Skip to main content
Annals of Intensive Care logoLink to Annals of Intensive Care
. 2021 Aug 19;11:127. doi: 10.1186/s13613-021-00915-4

Case fatality inequalities of critically ill COVID-19 patients according to patient-, hospital- and region-related factors: a French nationwide study

Antoine Guillon 1, Emeline Laurent 2,3, Antoine Duclos 4,5, Lucile Godillon 2, Pierre-François Dequin 1, Nelly Agrinier 6, Antoine Kimmoun 7, Leslie Grammatico-Guillon 2,8,
PMCID: PMC8375279  PMID: 34410543

Abstract

Background

The COVID-19 sanitary crisis inflicted different challenges regarding the reorganization of the human and logistic resources, particularly in intensive care unit (ICU). Interdependence between regional pandemic burden and individual outcome remains unknown. The study aimed to assess the association between ICU bed occupancy and case fatality rate of critically ill COVID-19 patients.

Methods

A cross-sectional study was performed in France, using the national hospital discharge database from March to May, 2020. All patients admitted to ICU for COVID-19 were included. Case fatality was described according to: (i) patient’s characteristics (age, sex, comorbid conditions, ICU interventions); (ii) hospital’s characteristics (baseline ICU experience assessed by the number of ICU stays in 2019, number of ICU physicians per bed), and (iii) the regional outbreak-related profiles (workload indicator based on ICU bed occupancy). The determinants of lethal outcome were identified using a logistic regression model.

Results

14,513 COVID-19 patients were admitted to ICU; 4256 died (29.3%), with important regional inequalities in case fatality (from 17.6 to 33.5%). Older age, multimorbidity and clinical severity were associated with higher mortality, as well as a lower baseline ICU experience of the health structure. Regions with more than 10 days with ≥ 75% of ICU occupancy by COVID-19 patients experienced an excess of mortality (up to adjusted OR = 2.2 [1.9–2.6] for region with the highest occupancy rate of ICU beds).

Conclusions

The regions with the highest burden of care in ICU were associated with up to 2.2-fold increase of death rate.

Supplementary Information

The online version contains supplementary material available at 10.1186/s13613-021-00915-4.

Keywords: COVID-19, ICU, Determinant of lethal outcomes

Introduction

The COVID-19 has been recently called a syndemic [1, 2]. This concept aims to describe how COVID-19 spreads with pre-existing conditions, but also how it is driven by larger political, economic, and social factors [1, 3]. To reconfigure conventional understanding of COVID-19 mortality, we should integrate healthcare contexts in which it occurred. In France, from March to May 2020, the COVID-19 outbreak massively affected the country, but with substantial differences in regional incidence ranges. Metropolitan France (i.e., on the European continent) is divided into 13 administrative regions, sharing the same universal healthcare system. The French healthcare system is a universal service for every citizen, irrespective of wealth, age or social status, made up of a fully integrated network of public and private hospitals, and other medical service providers.

The SARS-CoV2 virus, equally virulent intrinsically in these 13 regions, brought the similar clinical presentation, suggesting that each critically ill patient in France had theoretically the same risk of surviving or dying. However, a more nuanced approach is needed because this threat had inflicted different challenges regarding the reorganization of the human and logistic resources, particularly in intensive care unit (ICU) hospitalizations for advanced monitoring and live support. High burden on the healthcare system has already been observed in France in responding to terrorist attack but on a short period and in a restricted area [4]. This time and without any precedent, the healthcare system has been overwhelmed in some French regions, the number of critical care beds and dedicated health workers being a critical factor [5]. The ICU bed occupancy, defined as the number of critically ill COVID-19 patients divided by the number of ICU beds, has emerged as a dynamic workload indicator to assess the ICU burden. However, the number of ICU beds was difficult to establish because there was a constant flow of ICU reorganization (i.e., expansion of ICU beds, novel ICU locations within hospital or in pop-up hospital). Thus, the ICU occupancy was defined based on the ICU bed resource that was present before the pandemic [6]. Whether the outcome of critically ill patient was affected by the ICU occupancy is unknown. Mortality rate was higher within ICUs located in Paris and the northeast regions but the direct influence of logistic and organizational aspects, along with the incidence rates, on patient outcomes has not been proven [5]. We need to take a more holistic approach including the environmental factors such as hospital structures and region-related factors, to improve the comprehension of outcome of critically ill COVID-19 patients. The objective of the study was to assess the impact of ICU bed occupancy on case fatality rate of critically ill COVID-19 patients.

Methods

Study design and data collection

A cross-sectional study, using medico-administrative data from the exhaustive French hospital discharge database (HDD) (Programme de Médicalisation des Systèmes d’Information—PMSI) was performed with the data available on the national dedicated French secured platform (Agence Technique de l’Information sur l’Hospitalisation—ATIH). In France, it is mandatory to report data from all hospital stays at public and private hospitals. All information from reported hospitalizations is stored in the HDD as medical codes [International Classification of Diseases, Tenth Revision (ICD-10)]. All patients are assigned a unique identification number, allowing the same individual to be followed over time. The encrypted anonymized patient number, allowing the estimation of pre-existing comorbidities based on their 2-year anteriority (PMSI 2018-19) [79].

