Abstract
Introduction
Studies investigating the risk factors associated with unfavorable maternal/neonatal outcomes in cases of shoulder dystocia are scarce. This study aims to uncover the predictive factors that give rise to unfavorable outcomes within the context of shoulder dystocia.
Materials and methods
Medical records of pregnancies complicated by shoulder dystocia was obtained between 2008–2022 from a single tertiary center. This study involved the comparison of sociodemographic, sonographic, and delivery characteristics among pregnancies complicated by shoulder dystocia resulting in favorable vs. unfavorable maternal/neonatal outcomes.
Results
A total of 275 pregnancies were analyzed, with 111 (40.3%) classified as unfavorable outcomes and 164 (59.7%) as favorable outcomes. Employing a multivariable regression analysis, several independent associations were identified with unfavorable maternal/neonatal outcomes. Specifically, short maternal stature, pre-gestational diabetes, vacuum extraction, Wood’s screw maneuver, and macrosomia merged as significant predictors of unfavorable maternal/neonatal outcomes.
Conclusion
Short maternal stature, pre-gestational diabetes, vacuum extraction, Wood’s screw maneuver, and macrosomia may all contribute to poor maternal/neonatal outcomes in shoulder dystocia cases. This knowledge allows clinicians to improve their decision-making, patient care, and counseling.
Keywords: Shoulder dystocia, Predictors, Maternal outcomes, Neonatal outcomes
What does this study add to the clinical work
Maternal shorter stature, pregestational diabetes, vacuum extraction, Wood's screw maneuver, and neonatal macrosomia are contributing factors to adverse maternal/neonatal outcomes in instances of shoulder dystocia. |
Introduction
Shoulder dystocia is a term used to describe a vaginal delivery in which after delivery of the fetal head, additional obstetric maneuvers are needed to enable delivery of the fetal shoulders [1].
This condition occurs in 0.2–3% of births [2] and presents a range of risk factors, which can be categorized as either antepartum or intrapartum. Antepartum risks encompass elements like high birth weight, maternal obesity, excessive gestational weight gain, diabetes, advanced maternal age at first birth, previous shoulder dystocia, post-term pregnancies, and male fetal sex [3–9]. Intrapartum risk factors include factors like abnormal labor progress and interventions such as assisted vaginal delivery [10–13].
The implications of shoulder dystocia extend to neonatal complications, including brachial plexus palsy, clavicular/humerus fractures, hypoxic–ischemic encephalopathy, and even intrapartum fetal death and neonatal mortality [14–17]. In terms of maternal consequences, the impact is also marked by significant morbidities, prominently characterized by instances of hemorrhage and perineal lacerations ranging from third to fourth degree [18, 19].
Studies investigating the risk factors associated with unfavorable maternal/neonatal outcomes in cases of shoulder dystocia are scarce. These studies specifically investigated risk factors associated with shoulder dystocia cases, focusing on specific neonatal morbidities like permanent brachial plexus palsy [20, 21]. Given the limited research on diverse adverse maternal/neonatal outcomes related to shoulder dystocia, there exists a significant knowledge gap. To bridge this gap, our study aims to offer valuable insights to clinicians by investigating the contributing factors to these unfavorable outcomes. By pinpointing the specific characteristics and circumstances linked to adverse outcomes, clinicians can customize their approaches for individual patients and provide more comprehensive counseling to expectant parents.
Materials and methods
Study population
In this retrospective study, the medical records, sonographic reports, delivery charts, and neonatal charts of all singleton deliveries which resulted in shoulder dystocia between December 2008 and April 2022 from a single university hospital were reviewed. We excluded multiple pregnancies, terminations of pregnancy, cases of prior to delivery intrauterine fetal deaths, pregnancies with a known major fetal malformation, and cases with missing data. Shoulder dystocia was diagnosed in a vaginal delivery in which after delivery of the fetal head, additional obstetric maneuvers were needed to enable delivery of the fetal shoulders.
