =.014) was higher and a history of preterm delivery (p =.0010) was more common in the preterm delivery group than in the term delivery group. Furthermore, the proportion of women diagnosed with adenocarcinoma in situ (AIS) and cervical cancer in the preterm delivery group was higher than that in the term delivery group (p =.0099 and.0004, respectively). In multiple regression models in nulliparous women, cervical cancer or AIS (Odds ratio [OR]: 4.16, 95% CI: 1.26–13.68, p =.019) and a short cervix in the second trimester (OR: 13.41, 95% CI: 3.88–46.42, p <.0001) increased the risk of preterm delivery. Furthermore, a history of preterm delivery (OR: 7.35, 95% CI: 1.55–34.86, p =.012), cervical cancer or AIS (OR: 5.07, 95% CI: 1.24–20.73, p =.024), and a short cervix in the second trimester (OR: 4.29, 95% CI: 1.11–16.62, p =.035) increased the risk of preterm delivery in the multiple regression models in primiparous women. Conclusion: Pregnant women who previously underwent conization are at risk for preterm delivery. The histological type of AIS and cervical cancer was evaluated as a risk factor for preterm delivery. KEY MESSAGES Prior preterm delivery, presence of a short cervix, and cervical cancer or AIS were predictors of preterm delivery after conization. The depth of conization in cervical cancer or AIS group was significantly larger than that in the CIN group.
AB - Objective: Pregnancy after conization is associated with a high risk of preterm delivery. However, because risk factors for preterm delivery after conization remain unknown, we conducted a multicenter observational study to investigate risk factors associated with preterm delivery. Methods: We selected patients who had previously undergone conization and reviewed medical records from 18 hospitals in cooperation with Keio University School of Medicine between January 2013 and December 2019. Women were classified as nulliparous and primiparous, and a multiple logistic regression analysis was performed to evaluate the relative contributions of the various maternal risk factors for preterm delivery (i.e. delivery before 37 gestational weeks). Results: Among 409 pregnant women after conization, 68 women delivered preterm (17%). The incidence of nulliparity (p =.014) was higher and a history of preterm delivery (p =.0010) was more common in the preterm delivery group than in the term delivery group. Furthermore, the proportion of women diagnosed with adenocarcinoma in situ (AIS) and cervical cancer in the preterm delivery group was higher than that in the term delivery group (p =.0099 and.0004, respectively). In multiple regression models in nulliparous women, cervical cancer or AIS (Odds ratio [OR]: 4.16, 95% CI: 1.26–13.68, p =.019) and a short cervix in the second trimester (OR: 13.41, 95% CI: 3.88–46.42, p <.0001) increased the risk of preterm delivery. Furthermore, a history of preterm delivery (OR: 7.35, 95% CI: 1.55–34.86, p =.012), cervical cancer or AIS (OR: 5.07, 95% CI: 1.24–20.73, p =.024), and a short cervix in the second trimester (OR: 4.29, 95% CI: 1.11–16.62, p =.035) increased the risk of preterm delivery in the multiple regression models in primiparous women. Conclusion: Pregnant women who previously underwent conization are at risk for preterm delivery. The histological type of AIS and cervical cancer was evaluated as a risk factor for preterm delivery. KEY MESSAGES Prior preterm delivery, presence of a short cervix, and cervical cancer or AIS were predictors of preterm delivery after conization. The depth of conization in cervical cancer or AIS group was significantly larger than that in the CIN group.
KW - Conization
KW - cervical cancer
KW - pregnancy
KW - preterm delivery
KW - ultrasound
UR - http://www.scopus.com/inward/record.url?scp=85127331047&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85127331047&partnerID=8YFLogxK
U2 - 10.1080/14767058.2022.2056835
DO - 10.1080/14767058.2022.2056835
M3 - Article
C2 - 35341455
AN - SCOPUS:85127331047
SN - 1476-7058
VL - 35
SP - 9837
EP - 9842
JO - Journal of Maternal-Fetal and Neonatal Medicine
JF - Journal of Maternal-Fetal and Neonatal Medicine
IS - 25
ER -