Patients were included according to the following inclusion criteria: adults (≥ 18 years old), admitted to one French ICU (public or private sector), between March, 1st and May 31st 2020, with at least one night spent in ICU (including ICU and step-down units), and at least one ICD-10 diagnosis code of COVID-19 whatever their position in the hospital stay resume (Additional files 1, 2: Supplementary data).

Socio-demographic and clinical data related to these patients were extracted from the French HDD. Hospital and regional data were selected in the administrative section of the HDD from the Statistique Annuelle des Etablissements (SAE) available through the ATIH secured platform [6]. In case of transfer, the region retained for the analyses was the one with the longest ICU stay.

Variables of interest

Outcomes of COVID-19 patients hospitalized in ICU in France were analyzed according to three levels of variables:

Level 1—Patient characteristics: vital status at the end of the hospital stay (primary outcome), sociodemographics characteristics (age, sex), comorbid conditions (Additional files 1, 2), SAPS II (Simplified Acute Physiology Score II) at the first admission in the ICU (missing data if score < 5, n = 281), and specific care supports: mechanical ventilation (invasive or non-invasive, with/without prone position), renal replacement therapy, extra-corporeal membrane oxygenation, vasoactive treatments.

Level 2—Hospital characteristics: type of hospital (teaching or regional hospitals, local or private or mixed sector facilities), baseline ICU experience (approximated by the number of adult ICU stays in the hospital in 2019—before the pandemic), and number of ICU physicians per healthcare facility (expressed as the ratio of ICU physicians in 2019 divided by the number of ICU beds in the hospital).

Level 3—Regional characteristics: workload indicator based on the French indicator of ICU burden defined as the number of days with 75% or more of the ICU beds at baseline (before the COVID crisis) occupied by COVID-19 patients in the region, estimated per day over the study period.

Statistical methods

The continuous variables were described by their mean ± standard deviation (SD), whereas the qualitative variables were described with effectives and percentages. A description of the variables of interest was performed for the overall population, and then stratified according to: (i) the region of the longest COVID-19 ICU stay and (ii) the vital status at the end of the last COVID-19 ICU stay during the study period.

To identify the risk factors associated with the ICU case fatality, first, bivariate analyses were performed with the variables of interest above. Second, a logistic regression model was carried out, including variables with p < 0.2 in bivariate analysis, as well as variables considered as clinically relevant. Third, a descending stepwise process was used to select the final model of logistic regression, including all the statistically significant variables at the threshold p < 0.05. All variables, including those related to the patient, hospital and region, were included in the same model. Analyses were performed using SAS Enterprise Guide 71 64-bit (SAS Institute Inc., Cary, NC, USA), version available on the ATIH website at the moment of the analyses.

Ethical approval

No nominative, sensitive or personal data of patients have been collected. Our study involved the reuse of already recorded and anonymized data. The study falls within the scope of the French Reference Methodology MR-005 (declaration 2205437 v 0, August 22nd, 2018, subscripted by the Teaching Hospital of Tours), which require neither information nor consent of the included individuals. This study was consequently registered with the French Data Protection Board (CNIL MR-005 number #2018160620).

Results

We identified 14,513 adult patients with at least one ICU stay attributed to COVID-19, among 58,033 total ICU patients from March, 1rst to May, 31rst 2020. Critically ill COVID-19 patients represented 25% of all ICU-hospitalized patients in France during this period. However, important differences were observed at the regional level (Table 1): French administrative regions localized on the West part of the country (Bretagne, Pays de la Loire, Nouvelle Aquitaine) had 10 to 12% COVID-19 patients admitted to ICUs whereas this ratio reached 39 to 42% in North-East region (Grand Est) and in Paris with the surrounding area (Ile-de-France). Moreover, the occupancy of ICU beds by COVID-19 patients varied widely over time (Fig. 1). A simultaneous peak around April 1st was observed in all regions but with large differences in intensity and duration among them, whereas the patients’ characteristics were broadly similar across the country (Table 1). The patients were mainly male (78%; sex ratio 2.5), with a mean age of 63 ± 13 years old and 80.9% had at least one comorbid condition, the most frequent being high blood pressure, chronic heart diseases and diabetes mellitus (Table 1). The initial SAPS II was 39.5 (± 17) in France with little variability between regions (lowest value 36.0 ± 15.3; highest value 41.5 ± 17.4). The specific care supports were invasive mechanical ventilation for 68.1% of the cases and vasopressors for 58.8% (Table 1). Eventually, 4,256 COVID-19 patients died during their hospital stay, representing a 29.3% case fatality rate, varying from 17.6% to 33.5% according to the administrative region (Fig. 2A) and from 20.0% to 38.1% according to the period (Fig. 2B).

Table 1.

