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. 2022 Sep 19;2(9):e0000897. doi: 10.1371/journal.pgph.0000897

Meta-analysis of nationwide SARS-CoV-2 infection fatality rates in India

Lauren Zimmermann 1,2,*, Bhramar Mukherjee 1,2,3
Editor: Jong-Hoon Kim4
PMCID: PMC10021252  PMID: 36962545

Abstract

There has been much discussion and debate around underreporting of deaths in India in media articles and in the scientific literature. In this brief report, we aim to meta-analyze the available/inferred estimates of infection fatality rates for SARS-CoV-2 in India based on the existent literature. These estimates account for uncaptured deaths and infections. We consider empirical excess death estimates based on all-cause mortality data as well as disease transmission-based estimates that rely on assumptions regarding infection transmission and ascertainment rates in India. Through an initial systematic review (Zimmermann et al., 2021) that followed PRISMA guidelines and comprised a search of databases PubMed, Embase, Global Index Medicus, as well as BioRxiv, MedRxiv, and SSRN for preprints (accessed through iSearch) on July 3, 2021, we further extended the search verification through May 26, 2022. The screening process yielded 15 studies qualitatively analyzed, of which 9 studies with 11 quantitative estimates were included in the meta-analysis. Using a random effects meta-analysis framework, we obtain a pooled estimate of nationwide infection fatality rate (defined as the ratio of estimated deaths over estimated infections) and a corresponding confidence interval. Death underreporting from excess deaths studies varies by a factor of 6.1–13.0 with nationwide cumulative excess deaths ranging from 2.6–6.3 million, whereas the underreporting from disease transmission-based studies varies by a factor of 3.5–7.3 with SARS-CoV-2 related nationwide estimated total deaths ranging from 1.4–3.4 million, through June 2021 with some estimates extending to 31 December 2021. Underreporting of infections was found previously (Zimmermann et al., 2021) to be 24.9 (relying on the latest 4th nationwide serosurvey from 14 June-6 July 2021 prior to launch of the vaccination program). Conservatively, by considering the lower values of these available estimates, we infer that approximately 95% of infections and 71% of deaths were not accounted for in the reported figures in India. Nationwide pooled infection fatality rate estimate for India is 0.51% (95% confidence interval [CI]: 0.45%– 0.58%). We often tend to compare countries across the world in terms of total reported cases and deaths. Although the US has the highest number of reported cumulative deaths globally, after accounting for underreporting, India appears to have the highest number of cumulative total deaths (reported + unreported). However, the large number of estimated infections in India leads to a lower infection fatality rate estimate than the US, which in part is due to the younger population in India. We emphasize that the age-structure of different countries must be taken into consideration while making such comparisons. More granular data are needed to examine heterogeneities across various demographic groups to identify at-risk and underserved populations with high COVID mortality; the hope is that such disaggregated mortality data will soon be made available for India.

Introduction

The second wave of SARS-CoV-2 in the 2nd most populous country in the world, India, registered 414 thousand daily cases and 4.5 thousand daily deaths at its peak in May of 2021 [2], and led to a collapse of healthcare infrastructure [3]. Multiple studies indicate that the true number of infections and deaths are orders of magnitude larger [1, 4, 5]. Considerable effort has been devoted towards investigating the true number of SARS-CoV-2 attributed deaths and inferred infection fatality rates (IFR) in India. This brief report systematically synthesizes the existent literature on the true SARS-CoV-2 IFR in India (as of 26 May 2022), through a meta-analysis of studies based on excess deaths and studies based on epidemiological disease transmission models that present relevant estimates through at least June 2021, capturing most of the second wave in India.

Methods

In brief, we describe the systematic review framework that has previously been detailed in full with the complete search strategy [1]. Adhering to PRISMA guidelines (Table A in S1 Text includes the PRISMA checklist), the databases PubMed, Embase, Global Index Medicus, as well as BioRxiv, MedRxiv, and SSRN for preprints (accessed through iSearch), were searched on July 3, 2021 and results were updated through May 26, 2022. Using this approach, 4,971 citations were screened resulting in 15 studies classified into the following three groups: excess deaths studies (9 articles), disease transmission-based studies estimating unreported deaths (5 articles), disease transmission-based studies using reported deaths only (1 article). Since the three groups are not directly comparable, among the 15 studies, the 9 excess deaths studies with 11 datapoints are included in the nationwide quantitative synthesis. We were unable to stratify and separately meta-analyze disease transmission-based estimates (less than 3 studies rendered through at least June 2021 in the search verification). Several measures of fatality have been used in the literature as indicated in the glossary box. Using a random effects model with DerSimonian-Laird estimates and corresponding confidence intervals (CI), we meta-analyze IFR2 (defined as the infection fatality rate that accounts for death underreporting, as well as case underreporting). We provide a pooled estimate of nationwide IFR2 for SARS-CoV-2 in India with corresponding 95% CI. While this meta-analysis focuses on nationwide studies in India, we summarize the 18 other subnational/regional studies (not meta-analyzed) in Table B in S1 Text. A detailed explanation of the meta-analysis framework is provided in Methods B in S1 Text and Methods C in S1 Text, including Fig A in S1 Text displaying the process from data extraction to obtaining meta-analyzable IFRs.

