This is an update of the results from the previous report of the CORONADO (Coronavirus SARS-CoV-2 and Diabetes Outcomes) study, which aims to describe the outcomes and prognostic factors in patients with diabetes hospitalised for coronavirus disease-2019 (COVID-19).
Methods
The CORONADO initiative is a French nationwide multicentre study of patients with diabetes hospitalised for COVID-19 with a 28-day follow-up. The patients were screened after hospital admission from 10 March to 10 April 2020. We mainly focused on hospital discharge and death within 28 days.
Results
We included 2796 participants: 63.7% men, mean age 69.7 ± 13.2 years, median BMI (25th–75th percentile) 28.4 (25.0–32.4) kg/m2. Microvascular and macrovascular diabetic complications were found in 44.2% and 38.6% of participants, respectively. Within 28 days, 1404 (50.2%; 95% CI 48.3%, 52.1%) were discharged from hospital with a median duration of hospital stay of 9 (5–14) days, while 577 participants died (20.6%; 95% CI 19.2%, 22.2%). In multivariable models, younger age, routine metformin therapy and longer symptom duration on admission were positively associated with discharge. History of microvascular complications, anticoagulant routine therapy, dyspnoea on admission, and higher aspartate aminotransferase, white cell count and C-reactive protein levels were associated with a reduced chance of discharge. Factors associated with death within 28 days mirrored those associated with discharge, and also included routine treatment by insulin and statin as deleterious factors.
Conclusions/interpretation
In patients with diabetes hospitalised for COVID-19, we established prognostic factors for hospital discharge and death that could help clinicians in this pandemic period.
Matthieu Wargny and Louis Potier contributed equally to the manuscript and must be considered as joint first authors.
Bertrand Cariou and Samy Hadjadj contributed equally to the manuscript and must be considered as joint senior authors.
A complete list of the CORONADO trial investigators is provided in the electronic supplementary material (ESM).
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
ARB
Angiotensin-2 receptor blockers
AST
Aspartate aminotransferase
CCB
Calcium channel blocker
COPD
Chronic obstructive pulmonary disease
CORONADO
Coronavirus-SARS-CoV-2 and Diabetes Outcomes
COVID-19
Coronavirus disease-2019
CRP
C-reactive protein
CT
Computed tomography
DPP-4
Dipeptidyl peptidase 4
ICU
Intensive care unit
MRA
Mineralocorticoid receptor antagonist
OSA
Obstructive sleep apnoea
SARS-CoV-2
Severe acute respiratory syndrome coronavirus-2
Introduction
Soon after the coronavirus disease-2019 (COVID-19) pandemic outbreak, diabetes was rapidly identified as a risk factor for poor outcome [1, 2]. Diabetes has been previously recognised as a major risk factor for mortality in people infected with either the 2009 H1N1 pandemic influenza or the Middle East respiratory syndrome-related coronavirus (MERS-CoV) [3, 4]. More recently, diabetes consistently appeared as one of the major comorbidities associated with COVID-19 [1, 2, 5, 6].
Moreover, diabetes has been shown to be associated with worse prognosis. Indeed, the prevalence of diabetes was two- to threefold higher in patients admitted to intensive care units (ICUs) compared with those with less severe disease and the mortality rate was consistently higher in patients with diabetes [1, 2, 7‐10]. Altogether, diabetes received considerable attention and was very often considered as a top risk factor for fatal COVID-19. In this context, contracting COVID-19 is a major source of worry in people with diabetes [11‐13].
Anzeige
Diabetes-related worse COVID-19 prognosis has been extensively documented so far. In a short-term interim analysis of the CORONADO (Coronavirus-SARS-CoV-2 and Diabetes Outcomes) study, we showed that, in 1317 people with diabetes admitted for COVID-19, poor outcomes within 7 days were independently associated with BMI, age, diabetic complications, treated obstructive sleep apnoea (OSA), and some biological features [14]. However, to the best of our knowledge, no study has specifically focused on factors associated with favourable prognosis enabling hospital discharge in patients with diabetes admitted for COVID-19 infection.
Here, compared with our previous report, we expand our data to a larger sample size and a longer duration of follow-up. The current study describes the complete results of the CORONADO study, a French nationwide multicentre observational study aimed at identifying the clinical and biological features associated with disease severity and mortality in patients with diabetes hospitalised for COVID-19, with a specific focus on the clinical and biological characteristics of patients discharged home or to a long-term care facility by day 28.