Characteristics of COVID-19 patients admitted in the ICU, according to the French administrative region, March, 1st to May, 31st 2020

Population 2017 (n) Overall population Auvergne-Rhône-Alpes Bourgogne-Franche-Comté Bretagne Centre-Val de Loire Corse Grand Est
64,639,133 7,949,036 2,810,551 3,318,904 2,577,191 334,938 5,549,586
Patient in ICU—all causes (n) 58,033 6942 2235 2166 1831 202 5500
Critically ill COVID-19 patients in ICU (n, %) 14,513 25.0% 1358 19.6% 580 26.0% 256 11.8% 410 22.4% 44 21.8% 2130 38.7%
Age class (n, %)
 < 65 y.o 7145 49.2% 521 38.4% 213 36.7% 110 43.0% 182 44.4% 14 31.8% 928 43.6%
 65–79 y.o 6280 43.3% 698 51.4% 299 51.6% 129 50.4% 196 47.8% 25 56.8% 1066 50.0%
 ≥ 80 y.o 1088 7.5% 139 10.2% 68 11.7% 17 6.6% 32 7.8% 5 11.4% 136 6.4%
Age (mean ± s.d.) 63 ± 13 65.9 ± 12.4 66.9 ± 11.5 63.4 ± 13.3 64.2 ± 12.6 67.2 ± 13.2 64.4 ± 11.9
Sex ratio (M/F) 2.5 2.7 2.3 2.4 2.3 2.4 2.6
SAPS II (mean ± s.d.) 39.47 ± 17 38.85 ± 16.1 41.46 ± 15.6 37.69 ± 16.6 37.73 ± 15.9 39.91 ± 15.3 42.09 ± 17.4
Comorbidities (n, %) 11,739 80.9% 1132 83.4% 494 85.2% 196 76.6% 356 86.8% 33 75.0% 1782 83.7%
 High blood pressure 7131 49.1% 695 51.2% 293 50.5% 122 47.7% 229 55.9% 16 36.4% 1158 54.4%
 Chronic heart disease 4971 34.3% 545 40.1% 243 41.9% 84 32.8% 157 38.3% 14 31.8% 893 41.9%
 Diabetes 4487 30.9% 447 32.9% 189 32.6% 73 28.5% 150 36.6% 8 18.2% 667 31.3%
 Obesity 3549 24.5% 328 24.2% 139 24.0% 59 23.0% 129 31.5% 5 11.4% 563 26.4%
 Cancer 3078 21.2% 370 27.2% 174 30.0% 64 25.0% 128 31.2% 14 31.8% 567 26.6%
 Chronic renal disease 2352 16.2% 310 22.8% 93 16.0% 46 18.0% 84 20.5% 4 9.1% 448 21.0%
 Chronic pulmonary disease 1913 13.2% 218 16.1% 96 16.6% 34 13.3% 75 18.3% 6 13.6% 319 15.0%
 Neurological disease 1120 7.7% 166 12.2% 64 11.0% 12 4.7% 33 8.0% 2 4.5% 204 9.6%
 Chronic liver disease 1046 7.2% 102 7.5% 41 7.1% 16 6.3% 35 8.5% 1 2.3% 184 8.6%
ICU specific care supports (n, %)
 Central venous catheter 7407 51.0% 697 51.3% 258 44.5% 137 53.5% 215 52.4% 25 56.8% 1389 65.2%
 Continuous hemodynamic monitoring 7601 52.4% 774 57.0% 225 38.8% 114 44.5% 238 58.0% 30 68.2% 1319 61.9%
 Vasoactive treatment* 8528 58.8% 772 56.8% 367 63.3% 142 55.5% 230 56.1% 16 36.4% 1438 67.5%
  Renal replacement therapy 2165 14.9% 212 15.6% 64 11.0% 31 12.1% 49 12.0% 3 6.8% 259 12.2%
  ECMO 587 4.0% 25 1.8% 13 2.2% 6 2.3% 13 3.2% 2 4.5% 82 3.8%
Mechanical ventilation** (n, %)
 Non invasive/high flow oxygenotherapy 6546 45.1% 664 48.9% 241 41.6% 105 41.0% 191 46.6% 16 36.4% 824 38.7%
 Invasive 9885 68.1% 866 63.8% 430 74.1% 165 64.5% 276 67.3% 21 47.7% 1,652 77.6%
 Invasive with prone position 5534 38.1% 534 39.3% 257 44.3% 101 39.5% 165 40.2% 14 31.8% 967 45.4%