Glossary

CFR=ReportedCumulativeDeaths(ata14daylag)ReportedCumulativeCases
ExcessDeaths=ObservedAllCauseMortalityExpectedAllCauseMortality
URF(C)=EstimatedTotalCumulativeInfectionsReportedCumulativeCases
URF(D)=EstimatedTotalCumulativeDeathsReportedCumulativeDeaths(ata14daylag)
IFR1=ReportedCumulativeDeaths(ata14daylag)EstimatedTotalCumulativeInfections
IFR2=EstimatedTotalCumulativeDeathsEstimatedTotalCumulativeInfections

Lastly, ethical approval is not applicable to the present study. The research uses publicly available data, and is IRB exempt.

Results

Fig 1 displays the PRISMA flow diagram reflecting the number of included articles from the updated search verification through May 26, 2022. For India countrywide, underreporting factors (URF) for deaths based on excess deaths studies range from 6.1–13.0 with cumulative excess deaths ranging from 2.6–6.3 million (as shown in Table 1). Considering estimates from disease transmission-based studies, URF ranges from 3.5–7.3 for India with total estimated deaths attributed to SARS-CoV-2 ranging from 1.4–3.4 million (see Table 1). As previously reported [1], URF for cases/infections (inferred from the most recent seroprevalence estimate) is 24.9 using the 4th nationwide serosurvey [6]. As such, the evidence suggests that even by the lowest of these estimates roughly 95% of cases (URF (Case) is reportedly 24.9) and 71% of deaths (URF (Death) is at least 3.5) were missed in India.

Fig 1. PRISMA flow diagram.

Fig 1

Table 1. Summary of nationwide mortality data from included studies in India from 2020–2021.

Seroprevalence of 67.6% is used with 765 million infectionsa from an age-adjusted population as of 14 Jun-6 Jul 2021 from the 4th nationwide serosurvey [6].