The study population was further divided into two groups allowing for a clear differentiation between cases leading to adverse outcomes and those resulting in more favorable results within the study population:
The “Unfavorable Outcome” group encompassed cases complicated by any of the following conditions: maternal—perineal tear grade 3/4, postpartum fever, postpartum hemorrhage, or blood transfusion; neonatal—Apgar score at 5 min < 7, umbilical pH < 7.1, Erb’s palsy, clavicular fracture, cerebral complications (intra-ventricular hemorrhage, seizures or hypoxic–ischemic encephalopathy), respiratory complications (respiratory distress syndrome, mechanical ventilation or need for respiratory support), necrotizing enterocolitis, sepsis, blood transfusion, or neonatal death.
The “Favorable Outcome” group comprised all other cases that did not meet the criteria for unfavorable outcomes.
Maternal demographics, sonographic parameters, and delivery characteristics were compared between deliveries complicated with shoulder dystocia, which resulted with either an unfavorable or favorable outcomes.
Ethical approval and informed consent
All procedures were in accordance with the ethical standards of the institutional Review Board and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Decision number 0013–22-WOMCE dated 18/01/2022. Since the study used anonymous archival data and was retrospective in nature, informed consent was not obtained.
Data collection
The following maternal characteristics were collected from the medical chart of the patients: maternal age, maternal stature, pre-pregnancy weight and height (from which the body mass index (BMI) was calculated), diabetes mellitus, hypertensive disorder, smoking, nulliparity, and previous shoulder dystocia. Short maternal stature was defined as height less than 160 cm. Although a height of less than 155 cm is commonly accepted as the threshold for short stature, only 5.2% of the women in our study were below this height. To ensure a sufficient sample size for meaningful analysis, we set the cutoff value for short stature at less than 160 cm.
Sonographic characteristics were collected as well and included: fetal weight estimation, abdominal circumference > 90%, head circumference/ abdomen circumference ratio.
Delivery characteristics were collected as well and included: gestational age at delivery, second stage of labor > 1 h, vacuum extraction, the use of maneuvers including McRoberts, suprapubic pressure, posterior shoulder extraction, Rubin and wood’s screw maneuver, shoulder dystocia time ≥ 90 s (in cases in which the time from head to shoulders delivery was documented in the medical record), induction of labor, episiotomy, epidural analgesia, neonatal weight, macrosomia, and whether the delivery took place on a night shift.
Gestational age was calculated based on the woman’s first ultrasound examination in the pregnancy and last menstrual period [22]. A woman was considered to have diabetes mellitus if she had a diagnosis of type 1/type 2 in the medical record or gestational diabetes mellitus based on the two-step approach described in the National Diabetes Group criteria [23]. Chronic hypertension and preeclampsia were diagnosed according to the current American College of Obstetricians and Gynecologists criteria [24] which were fully adapted by our institution for hypertensive disorders diagnosis and management.
Immediately after birth, all neonates were examined by pediatricians. Birth weight percentiles for gestational age were assigned using the updated local growth charts [25]. Macrosomia was defined as actual birthweight ≥ 90th percentile for gestational age/absolute weight ≥ 4000 g.
In all cases, estimated fetal weight and Doppler findings were determined at the departmental ultrasound unit < 7 days from delivery, by expert sonographers. All ultrasound examinations were performed using the Voluson series ultrasound machines (E6, E8, E10, GE Healthcare, Gretz Ultrasound, Zipf, Austria) using a 6 MHz transabdominal transducer. The following data were collected from the sonographic records: gestational age at sonographic study, abdominal circumference, head circumference, biparietal diameter, femur length from which the estimated fetal weight was calculated [26].
The following data were collected from the neonatal records: birthweight, cord blood pH, Apgar score, respiratory morbidity (defined as—respiratory distress syndrome/need for mechanical ventilation or support), cerebral morbidity (defined as—intra-ventricular hemorrhage, hypoxic ischemic encephalopathy, seizures), hypoglycemia, necrotizing enterocolitis, sepsis, need for blood transfusion, and death.