Death (n, %) 4256 29.3% 347 25.6% 175 30.2% 45 17.6% 87 21.2% 12 27.3% 660 31.0%
Hauts-de-France Ile-de-France Normandie Nouvelle-Aquitaine Occitanie Pays de la Loire Provence-Alpes-Côte D’azur
Population 2017 (n) 6,003,815 12,174,880 3,330,478 5,956,039 5,845,209 3,757,600 5,030,906
Patient in ICU—all causes (n) 5464 13,620 2451 4833 5142 2964 4683
Critically ill COVID-19 patients in ICU (n, %) 1333 24.4% 5650 41.5% 387 15.8% 503 10.4% 667 13.0% 355 12.0% 840 17.9%
Age class (n, %)
 < 65 y.o 624 46.8% 3321 58.8% 177 45.7% 248 49.3% 286 42.9% 170 47.9% 351 41.8%
 65–79 y.o 579 43.4% 2016 35.7% 180 46.5% 212 42.1% 318 47.7% 166 46.8% 396 47.1%
 ≥ 80 y.o 130 9.8% 313 5.5% 30 7.8% 43 8.5% 63 9.4% 19 5.4% 93 11.1%
Age (mean ± s.d.) 63.9 ± 12.9 61 ± 13.2 63.6 ± 12.2 63.7 ± 12.6 64.2 ± 13.3 62.4 ± 13.2 65.3 ± 13.2
Sex ratio (M/F) 2.3 2.6 2.4 2.5 2.3 2.7 2.3
SAPS II (mean ± s.d.) 41.79 ± 18.6 38.76 ± 17.2 36.81 ± 14.8 39.5 ± 18.2 37.19 ± 16.1 35.95 ± 15.3 39.27 ± 15.6
Comorbidities (n, %) 1151 86.3% 4364 77.2% 326 84.2% 403 80.1% 537 80.5% 285 80.3% 680 81.0%
 High blood pressure 740 55.5% 2571 45.5% 207 53.5% 236 46.9% 306 45.9% 154 43.4% 404 48.1%
 Chronic heart disease 524 39.3% 1505 26.6% 140 36.2% 199 39.6% 245 36.7% 99 27.9% 323 38.5%
 Diabetes 413 31.0% 1746 30.9% 115 29.7% 135 26.8% 187 28.0% 87 24.5% 270 32.1%
 Obesity 358 26.9% 1286 22.8% 117 30.2% 121 24.1% 165 24.7% 88 24.8% 191 22.7%
 Cancer 420 31.5% 666 11.8% 78 20.2% 116 23.1% 186 27.9% 82 23.1% 213 25.4%
 Chronic renal disease 266 20.0% 627 11.1% 57 14.7% 85 16.9% 139 20.8% 51 14.4% 142 16.9%
 Chronic pulmonary disease 209 15.7% 535 9.5% 55 14.2% 82 16.3% 110 16.5% 34 9.6% 140 16.7%
 Neurological disease 102 7.7% 301 5.3% 16 4.1% 60 11.9% 75 11.2% 26 7.3% 59 7.0%
 Chronic liver disease 130 9.8% 352 6.2% 21 5.4% 31 6.2% 52 7.8% 22 6.2% 59 7.0%
ICU specific care supports (n, %)
 Central venous catheter 695 52.1% 2700 47.8% 197 50.9% 284 56.5% 322 48.3% 161 45.4% 327 38.9%
 Continuous hemodynamic monitoring 799 59.9% 2726 48.2% 198 51.2% 318 63.2% 368 55.2% 144 40.6% 348 41.4%
 Vasoactive treatment* 746 56.0% 3234 57.2% 243 62.8% 315 62.6% 369 55.3% 192 54.1% 464 55.2%
Renal replacement therapy 212 15.9% 1007 17.8% 50 12.9% 57 11.3% 77 11.5% 46 13.0% 98 11.7%
ECMO 52 3.9% 306 5.4% 10 2.6% 7 1.4% 17 2.5% 20 5.6% 34 4.0%
Mechanical ventilation** (n, %)
 Non invasive/high flow oxygenotherapy 696 52.2% 2450 43.4% 229 59.2% 229 45.5% 339 50.8% 99 27.9% 463 55.1%
 Invasive 849 63.7% 3823 67.7% 278 71.8% 334 66.4% 419 62.8% 242 68.2% 530 63.1%
 Invasive with prone position 389 29.2% 2158 38.2% 143 37% 143 28.4% 224 33.6% 137 38.6% 302 36.0%
Death (n, %) 406 30.5% 1894 33.5% 98 25.3% 93 18.5% 151 22.6% 80 22.5% 208 24.8%

