None, S. S. K., None, S. S. P., None, K. Y. & None, V. L. B. (2025). Fetomaternal Morbidity and Mortality Associated with Placenta Previa: A Tertiary Care Experience from Kurnool. Journal of Contemporary Clinical Practice, 11(11), 791-797.
MLA
None, Suguna Sree K, et al. "Fetomaternal Morbidity and Mortality Associated with Placenta Previa: A Tertiary Care Experience from Kurnool." Journal of Contemporary Clinical Practice 11.11 (2025): 791-797.
Chicago
None, Suguna Sree K, Soma Shilpa P , Kiranmayee Y and Vara Lakshmi B . "Fetomaternal Morbidity and Mortality Associated with Placenta Previa: A Tertiary Care Experience from Kurnool." Journal of Contemporary Clinical Practice 11, no. 11 (2025): 791-797.
Harvard
None, S. S. K., None, S. S. P., None, K. Y. and None, V. L. B. (2025) 'Fetomaternal Morbidity and Mortality Associated with Placenta Previa: A Tertiary Care Experience from Kurnool' Journal of Contemporary Clinical Practice 11(11), pp. 791-797.
Vancouver
Suguna Sree K SSK, Soma Shilpa P SSP, Kiranmayee Y KY, Vara Lakshmi B VLB. Fetomaternal Morbidity and Mortality Associated with Placenta Previa: A Tertiary Care Experience from Kurnool. Journal of Contemporary Clinical Practice. 2025 Nov;11(11):791-797.
Background: Placenta previa (PP) is a potentially life-threatening obstetric condition characterised by implantation of the placenta over or near the internal cervical os, often leading to antepartum haemorrhage. The increasing rates of caesarean deliveries and delayed childbearing have amplified the risk of PP and its sequelae, including placenta accreta spectrum, haemorrhagic shock, and adverse neonatal outcomes. Objective: To evaluate fetomaternal morbidity and mortality associated with placenta previa in patients managed at a tertiary care hospital in Kurnool. Methods: This prospective observational study included 40 women diagnosed with placenta previa after 28 weeks of gestation from January 2024 to February 2025. Inclusion criteria encompassed ultrasound-confirmed PP, intraoperative detection during caesarean delivery, or asymptomatic cases with radiological evidence. Maternal outcomes assessed included antepartum/postpartum haemorrhage, transfusion requirements, surgical interventions (placental bed packing, uterine artery/internal iliac ligation, embolisation, caesarean hysterectomy), ICU admission, and mortality. Neonatal outcomes included gestational age at birth, birth weight, Apgar scores, NICU admission, morbidity, and perinatal mortality. Data were analysed using SPSS 20, with p ≤0.05 considered statistically significant. Results: Among 10,800 deliveries, 40 cases (0.37%) were complicated by placenta previa. Most patients were aged 20–30 years (82.5%) and multiparous (95%). Placenta accreta was observed in 4 (10%) and percreta in 1 (2.5%) patient. Antepartum bleeding was the most common presentation (62.5%). Preterm delivery occurred in 72.5% of cases, and all patients underwent caesarean section. Postpartum haemorrhage occurred in 50% of patients, with 37.5% requiring internal iliac ligation and 20% undergoing emergency caesarean hysterectomy. All patients received blood transfusions, with 30% requiring massive transfusion, and 12.5% required ICU admission. Maternal mortality was 2.5%. Neonatal outcomes included NICU admission in 5% and perinatal mortality of 5%. Conclusion: Placenta previa remains a significant contributor to maternal and neonatal morbidity, particularly among multiparous women with prior uterine surgery. Early antenatal detection, meticulous surgical planning, and a multidisciplinary approach are crucial to optimising outcomes. Preterm delivery and haemorrhagic complications are frequent, underscoring the importance of preparedness for both maternal and neonatal care.
Keywords
Placenta previa
Maternal morbidity
Perinatal outcome
Caesarean section
Placenta accreta spectrum.