The following data were collected from the maternal post-delivery records: perineal tear grade 3/4, postpartum fever, postpartum hemorrhage (defined as estimated blood loss > 500 ml), blood transfusion.
Data analysis
Data analysis was performed utilizing SPSS software version 22.0 (SPSS Inc., Chicago, IL, USA). Data were presented as follows: continuous variables are presented either as mean ± SD or as median and range, as appropriate. Categorical variables are presented as n (%). Continuous parameters were compared by the Student t test and categorical variables by the Chi2 with Yates’ correction test or the Fisher exact test, as appropriate. A statistically significant p < 0.05 was defined.
A multivariable regression analysis was performed in which composite of unfavorable maternal/ neonatal outcome served as the dependent variable while short maternal stature, BMI, pre-gestational diabetes, smoking, vacuum extraction, wood's screw maneuver, shoulder dystocia ≥ 90 s, and macrosomia served as independent variables.
Results
A total of 275 deliveries were included in the study: 111 (40.3%) in the unfavorable outcome group and 164 (59.6%) in the favorable outcome group. In our institution, there are approximately 3,600 vaginal deliveries per year, which corresponds to 50,4000 delivers in the study period. The rate of shoulder dystocia in our institution was approximately 0.5% (275/50400).
Maternal and sonographic characteristics of the two groups are presented and compared in Table 1. Patients in the unfavorable outcome group were shorter, had higher BMI, higher rate of pre-gestational diabetes, and smoking.
Table 1.
Unfavorable outcome n = 111 |
Favorable outcome n = 164 |
p value | |
---|---|---|---|
Maternal characteristics | |||
Age (years) | 31.1 ± 5 | 31.1 ± 5.2 | 1 |
Short maternal stature (≤ 160 cm) | 41/74 (55.4) | 40/115 (34.8) | < 0.01 |
BMI (kg/m2) | 25.95 ± 6.3 | 24.84 ± 4.5 | 0.05 |
Obesity (BMI > 30 kg/m2) | 14/61 (23.0) | 12/88 (13.6) | 0.14 |
GDMA1 | 13 (11.7) | 16 (9.8) | 0.6 |
GDMA2 | 3 (2.7) | 9 (5.5) | 0.26 |
Pre-gestational diabetes | 7 (6.3) | 3 (1.8) | 0.05 |
Hypertensive disorder | 5 (4.5) | 4 (2.4) | 0.34 |
Preeclampsia | 6 (5.4) | 3 (1.8) | 0.10 |
Smoking | 17/110 (15.5) | 11/157 (7.0) | 0.02 |
Nulliparity | 29 (26.1) | 31 (18.9) | 0.15 |
Previous shoulder dystocia | 3 (2.7) | 0 (0) | 0.06 |
Sonographic characteristics prior to delivery | |||
Fetal weight estimation (g) | 3418 ± 541.8 | 3444.9 ± 442.5 | 0.65 |
Abdomen circumference > 90% | 19/48 (39.6) | 20/50 (40) | 0.96 |
Head circumference/abdomen circumference | 0.94 ± 0.05 | 0.93 ± 0.05 | 0.1 |
All data are shown as number (%), mean ± standard deviation or median (range), as appropriate. BMI body mass index. Values in bold are statistically significant (p < 0.05)
There were no differences in sonographic parameters between the study groups.
Delivery characteristics of the two groups are presented and compared in Table 2. Patients in the unfavorable outcome group had higher rate of vacuum extraction, Wood’s screw maneuver, shoulder dystocia time ≥ 90 s, and macrosomia.
Table 2.