*Dobutamine, dopamine, epinephrine, norepinephrine

**One patient can have both invasive and non-invasive mechanical ventilation during their ICU stay

Fig. 1.

Fig. 1

Evolution of occupancy rate of ICU beds by COVID-19 patients, according to the French administrative region. The number of beds refers to ICU beds pre-existing before the COVID-19 crisis

Fig. 2.

Fig. 2

Case fatality rate of COVID-19 patients admitted to ICU in France, March 1st to May 31st, 2020. Case fatality rate of COVID-19 patients according to: A the French administrative region, B the date of admission

The factors significantly associated with the case fatality in the adjusted analyses are presented in Table 2 (all the variables initially tested are presented in Additional file 2: Table S1; all the variables ultimately included in the final model are presented in Table 2).

Table 2.

Factors associated with case fatality in COVID-19 patients admitted in the ICU in France, March, 1st to May, 31st 2020, analyzed by logistic regression model

Univariate Multivariate
N = 14,513 N =  14,232
p Adjusted OR 95% CI p
Patient level
Age
 < 65 y–o < .0001 Ref
 65–79 y–o 2.5 [2.3–2.8] < .0001
 ≥ 80 y–o 10.2 [8.7–12] < .0001
Sex
 Female 0.0009 1.1 [1–1.2] 0.16
SAPS II*
 < 30  < .0001 Ref
 [30–40] 1.4 [1.3–1.6] < .0001
 ≥ 40 2.3 [2.1–2.6] < .0001
Comorbid conditions
 0  < .0001 Ref
 1 1.0 [0.9–1.2] 0.9
 2 1.0 [0.9–1.1] 1.0
 ≥ 3 1.2 [1.0–1.3] 0.01
ICU specific care supports
 Invasive ventilation < .0001 1.7 [1.5–1.9] < .0001
 Vasoactive treatment** < .0001 1.7 [1.5–1.9] < .0001
 Renal replacement therapy < .0001 2.9 [2.6–3.2] < .0001
 ECMO < .0001 2.9 [2.4–3.5] < .0001
Hospital level
Number of ICU stays in hospital 2019, age ≥ 18 y–o***
< 100 0.003 1.3 [1.1–1.4]  < .0001
 [1000–2000] 1.0 [0.9–1.2] 0.73
 ≥ 2000 Ref
Regional level
Number of days with 75% or more of ICU beds occupied by COVID-19 patients
 < 10 days  < .0001 Ref
 10–19 days 1.2 [1.0–1.5] 0.03
 20–29 days 1.5 [1.2–1.7]  < .0001
 ≥ 30 days 2.2 [1.9–2.6]  < .0001

*Missing data SAPS II n = 281

**Dobutamine, dopamine, epinephrine, norepinephrine

***For hospitals with several ICUs, all ICU stays were included

At the patient level, the risk of death increased with age (odds ratio [OR]: 2.5 [2.3–2.8] for patients of 65 to 79 years old and OR: 10.2 [8.7–12.0] for patients over 80 years old), SAPS II and comorbid conditions (Table 2).

At the hospital level, the previous experience of the health structure, assessed by the number of 2019 ICU hospitalizations, was significantly associated with the case fatality in the adjusted analyses. Healthcare facilities with less than 1000 ICU stays in 2019 were associated with a higher risk of death for patients admitted to ICU for COVID-19 (Table 2).

At the regional level, we observed an exposure–response relationship between ICU bed occupancy and case fatality rate: adjusted OR were 1.2 [1.0–1.5], 1.5 [1.2–1.7], 2.2 [1.9–2.6] for patients hospitalized in regions from 10–19 days up to ≥ 30 days of high occupancy rate of ICU beds, as compared with regions with less than 10 days of high bed occupancy rate of ICU beds (Table 2).

Discussion

In this study, we found that the overall death rate of COVID-19 patients hospitalized in ICU during the first outbreak in France was 29.3%, but that masked tremendous inequalities at the regional level. We demonstrated that the burden of the COVID-19 crisis at the regional level (assessed by the ICU bed occupancy) was associated with higher COVID-19 mortality rate. We also demonstrated that the experience of the hospital structures (e.g., number of ICU hospitalizations in the previous year) was statistically associated with COVID-19 mortality rate. Our approach differed from conventional understanding of diseases based on patients’ characteristics and severity at presentation; instead, we investigated how healthcare organization and immediate logistic resources affected the death rate in critically ill COVID-19 patients. Results from our study showed that French regions that were overwhelmed by the COVID-19 sanitary crisis had a twofold increase in adjusted case fatality rate.

All levels components (patient, hospital, and region) were independently associated with mortality. At the patient’s level, expected results were observed: aging had the strongest association with lethal outcome [7, 8, 10]; multimorbidity and severity at presentation (SAPS II) were also linked with mortality [11]. At the regional level, the ICU bed occupancy rate was used as a surrogate of the importance of the sanitary crisis, and of ICU burden in particular. The majority of French regions have experienced occupancy rates superior to 100% of pre-existing bed capacity, demonstrating an extraordinary expansion of ICU beds by implementation of new ICU locations, within hospital or in pop-up hospital. For example in the Grand Est region, the number of critically ill COVID-19 patients was superior to the pre-existing ICU bed capacity of the region in 3 weeks. The expanse of critical care capacity during the pandemic has not been without any cost. Indeed, we observed that the risk of death increased gradually with the ICU occupancy rates at the regional level. Regions with more than 10 days with 75% or more of ICU beds occupied by COVID-19 patients had experienced an excess of mortality, independently to the other parameters. Intensive care medicine is a highly skill- and experienced-based medical specialty. One can assume that the implantation of temporary ICU structures has been a tremendous effort to limit the dramatic consequences of crude ICU bed shortage, but the quality of care that was provided in these conditions could hardly guaranty the highest standards of care. In agreement with this assumption, we observed that the importance of the experience of the hospital structures, assessed by the number of ICU patients treated yearly before the pandemic, was also an independent protective factor. At last, the cut-off threshold of 75% or more of ICU beds occupied by COVID-19 patients could hardly be considered as an operational marker, but is rather a late indicator. With median duration of mechanical ventilation and ICU stay of 13 (8–18) and 21 (13–36) [12], an important effort of anticipation should be performed to avoid reaching this level of ICU shortage.