Study Time Period Estimated Total Deaths (LL, UL) in Millions COVID-19 Reported Deaths1 Under Reporting Factor (LL, UL)2 Data Source(s) Infection Fatality Rate (%)
Excess Deaths Studies
Wang et al., 20223 * Jan ’20-Dec ’21 4.0 (95% UI: 3.7, 4.3) 481,080 8.3 (7.5, 8.9) CRS 0.52
[5]
World Health Organization & Knutson, 2022 * Jan ’20-Dec ’21 4.7 (95% CI: 3.3, 6.4) 481,080 9.8 (6.8, 13.4) Human Mortality Database, World Mortality Dataset, ACM subnational data 0.61
[9]
The Economist & Solstad, 2021 * Jan ‘20-Dec ‘21 4.8 (95% CI: 1.2, 8.2) 481,080 10.1 (2.6, 17.2) Human Mortality Database, World Mortality Dataset, ACM subnational data 0.63
[12]
Jha et al., 20223 July ‘20-May ‘21 630 th (95% CI: 531, 730) N/A N/A Facility-based deaths sample from HMIS --
[4]
July ‘20-May ‘215 1.2 (95% CI: 1.0, 1.4) 204,330 6–7 CRS 0.15
* Jun ’20-Jul ’216 3.2 (95% CI: 3.1, 3.4) 450,000 6–7 CVoter 0.42
Anand et al., 20214 * Apr ’20-Jun ’21 3.4 (range:1.1, 4.0) 400,000 8.5 (2.7, 10.0) CRS 0.44
[14]
* Apr ’20-Jun ’21 4.0 400,000 10.0 International age-specific infection fatality rates 0.52
* Apr ’20-Jun ’21 4.9 400,000 12.2 CMIE 0.64
Guilmoto, 20223 Mar ’20-May ’21 3.2 458,900 7.0 Indian Railways, Kerala age & sex-specific death rates 0.41
[15]
* Mar ’20-Nov ’21 3.7 458,900 8.6 MLA, Kerala age & sex-specific death rates 0.48
Leffler et al., 20224 * Jan ’20-Aug ’21 2.6 (range:1.9, 3.5) 438,560 6.1 (4.5, 8.1) CRS 0.34
[16]
Malani & Ramachandran, 20213 * Feb ’20-Aug ’21 6.3 458,470 13 CMIE 0.82
[17]
Banaji & Gupta, 20213 * Apr ’20-Jun ’21 3.8 (range:2.8, 5.2) 399,489 9.5 (6.9, 13.0) CRS 0.50
[18]
Study Time Period Estimated Total Deaths (LL, UL) in Millions COVID-19 Reported Deaths 1 Under Reporting Factor (LL, UL) 2 Data Source(s) Infection Fatality Rate (%)
Disease Transmission-based Studies
Using Reported and Unreported COVID-19 Deaths
Barber et al., 2022 Jan ’20-Nov ’21 3.4 (95% UI: 2.5, 4.9) 470,810 7.3 (5.3, 10.4) COVID-19 reported cases and deaths from covid19india.org, nationwide and state level serosurveys, hospitalizations from IDSP, excess death estimates from Wang et al. (2022) 0.3 (95% UI: 0.3, 0.5)
[7]
Zimmermann et al., 2021 Apr ’20-Jun ’21 1.4 (95% CrI: 1.3, 1.4) 412,019 3.5 COVID-19 reported cases and deaths from covid19india.org, COVID-19 infections from nationwide serosurvey 0.36 (95% CrI: 0.35, 0.38)
[1]
Rahmandad et al., 20217 Jan-Dec 2020 N/A N/A N/A COVID-19 reported cases and deaths from JHU CSSE, testing data from Indian Council of Medical Research, World Bank indicators 0.35 (95% CrI: 0.32, 0.39)
[19]
Shewade et al., 2021 Jan-Jul 2020 197 th 173,153 5.5–11.0 COVID-19 reported cases and deaths from worldometers.info/coronavirus, CRS deaths registration coverage and errors in MCCD 0.58–1.16
[20]
Campbell & Gustafson, 2021 May-Jun 2020 46 th 12,573 3.6 COVID-19 reported deaths from ourworldindata.org/coronavirus/country/india, COVID-19 infections from nationwide serosurvey, death underreporting factor from Purkayastha et al. (2021), WDI nationwide age proportions 0.29 (95% CrI: 0.09, 0.90)
[21]
Using Reported COVID-19 Deaths
Song et al., 2021 Mar ’20-Jun ’21 532 th (95% CI: 513, 552) 399,489 1.3 (1.2, 1.4) COVID-19 reported cases and deaths from WHO COVID-19 Dashboard, Influenza reported cases from WHO FLUNET 0.06
[22]

Notes: Asterisk (*) denotes that the excess deaths study was included in the quantitative meta-analysis, being through at least June 2021.

N/A = Not available, CRS = Civil Registration System, MLA = Member of the Legislative Assembly sample, CVoter = CVoter India Omnibus telephone survey, HMIS = Health Management Information System, ACM = all-cause mortality, CMIE = Center for Monitoring Indian Economy Consumer Pyramids Household survey, IDSP = Integrated Disease Surveillance Programme (for Goa, India). JHU CSSE = Johns Hopkins University Center for Systems Science and Engineering, MCCD = Medical Certification of Cause of Death from Ministry of Home Affairs, WDI = World Bank’s World Development Indicators. Lower and upper uncertainty bounds for all-cause excess deaths estimates are included in this table, when provided in the study.

[a] Estimated total cumulative infections is calculated as the seroprevalence of 67.6% among ages ≥ 6 years from the latest 4th nationwide serosurvey study in India [6] multiplied by the age-adjusted population (additional details are included in Methods B in S1 Text and Fig A in S1 Text).

[1] COVID-19 Reported Deaths are obtained from covid19india.org, unless otherwise noted.

[2] Underreporting Factor is computed as Excess Deaths divided by COVID-19 Reported Deaths, unless otherwise noted.

[3] Underreporting Factor (URF), as well as COVID-19 Reported Deaths are directly reported in this study. Hence, the URF in this table is the precalculated estimate provided.

[4] Excess Deaths, as well as COVID-19 Reported Deaths, are directly reported in this study.

[5] The COVID-19 Reported Deaths provided in this study are across select states in the Civil Registration System (CRS).

[6] The precalculated Underreporting Factor and COVID-19 Reported Deaths reported in this study are through September 2021.

[7] Numerical estimates for total deaths are unavailable for Rahmandad et al. (2021) [19], and are thereby displayed as not available in this table.