Unfavorable outcome n = 111 |
Favorable outcome n = 164 |
p value | |
---|---|---|---|
Gestational age at delivery (weeks) | 39.4 ± 1.3 | 39.6 ± 1.2 | 0.19 |
Second stage of labor > 1 h | 20/108 (18.5) | 20/158 (12.7) | 0.18 |
Vacuum extraction | 19 (17.1) | 12 (7.3) | 0.01 |
McRoberts maneuver | 100 (90.1) | 145 (87.9) | 0.66 |
Suprapubic pressure | 96 (86.5) | 148 (89.7) | 0.33 |
Posterior shoulder extraction | 12 (10.8) | 9 (5.5) | 0.10 |
Rubin’s maneuver | 0 (0) | 0 (0) | 1 |
Wood’s screw maneuver | 14 (12.6) | 2 (1.2) | < 0.001 |
Shoulder dystocia time ≥ 90 s | 13/48 (27.1) | 4/46 (8.7) | 0.02 |
Induction of labor | 37 (33.3) | 51 (31.1) | 0.69 |
Episiotomy | 44 (39.6) | 48 (29.1) | 0.07 |
Epidural analgesia | 83 (74.8) | 107 (64.8) | 0.09 |
Neonatal weight (g) | 3856.1 ± 396.9 | 3804.6 ± 390.3 | 0.28 |
Macrosomia (birthweight ≥ 90th percentile for gestational age/absolute weight ≥ 4000 g) | 70 (63.1) | 80 (48.7) | 0.02 |
Night shift | 86 (77.5) | 132 (82.1) | 0.54 |
All data are shown as number (%), mean ± standard deviation or median (range), as appropriate. Values in bold are statistically significant (p < 0.05)
Description of the individual complications that formed the unfavorale outcome group is presented in Table 3.
Table 3.
Unfavorable outcome n = 111 | |
---|---|
Maternal complications | |
Perineal tear grade 3 | 4 (3.6) |
Perineal tear grade 4 | 1 (0.9) |
Postpartum fever | 11 (9.9) |
Postpartum hemorrhage | 25 (22.5) |
Blood transfusion | 15 (13.5) |
Neonatal complications | |
Apgar 5 min < 7 | 5 (4.5) |
pH < 7.1 | 5 (4.5) |
Respiratory morbidity | 58 (52.2) |
Cerebral morbidity | 2 (1.8) |
Erb’s palsy | 24 (21.6) |
Clavicular fracture | 13 (11.7) |
Necrotizing enterocolitis | 0 (0) |
Sepsis | 4 (3.6) |
Transfusion | 3 (2.7) |
Neonatal death | 0 (0) |
All data are shown as number (%). Respiratory morbidity include respiratory distress syndrome, mechanical ventilation or need for respiratory support; cerebral morbidity include intra-ventricular hemorrhage, seizures or hypoxic–ischemic encephalopathy
Table 4 presents the results of a multivariable regression analysis to identify independent associations with compositeunfavorable maternal/neonatal outcomes in deliveries complicated with shoulder dystocia. In this analysis, short maternal stature (aOR = 1.12, 95% CI 1.04–2.01), pre-gestational diabetes (aOR = 1.22, 95% CI 1.03–3.09), vacuum extraction (aOR = 1.95, 95% CI 1.22–4.36), Wood’s screw maneuver (aOR = 2.66, 95% CI 1.77–6.39), and macrosomia (aOR = 1.04, 95% CI 1.01–2.77) were associated with unfavorable maternal/neonatal outcome in deliveries complicated with shoulder dystocia.
Table 4.
Variable | aOR | 95% CI |
---|---|---|
Short maternal stature (≤ 160 cm) | 1.12 | 1.04–2.01 |
BMI (kg/m2) | NS | NS |
Pre-gestational diabetes | 1.22 | 1.03–3.09 |
Smoking | NS | NS |
Vacuum extraction |
1.95 2.66 |
1.22–4.36 |
Wood’s screw maneuver | 1.77–6.39 | |
Shoulder dystocia time ≥ 90 s | NS | NS |
Macrosomia (birthweight ≥ 90th percentile for gestational age/absolute weight ≥ 4000 g) | 1.04 | 1.01.2.77 |
BMI body mass index. Values in bold were significant in the regression analysis. NS = not significant
Discussion
Principal findings
This study sought to identify discerning factors contributing to adverse maternal/neonatal outcomes in instances of shoulder dystocia. Within the purview of our investigation, we identified specific predictors, namely: maternal shorter stature, pre-gestational diabetes, employment of vacuum extraction, implementation of the Wood’s screw maneuver, and neonatal macrosomia.
