Dear Editor,
We observed that there is a limited information on the impact of the SARS-CoV-2 infection on pregnant women with heart disease (HD). Aim of our study was to investigate the impact of COVID-19 on pregnancy and neonate retrospectively at BYL Nair Charitable Hospital (NH), a dedicated COVID-19 hospital [1] in women with HD in Mumbai, India. In the initial phase of COVID-19 pandemic of 6 months, NH received five RT-PCR confirmed COVID-19 pregnant women with heart disease [Rheumatic HD (RHD; n = 3), Peripartum Cardiomyopathy (PPCM; n = 2)], out of 879 COVID-19 pregnant and post-partum women (Table 1 ). To address if COVID-19 poses additional risk in pregnancy with HD, we compared outcomes in uninfected pregnant women with HD (n = 43) in pre-pandemic period from the same center (Table S1). We found around 1% of heart disease in pregnant women with COVID-19. Adverse outcomes such as preterm delivery, PPROM, low birth weight, neonatal death were observed in pregnant women with HD (RHD/PPCM) and COVID-19. Pre-term delivery was nearly three times higher in women with HD and COVID-19 (95 % CI 0.33–20.48). PPROM/PROM was observed 14 times higher in women with HD and SARS-CoV-2 infection (95 % CI 0.69–283.79). Preterm vaginal delivery was reported in one woman with RHD and COVID-19 (Case-2) and her new-born required neonatal intensive care due to low birth weight.
Table 1.
Demographic, epidemiological, clinical characteristics and management of pregnant women with RHD or PPCM and COVID-19.
Parameters | RHD1 | RHD2 | RHD3 | PPCM1 | PPCM2 |
---|---|---|---|---|---|
Heart Disease history | RHD since childhood | RHD diagnosed during first pregnancy | RHD since childhood | PPCM | PPCM |
No. of referrals before reaching NH | 2 | 1 | 2 | 4 | 5 |
Demographic | |||||
Age in years | 27 | 31 | 26 | 26 | 21 |
Gravida (G) /Parity (P) | Primigravida | G3P2L2 | G4P2L2 | G3P2L2 | Primigravida |
BMI kg/m2 | 22.6 | 23.1 | Not available | 34.5 | 23 |
Containment/Sealed zone | No | Yes | No | No | Yes |
Indication for COVID-19 RT-PCR testing | Symptomatic | Universal Testing | Universal Testing | Symptomatic | Universal Testing |
Clinical | |||||
Asymptomatic/Symptomatic (Mild/Moderate/Severe) | Symptomatic Mild cough with expectoration and breathlessness b |
Asymptomatic | Asymptomatic | Symptomatic Mild (palpitations and dyspnoea) |
Asymptomatic |
Fever | No | No | No | No | No |
Cough | Yes | No | No | Yes | No |
Breathing Difficulty | Yes | No | No | Yes | No |
Investigations | |||||
Hemoglobin, g/dL (Reference range - >11.0) | 12.1 | 11.1 | 9.9 | 12 | 10.6 |
White blood cell count, /μL (Reference range - 3500−9500) | 7300 | 6700 | 9800 | 10900 | 6000 |
Platelet count, ×103/μL (Reference range - 125−350) | 1.21 | 1.20 | 1.3 | 3.09 | 4.11 |
Serum Creatinine, mg/dL (Reference range - 0.84–1.21) | 2.3 | 1.0 | 0.9 | 0.4 | 0.9 |
Echocardiogram | Moderate MS, moderate MR, mild TR, dilated LA with mildly dilated LV, Moderate PAH, MVOA 1.3 cm2 LVEF-65 % | Severe MS, moderate MR, trivial AR Severe TR | Moderate MS severe PAH LVEF 60 % | Dilated LV, severe generalised LV hypokinesia, LVEF 20 %, LV diastolic dysfunction, LV non-compaction, Mild MR, Mild PAH, Mild TR, RVSP 48mmhg | Global LV Hypokinesia, LVEF of 30−35 %, LV non-compaction, Mild MR, Moderately Compromised LV Systolic Function |
Blood Pressure in mmHg | 100/70 | 110/70 | 100/70 | 130/80 | 110/70 |
Oxygen Saturation % | 95 | 99 | 98 | 96 | 99 |
Chest X-ray changes | Yes | Not done | Not done | Normal | Not done |
Consolidation | Yes | No | No | No | No |
ARDS | No | No | No | No | No |
Arterial blood gas analysis | Normal | Normal | Normal | Normal | Normal |
Relevant Ultrasound | Ultrasound - bilateral bright kidney. | – | – | – | Level-II ultrasound at 21 weeks - severe oligohydramnios, bilateral hydro-nephrosis, hydro-ureter, key-hole bladder, posterior urethral valves. |
Weeks of Gestation at delivery | 39 weeks | 36 weeks | 37 weeks at admission | 36weeks 5days | 38weeks 1day |
Mode of delivery | Vaginal Delivery | Vaginal Delivery | Undelivered | Cesarean section | Vaginal Delivery a |
PROM/PPROM | No | No | – | Yes | No |
Preterm labour | No | Yes | – | Yes | No |
Neonatal Outcome | Good | NICU admission, Baby survived | – | Good | Multiple congenital anomalies, poor APGAR, NICU admission, NND |
Birth Weight in Kg | 2.470 | 1.790 | – | 2.240 | 2.229 |
Complications intrapartum & postpartum | No | No | – | No | No |
Treatment | frusemide, lacilactone (with-held) and metoprolol | spironolactone, frusemide, metoprolol, penicillin | atenolol, frusemide, penicillin | frusemide, bisoprolol, isosorbide dinitrate, digoxin | carvedilol, ramipril |
Hospital Stay | 14 | 17 | 4 | 13 | 5 |
Mortality | No | No | No | No | No |
SARS-CoV-2, Severe Acute Respiratory Syndrome Corona virus 2; RT-PCR, Reverse Transcriptase Polymerase Chain Reaction; COVID-19, coronavirus disease 2019; PROM, premature rupture of membranes ; PPROM, preterm premature rupture of membranes; NICU, neonatal intensive care unit; NND, neonatal death; RHD, rheumatic heart disease ; PPCM, peripartum cardiomyopathy; MS, mitral stenosis; MR, mitral regurgitation; TR, tricuspid regurgitation; LA- Left Atrium, LV-Left ventricular; PAH, pulmonary artery hypertension; MVOA, Mitral Valve Orifice Area; LVEF, left ventricle ejection fraction; AR, aortic regurgitation; RVSP, right ventricular systolic pressure; ARDS, Acute Respiratory Distress Syndrome.