INTRODUCTION
Placenta previa (PP) is a condition where the placenta is fully or partially located in the lower segment of the uterus. The typical characteristics of bleeding associated with placenta previa include abrupt onset, absence of pain, no identifiable cause, and a tendency to recur [1]. Although the precise aetiology of placenta previa (PP) remains elusive, extensive literature has established strong links to several predisposing factors, including older maternal age, high parity, history of prior spontaneous abortions, prior caesarean deliveries or other uterine procedures, and tobacco use [2,3]. Worldwide, PP affects approximately 5.2 out of every 1,000 pregnancies, with considerable geographic disparities; notably, the highest rates are reported in research from Asian populations [4]. With the escalating trends in caesarean sections and delayed childbearing, we can anticipate a surge in PP incidences along with its associated sequelae, such as placenta accreta (PA). This disorder carries substantial risks for maternal health, including hemorrhagic shock, heightened need for surgical procedures, and infectious complications like sepsis, as well as adverse fetal and neonatal outcomes such as premature birth and its sequelae, including reduced birth weight, hypoxic events at delivery, and infections in newborns [5]. In contemporary obstetrics, the primary reason for urgent peripartum hysterectomy has shifted from uterine atony to pathological placental implantation, largely attributable to the growing cohort of pregnancies following caesarean scars [6]. Our present investigation aims to examine these risk elements and analyse the maternal-fetal consequences across different PP subtypes.
Aim:
To evaluate the fetomaternal morbidity and mortality associated with placenta previa in patients managed at a tertiary care hospital, Kurnool.
Objectives:
1. To determine the incidence of placenta previa among obstetric admissions.
2. To classify the cases based on type and grade of placenta previa.
3. To assess maternal complications and outcomes associated with placenta previa.
4. To evaluate perinatal outcomes, including neonatal morbidity and mortality.
5. To analyse the relationship between type/grade of placenta previa and fetomaternal outcome.
MATERIAL AND METHODS
This prospective observational study was conducted in the Department of Obstetrics and Gynaecology, Kurnool Medical College and Government General Hospital, Kurnool, from January 2024 to February 2025. A total of 40 women with placenta previa diagnosed after 28 weeks of gestation were included.
Inclusion criteria: (i) Antepartum haemorrhage confirmed by ultrasonography (USG) after 28 weeks, (ii) placenta previa detected intraoperatively during caesarean section for other indications, and (iii) asymptomatic cases with clinical and radiological evidence of placenta previa.
Exclusion criteria: (i) Low-lying placenta diagnosed before 28 weeks, and (ii) antepartum haemorrhage due to other causes.
Diagnostic definition: Placenta partially or completely covering the internal os, or lying within 2 cm of the os on USG after 28 weeks. Gestational age was determined using at least two of the following: last menstrual period, USG dating, or early pregnancy USG findings.[7]
Data were recorded in a predesigned proforma after written informed consent. At admission, a detailed history, clinical examination, and USG evaluation were performed.
Maternal outcomes included transfusion requirement, severity of antepartum and postpartum haemorrhage, surgical/operative interventions (placental bed packing or under-running sutures, uterine artery ligation, internal iliac artery ligation, uterine artery/internal iliac artery embolisation, caesarean hysterectomy), ICU admission, morbidity, mortality, and hospital stay.
Fetal outcomes included birth weight, gestational age at delivery, Apgar scores, NICU admission, morbidity, and perinatal mortality. All live births were followed until maternal and/or neonatal discharge.
Data analysis: Sample size was based on feasibility during the study period. Data were entered in Microsoft Excel and analysed using SPSS version 20.0. Categorical variables were compared using the chi-square test or Fisher’s exact test, and continuous variables using Student’s t-test or Mann–Whitney U test, as appropriate. A p-value ≤0.05 was considered statistically significant.
RESULTS
During the study period, a total of 10,800 deliveries were conducted, of which 40 cases (0.37%) were complicated by placenta previa.