Results in the context of what is known
Shoulder dystocia is an obstetrical emergency associated with adverse maternal and neonatal outcomes, and while there are instances with identifiable predictors, a substantial portion of cases remains elusive in terms of predictive factors. Numerous studies have tried to find predictors for shoulder dystocia; however, a significant proportion—ranging from 50 to 75%—of shoulder dystocia cases arises without the presence of discernible risk factors [27, 28].
Studies focusing on predictors for adverse outcomes in shoulder dystocia cases are limited. Narendran et al. [20] conducted a study in 2021 encompassing 1134 instances of shoulder dystocia, shedding light on predictive markers for neonatal brachial plexus palsy. Their findings underscored associations with diabetes, birthweight exceeding 4000 g, the act of seeking assistance during shoulder dystocia, and a shoulder dystocia duration of 120 s or more. Harari et al. [29] found in a study from 2021 that while fetal macrosomia, maternal diabetes mellitus, male gender, and advanced maternal age are associated with shoulder dystocia, no association was found between shoulder dystocia and long-term neonatal neurological morbidity. Other studies [21, 30, 31] reinforced these findings by revealing significant associations. Factors such as macrosomia, lower maternal height, elevated maternal weight, excessive maternal weight gain, as well as gestational age and parity, were implicated in neonatal birth injuries. In addition, Hehir et al. conducted a study in 2018 involving 685 cases of shoulder dystocia, identifying predictors for maternal sphincter injury. Nulliparity, operative vaginal delivery, and the utilization of internal maneuvers emerged as substantial predictors [32].
Clinical and research implications
In the present study, we tried to establish a comprehensive framework encompassing maternal, obstetrical, and neonatal parameters collectively, as opposed to analyzing them individually. This holistic approach aims to uncover potential interconnections among these parameters, recognizing their mutual influence, and to ascertain whether they collectively correlate with unfavorable maternal and neonatal outcomes. For instance, maternal height below 160 cm is suggested as a potential risk factor for an inadequate pelvis, leading to cephalopelvic disproportion [33] and consequent shoulder dystocia. Pre-gestational diabetes is another recognized risk factor for shoulder dystocia, primarily attributed to typical fetal muscle and fat distribution patterns [34, 35] often resulting in increased birthweight [36]. Furthermore, macrosomia [37] and interventions like vacuum extraction [13] and Wood’s screw maneuver [38, 39] might contribute to traumatic labor for both the mother and the neonate. These suppositions align with the findings of our study.
Strengths and limitations
The current study is unique in several aspects. First, it investigated a relatively large cohort of labors complicated with shoulder dystocia. Second, this study, in contrast to most previous studies, examined a large spectrum of neonatal complications. Third, this study concentrated not only on neonatal complications resulting from shoulder dystocia, but also maternal complications. Our study is not without limitations. First, we have only collected short-term neonatal outcomes. Second, since shoulder dystocia is a relatively uncommon event, and the separate adverse maternal and neonatal outcomes are each uncommon themselves, we had to apply the current methodology combining the two to a composite adverse outcome. When trying to investigate each separately, each of the important findings did not reach statistical significance. While we are conscious that using a composite outcome may be seen as a research constraint, we think it was necessary to utilize one because the individual components of the composite are uncommon problems. We have described and validated the same composite neonatal outcomes in our previous publications with other pregnancy complications [40]. Third, shoulder dystocia is a clinical diagnosis biased by the individual caregiver, and all cases participated in this study were retrieved based on this subjective computerized diagnosis. Lastly, cases of shoulder dystocia that were immediately and easily managed were probably underreported and, therefore, underrepresented in this study.