Methods
Study design and participants
The design of the CORONADO study has been previously reported [14]. The aim of the study was to describe the phenotypic characteristics and prognosis of patients with diabetes presenting with COVID-19 between 10 March and 10 April 2020, in 68 French hospitals. Inclusion criteria were: (1) hospitalisation in a dedicated COVID-19 unit for biologically attested (PCR for severe acute respiratory syndrome coronavirus-2 [SARS-CoV-2]) and/or clinically/radiologically attested COVID-19 (i.e. as ground-glass opacity and/or crazy paving on chest computed tomography [CT] scan); (2) personal history of diabetes or newly diagnosed diabetes on admission (i.e. HbA1c ≥6.5% [48 mmol/mol] during hospitalisation).
The study was designed in accordance with the Declaration of Helsinki and conducted in accordance with French legislation with approvals obtained from one local and two national committees: the local ethics committee (IRB/IEC – GNEDS; Ref. CORONADOV2), the CEREES (n° INDS:1544730) and the CNIL (DR-2020-155/920129). The latter waived informed consent owing to the purely observational approach using only retrospective data [14].
Anzeige
This article follows the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guidelines for cohort studies.
Data collection
Data collection was retrospectively performed by clinical research associates and physicians in participating centres from medical files. They systematically reviewed the medical files of all COVID-19 inpatients, selected those with diabetes and, if necessary, contacted the patient’s general and/or specialist practitioners, regular pharmacist and biomedical laboratory. Collected data included clinical characteristics prior to admission including complications, comorbidities and routine treatments. Moreover, COVID-19-related clinical, radiological and biological characteristics were collected on admission. Regarding liver enzymes, the upper limit of normal was different between centres (see electronic supplementary material [ESM] Table 1).
Patient follow-up and clinical outcomes
The composite primary outcome was combined tracheal intubation for mechanical ventilation and/or death within 7 days of admission. Participants discharged before day 7 were systematically contacted to check for the non-occurrence of these events on day 7.
Secondary outcomes included death, tracheal intubation, admission to ICUs and hospital discharge. A secondary time point was considered at day 28 for all patients alive and not discharged by day 7 in order to consider outcomes between admission and day 28. Outcomes were no longer collected after discharge on day 7 or later and no further follow-up was organised after day 28. Moreover, patients transferred to rehabilitation centres or to other hospitals were classified as ‘transferred’ and no follow-up information could be ascertained after the transfer. Those who remained in the hospital of their initial admission were classified as ‘in-hospital’. Only those returning home or to a long-term care facility were classified as ‘discharged’.
The current analysis mainly focused on hospital discharge and death within 28 days of follow-up.
Statistical analyses
Quantitative data were expressed as mean ± SD or median (25th–75th percentile). Categorical variables were given as n (%) of participants. We described covariates according to time of admission, splitting data prior to and on admission, which corresponds to a clinician’s perspective. As specified in the protocol, the main objective of the study was descriptive. Originally, we calculated that, with a population of 300 participants and an attrition rate of 20%, an occurrence of 16% of the composite outcome would give a 95% CI equal to 11.7, 21.1% using the Clopper–Pearson estimate. In this analysis, we considered two main outcomes: hospital discharge and death within 28 days. The composite outcome (death and/or tracheal intubation) is only presented as ESM (ESM Tables 2–4).
Univariate logistic regression models were used to calculate ORs associated with study outcomes. Natural-log transformation was consistently considered in order to comply with linearity assumptions, which applied for diabetes duration, BMI and biological features.
Multivariable logistic regression models were used to assess the association between clinical and biological features and study outcomes (discharge and death within 28 days and primary outcome within 7 days). A standardisation process (z score) was also applied to quantitative variables to allow for direct comparison. Covariates included in the model were chosen according to a clinician’s point of view, based on background knowledge. The multivariate model included elementary clinical characteristics (sex, age, BMI); the patient’s history (hypertension, micro- and macrovascular complications, chronic obstructive pulmonary disease [COPD], treated OSA); routine medication (metformin, insulin, angiotensin-2 receptor blockers [ARBs] and/or ACE inhibitors and/or mineralocorticoid receptor antagonists [MRAs], statins, anticoagulation therapy); symptoms on admission (time between symptom onset and hospital admission, dyspnoea); and biological features (eGFR [determined using the CKD-EPI formula], aspartate aminotransferase [AST], white cell count, platelets, C-reactive protein [CRP]). Of note, the event-per-variable was always ≥10 in the main multivariable analyses.