The use of administrative hospital databases for epidemiological purpose has sometime been challenged or criticized. Strengths and weaknesses of this method has been already discussed [7, 8, 1317]. Herein, there is an unprecedented opportunity to compare results obtained from prospective cohorts or from retrospective analysis of hospital discharge database HDD (present study or [12]). Indeed, the COVID-ICU study [12] was a multi-center, prospective cohort conducted in 138 hospitals (135 in France, 3 in Belgium and Switzerland) that studied 4,643 COVID-19 patients hospitalized in ICU during the same study period [12]. Consequently, a large proportion of patient overlap is expected with our 14,513-patient nationwide cohort generated from French HDD. The patients’ characteristics at admission were comparable whatever the methodology used, in COVID-ICU or the present study, respectively: sex ratio (26% of female vs 28%), mean age (63 years old, both study), proportion of hypertension (48% vs 49%) and diabetes mellitus (28% vs 31%), whereas obesity was different (41% vs 24.5%). Ventilation support characteristics in the two studies were: invasive mechanical ventilation during the ICU stay 80% vs 68.1%, extra-corporeal membrane oxygenation (ECMO) 8% vs 4%, respectively, in COVID-ICU or the present study. The few observed differences may be explained by a certain degree of inaccuracy that is an inherent bias of administrative hospital database. For example, there is probably an underestimation of obesity rate in our report. However, selective bias could also be generated by prospective database. For example, the use of ECMO was double in COVID-ICU prospective study compared to our report, but 56% of the patients in COVID-ICU were recruited in Paris where there is a worldwide expert center for ECMO [12]. Rather than opposing studies based on retrospective administrative data with studies based on prospective clinical databases, future challenges will probably be to implement novel complementary strategies combining the advantages of both approaches. The major interest of the HDD is the exhaustive record of all patients hospitalized during the studied period without initial selection bias, giving reliable information on healthcare in real life. Patients from all regions and all healthcare structures were included, and not only health structures involved in clinical research. The major interest of prospective clinical database is to provide a granularity that is indispensable to further decipher these observations.

This study had limitations. Due to the cross-sectional study design, exposure and outcome are simultaneously assessed. Thus, we cannot establish a true cause-and-effect relationship without longitudinal data. We assumed that discharge from the hospital was not a competing event for death because we, and others, observed that the death in COVID-19 critical patients occurred almost exclusively in ICU or in ward following ICU-discharge, and rarely after hospital discharge [9, 12]. Regarding the choice of the statistical methods, it is difficult to clearly identify the best method between multivariable methods and propensity scores to adjust for confounders in non-randomized studies [18]. Both standard multivariable methods and propensity scores have key limitations, and none is able to take into account unknown confounders. Debate persists on the real usefulness of propensity scores in comparison to standard multivariable approaches such as logistic regression [18, 19], but it is important to keep in mind that in many cases both approaches provide similar results [20, 21]. The use of propensity score with matching could have been used here and may have reduced errors in the estimation of the effect of the confounders on the outcome. However, the propensity score empirical coverage probability decreased after eight or more events per confounder [19] and the logistic regression seems to be a relevant choice when there are at least eight events per confounder. Because there was similar follow-up, no censored data and important number of events per covariate, we preferred to use a commonly used method, easy to understand by non-specialized readers, and to carefully report all available information (Additional file 2: Table S1 for bivariate analysis, Table 2 for logistic regression model). Next, nurse/bed ratio might have been an important factor to take into consideration but incoherencies were found in the declarative data between the number of full-time equivalents and the number of persons. We preferred not to use this information. Finally, the reliability of national health administrative systems for epidemiology purpose may vary according to case definition and could generate false positive diagnosis, whereas false-negative rate remained relatively low whatever the definition [13, 15, 22]. However, the implementation of straightforward coding for COVID-19 limited the risk of information bias. Another limitation is the potential for biases related to under-detection or misclassification, particularly for comorbidities (as discussed earlier for obesity rate). However, a good agreement between patients’ characteristics in the concomitant prospective cohort [12] was observed. For some variables, information is not recorded when there is no direct impact on patient care during hospitalization (e.g., tobacco use). Overall, rigorous acknowledgment of strength and limitation of HDD are critical to provide epidemiological data. In the context of the COVID-19 sanitary crisis, HDD-based surveillance has been promoted as a cost-effective method for healthcare service studies with real life dynamic approach, as previously demonstrated [5, 23, 24].

In conclusion, we studied critically ill COVID-19 patients during the first French outbreak and observed significant differences in adjusted case fatality rate between French regions. The regions with the highest burden of care in ICU were associated with up to 2.2-fold increase of death rate.

Supplementary Information

13613_2021_915_MOESM1_ESM.docx (27.4KB, docx)

Additional file 1. ICD-10 diagnosis codes.

