Utilizing Maternal Morbidity as a Novel Screening (MMS) Tool for Predicting Peripartum Morbidity at a Rural Tertiary Care Teaching Hospital in Central India
Arti M Wasnik, Neema Acharya, Manjusha G Mahakalkar

TL;DR
This study introduces a new maternal morbidity screening tool that better predicts childbirth complications than existing methods in a rural Indian hospital.
Contribution
A novel maternal morbidity screening (MMS) tool was developed and shown to outperform the MEOWS chart in predicting peripartum morbidity.
Findings
The MMS tool achieved 90.50% accuracy in predicting peripartum morbidity.
MMS had higher sensitivity (95.24%) and specificity (89.50%) compared to the MEOWS chart.
Obstetric morbidity was 66.66% in the maternal morbidity group using MMS versus 32% with MEOWS.
Abstract
Background The majority of complications and deaths related to childbirth are concentrated in developing and disadvantaged nations, where the rates are unacceptably elevated. These incidents predominantly occur in the vicinity during the intrapartum period and immediately after childbirth. The peripartum period is especially critical for expectant mothers, as it represents the time when a significant number of complications and deaths occur. This study aimed to develop, validate, and assess the efficacy of the maternal morbidity screening (MMS) tool for predicting peripartum morbidity. Methodology The study was conducted in two phases: Phase one involved developing, validating, and piloting the MMS tool, while Phase two focused on evaluating and comparing the MMS tool with the modified early obstetric warning system (MEOWS) chart for predicting peripartum morbidity. An observational…
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| Sr. No. | Parameters | Normal (Green) | Low Risk (Orange Alert) | High Risk (Red Alert) |
| 1 | Temperature | 36-38 °C | 35-<36 °C | >38 °C or <35 °C |
| 2 | O2 saturation | 95-100% | - | <95% |
| 3 | Heart rate | 50-100 | >100-120 or 40-<50 | <40 or >120 |
| 4 | Respiratory rate | 10-20 | 21-30 | <10 or >30 |
| 5 | Systolic BP | 100-140 | 90-<100 or >140-160 | <90 or >160 |
| 6 | Diastolic BP | <90 | 90-100 | >100 |
| 7 | Proteinuria | nil-trace | 1+ to 2+ | >2+ |
| 9 | Neural response | Alert | Responds to verbal stimuli | Unresponsive, responds to pain |
| 10 | General condition | Looks well | Looks unwell | - |
| 11 | Blood investigation Hb | 11-12 g/dL | <11 g/dL | <6 g/dL |
| 12 | WBC | 4.5-11.0x109/L | <4.5-11.0x109/L | <3.5 or irrespective |
| 13 | Platelet | 150-400x109/L | <150-400x109/L | <10-20x109/L |
| 14 | SGPT | 7-56 IU/L | - | >7-56 IU/L |
| 15 | Bilirubin | 1.2 mg/dL | - | >1.2 mg/dL |
| 16 | Urea | 17-43 mg/dL | - | >17-43 mg/dL |
| 17 | Creatinine | 0.7-1.2 mg/dL | - | >0.7-1.2 mg/dL |
| 18 | RBS | <200 mg/dL | - | >200 mg/dL |
| MMS Tool (221) | MEOWS Chart (221) | ||
| Triggered group | Non-trigger group | Triggered group | Non-trigger group |
| 57 | 164 | 51 | 170 |
| 25.79% | 74.20% | 23.07% | 76.92% |
| Parameters | Total Orange + Red Trigger (Abnormal Zone) MMS Tool | Total Orange + Red Trigger (Abnormal Zone) MEOWS Chart | Difference |
| Respiratory rate | 12 (5.42%) | 9 (4.07%) | 1.35% |
| Oxygen saturation | 3 (1.35%) | 4 (1.80%) | 0.45% |
| Temperature | 4 (1.80%) | 5 (2.26%) | 0.45% |
| Heart rate | 10 (4.52%) | 11 (4.97%) | 0.45% |
| Systolic BP | 12 (5.42%) | 12 (5.42%) | 0 |
| Diastolic BP | 16 (7.23%) | 11 (4.97%) | 2.26% |
| Colour of liquor | 2 (0.90%) | 2 (0.90%) | 0 |
| Neural response | 4 (1.80%) | 3 (0.90%) | 0.90% |
| General condition | 3 (1.35%) | 5 (2.26%) | 0.91% |
| Parameters | Green Zone (Normal Zone) | Orange Zone | Red Zone | Total Orange + Red Trigger (Abnormal Zone) |
| Hb | 208 | 10 | 3 | 13 (5.88%) |
| RBS | 214 | 5 | 2 | 7 (3.16%) |
| WBC | 212 | 6 | 3 | 9 (4.07%) |
| Platelets | 218 | 2 | 1 | 3 (1.35%) |
| SGPT | 212 | 9 | - | 9 (4.07%) |
| Bilirubin | 219 | - | 2 | 2 (0.90%) |
| Proteinuria | 206 | 7 | 8 | 15 (6.78%) |
| Creatinine | 213 | 5 | 3 | 8 (3.61%) |
| Urea | 217 | 3 | 1 | 4 (1.80%) |
| MMS Tool | MEOWS Chart | |||
| Obstetric morbidity during hospital stay | Triggered group (n=57) | Non-triggered group (n=164) | Triggered group (n=51) | Non-triggered group (n=170) |