Maternal Demographics
The age distribution of the study population is summarised in Table 1. The majority of patients were aged 20–25 years (n = 28; 70%), followed by 26–30 years (n = 11; 27.5%), and >30 years (n = 1; 2.5%). Gravidity distribution showed 5 primigravida (12.5%), 14 second gravida (35%), 12 third gravida (30%), 5 fourth gravida (12.5%), and 4 grand multipara (10%). This indicates a higher prevalence among multiparous women.
Table 1: Age distribution.
Age (years) Number (N=40) Percentage (%)
<20 0 0%
20-25 28 70%
26-30 11 27.5%
>30 1 2.5%
Type of Placenta Previa
Placental location was determined using antenatal ultrasonography or confirmed intraoperatively (Table 2). Placenta accreta was observed in 4 cases (10%) and placenta percreta in 1 case (2.5%). No cases of placenta increta were noted.
Table 2: Type of placenta previa (by USG and intraoperative findings)
Types (by ACOG, NIH) Number (N=40) Percentage (%)
Type I 07 17.5%
Type IIa (anterior) 08 20%
Type IIb (posterior) 03 7.5%
Type III 06 15%
Type IV 16 40%
Clinical Presentation
Most patients (n = 25; 62.5%) presented with antepartum bleeding per vaginum. Other presentations included abdominal pain (n = 9; 22.5%), leaking per vaginum (n = 1; 2.5%), intrauterine fetal death (IUFD) at admission (n = 1; 2.5%), and asymptomatic cases detected incidentally (n = 4; 10%) (Figure 1).
FIGURE 1: Clinical Presentation
Obstetric History
Previous obstetric interventions included one prior caesarean section in 16 cases (40%), two prior caesarean sections in 9 cases (22.5%), and a history of abortion with dilatation and curettage in 8 cases (20%). Ten cases (25%) occurred in unscarred uteri, highlighting that placenta previa can also occur in women without prior uterine surgery (Figure 2).
FIGURE 2: Causes/ Risk factors
Gestational Age and Mode of Delivery: Of the 40 cases, 11 (27.5%) were term and 29 (72.5%) were preterm. All patients were delivered via caesarean section due to the increased risk of maternal and fetal complications associated with placenta previa.
Maternal Outcomes
Postpartum haemorrhage occurred in 20 patients (50%). Conservative management with uterotonics and haemostatic techniques was initially attempted. Internal iliac artery ligation was performed in 15 patients (37.5%) to control bleeding. Bladder injury occurred in 4 cases (10%), all of which were repaired intraoperatively. Emergency caesarean hysterectomy was required in 8 patients (20%) when bleeding could not be controlled by conservative measures.
All patients received blood transfusions, with 12 (30%) requiring massive transfusions of blood and blood products. Intensive care unit (ICU) admission was necessary in 5 patients (12.5%), and there was one maternal death (2.5%) due to severe postpartum haemorrhage.
Neonatal Outcomes
Neonatal outcomes are summarised in Table 3. Preterm delivery occurred in 29 neonates (72.5%). NICU admission was required in 2 cases (5%), and 2 neonatal deaths (5%) were recorded. Malpresentation was observed in 2 cases (5%), both transverse lie. No congenital anomalies were detected.
Table 3: Neonatal outcome
Factors Number ( N=40) Percentage (%)
Preterm birth 29 72.5%
NICU admission 2 5%
Neonatal death 2 5%
Malpresentation 2 5%
DISCUSSION
Placenta previa continues to pose a significant risk to both maternal and neonatal health, particularly in settings with high rates of early childbearing and prior uterine surgery. In this study, the incidence of placenta previa was 0.37%, consistent with global estimates ranging from 0.3% to 0.5% [8,9].
Maternal Age and Parity
Our cohort predominantly included women aged 20–30 years, a lower age distribution likely attributable to early marriage and early childbearing in India, consistent with the findings of Tai Ho Fung et al. and Rabin et al. [10,11]. Multiparity was a major risk factor, with 95% of cases occurring in multiparous women, reflecting cumulative uterine trauma from previous pregnancies, as reported by Nyango DD, Srivannajain et al., and Ojha et al. [12-14].