13613_2021_915_MOESM2_ESM.docx (29.5KB, docx)

Additional file 2. Bivariate analysis of case fatality in COVID-19 patients admitted in the ICU in France, March–May 2020.

Acknowledgements

We thank all staffs of health care facilities who contributed to the Hospital Discharge Database implementation.

Abbreviations

ATIH

Agence Technique de l’Information sur l’Hospitalisation

HDD

Hospital discharge database

ICU

Intensive care unit

PMSI

Programme de Médicalisation des Systèmes d’Information

SAE

Statistique Annuelle des Etablissements

SAPS II

Simplified Acute Physiology Score II

SD

Standard deviation

Authors' contributions

AG, LGG, LG conceived and designed the study and were involved in drafting the manuscript. LG performed the data retrieval and LG EL AG and LGG performed the statistical analysis. AG LGG and EL made substantial contributions to the conception of the study; all the authors were involved in the interpretation of the data, in drafting the manuscript and made critical revisions to the discussion section. All authors read and approved the final manuscript.

Funding

The authors declare that they have no sources of funding for the research.

Availability of data and materials

Restrictions apply to the availability of these data and so are not publicly available. However, data are available from the authors upon reasonable request and with the permission of the institution.

Declarations

Ethics approval and consent to participate

No nominative, sensitive or personal data of patients have been collected. Our study involved the reuse of already recorded and anonymized data. The study falls within the scope of the French Reference Methodology MR-005 (declaration 2205437 v 0, August 22nd, 2018, subscripted by the Teaching Hospital of Tours), which require neither information nor consent of the included individuals. This study was consequently registered with the French Data Protection Board (CNIL MR-005 number #2018160620).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflict of interest.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Antoine Guillon, Email: antoine.guillon@univ-tours.fr.

Emeline Laurent, Email: E.LAURENT@chu-tours.fr.

Antoine Duclos, Email: antoine.duclos@chu-lyon.fr.

Lucile Godillon, Email: L.GODILLON@chu-tours.fr.

Pierre-François Dequin, Email: pierre-francois.dequin@univ-tours.fr.

Nelly Agrinier, Email: N.AGRINIER@chru-nancy.fr.

Antoine Kimmoun, Email: akimmoun@gmail.com.

Leslie Grammatico-Guillon, Email: leslie.guillon@univ-tours.fr.