| Category 1 | 19 (33.33%) | 162 (98.78%) | 27 (68%) | 158 (88.77%) |
| Category 2 | 38 (66.66%) | 2 (1.21%) | 24 (32%) | 12 (11.22%) |
| Total | 57 (100%) | 164 (100%) | 51 (100%) | 170 (100%) |
| Mode of Delivery and Obstetric Intervention | Normal (Triggered) Group (n=57) | Abnormal (Non-Triggered) Group (n=164) | χ2-value |
| Normal delivery | 35 (61.40%) | 54 (32.92%) | 16.65, p=0.0002, S |
| LSCS | 20 (30.08%) | 108 (65.85%) | |
| Assisted | 2 (3.50) | 2 (3.50%) | |
| Total | 57 (100%) | 164 (100%) |
| Maternal Morbidity | MMS Tool | MEOWS Chart |
| Sensitivity | 95.24% | 70.51% |
| Specificity | 89.50% | 86.81% |
| Positive predictive value | 70.24% | 52.95% |
| Negative predictive value | 98.50% | 92.94% |
| Accuracy | 90.50% | 83.71% |
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Taxonomy
TopicsMaternal and fetal healthcare · Global Maternal and Child Health · Maternal and Perinatal Health Interventions
Introduction
High rates of obstetric morbidity and mortality remain a persistent problem in underdeveloped nations, even with the implementation of national and international healthcare programs [1]. By 2030, the worldwide maternal mortality rate (MMR) is expected to drop to below 70 per 100,000 live births, according to the Sustainable Development Goals (SDG) [2]. The MMR in India is currently 97 per 100,000 live births, with noticeable regional differences. Maharashtra's MMR is 33 per 100,000 live births, while Kerala boasts a unique MMR of 19 per 100,000 live births, attributed to strong referral networks and efficient screening procedures [3]. Despite continuous endeavours, India has not achieved the Millennium Development Goal's (MDG) objective of reducing maternal mortality. There is now a shift in focus to indicators such as obstetric morbidity and the ratio of severe maternal morbidity to mortality [4,5].
In India, anaemia stands as the second leading cause of maternal mortality, accounting for approximately 20% of deaths attributed to this condition [6]. A patient diagnosed with mild preeclampsia on clinical examination may have underlying multisystem involvement and related complications, primarily detected through biochemical tests [7]. The International Federation of Gynecology and Obstetrics (FIGO) also recommends that patients with preeclampsia undergo timely diagnostic biochemical testing for systemic involvement. Gestational diabetes mellitus (GDM) impacts 2%-5% of pregnancies each year. Throughout pregnancy, there is a 50% rise in the glomerular filtration rate. Nevertheless, elevated creatinine levels nearing the upper threshold of normal serve as an indicator of potential renal issues in GDM. Elevated uric acid levels observed in GDM are part of the metabolic syndrome, causing insulin resistance. The pathophysiology, biochemical, and metabolic abnormalities in GDM affect the renal system [8].
This study compares obstetric morbidity in patients using a newly developed maternal morbidity screening (MMS) tool and the modified early obstetric warning system (MEOWS) chart, assessing sensitivity, specificity, predictive value, and accuracy. To enhance predictability, we propose incorporating biochemical parameters into the screening tool format for comprehensive and accessible use by healthcare professionals. This will facilitate early identification and management of peripartum morbidity in both high- and low-risk groups.
Materials and methods
Study setting, study design, and sample size
The present study was conducted in the Obstetrics and Gynaecology Department of Acharya Vinoba Bhave Rural Hospital (AVBRH), Sawangi (M) Wardha. The study design was an observational analytical clinical study. The study population consisted of 441 prenatal women in labour with a gestational age greater than 28 weeks. The study was approved by Datta Meghe Institute of Medical Sciences (Deemed to be University) Institutional Ethics Committee (DMIMS (DU)/IEC/2020-21/9155).
Inclusion and exclusion criteria
Eligible participants were those who were in labour and had a gestational age of more than 28 weeks. Patients who did not give consent and cases where the pregnancy continued beyond the following day were excluded.