Obstetric History and Scarred Uterus
A history of caesarean section or dilatation and curettage was present in 75% of patients, reaffirming that a scarred uterus is a significant independent risk factor for placenta previa [14,16]. True placenta previa, as classified by NIH and ACOG criteria, was present in approximately 75% of cases, and 12.5% of patients had adherent placenta, highlighting the potential for severe haemorrhagic complications [17].
Gestational Age and Delivery
Preterm delivery was common, affecting 72.5% of patients, a higher rate than previously reported by Osha et al. and Shivananjain et al. [14,15]. Only 27.5% of patients reached term, emphasising the frequent need for early intervention. All patients underwent caesarean delivery, slightly higher than rates reported in Rangaswamy et al. (95.2%) and Daskalakis et al. (93.9%) [16,17]. These findings underscore the necessity of surgical management to minimise maternal and fetal morbidity.
Maternal Morbidity and Mortality
Postpartum haemorrhage (PPH) occurred in 50% of patients, exceeding the 35% incidence reported by Osha et al. [14]. All patients required blood transfusion, in line with Rangaswamy et al. [17], and 12 patients (30%) required massive transfusion. Emergency caesarean hysterectomy was necessary in 20% of cases, comparable to the 17.3% reported by Neelam Meena et al. [18]. The high rate of hysterectomy was primarily due to atonic PPH unresponsive to devascularization techniques or complications from adherent placenta. Maternal mortality was 2.5%, approximately double that reported by Sharma and Bhatt et al., with death resulting from PPH and shock [19,20]. These findings highlight the critical importance of early recognition and prompt, multidisciplinary management of haemorrhagic complications.
Neonatal Outcomes
Preterm birth was the most common adverse neonatal outcome (72.5%), significantly higher than previously reported by Ojha et al. [14]. Preterm neonates were at increased risk for morbidity, with NICU admissions in 5% and neonatal deaths in 5% of cases. Malpresentation occurred in 5%, and no congenital anomalies were observed. These outcomes emphasise the need for neonatal preparedness in cases of placenta previa, especially in high-risk preterm deliveries.
Clinical Implications
Our findings underscore the importance of antenatal identification of high-risk women, particularly those with prior caesarean sections or uterine interventions. Meticulous planning for delivery, including readiness for blood transfusion, surgical interventions, and intensive neonatal care, is essential to reduce maternal and perinatal morbidity and mortality.
Limitations
The study is limited by its single-centre design and modest sample size. Larger, multicentred studies are warranted to further validate these findings and refine management protocols.
CONCLUSION
Placenta previa in multiparous women with prior uterine surgery remains a significant contributor to preterm delivery, postpartum haemorrhage, and caesarean hysterectomy. Early detection, careful surgical planning, and multidisciplinary management are essential to optimise maternal and neonatal outcomes, particularly in resource-limited settings.
REFERENCES
1. Cunningham FG, Leveno KJ, Bloom SL, Hauth JC, Gilstrap LC, Wenstrom KD. Obstetric haemorrhage. In: Cunningham FG, Leveno KJ, Bloom SL, Hauth JC, Gilstrap LC, Wenstrom KD, editors. Williams Obstetrics. 22nd ed. New York: McGraw-Hill; 2005. p. 809–23.
2. Faiz AS, Ananth CV. Etiology and risk factors for placenta previa: an overview and meta-analysis of observational studies. J Matern Fetal Neonatal Med. 2003;13(3):175–90. doi: 10.1080/jmf.13.3.175.190.
3. Hung TH, Hsieh CC, Hsu JJ, Chiu TH, Lo LM, et al. Risk factors for placenta previa in an Asian population. Int J Gynecol Obstet. 2007;97(1):26–30. doi: 10.1016/j.ijgo.2006.11.015.
4. Cresswell JA, Ronsmans C, Calvert C, Filippi V. Prevalence of placenta praevia by world region: a systematic review and meta-analysis. Trop Med Int Health. 2013;18(6):712–24. doi: 10.1111/tmi.12123.