Conclusion
In conclusion, shoulder dystocia is an unpredictable obstetrical emergency with numerous potential maternal and neonatal adverse outcomes. This study puts the focus on risk factors which are associated with unfavorable maternal and neonatal outcome in cases of shoulder dystocia: short maternal stature, pre-gestational diabetes, vacuum extraction, Wood’s screw maneuver, and macrosomia. Understanding these risk factors might help clinicians give a better consultation for women at risk of labor complicated with shoulder dystocia and avoid poor maternal and neonatal outcomes.
Author contributions
All authors have participated sufficiently in the work and agreed to be accountable for all aspects of the work. Daniel Tairy: collected the data, wrote the manuscript, Shalhevet Frank: collected the data, performed statistical analysis, Shir Lev: collected the data, performed statistical analysis. Yael Ganor Paz: revised the manuscript, designed the research. Jacob Bar: revised the manuscript, designed the research. Giulia Barda: revised the manuscript, designed the research. Eran Weiner: revised the manuscript, performed statistical analysis. Michal Levy: wrote the manuscript, designed the research.
Funding
Open access funding provided by Tel Aviv University.
Data availability
The data that support the findings of this study are available from the corresponding author, DT, upon reasonable request.
Declarations
Conflict of interest
All authors declare that they have no conflict of interest.
Ethical approval
All procedures were in accordance with the ethical standards of the institutional Review Board and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Informed consent
Since the study used anonymous archival data and was retrospective in nature, informed consent was not obtained.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Davis DD, Roshan A, Canela CD, Varacallo M. Shoulder Dystocia. In Treasure Island (FL); 2023.
- 2.Practice Bulletin No 178: Shoulder Dystocia. Obstet Gynecol. 2017 129(5):e123–33. [DOI] [PubMed]
- 3.Ouzounian JG, Gherman RB (2005) Shoulder dystocia: are historic risk factors reliable predictors? Am J Obstet Gynecol 192(6):1933–1938 [DOI] [PubMed] [Google Scholar]
- 4.Vidarsdottir H, Geirsson RT, Hardardottir H, Valdimarsdottir U, Dagbjartsson A (2011) Obstetric and neonatal risks among extremely macrosomic babies and their mothers. Am J Obstet Gynecol 204(5):423.e1–6 [DOI] [PubMed] [Google Scholar]
- 5.Øverland EA, Vatten LJ, Eskild A (2014) Pregnancy week at delivery and the risk of shoulder dystocia: a population study of 2,014,956 deliveries. BJOG 121(1):34–41 [DOI] [PubMed] [Google Scholar]
- 6.Overland EA, Spydslaug A, Nielsen CS, Eskild A (2009) Risk of shoulder dystocia in second delivery: does a history of shoulder dystocia matter? Am J Obstet Gynecol 200(5):506.e1–6 [DOI] [PubMed] [Google Scholar]
- 7.Lewis DF, Raymond RC, Perkins MB, Brooks GG, Heymann AR (1995) Recurrence rate of shoulder dystocia. Am J Obstet Gynecol 172(5):1369–1371 [DOI] [PubMed] [Google Scholar]
- 8.Kim SY, Sharma AJ, Sappenfield W, Wilson HG, Salihu HM (2014) Association of maternal body mass index, excessive weight gain, and gestational diabetes mellitus with large-for-gestational-age births. Obstet Gynecol 123(4):737–744 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Zhang C, Wu Y, Li S, Zhang D (2018) Maternal prepregnancy obesity and the risk of shoulder dystocia: a meta-analysis. BJOG 125(4):407–413 [DOI] [PubMed] [Google Scholar]