Nationwide pooled IFR2 estimate for India is 0.51% (95% confidence interval [CI]: 0.45%– 0.58%), as presented in Fig 2. This estimate attributes 100% of excess deaths to SARS-CoV-2 during 2020–2021. In actuality, the proportion of excess deaths resulting from COVID-19 is not likely to wholly account for the total excess deaths during the pandemic period, and as such this estimate of 0.51% is likely an overestimate. However, disease transmission-based studies give us a nationwide pooled IFR2 estimate of 0.34% (95% CI: 0.28%– 0.41%), although we caution that this second estimate relies on less than 3 data points. Overall, comparing IFR2 to the nationwide pooled IFR1 (calculated based on reported deaths) of 0.10% (95% CI: 0.07%– 0.14%) [1], we find that IFR2 is roughly 4 times greater than IFR1. Lastly, Fig B in S1 Text presents a visualization of the publication bias assessment among the included studies, and the Egger and Begg tests for asymmetry, as well as the Joanna Briggs Institute (JBI) risk of bias results are presented in the supplementary content (see Methods D in S1 Text and Methods E in S1 Text).

Fig 2. Nationwide estimated pooled IFR2 of SARS-CoV-2 for India, through June 2021 and extending to December 2021.

Fig 2

Included studies listed in this forest plot are categorized as excess deaths studies. There were too few disease transmission-based studies (less than 3 studies through June 2021) identified by the search, and therefore, further meta-analyzing the additional category of disease transmission-based studies was not feasible.

Discussion and conclusions

Over two years since the start of the pandemic, numerous peer-reviewed studies have focused on understanding the actual death toll of SARS-CoV-2 in India, primarily either via excess deaths or disease transmission-focused modeling, enabling the meta-analysis herein of the 11 identified excess deaths estimates. When appropriately accounting for case and death underreporting, the cumulative SARS-CoV-2 infection fatality rate in India varies within a 95% CI of 0.45%-0.58%, which indicates that IFR2 is 4–6 times more than what is being reported based on tabulated deaths due to COVID-19. The disease transmission-based estimates qualitatively appear to be more conservative than the ones that originated from excess deaths studies. One possible explanation could stem from the fact that most of the excess death studies are based on all-cause-mortality data and do not quantify the proportion of the excess deaths attributable to COVID-19. The pooled IFR2 estimate from COVID-specific transmission model-based studies is largely congruent to the estimated IFR of 0.3% (as of 14 November 2021) for India reported in the global IFR study by Barber et al. (2022) [7].

Limitations of the meta-analysis are as follows. First, insufficient data on age and sex-disaggregated mortality for India precluded investigation into heterogeneity by such demographics. Second, multiple studies rely on excess deaths derived from common sources, such as the civil registration system (CRS) data, as well as infections derived from nationwide serosurveys, which rules out independence between included studies and may bias the resulting pooled estimate. India recently released the CRS data for 2020, but most studies estimate largest excess deaths during April-June of 2021 and no CRS data are available for this period. Moreover, the incompleteness of CRS data may hinder representativeness and, thereby, complicates the interpretability of excess deaths estimates relying on CRS data. The more nationally representative sample registration system (SRS) is often used to adjust for missing death information in CRS, but SRS data are not yet available for 2020 and 2021. Lastly, while we use the latest available nationwide serosurvey to obtain an age-adjusted infections estimate in computing the IFR for SARS-CoV-2, we acknowledge that this approach does not incorporate factors of waning immunity and re-infections. If such components were able to be accounted for, the denominator of the IFR (estimated infections) may have been larger and thereby the true IFR will be attenuated to a degree. Such limitations inherent to sero-surveillance studies also include sero-reversion which concerns reduced detection of SARS-CoV-2 antibodies and leads to an upward bias in IFR estimates [8].

It is critical to contextualize the uncaptured SARS-CoV-2 infections and deaths in India, and how such underreporting could distort comparisons of disease spread and mortality within countries across the world. Considering the three countries with the highest cumulative reported deaths (as of December 31, 2021), namely, India, Brazil, and the United States (in ascending order), the IFR2 (as of 14 November 2021) reported by Barber et al. (2022) appears to be the lowest in India (IFR2 of 0.3%) compared to the US (IFR2 of 0.9%) and Brazil (IFR2 of 0.5%) [7]. This is due to the very large number of estimated cumulative infections in India (approximately 1 billion, through mid-November 2021 [7]). With respect to the total number of deaths, Wang et al. (2022) estimate deaths to be underreported by a factor of 8.3, 1.3, and 1.2 for India, the US, and Brazil, respectively [5]. This is qualitatively similar to the death underreporting factors reliant on WHO estimates (similarly through 31st December 2021) of 9.8, 1.1, and 1.1 for India (4.7 million excess deaths and 481,080 reported deaths), the US (933,547 excess deaths and 818,464 reported deaths), and Brazil (681,514 excess deaths and 618,817 reported deaths), respectively [9]. These rankings indicate that underreporting of deaths (through 31st December 2021) is particularly acute for India.