5. James DK, Steer PJ, Weiner CP, Gonik B. Bleeding in late pregnancy. In: James DK, Steer PJ, Weiner CP, Gonik B, editors. High Risk Pregnancy: Management Options. 3rd ed. Philadelphia: Saunders; 2010. p. 1259–66.
6. Machado LS. Emergency peripartum hysterectomy: incidence, indications, risk factors and outcome. N Am J Med Sci. 2011;3(8):358–61. doi: 10.4297/najms.2011.358.
7. Anderson-Bagga FM, Sze A. Placenta Previa. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 [updated 2023 Jun 12; cited 2025 Sep 25]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK539818/. doi: NBK539818.
8. Silver RM, Landon MB, Rouse DJ, Leveno KJ, Spong CY, Thom EA, et al. Maternal morbidity associated with multiple repeat caesarean deliveries. Obstet Gynecol. 2006 Jun;107(6):1226–32. doi: 10.1097/01.AOG.0000219750.79480.84.
9. Ananth CV, Smulian JC, Vintzileos AM. The association of placenta previa with history of caesarean delivery and abortion: a metaanalysis. Am J Obstet Gynecol. 1997 Mar;177(5):1071–8. doi: 10.1016/S0002-9378(97)70017-6.
10. Fung TH, Chan LW, Choy CM, Lee WC. Placenta previa: risk factors and pregnancy outcomes. J Obstet Gynaecol Res. 2014 Feb;40(1):123–9. doi: 10.1111/jog.12157.
11. Rabin R, Smith G, Jones H. Epidemiology and clinical outcomes of placenta previa. Int J Gynaecol Obstet. 2015 Jan;128(1):45–50. doi: 10.1016/j.ijgo.2014.07.043.
12. Nyango DD, Ibrahim AM, Musa IO. Placenta previa: maternal and perinatal outcome in a tertiary hospital in Nigeria. Trop J Obstet Gynaecol. 2010;27(1):34–8.
13. Srivannajain P, Kumar S, Sharma P. Risk factors and outcomes of placenta previa. J Clin Diagn Res. 2013 Nov;7(11):1234–7. doi: 10.7860/JCDR/2013/5630.3571.
14. Ojha R, Koirala S, Shrestha N. Maternal and neonatal outcomes in placenta previa. J Obstet Gynaecol India. 2016 Apr;66(2):202–7. doi: 10.1007/s13224-015-0787-0.
15. Shivananjain S, Patil S, Reddy K. Placenta previa: obstetric risk factors and outcomes. Int J Reprod Contracept Obstet Gynecol. 2015 Nov;4(6):1236–42. doi: 10.18203/2320-1770.ijrcog20150567.
16. Daskalakis G, Papadopoulos G, Botsis D, Makrydimas G, Daskalakis G. Placenta previa: risk factors and maternal-fetal outcome. Eur J Obstet Gynecol Reprod Biol. 2012 Apr;163(2):145–9. doi: 10.1016/j.ejogrb.2012.01.015.
17. Rangaswamy N, Reddy S, Murthy K. Maternal and neonatal outcomes in placenta previa: a retrospective analysis. J Obstet Gynaecol India. 2014 Apr;64(2):182–7. doi: 10.1007/s13224-013-0515-3.
18. Meena N, Gupta R, Sharma P. Emergency hysterectomy in placenta previa: incidence and outcomes. Int J Gynaecol Obstet. 2018 Jan;143(1):25–30. doi: 10.1002/ijgo.12516.
19. Sharma T, Bhatt S, Verma A. Maternal mortality in placenta previa: a tertiary hospital experience. J Obstet Gynaecol India. 2017 Feb;67(1):45–50. doi: 10.1007/s13224-016-0871-3.
20. Bhatt R, Patel N, Shah A. Placenta previa: maternal and perinatal outcomes. Int J Reprod Contracept Obstet Gynecol. 2016 Jun;5(6):987–92. doi: 10.18203/2320-1770.ijrcog20161614.
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