- 10.Laughon SK, Berghella V, Reddy UM, Sundaram R, Lu Z, Hoffman MK (2014) Neonatal and maternal outcomes with prolonged second stage of labor. Obstet Gynecol 124(1):57–67 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Gemer O, Bergman M, Segal S (1999) Labor abnormalities as a risk factor for shoulder dystocia. Acta Obstet Gynecol Scand 78(8):735–736 [PubMed] [Google Scholar]
- 12.Poggi SH, Stallings SP, Ghidini A, Spong CY, Deering SH, Allen RH (2003) Intrapartum risk factors for permanent brachial plexus injury. Am J Obstet Gynecol 189(3):725–729 [DOI] [PubMed] [Google Scholar]
- 13.DallAsta A, Ghi T, Pedrazzi G, Frusca T (2016) Does vacuum delivery carry a higher risk of shoulder dystocia? Review and meta-analysis of the literature. Eur J Obstet Gynecol Reprod Biol. 10.1016/j.ejogrb.2016.07.506 [DOI] [PubMed] [Google Scholar]
- 14.Foad SL, Mehlman CT, Ying J (2008) The epidemiology of neonatal brachial plexus palsy in the United States. J Bone Joint Surg Am 90(6):1258–1264 [DOI] [PubMed] [Google Scholar]
- 15.Turnpenny PD, Nimmo A (1993) Fractured clavicle of the newborn in a population with a high prevalence of grand-multiparity: analysis of 78 consecutive cases. Br J Obstet Gynaecol 100(4):338–341 [DOI] [PubMed] [Google Scholar]
- 16.Davidesko S, Levitas E, Sheiner E, Wainstock T, Pariente G (2023) Critical analysis of risk factors for intrapartum fetal death. Arch Gynecol Obstet 308(4):1239–1245 [DOI] [PubMed] [Google Scholar]
- 17.Tsur A, Sergienko R, Wiznitzer A, Zlotnik A, Sheiner E (2012) Critical analysis of risk factors for shoulder dystocia. Arch Gynecol Obstet 285(5):1225–1229 [DOI] [PubMed] [Google Scholar]
- 18.Gachon B, Desseauve D, Fritel X, Pierre F (2016) Is fetal manipulation during shoulder dystocia management associated with severe maternal and neonatal morbidities? Arch Gynecol Obstet 294(3):505–509 [DOI] [PubMed] [Google Scholar]
- 19.Gauthaman N, Walters S, Tribe I-A, Goldsmith L, Doumouchtsis SK (2016) Shoulder dystocia and associated manoeuvres as risk factors for perineal trauma. Int Urogynecol J 27(4):571–577 [DOI] [PubMed] [Google Scholar]
- 20.Narendran LM, Mendez-Figueroa H, Chauhan SP, Folh KL, Grobman WA, Chang K et al (2022) Predictors of neonatal brachial plexus palsy subsequent to resolution of shoulder dystocia. J Matern neonatal Med 35(25):5443–5449 [DOI] [PubMed] [Google Scholar]
- 21.Yenigül AE, Yenigül NN, Başer E, Özelçi R (2020) A retrospective analysis of risk factors for clavicle fractures in newborns with shoulder dystocia and brachial plexus injury: a single-center experience. Acta Orthop Traumatol Turc 54(6):609–613 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.ACOG Practice Bulletin No (2009) 101: Ultrasonography in pregnancy. Obstet Gynecol 113(2 Pt 1):451–461 [DOI] [PubMed] [Google Scholar]
- 23.Report of the expert committee on the diagnosis and classification of diabetes mellitus. Diabetes Care. 2003 26 Suppl 1:S5–20. [DOI] [PubMed]
- 24.Hypertension in pregnancy (2013) Report of the American College of Obstetricians and Gynecologists’ Task Force on Hypertension in Pregnancy. Obstet Gynecol 122(5):1122–1131 [DOI] [PubMed] [Google Scholar]
- 25.Dollberg S, Haklai Z, Mimouni FB, Gorfein I, Gordon ES (2005) Birthweight standards in the live-born population in Israel. Isr Med Assoc J 7(5):311–314 [PubMed] [Google Scholar]