While metrics are useful for evaluating public health policies, we caution against such crude comparisons based on a single metric. Although we use cumulative excess deaths as a measure of comparison in mortality ranking, population counts are not factored in and deaths per million may be preferrable in another context. In addition, such overall mortality comparisons must be placed in the context of the age-structure of the different countries. India has a younger population (Median age 28 years) than the US (Median age 38 years) or Brazil (Median age 34 years) [10]. Age-specific IFR2 should be used, if possible, when examining COVID-19 mortality burden within and across countries and in subsequent decision making. Recent studies underscore the importance of adjusting for age structures, when performing related deaths estimations. For example, The Economist recently made available an age-adjusted IFR source [11], which is further incorporated into their published estimates [12]. Disaggregated mortality data are necessary to validate these age-specific estimates for India.

Many of the included studies in this meta-analysis also sought to account for changes in mortality and subsequently changes in IFR over time often by incorporating as granular, longitudinal data as possible. This is important as the lethality of the virus is subject to multiple time-varying components, especially the roll-out of vaccines (starting in January 2021 within India), as well as the changing variant landscape wherein the milder SARS-CoV-2 variant Omicron and sub-lineages became dominant.

We look forward to the release of timely, disaggregated data on SARS-CoV-2 deaths within India to assess the burden of COVID-19 among various demographic groups [13], as well as to enable targeted policy interventions. Once nationwide 2021 CRS reports are released, the findings with respect to the excess death estimates will be further validated. In the absence of data, we must rely on curated estimates computed by multiple teams of dispassionate scientists and a systematic review and synthesis of such evidence.

Supporting information

S1 Table. Results of risk of bias assessment for included articles.

(XLSX)

S1 Text

(DOCX)

S1 Data

(XLSX)

S2 Data

(R)

S1 Code

(R)

Acknowledgments

The authors thank the information specialists from the University of Michigan Taubman Health Sciences Library for their prior guidance on the search strategy for the systematic review that enabled this meta-analysis. The authors also wish to thank Maxwell Salvatore for providing technical advice and feedback regarding the graphics in this report.

Data Availability

Data and code files are available as Supporting Information files in S1 Data and S1 Code, respectively.

Funding Statement

LZ and BM were supported by funding from the University of Michigan School of Public Health and Center for Precision Health Data Science. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0000897.r001

Decision Letter 0

Jong-Hoon Kim

26 Apr 2022

PGPH-D-21-01072

Meta-analysis of nationwide SARS-CoV-2 infection fatality rates in India

PLOS Global Public Health

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Comments to the Author

1. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Partly

Reviewer #2: Yes

Reviewer #3: Yes

Reviewer #4: Yes

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2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I don't know

Reviewer #2: Yes

Reviewer #3: I don't know

Reviewer #4: Yes

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3. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

Reviewer #4: Yes

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4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

Reviewer #4: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The paper is potentially a valuable addition to the literature on the impact of the pandemic in LMICs. In a context of hugely variable surveillance and major gaps in our knowledge of the impact of the pandemic in the Global South, such work is of high importance. Given India's sheer size and weak surveillance, understanding pandemic mortality in India is perhaps the most critical challenge to understanding pandemic mortality worldwide.

However, there are some limitations to the work, which the authors would do well to address. First some general observations and questions:

It would be helpful if the 15 studies which were included in the meta-analysis are listed clearly, perhaps in a table, along with an outline of what kind of data or analysis appears in each, and how this data is used to arrive at IFR estimates.

The eligibility criteria for included and excluded papers (Figure 2) are not clear - it appears that papers which either model pandemic mortality or include prevalence or mortality data were included. Were papers focussing on subnational data excluded, or were no such papers found to meet the eligibility criteria? In sum, the framework needs to be spelled out more clearly - Figure 2 does not seem adequate.

In reading a meta-analysis there is often the assumption in the reader's mind - rightly or wrongly - that the studies are in some sense "independent". They may involve different data-sets, different geographical regions, different methodologies, etc. Here, however, it appears that many of the estimates are based around overlapping data and techniques. This applies for example to the estimates of excess mortality based on civil registration data, and also perhaps to estimates of prevalence based on serosurveys. Overall, it appears that there is relatively little "independent" data behind the numbers from different papers, increasing the risk of systematic bias (more on this below). This warrants at least some discussion.