References

  • 1.Mendenhall E. The COVID-19 syndemic is not global: context matters. Lancet. 2020;396:1731. doi: 10.1016/S0140-6736(20)32218-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Horton R. Offline: COVID-19 is not a pandemic. Lancet Lond Engl. 2020;396:874. doi: 10.1016/S0140-6736(20)32000-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Singer M, Bulled N, Ostrach B, Mendenhall E. Syndemics and the biosocial conception of health. Lancet Lond Engl. 2017;389:941–950. doi: 10.1016/S0140-6736(17)30003-X. [DOI] [PubMed] [Google Scholar]
  • 4.Hirsch M, Carli P, Nizard R, Riou B, Baroudjian B, Baubet T, et al. The medical response to multisite terrorist attacks in Paris. Lancet. 2015;386:2535–2538. doi: 10.1016/S0140-6736(15)01063-6. [DOI] [PubMed] [Google Scholar]
  • 5.Rimmelé T, Pascal L, Polazzi S, Duclos A. Organizational aspects of care associated with mortality in critically ill COVID-19 patients. Intensive Care Med. 2020;47(1):119–21. doi: 10.1007/s00134-020-06249-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Beyond 20/20 WDS - Rapports. http://www.data.drees.sante.gouv.fr/ReportFolders/reportFolders.aspx. Accessed 12 Jan 2021.
  • 7.Laporte L, Hermetet C, Jouan Y, Gaborit C, Rouve E, Shea KM, et al. Ten-year trends in intensive care admissions for respiratory infections in the elderly. Ann Intensive Care. 2018;8:84. doi: 10.1186/s13613-018-0430-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Guillon A, Hermetet C, Barker KA, Jouan Y, Gaborit C, Ehrmann S, et al. Long-term survival of elderly patients after intensive care unit admission for acute respiratory infection: a population-based, propensity score-matched cohort study. Crit Care. 2020;24:384. doi: 10.1186/s13054-020-03100-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Guillon A, Laurent E, Godillon L, Kimmoun A, Grammatico-Guillon L. Long-term mortality of elderly patients after intensive care unit admission for COVID-19. Intensive Care Med. 2021 doi: 10.1007/s00134-021-06399-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Guillon A, Mizgerd JP, Grammatico-Guillon L. 2-year survival among elderly hospitalised for acute respiratory infection versus hip fracture: a useful comparison to raise awareness. Eur Respir Rev Off J Eur Respir Soc. 2020;29:200156. doi: 10.1183/16000617.0156-2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Le Gall JR, Lemeshow S, Saulnier F. A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA. 1993;270:2957–2963. doi: 10.1001/jama.1993.03510240069035. [DOI] [PubMed] [Google Scholar]
  • 12.COVID-ICU Group on behalf of the REVA Network and the COVID-ICU Investigators Clinical characteristics and day-90 outcomes of 4244 critically ill adults with COVID-19: a prospective cohort study. Intensive Care Med. 2020;47(1):60–73. doi: 10.1007/s00134-020-06294-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Jouan Y, Grammatico-Guillon L, Espitalier F, Cazals X, François P, Guillon A. Long-term outcome of severe herpes simplex encephalitis: a population-based observational study. Crit Care Lond Engl. 2015;19:345. doi: 10.1186/s13054-015-1046-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Grammatico-Guillon L, Baron S, Gettner S, Lecuyer A-I, Gaborit C, Rosset P, et al. Bone and joint infections in hospitalized patients in France, 2008: clinical and economic outcomes. J Hosp Infect. 2012;82:40–48. doi: 10.1016/j.jhin.2012.04.025. [DOI] [PubMed] [Google Scholar]
  • 15.Grammatico-Guillon L, Baron S, Gaborit C, Rusch E, Astagneau P. Quality assessment of hospital discharge database for routine surveillance of hip and knee arthroplasty-related infections. Infect Control Hosp Epidemiol. 2014;35:646–651. doi: 10.1086/676423. [DOI] [PubMed] [Google Scholar]
  • 16.Grammatico-Guillon L, Baron S, Rosset P, Gaborit C, Bernard L, Rusch E, et al. Surgical site infection after primary hip and knee arthroplasty: a cohort study using a hospital database. Infect Control Hosp Epidemiol. 2015;36:1198–1207. doi: 10.1017/ice.2015.148. [DOI] [PubMed] [Google Scholar]
  • 17.Quantin C, Chatellier G, Le Goaster C, Taright N, Kohler F, Toussaint E, et al. Système d’information hospitalier et Epidémiologie. Rev Epidemiol Sante Publique. 2014;62:S69. doi: 10.1016/j.respe.2014.01.068. [DOI] [PubMed] [Google Scholar]
  • 18.Biondi-Zoccai G, Romagnoli E, Agostoni P, Capodanno D, Castagno D, D’Ascenzo F, et al. Are propensity scores really superior to standard multivariable analysis? Contemp Clin Trials. 2011;32:731–740. doi: 10.1016/j.cct.2011.05.006. [DOI] [PubMed] [Google Scholar]
  • 19.Cepeda MS, Boston R, Farrar JT, Strom BL. Comparison of logistic regression versus propensity score when the number of events is low and there are multiple confounders. Am J Epidemiol. 2003;158:280–287. doi: 10.1093/aje/kwg115. [DOI] [PubMed] [Google Scholar]
  • 20.Kurth T, Walker AM, Glynn RJ, Chan KA, Gaziano JM, Berger K, et al. Results of multivariable logistic regression, propensity matching, propensity adjustment, and propensity-based weighting under conditions of nonuniform effect. Am J Epidemiol. 2006;163:262–270. doi: 10.1093/aje/kwj047. [DOI] [PubMed] [Google Scholar]
  • 21.Stürmer T, Joshi M, Glynn RJ, Avorn J, Rothman KJ, Schneeweiss S. A review of the application of propensity score methods yielded increasing use, advantages in specific settings, but not substantially different estimates compared with conventional multivariable methods. J Clin Epidemiol. 2006;59:437–447. doi: 10.1016/j.jclinepi.2005.07.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Grammatico-Guillon L, Maakaroun Vermesse Z, Baron S, Gettner S, Rusch E, Bernard L. Paediatric bone and joint infections are more common in boys and toddlers: a national epidemiology study. Acta Paediatr Oslo Nor. 1992;2013(102):e120–125. doi: 10.1111/apa.12115. [DOI] [PubMed] [Google Scholar]
  • 23.Piroth L, Cottenet J, Mariet A-S, Bonniaud P, Blot M, Tubert-Bitter P, et al. Comparison of the characteristics, morbidity, and mortality of COVID-19 and seasonal influenza: a nationwide, population-based retrospective cohort study. Lancet Respir Med. 2020;9(3):251–259. doi: 10.1016/S2213-2600(20)30527-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lantelme P, Couray Targe S, Metral P, Bochaton T, Ranc S, Le Bourhis ZM, et al. Worrying decrease in hospital admissions for myocardial infarction during the COVID-19 pandemic. Arch Cardiovasc Dis. 2020;113:443–447. doi: 10.1016/j.acvd.2020.06.001. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

13613_2021_915_MOESM1_ESM.docx (27.4KB, docx)

Additional file 1. ICD-10 diagnosis codes.

13613_2021_915_MOESM2_ESM.docx (29.5KB, docx)

Additional file 2. Bivariate analysis of case fatality in COVID-19 patients admitted in the ICU in France, March–May 2020.

Data Availability Statement

Restrictions apply to the availability of these data and so are not publicly available. However, data are available from the authors upon reasonable request and with the permission of the institution.


Articles from Annals of Intensive Care are provided here courtesy of Springer-Verlag

RESOURCES