Data collection process and instrument
The Confidential Enquiry into Maternal and Child Health (CEMACH) report's recommended MEOWS chart was used, and parameters were entered for every patient in accordance with the usual procedure [9]. The trigger zone type was derived using standard values from the MEOWS chart. Both groups' baseline measurements included heart rate, respiration rate, blood pressure, temperature, overall health, neural responsiveness, and oxygen saturation. Physiological and biochemical parameters were monitored using the MMS tool, categorizing them into trigger and non-trigger zones, as detailed in Table 1. Monitoring occurred every four hours until 24 hours post-delivery in both groups.
Statistical analysis
The gathered data were analyzed using both inferential and descriptive statistical techniques. This involved performing chi-square tests and examining key test statistics such as specificity, sensitivity, accuracy, and predictive value. Statistical analysis were conducted using IBM SPSS Statistics for Windows, Version 26 (Released 2019; IBM Corp., Armonk, New York), revealing significant findings with a threshold set at p<0.05.
Results
The MMS tool identified trigger zones with a rate of 25.79%, compared to 23.07% in the MEOWS chart. The non-trigger group in the MMS observed a rate of 74.20%, while the MEOWS chart showed 76.92% (Table 2).
The MMS tool and MEOWS chart showed variations in the following parameters: respiratory rate (1.35%), oxygen saturation (0.45%), temperature (0.45%), heart rate (0.45%), diastolic blood pressure (2.26%), neural response (0.90%), and general condition (0.91%). There was no significant difference found between both groups (Table 3).
The most common parameters leading to derangement and placing the patient into the trigger zone were haemoglobin (Hb) (5.88%), proteinuria (6.78%), serum glutamic pyruvic transaminase (SGPT) (4.07%), white blood cell (WBC) (4.07%), and random blood sugar (RBS) (3.16%) (Table 4).
The analysis demonstrated significant improvement in morbidity during hospital stay, 66.66% in the MMS tool and 32% in the MEOWS chart. The MMS tool had more likelihood of developing morbidity than the MEOWS chart (Table 5).
The normal delivery rate in the MMS tool for the triggered group is 61.40%, while the rate for the lower-segment caesarean section (LSCS) is 30.08 % (Table 6).
Table 6: Comparison of the delivery methods and obstetric interventions in the normal (trigger and non-trigger) groupsp-value<0.05 is considered significantLSCS: lower-segment caesarean section; x2: chi-square
The sensitivity of the MMS tool was found to be 95.24%, compared to 70.51% for the MEOWS chart. The specificity of the MMS tool was 89.50% compared to 86.81% for the MEOWS. The predictive value of the MMS was 98.50% compared to 92.94% for the MEOWS, and the accuracy of the MMS was 90.50% as opposed to 83.71% for the MEOWS chart. The MMS tool had more sensitivity, specificity, predictive value, and accuracy than the MEOWS chart (Table 7).
Discussion
In the MMS tool, the trigger zone was 25.79%, compared to 23.07% in the MEOWS chart. The non-trigger zone in the MMS group was 74.20%, while in the MEOWS chart, it was 76.92%. This comparison aligns with the studies conducted by Singh A et al. [10] and Singh S et al. [11]. In these studies, among the triggered group, 66.66% fell into category II, indicating those with obstetric morbidity in the MMS tool and 32% in the MEOWS chart. The MMS tool showed a higher likelihood of developing morbidity compared to the MEOWS chart. Similar results were observed in the study conducted by Singhal S et al. [12]. In the non-triggered group, 1.21% were categorized under category II, with the most prevalent obstetric morbidity being hypertensive disorders of pregnancy at 1.21%, followed by anaemia at 1.21% and gestational diabetes at 0.60%. Consequently, it can be deduced that the most common obstetric morbidities in both the category I and category II groups were hypertensive disorders of pregnancy and anaemia.
Research conducted by Singh et al. reported obstetric morbidity in 26.6% of the triggered group and 16.61% of the non-triggered group. The study noted one mortality in the triggered group, attributed to eclampsia. Hypertensive disorders of pregnancy emerged as the most prevalent morbidity in the triggered group, followed by anaemia, obstetric haemorrhage, and sepsis [10]. The findings were comparable with the current study. In a study by Singh S et al., there were no reported cases of maternal mortality [11]. However, in contrast to the present study, haemorrhage emerged as the predominant morbidity, followed by hypertensive disorders in pregnancy and anaemia. A study conducted in developing countries by Khan KS et al. examined the collective factors contributing to maternal deaths using various datasets. It was concluded that haemorrhage and hypertensive disorders were the primary factors leading to maternal deaths in developing nations [13].