Anzeige
Sensitivity analyses were performed for all multivariable models. First, we restricted the study population to the 2547 participants (91.1%) with a positive SARS-CoV-2 PCR. Second, we restricted the study population to the 1551 participants (55.5%) with admission plasma glucose data available.
All statistical tests were two-sided with a type 1 error set at 5%. All analyses were performed on available data, without imputation, and using statistical software R version 4.0.0 (https://cran.r-project.org).
Results
Study population and characteristics of COVID-19
The different centres originally screened 2951 patients suspected of hospitalisation or prolongation of hospitalisation related to COVID-19 between 10 March and 10 April 2020, with a diagnosis of diabetes mellitus (see flow diagram, ESM Fig. 1). After further investigations, 97 patients (3.3%) were ruled out for not meeting inclusion criteria (including 47 patients without diabetes mellitus and 35 without COVID-19). From the 2854 patients meeting inclusion criteria, 58 patients (2.0%) were excluded from the present analysis because of at least one unavailable key outcome, including seven with missing data on death during hospital stay and 25 with missing data on discharge. Finally, 2796 patients were analysed. Among those participants, 1317 (47.1%) were previously described in a recent interim analysis [14].
The baseline characteristics of the study participants are detailed in Tables 1 and 2. Briefly, participants were mostly male (63.7%), classified as having type 2 diabetes (88.2%), of Europid origin (58.1%), and with a mean ± SD age of 69.7 ± 13.2 years, a median (25th–75th percentile) BMI of 28.4 (25.0–32.4) kg/m2 and a median (25th–75th percentile) HbA1c value of 60.7 mmol/mol (50.8–74.9 mmol/mol) (7.7% [6.8–9.0%]). On admission, a positive SARS-CoV-2 PCR was found in 2547/2705 (94.2%) patients and median (25th–75th percentile) CRP was 86 (40–148) mg/l.
Table 1
Clinical characteristics prior to admission of CORONADO participants according to the discharge within 28 days
Discharge within 28 days
Clinical features
Available data
All (N = 2796)
No (n = 1392)
Yes (n = 1404)
Unadjusted OR (95% CI)
Age-adjusted OR (95% CI)
Age-adjusted p value
Sex (female)
2796
1014/2796 (36.3)
467/1392 (33.5)
547/1404 (39.0)
1.26 (1.08, 1.48)
1.38 (1.18, 1.62)
<0.001
Age (years)
2796
69.7 ± 13.2
73.1 ± 12.4
66.3 ± 13.1
0.96 (0.95, 0.97)
–
<0.001
Age class (years)
2796
<0.001
<55
367/2796 (13.1)
117/1392 (8.4)
250/1404 (17.8)
1
55–64
565/2796 (20.2)
209/1392 (15.0)
356/1404 (25.4)
0.80 (0.60, 1.05)
–
0.11
65–74
797/2796 (28.5)
394/1392 (28.3)
403/1404 (28.7)
0.48 (0.37, 0.62)
–
<0.001
≥75
1067/2796 (38.2)
672/1392 (48.3)
395/1404 (28.1)
0.28 (0.21, 0.35)
–
<0.001
Ethnicity
2384
0.13
EU
1385/2384 (58.1)
745/1193 (62.4)
640/1191 (53.7)
1
1
MENA
497/2384 (20.8)
227/1193 (19.0)
270/1191 (22.7)
1.38 (1.13, 1.70)
1.17 (0.95, 1.45)
0.15
AC
415/2384 (17.4)
174/1193 (14.6)
241/1191 (20.2)
1.61 (1.29, 2.01)
1.06 (0.83, 1.34)
0.65
AS
87/2384 (3.6)
47/1193 (3.9)