The study includes both data- and model-based estimates, and it is observed that the model-based estimates of IFR are more conservative than data-based ones. However, model-based estimates reflect a complex array of assumptions - including, perhaps, about ascertainment of infections and deaths, and even sometimes about IFR itself. This leads to the possibility of circularity. Without some discussion of the assumptions behind the models it is very hard to interpret model-based IFR estimates, or to know whether they deserve the same weight as data-based ones. (Although data-based estimates also rely on a host of assumptions, these are in general more obvious to see). This seems to me to be of critical importance in a meta-analysis which relies on a small number of papers, a sizeable fraction of which are modelling papers.

On the theme of model-based estimates, disproportionate weight appears to be given in the text to the IHME modelling, whose estimates appear to be outliers even amongst the model-based estimates (and certainly amongst the estimates from all sources). Are the IHME projections available in any kind of preprint, perhaps submitted for peer-review? Is this work sufficiently transparent to meet the criteria for this kind of analysis? (I have some doubts about this, but these would be allayed if the authors referenced a technical document which included details of how the IHME estimates are arrived at, specifically for India.)

Overall, potential systematic biases deserve much more discussion. For example, in estimates based on survey or civil registration data: the possibility of non-COVID excess mortality, particularly during periods when healthcare infrastructure is overwhelmed; potential sampling biases in survey-based estimates; issues around incompleteness of death registration and possible differential impact of the pandemic on communities where registration is higher/lower; possible issues with the fact that available data is often from sources (e.g. online systems) which are incomplete. Although a meta-analysis may not be the place to discuss in detail potential biases in each study, it is important for readers to understand the limitations to the work, which are often common to many papers.

Some specific observations and questions:

What is the relationship between this paper and reference (1) Zimmermann et al? It would be helpful if the authors could clarify whether this paper is a presentation of the key findings of their earlier work, whether it includes further data and analysis, and so forth.

The line: "Supplementary Figure 2 shows a nationwide pooled IFR 2 estimate for India of 0.499%" does not seem to accord with Figure 2, where the pooled estimate appears to be 0.44%.

IFR1 (i.e., IFR based on recorded COVID-19 deaths) is fairly easy to calculate, but the origin of the IFR1 estimates quoted in the paper are not clear. If they are national estimates, then they are too high. For example, taking national level reported COVID-19 deaths, IFR1=0.1% would be consistent with an infection rate of a mere 34%, considerably lower than the estimates from recent serosurveys. The source of this mismatch requires clarification. Data from a few well-surveilled urban localities generally gives much higher values of IFR1 - is this the source of the high IFR1 estimate? If so, the aggregate IFR1 estimate should not be used to provide national estimates of URF (D). These matters are vitally important from the point of view of understanding the scale, geographical variation, and reasons behind COVID-19 death under-reporting in India.

Although the aggregate estimates of IFR2 are plausible, the calculations which underlie the individual estimates are not transparent. For example, some estimates are based on prevalence estimates in Murhekar et al (June 2020); but it is unclear what mortality data has been used as the numerator in these estimates. Do many of the papers include mortality data up to June-July 2020? If so, how reliable are these figures given, for example, the various delays and disruption to death registration during national lockdown? It would seem that a multiplicity of possible errors make the early estimates highly unreliable.

In Table 1, the Wave 2 estimate for Banaji and Gupta is empty, but the preprint does include a point estimate (11.3) of the death underreporting factor during March-May 2021 in the subsection "Increasing under-ascertainment of COVID-19 deaths?" Is there a reason this was omitted?

In Figure 3, an IFR2 estimate for India of 0.135% is given based on IHME projections. But the IHME seemed to estimate 2.8M total deaths on Sept. 20, 2021, and a 66% infection rate, which would together give an IFR2 estimate of around 0.3%. Could the authors clarify the source of the IFR2 estimate of 0.135% attributed to the IHME?

Reviewer #2: The studies reviewed could be updated and expanded:

The following study has India data which could be incorporated:

Wang H, Paulson KR, Pease SA, Watson S, Comfort H, Zheng P, Aravkin AY, Bisignano C, Barber RM, Alam T, Fuller JE. Estimating excess mortality due to the COVID-19 pandemic: a systematic analysis of COVID-19-related mortality, 2020–21. The Lancet. 2022 Mar 10.