The study conducted by Geller SE et al. assessed factors associated with maternal outcomes, revealing haemorrhage and hypertensive disorders as the principal causes, although with some regional variations [14]. In the current study, hypertensive disorders of pregnancy stand out as the predominant cause of obstetric morbidity. One possible reason for this could be the low awareness levels among patients. Anaemia, being the second most common cause of morbidity in triggered patients in the present study, might reflect a lack of proper iron supplementation, poor nutritional status, and the occurrence of multiple and more frequent births among Indian females. Therefore, addressing this issue requires intensive care and efforts to improve maternal outcomes significantly.
Haemoglobin levels found at 5.88%, which is considered abnormal, are a crucial biochemical parameter in pregnancy. Early recognition of low haemoglobin can prevent further complications during pregnancy. Several studies have reported it to be one of the most common issues encountered [15,16]. There was an elevation in proteinuria by 6.78%, with 5.42% and 4.97% increases in systolic blood pressure (SBP) and diastolic blood pressure (DBP), respectively. Both SBP and DBP were significantly higher in preeclampsia patients. Several studies have also reported these findings [17,18]. Routine measurement of blood pressure during pregnancy has long been a standard part of prenatal care [19].
The sensitivity of the MMS screening tool was 95.24%, the specificity was 89.50 %, and the predictive value was 98.50%. The accuracy of the MMS tool was 90.50%. The MEOWS chart showed a sensitivity of 70.51%, specificity of 86.81%, predictive value of 92.94%, and accuracy of 83.71%. It indicates that the MMS tool was more efficacious for predicting peripartum morbidity. The sensitivity in the MMS tool is higher than in the previous research by Singhal S et al. [12,20]. Healthcare workers should consider researching common disease entities leading to obstetric morbidity at healthcare systems' primary, secondary, and tertiary levels.
Clinical implications
The MMS tool is a potentially valuable and cost-effective resource, providing a straightforward means for healthcare workers to promptly identify, treat, and urgently refer cases.
Strengths
This study categorizes the trigger and non-trigger zones and compares them with the MEOWS chart. The MMS tool includes both physiological and biochemical parameters, enabling the early detection of peripartum morbidity before it reaches severe levels.
Limitations
As such, there are no palpable weaknesses; however, long-term follow-up is required to assess.
Conclusions
The occurrence of maternal morbidity in the trigger zone was significantly higher than in the non-trigger zone in the MMS tool compared with the MEOWS chart. The MMS tool demonstrated superior predictive capability for peripartum morbidity compared to the existing chart. Overall, the accuracy of the MMS tool in predicting peripartum morbidity was significantly higher than that of the MEOWS chart. Consequently, employing the MMS screening tool to anticipate peripartum morbidity is recommended.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Evaluation of obstetric near miss and maternal deaths in a tertiary care hospital in north India: shifting focus from mortality to morbidity J Obstet Gynaecol India Pandey A Das V Agarwal A Agrawal S Misra D Jaiswal N 3943996420142548914110.1007/s 13224-014-0552-1PMC 4257929 · doi ↗ · pubmed ↗
- 2Sustainable development goal 3 5 2024 2017 https://sustainabledevelopment.un.org/sdg 3.
- 3Special bulletin on maternal mortality in India 2018-20 5 2024 2022 https://censusindia.gov.in/nada/index.php/catalog/44379/download/48052/SRS_MMR_Bulletin_2018_2020.pdf
- 4Predictors of maternal mortality and near-miss maternal morbidity J Perinatol Goffman D Madden RC Harrison EA Merkatz IR Chazotte C 5976012720071770318110.1038/sj.jp.7211810 · doi ↗ · pubmed ↗
- 5Maternal critical care in obstetrics J Obstet Gynaecol Can Baskett TF O’Connell CM 2182213120091941656710.1016/S 1701-2163(16)34119-6 · doi ↗ · pubmed ↗
- 6The prevalence of anaemia and associated factors in pregnant women in a rural Indian community J Australasian Med Ahmad N Kalakoti P Bano R Aarif SMM 27628032010 https://api.semanticscholar.org/Corpus ID:73992937
- 7A study of HELLP syndrome among cases of pre-eclampsia and eclampsia: incidence and correlation of laboratory parameters J Oalib Tiwari P Bhalavi S Nayak S Tiwari R 022015 https://www.scirp.org/journal/paperinformation?paperid=68595
- 8Exploration of the clinico-biochemical parameters to explain the altered renal mechanism in gestational diabetes mellitus J Clin Diagn Res Nagalakshmi CS Devaki RN Akila P 36937162012 https://www.jcdr.net/articles/PDF/1987/3812_E(C)_F(T)_PF(V)_PFA(A)_P(_).pdf