40/1191 (3.4)
0.99 (0.64, 1.53)
0.68 (0.43, 1.08)
0.10
BMI (kg/m2)
2460
28.4 (25–32.4)
28.2 (24.8–32.2)
28.7 (25.3–32.5)
1.09 (1.01, 1.18)
0.99 (0.91, 1.07)
0.77
BMI class
2460
0.66
<25 kg/m2
611/2460 (24.8)
325/1226 (26.5)
286/1234 (23.2)
1
1
25–29.9 kg/m2
890/2460 (36.2)
437/1226 (35.6)
453/1234 (36.7)
1.18 (0.96, 1.45)
1.09 (0.88, 1.35)
0.42
30–39.9 kg/m2
823/2460 (33.5)
398/1226 (32.5)
425/1234 (34.4)
1.21 (0.98, 1.50)
1.00 (0.80, 1.25)
0.99
≥40 kg/m2
136/2460 (5.5)
66/1226 (5.4)
70/1234 (5.7)
1.21 (0.83, 1.75)
0.90 (0.61, 1.32)
0.58
Diabetes duration (years)
1767
11 (5–20)
12 (5–20)
10 (4–18)
0.84 (0.76, 0.92)
0.99 (0.90, 1.10)
0.92
HbA1c (mmol/mol)a
1800
60.7 (50.8–74.9)
59.6 (50.8–72.7)
61.8 (50.8–77.1)
1.19 (1.08, 1.31)
1.06 (0.96, 1.17)
0.24
HbA1c (%)a
1800
7.7 (6.8–9.0)
7.6 (6.8–8.8)
7.8 (6.8–9.2)
1.19 (1.08, 1.31)
1.06 (0.96, 1.17)
0.24
Hypertension
2769
2126/2769 (76.8)
1122/1379 (81.4)
1004/1390 (72.2)
0.60 (0.50, 0.71)
0.80 (0.66, 0.97)
0.025
Dyslipidaemia
2710
1267/2710 (46.8)
661/1342 (49.3)
606/1368 (44.3)
0.82 (0.70, 0.95)
0.93 (0.79, 1.08)
0.35
Current tobacco use
2288
131/2288 (5.7)
63/1109 (5.7)
68/1179 (5.8)
1.02 (0.71, 1.45)
0.93 (0.65, 1.34)
0.69
Long-term diabetes complications
Microvascular complicationsb
1966
869/1966 (44.2)
516/939 (55.0)
353/1027 (34.4)
0.43 (0.36, 0.52)
0.59 (0.49, 0.72)
<0.001
Macrovascular complicationsc
2627
1014/2627 (38.6)
586/1297 (45.2)
428/1330 (32.2)
0.58 (0.49, 0.67)
0.74 (0.63, 0.88)
<0.001
Comorbidities
Heart failure
2651
302/2651 (11.4)
190/1308 (14.5)
112/1343 (8.3)
0.54 (0.42, 0.69)
0.71 (0.55, 0.92)
0.009
NAFLD or liver cirrhosis
2640
218/2640 (8.3)
102/1310 (7.8)
116/1330 (8.7)
1.13 (0.86, 1.49)
0.98 (0.73, 1.30)
0.87
Active cancer
2742
253/2742 (9.2)
137/1362 (10.1)
116/1380 (8.4)
0.82 (0.63, 1.06)
1.05 (0.80, 1.37)
0.73
COPD
2732
263/2732 (9.6)
162/1359 (11.9)
101/1373 (7.4)
0.59 (0.45, 0.76)
0.70 (0.54, 0.92)
0.009
Treated OSA
2593
273/2593 (10.5)
144/1284 (11.2)
129/1309 (9.9)
0.87 (0.67, 1.11)
0.84 (0.65, 1.09)
0.20
Routine treatment before admission
Metformin
2794
1553/2794 (55.6)
690/1391 (49.6)
863/1403 (61.5)
1.62 (1.40, 1.89)
1.46 (1.25, 1.71)
<0.001
Sulfonylurea/glinides
2794
782/2794 (28.0)
378/1391 (27.2)
404/1403 (28.8)
1.08 (0.92, 1.28)
1.13 (0.96, 1.34)
0.15
DPP4-inhibitors
2794
615/2794 (22.0)
286/1391 (20.6)
329/1403 (23.4)
1.18 (0.99, 1.42)
1.22 (1.02, 1.47)
0.033
GLP-1RA
2794
254/2794 (9.1)
108/1391 (7.8)
146/1403 (10.4)
1.38 (1.06, 1.79)
1.11 (0.85, 1.45)
0.45
Insulin
2796
1039/2796 (37.2)
563/1392 (40.4)
476/1404 (33.9)
0.76 (0.65, 0.88)
0.78 (0.67, 0.92)
0.002
Diureticsd
2794
1058/2794 (37.9)
602/1391 (43.3)
456/1403 (32.5)
0.63 (0.54, 0.74)
0.78 (0.66, 0.91)
0.002
β-Blockers
2794
988/2794 (35.4)
552/1391 (39.7)
436/1403 (31.1)
0.69 (0.59, 0.80)
0.84 (0.71, 0.99)
0.033
CCB
2794
924/2794 (33.1)
487/1391 (35.0)
437/1403 (31.1)
0.84 (0.72, 0.98)
0.91 (0.77, 1.07)
0.25
ARBs and/or ACE inhibitors and/or MRAe
2794
1570/2794 (56.2)
800/1391 (57.5)
770/1403 (54.9)
0.90 (0.77, 1.04)
1.03 (0.88, 1.20)
0.75