Your fourth reference by Deshmukh doesn’t list the title of the report:

Y. Deshmukh, W. Suraweera, C. Tumbe, A. Bhowmick, S. Sharma, P. Novosad, S.

H. Fu, L. Newcombe, H. Gelband, P. Brown, P. Jha, medRxiv, in press,

doi:10.1101/2021.07.20.21260872.

I think that study is the same is this one by Jha, which is now published:

Jha P, Deshmukh Y, Tumbe C, Suraweera W, Bhowmick A, Sharma S, Novosad P, Fu SH, Newcombe L, Gelband H, Brown P. COVID mortality in India: National survey data and health facility deaths. Science. 2022 Jan 6:eabm5154.

The study by Leffler et al is now published in a journal:

Preliminary Analysis of Excess Mortality in India During the COVID-19 Pandemic.

Leffler CT, Lykins V JD, Das S, Yang E, Konda S.

Am J Trop Med Hyg. 2022 Apr 4:tpmd210864. doi: 10.4269/ajtmh.21-0864. Online ahead of print. PMID: 35378508.

The published version of the study by Leffler now has mortality data through August 31, 2021.

The study by Guilmoto is now published:

Christophe Z Guilmoto. An alternative estimation of the death toll of the Covid-19 pandemic in India., PLoS One. 2022 Feb 16;17(2):e0263187. doi: 10.1371/journal.pone.0263187. eCollection 2022.

Reviewer #3: The study appears an important meta-analysis of model and excess-deaths based studies of the pandemic's death toll in India, and using undercounting-ratios of infections based on seroprevalence studies, what a plausible range of the covid-19 IFR in India might be.

I believe that provided my below recommendations are followed and/or comments addressed, the study should be published and would be a valuable contribution. (This is also my understanding of the selection "minor revision"). I defer to discipline specialists on the fitness of article to journal. I also defer to discipline specialists on the statistical methodology employed, and the soundness and completeness of the replication package.

My comments will be restricted to the data used, and a few of the assumptions underlying the IFR estimations, and presentation. My apologies if I missed something obvious, including elements which address the concerns I raise below.

Comments:

1. The Anand et al study has three estimates, but the study as far as I can tell only includes one of these. I would have liked to have seen an explicit justification of the choice of which to use. While I see a clear reason to exclude the IFR-based estimate, I wonder why the estimation based on the civil-state registration system was not included.

2. Acknowledging that I am an interested party, I find it puzzling that The Economist's estimates of excess deaths in India are not included, despite their global model being widely cited in other academic research (including that cited here), and having estimates on both the first and second wave.

3. Sero-prevalence based estimates are problematic beyond the early stages of the pandemic, because sero-reversion means that infections become progressively less probable to be detected, and because re-infections are possible. (They are also problematic in many contexts because of vaccines.) This should be acknowledged explicitly, and the implications discussed.

4. I found it hard to follow where infection estimates were from - I would have liked something like what was done for table 1 except for infection estimates. Table 2 was confusing to me - I would try to improve this presentation.

3. The use of the IHME estimate of infections is problematic in figure 3, because, unless I am mistaken, this estimate is based on an estimated IFR and estimated death rates, meaning the implied IFR is "baked in". The figure is also unclear (that is, if the bars are meant to mutually exclusive).

5. For reasons discussed elsewhere, see e.g. Andrew Gelman (2021), I would consider avoiding reliance on IHME estimates regarding the pandemic in general.

6. My recommendation would be to drop this comparison to other the US and Brazil, and rather here summarize other estimates of IFR (of which there are many - see e.g. Brazeau et al 2020 and the papers citing this study).

7. With regards to discussion on age structure, the following might be of interest: https://github.com/TheEconomist/covid-19-age-adjusted-ifr -- these also figure in The Economist's global model.

8. I find it strange that there is no mention of changes in IFR over time. This has been known to respond to health care capacity, treatment quality changes, vaccines, and variants. This must at a minimum be acknowledged.

Recommendations:

1. Add justification of selection of which Anand et al study estimate to use

2. Clearer presentation of sources for infection estimates, and a discussion of their limitations (sero-reversion being an important one)

3. Include The Economist's estimate for India's death toll

4. Drop figure 3, which is both confusing, is based on a different approach than the rest of the study, and presents information which is already widely known

5. Replace this with a discussion, and perhaps a table, of how this compares to other studies' estimates of IFRs.

6. Consider including a mention of age-adjusted implied IFR by country.

8. Add to discussion the limitations of the study as it relates to varying IFRs over time: this should mention vaccines, the sars-cov-2 variants, treatment quality, and how this study is based on data from a certain such context, and how this context has changed.