- 26.Hadlock FP, Harrist RB, Sharman RS, Deter RL, Park SK (1985) Estimation of fetal weight with the use of head, body, and femur measurements–a prospective study. Am J Obstet Gynecol 151(3):333–337 [DOI] [PubMed] [Google Scholar]
- 27.Deneux-Tharaux C, Delorme P (2015) Epidemiology of shoulder dystocia. J Gynecol Obstet Biol Reprod (Paris) 44(10):1234–1247 [DOI] [PubMed] [Google Scholar]
- 28.Mehta SH, Sokol RJ (2014) Shoulder dystocia: risk factors, predictability, and preventability. Semin Perinatol 38(4):189–193 [DOI] [PubMed] [Google Scholar]
- 29.Harari Z, Zamstein O, Sheiner E, Wainstock T (2021) Shoulder Dystocia during Delivery and Long-Term Neurological Morbidity of the Offspring. Am J Perinatol 38(3):278–282 [DOI] [PubMed] [Google Scholar]
- 30.Robinson R, Walker KF, White VA, Bugg GJ, Snell KIE, Jones NW (2020) The test accuracy of antenatal ultrasound definitions of fetal macrosomia to predict birth injury: A systematic review. Eur J Obstet Gynecol Reprod Biol 246:79–85 [DOI] [PubMed] [Google Scholar]
- 31.Dyachenko A, Ciampi A, Fahey J, Mighty H, Oppenheimer L, Hamilton EF (2006) Prediction of risk for shoulder dystocia with neonatal injury. Am J Obstet Gynecol 195(6):1544–1549 [DOI] [PubMed] [Google Scholar]
- 32.Hehir MP, Rubeo Z, Flood K, Mardy AH, O’Herlihy C, Boylan PC et al (2018) Anal sphincter injury in vaginal deliveries complicated by shoulder dystocia. Int Urogynecol J 29(3):377–381 [DOI] [PubMed] [Google Scholar]
- 33.Toh-Adam R, Srisupundit K, Tongsong T (2012) Short stature as an independent risk factor for cephalopelvic disproportion in a country of relatively small-sized mothers. Arch Gynecol Obstet 285(6):1513–1516 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Khoury JC, Dolan LM, Vandyke R, Rosenn B, Feghali M, Miodovnik M (2012) Fetal development in women with diabetes: imprinting for a life-time? J Matern neonatal Med 25(1):11–14 [DOI] [PubMed] [Google Scholar]
- 35.Pylypjuk CL, Day C, ElSalakawy Y, Reid GJ (2022) The Significance of Exposure to Pregestational Type 2 Diabetes in Utero on Fetal Renal Size and Subcutaneous Fat Thickness. Int J Nephrol 2022:3573963 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Dildy GA, Clark SL (2000) Shoulder dystocia: risk identification. Clin Obstet Gynecol 43(2):265–282 [DOI] [PubMed] [Google Scholar]
- 37.Nesbitt TS, Gilbert WM, Herrchen B (1998) Shoulder dystocia and associated risk factors with macrosomic infants born in California. Am J Obstet Gynecol 179(2):476–480 [DOI] [PubMed] [Google Scholar]
- 38.Chauhan SP, Laye MR, Lutgendorf M, McBurney JW, Keiser SD, Magann EF et al (2014) A multicenter assessment of 1,177 cases of shoulder dystocia: lessons learned. Am J Perinatol 31(5):401–406 [DOI] [PubMed] [Google Scholar]
- 39.McFarland MB, Langer O, Piper JM, Berkus MD (1996) Perinatal outcome and the type and number of maneuvers in shoulder dystocia. Int J Gynaecol Obstet 55(3):219–224 [DOI] [PubMed] [Google Scholar]
- 40.Tairy D, Gluck O, Tal O, Bar J, Katz N, Hiaev Z et al (2019) Amniotic fluid transitioning from clear to meconium stained during labor—prevalence and association with adverse maternal and neonatal outcomes. J Perinatol. 10.1038/s41372-019-0436-4 [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author, DT, upon reasonable request.