Statins
2794
1282/2794 (45.9)
664/1391 (47.7)
618/1403 (44.0)
0.86 (0.74, 1.00)
0.96 (0.82, 1.12)
0.63
Anti-platelet therapy
2794
1125/2794 (40.3)
594/1391 (42.7)
531/1403 (37.8)
0.82 (0.70, 0.95)
1.03 (0.88, 1.20)
0.75
Anticoagulation therapy
2794
501/2794 (17.9)
321/1391 (23.1)
180/1403 (12.8)
0.49 (0.40, 0.60)
0.65 (0.53, 0.80)
<0.001
Population size was N = 2796. Data shown are n (%), and mean ± SD or median (25th–75th percentile) if not normally distributed
p values are calculated using Wald test (unadjusted and age-adjusted logistic regression, except for ‘age’ and ‘age class’, which were not adjusted). ORs correspond to an increase of 1 SD after natural-log transformation and standardisation for BMI, diabetes duration and HbA1c
aHbA1c determined in the 6 months prior to or in the first 7 days following hospital admission
bMicrovascular complication was defined as history of one or more of the following: diabetic kidney disease and/or severe diabetic retinopathy and/or diabetic foot ulcer
cMacrovascular complication was defined as history of one or more of the following: ischaemic heart disease (acute coronary syndrome and/or coronary artery revascularisation) and/or cerebrovascular disease (stroke and/or transient ischaemic attack) and/or peripheral artery disease (amputation owing to ischaemic disease and/or lower limb artery revascularisation)
dDiuretics include loop diuretics, thiazide diuretics and potassium-sparing diuretics
eMRAs include spironolactone and eplerenone
Abbreviations: EU, Europid; MENA, Middle East North Africa; AC, African or Caribbean; AS, Asian; NAFLD, non-alcoholic fatty liver disease; GLP-1RA, glucagon-like peptide 1-receptor agonist
Table 2
Characteristics on admission of CORONADO participants, according to discharge within 28 days
Discharge within 28 days
Variable
Available data
All (N = 2796)
No (n = 1392)
Yes (n = 1404)
Unadjusted OR (95% CI)
Age-adjusted OR (95% CI)
Age-adjusted p value
Time from symptom onset to hospital admission (days)
2743
5 (2–9)
4 (2–7)
6 (3–9)
1.05 (1.04, 1.07)
1.04 (1.02, 1.05)
<0.001
Clinical presentation
Fever
2755
2077/2755 (75.4)
1031/1364 (75.6)
1046/1391 (75.2)
0.98 (0.82, 1.16)
0.85 (0.71, 1.01)
0.068
Dyspnoea
2754
1771/2754 (64.3)
942/1364 (69.1)
829/1390 (59.6)
0.66 (0.57, 0.77)
0.62 (0.52, 0.73)
<0.001
Abnormal chest CT scan
1982
1919/1982 (96.8)
898/927 (96.9)
1021/1055 (96.8)
0.97 (0.59, 1.60)
0.83 (0.49, 1.39)
0.48
Biological findings
Positive SARS-CoV-2 PCR
2705
2547/2705 (94.2)
1286/1340 (96.0)
1261/1365 (92.4)
0.51 (0.36, 0.71)
0.46 (0.33, 0.66)
<0.001
Admission plasma glucose (mmol/l)
1551
9.5 (7.0–13.5)
10.0 (7.1–14.0)
9.1 (6.9–12.8)
0.89 (0.80, 0.98)
0.82 (0.73, 0.91)
<0.001
Plasma creatinine (μmol/l)
2602
91 (69–133)
103 (75–153)
84 (65–115)
0.69 (0.63, 0.75)
0.73 (0.67, 0.80)
<0.001
eGFR (ml min−1 [1.73 m]−2)a
2602
68.5 (41.8–89.7)
57.1 (34.5–82.7)
78.5 (52.0–95.6)
1.57 (1.44, 1.71)
1.36 (1.25, 1.49)
<0.001
ALT (%ULN)
2478
0.62 (0.42–1.00)
0.62 (0.40–0.99)
0.62 (0.43–1.00)
0.96 (0.89, 1.04)
0.87 (0.80, 0.95)