Best of luck in revisions of this important research

Reviewer #4: Major Comments

I wasn't totally sure of the methodology, and I see that estimates of the IFR can be obtained using lower bounds on under-reporting. But with a sampling-based approach (from the asymptotic distribution of your estimators), couldn't you obtain estimates of IFR that account for uncertainty in the underreporting?

It wasn't clear to me what was model-based and what wasn't. IHME and The Economist excess mortality estimates for India would be model-based, right?

Specific Comments

Abstract: ``Highly conservative'' could be misinterpreted as for the ratio (the IFR) but you are referring to the underreporting of numerator and denominator, which does not mean the ratio is highly conservative. To be clear, I'm not suggesting you report different IFRs, but am commenting on the wording.

P3 ``top three countries", via what metrics?

P3 ``obscur". Typo.

P3 Give 3 decimal places for 0.44\\% figure.

P4 Is there a reason why for URF(C) you have "Total Cumulative Infections" in the numerator and "Cumulative Cases" in the denominator. Is it important to distinguish between ``infections" and ``cases"? And no ``Total" in the denominator.

Table 1. I didn't fine this table very easy to take in. Having a column labeled ``excess deaths" would help.

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Reviewer #1: No

Reviewer #2: No

Reviewer #3: Yes: Sondre Ulvund Solstad

Reviewer #4: No

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PLOS Glob Public Health. doi: 10.1371/journal.pgph.0000897.r003

Decision Letter 1

Jong-Hoon Kim

22 Jul 2022

Meta-analysis of nationwide SARS-CoV-2 infection fatality rates in India

PGPH-D-21-01072R1

Dear Ms Zimmermann,

We are pleased to inform you that your manuscript 'Meta-analysis of nationwide SARS-CoV-2 infection fatality rates in India' has been provisionally accepted for publication in PLOS Global Public Health.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. A member of our team will be in touch with a set of requests.

Please note that your manuscript will not be scheduled for publication until you have made the required changes, so a swift response is appreciated.

IMPORTANT: The editorial review process is now complete. PLOS will only permit corrections to spelling, formatting or significant scientific errors from this point onwards. Requests for major changes, or any which affect the scientific understanding of your work, will cause delays to the publication date of your manuscript.

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Thank you again for supporting Open Access publishing; we are looking forward to publishing your work in PLOS Global Public Health.

Best regards,

Jong-Hoon Kim, Ph.D.

Academic Editor

PLOS Global Public Health

***********************************************************

There are a couple of minor editorial comments by Reviewer #3. Please address those when you make formatting changes for the final version.

Reviewer Comments (if any, and for reference):

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #3: All comments have been addressed

Reviewer #4: All comments have been addressed

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2. Does this manuscript meet PLOS Global Public Health’s publication criteria? Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe methodologically and ethically rigorous research with conclusions that are appropriately drawn based on the data presented.

Reviewer #1: Yes

Reviewer #3: Yes

Reviewer #4: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #3: I don't know

Reviewer #4: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available (please refer to the Data Availability Statement at the start of the manuscript PDF file)?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception. The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #3: Yes

Reviewer #4: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS Global Public Health does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #3: Yes

Reviewer #4: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors have carefully engaged with all the comments and criticisms, and the paper is much improved. The selection criteria for the studies, and methodological approach are presented more transparently, and it is now easier to understand the detail of the manuscript. Within the framework of incomplete data and multiple, overlapping uncertainties, the authors should be congratulated for drawing together, to the extent possible, a "consensus" on the questions of pandemic mortality/IFR in the Indian context. I recommend that the piece be published.

Reviewer #3: Thank for addressing my concerns. Just two tiny quibbles. First, in table 1, it says The Economist's estimate uses Mumbai data. But the full list of subnational data sources is Tamil Nadu State, Madhya Pradesh State, Andhra Pradesh State, Mumbai City, Kolkata City, and (in Indonesia) Jakarta Province. I would encourage "ACM subnational data" instead, or list all of them. Second, "" ext-link-type="uri" xlink:type="simple">github.com/TheEconomist/covid-19-age-adjusted-ifr" could easier be a standard reference to the article in which it was published: https://www.economist.com/graphic-detail/2020/11/16/why-rich-countries-are-so-vulnerable-to-covid-19

Thanks!

Reviewer #4: My comments have been adequately addressed.

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7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

Do you want your identity to be public for this peer review? If you choose “no”, your identity will remain anonymous but your review may still be made public.

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Reviewer #1: No

Reviewer #3: No

Reviewer #4: No

**********

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