Presented in the labour suite with a fully dilated cervix and delivered vaginally immediately on arrival, on the stretcher.
Increased in intensity since 5 days but she had similar complaints since long before pregnancy.
Pregnant woman with RHD and COVID-19 presented with fever, cough with expectoration, breathlessness, tachycardia with normal oxygen saturation. This suggests some diagnostic overlap between SARS-CoV-2 infection and new or recurrent acute respiratory failure with HD [2]. Two women with RHD were on secondary prophylaxis with penicillin in our study group. During the period of lockdown when there were transportation restrictions, the pregnant women with RHD faced several challenges in accessing the healthcare. Therefore, secondary prophylaxis must be ensured to all patients with RHD and more specifically to pregnant women by the public and private healthcare providers. Pregnancy is a state that is particularly susceptible to respiratory diseases like COVID-19 due to a compensated respiratory alkalosis with metabolic acidosis [3]. Despite this, both the cases with PPCM described in this report did not have worsening of PPCM due to COVID -19.
We faced multiple challenges because of COVID-19 status and comorbidities of the women presented in this report. During the early phase of pandemic, there was a delay in receiving appropriate treatment as all these women were denied treatment in multiple hospitals before being referred to our dedicated COVID-19 facility at NH. This observation suggested the significant challenges faced by these women, who are also likely to face difficulties in secondary prophylaxis and access to health care leading to additional risk for adverse pregnancy and neonatal outcomes.
One woman with PPCM (Case-5) had multiple congenital anomalies in the fetus at 21-weeks pregnancy but was denied medical termination of pregnancy (MTP) in multiple hospitals. The MTP Act (1971) in India permits the pregnancy termination until 20-weeks. Although MTP amendment Bill (2020) was passed in March, 2020 in the Lok-Sabha, it is yet to become an Act.
In the context of the COVID-19 pandemic, our study generated an evidence of impact of COVID-19 on pregnant women with RHD with COVID-19. Therefore, countries with endemic RHD with higher COVID-19 burden should make provision of cardiac assessment on ultrasound to improve RHD diagnosis and strengthen the healthcare system for multi-speciality management of pregnant women with RHD and COVID-19.
Funding
The study is funded by intramural grant of ICMR-NIRRH (MS/RA/951/07-2020).
Author contributions
NM and RG had full access to all data and take responsibility for data integrity and the accuracy of the analysis. NM and RG were responsible for study concept and design. NM, RG, SM supervised the study. AT, BJ, NK and SG acquired the data. All authors interpreted the data. RG and NM performed statistical analysis. NM, SM, and RG provided administrative, technical and material support. NM and AT drafted the manuscript. RG, NM revised the manuscript. All authors approved the manuscript.
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Declaration of Competing Interest
The authors report no declarations of interest.
Acknowledgements
The authors acknowledge the network of National Registry of Pregnant women with COVID-19 in India (PregCovid Registry, CTRI/2020/05/025423). The Dean, TNMC, Faculties, Resident doctors in the Department of Obstetrics and Gynaecology, Cardiology at TNMC, Mumbai are sincerely acknowledged. RG lab is funded by grants from Indian Council of Medical Research (ICMR). RG is an awardee of the DBT Wellcome India alliance clinical and public health intermediate fellowship (Grant no. IA/CPHI/18/1/503933). Dr Periyasamy Kuppusamy (NIRRH) is acknowledged for assistance in statistical analysis.
Footnotes
Supplementary material related to this article can be found, in the online version, at doi:https://doi.org/10.1016/j.ejogrb.2021.01.024.
Appendix A. Supplementary data
The following is Supplementary data to this article:
References
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