0.002
AST (%ULN)
2444
1.06 (0.75–1.60)
1.17 (0.80–1.85)
0.98 (0.70–1.38)
0.68 (0.62, 0.74)
0.64 (0.58, 0.71)
<0.001
GGT (%ULN)
2317
0.95 (0.55–1.77)
0.99 (0.56–1.88)
0.92 (0.55–1.63)
0.89 (0.82, 0.96)
0.85 (0.78, 0.92)
<0.001
Haemoglobin (g/l)
2728
127 (114–142)
125 (110–141)
129 (118–143)
1.28 (1.18, 1.38)
1.21 (1.12, 1.31)
<0.001
White cell count (103/mm3)
2726
6580 (5000–8818)
6800 (5150–9370)
6310 (4900–8400)
0.82 (0.76, 0.88)
0.82 (0.76, 0.89)
<0.001
Lymphocyte count (103/mm3)
2646
990 (690–1400)
900 (600–1300)
1100 (780–1470)
1.29 (1.19, 1.40)
1.23 (1.13, 1.33)
<0.001
Platelet count (103/mm3)
2725
201 (156–260)
196 (150–254)
205 (164–264)
1.17 (1.08, 1.26)
1.13 (1.04, 1.22)
0.003
CRP (mg/l)
2612
86.0 (40.3–148.0)
98.6 (49.2–166.5)
73.0 (33.4–128.0)
0.74 (0.68, 0.80)
0.70 (0.65, 0.76)
<0.001
LDH (U/l)
1427
351 (266–498)
402 (290–567)
319 (250–419)
0.60 (0.52, 0.70)
0.56 (0.48, 0.66)
<0.001
CPK (U/l)
1385
132 (67–305)
164 (72–416)
108 (61–222)
0.70 (0.62, 0.78)
0.67 (0.60, 0.75)
<0.001
Fibrinogen (g/l)
1424
6.3 (5.0–7.4)
6.3 (5.0–7.6)
6.2 (5.0–7.3)
0.99 (0.89, 1.10)
0.96 (0.87, 1.07)
0.51
Population size was N = 2796. Data shown are n (%) and or median (25th–75th percentile)
p values are calculated using Wald test (unadjusted and age-adjusted logistic regression). Quantitative variables were natural-log transformed and associated ORs correspond to an increase of 1 SD after standardisation, except for time from symptoms onset to hospital admission (1 day increase)
COVID-19-related clinical outcomes are detailed in ESM Table 5 and the timeframe for study outcomes is presented in Fig. 1.
Fig. 1
Distribution of patient outcomes according to time since hospital admission. Population size was N = 2796
×
Discharge within 28 days
As shown in Fig. 1, 50.2% of the CORONADO participants were discharged within 28 days. Their median (25th–75th percentile) length of stay before discharge was 9 (5–14) days with 156/1404 (11.1%) discharged in the first 3 days following admission. Since the management of COVID-19 has been rapidly evolving, we analysed the length of stay according to three consecutive admission periods (see ESM Fig. 2a,b) and highlighted no statistical difference, with 18/234 (7.7%), 104/886 (11.7%) and 34/284 (12.0%) patients discharged in the first 3 days who were admitted 10–19 March, 20–30 March, and 31 March to 10 April, respectively (p = 0.18).
The characteristics of the participants discharged by day 28 are presented in Table 1 and Table 2. Briefly, women were more likely than men to be discharged. Older age was associated with a lower chance of discharge (for a 1-year increment, OR 0.96; 95% CI 0.95, 0.97). Hypertension, micro- or macrovascular diabetic complications, heart failure and COPD were also associated with a lower chance of discharge. Regarding routine therapy, metformin and dipeptidyl peptidase 4 (DPP-4) inhibitors were associated with a higher chance of discharge, whereas insulin, diuretics, β-blockers and anticoagulation therapy were associated with a lower chance.
As regards patient characteristics on admission, dyspnoea, plasma creatinine, and almost all biological findings associated with an inflammatory profile (including higher AST, higher white cell and lower lymphocyte cell count, and higher CRP) were significantly associated with a lower chance of discharge.
Anzeige
The results of multivariable analysis of discharge within 28 days are presented in Fig. 2 (see ESM Table 6 for results of the raw multivariable analysis, without transformation). Predictors of discharge on day 28 were younger age, routine metformin therapy and longer time between symptom onset and hospital admission. Conversely, history of microvascular complications, routine anticoagulant therapy, dyspnoea, higher AST, white cell count and CRP levels were associated with a reduced chance of discharge.
Fig. 2
Multivariable analysis of hospital discharge and death within 28 days: covariates prior to and on admission. Models were applied to 1355 participants yielding 728 discharges (53.7%) and 225 deaths within 28 days (16.6%). Regarding quantitative variables: all were natural-log transformed, except for age and BMI, and the ORs correspond to an increase of 1 SD after standardisation. The model on the left uses discharge within 28 days as the dependent variable, and the model on the right uses death within 28 days. Microvascular complication was defined as history of one or more of the following: diabetic kidney disease and/or severe diabetic retinopathy and/or history of diabetic foot ulcer. Macrovascular complication was defined as history of one or more of the following: ischaemic heart disease (acute coronary syndrome and/or coronary artery revascularisation) and/or cerebrovascular disease (stroke and/or transient ischaemic attack) and/or peripheral artery disease (amputation owing to ischaemic disease and/or lower limb artery revascularisation) MRAs include spironolactone and eplerenone; eGFR was determined by the CKD-EPI formula. ULN, upper limit of normal
×
In the sensitivity analysis on the complete-case population restricted to the patients with positive SARS-CoV-2 PCR (n = 1249) or admission plasma glucose available and added to the model (n = 761), using the same variables as those used in the multivariable model applied to the whole population, we found very similar results (ESM Table 7).
Death within 28 days
Characteristics prior to admission of those patients who died within 28 days are presented in Table 3. In age-adjusted analysis, male sex, longer duration of diabetes, as well as history of micro- and macrovascular complications, heart failure and COPD were significantly associated with death.
Table 3
Clinical characteristics prior to admission of CORONADO participants, according to death within 28 days
Death within 28 days
Clinical features
Available data
No (n = 2219)
Yes (n = 577)
Unadjusted OR (95% CI)
Age-adjusted OR (95% CI)
Age-adjusted p value
Sex (female)
2796
826/2219 (37.2)
188/577 (32.6)
0.82 (0.67, 0.99)
0.69 (0.56, 0.84)
<0.001
Age (years)
2796
67.9 ± 13.0
76.8 ± 11.3
1.06 (1.05, 1.07)
–
<0.001
Age class (years)
2796
<0.001
<55
345/2219 (15.5)
22/577 (3.8)
1
55–64
511/2219 (23.0)
54/577 (9.4)
1.66 (0.99, 2.77)
–
0.054
65–74
657/2219 (29.6)
140/577 (24.3)
3.34 (2.09, 5.34)
–
<0.001
≥75
706/2219 (31.8)
361/577 (62.6)
8.02 (5.12, 12.6)
–
<0.001
Ethnicity
2384
0.35
EU
1065/1895 (56.2)
320/489 (65.4)
1
1
MENA
406/1895 (21.4)
91/489 (18.6)
0.75 (0.58, 0.97)
0.98 (0.74, 1.28)
0.86
AC
357/1895 (18.8)
58/489 (11.9)
0.54 (0.40, 0.73)
1.01 (0.73, 1.41)
0.94
AS
67/1895 (3.5)
20/489 (4.1)
0.99 (0.59, 1.66)
1.67 (0.96, 2.88)
0.068
BMI (kg/m2)
2460
28.6 (25.2–32.6)
27.8 (24.5–31.7)
0.91 (0.82, 1.00)
1.06 (0.95, 1.18)
0.31
BMI class
2460
0.17
<25 kg/m2
473/1973 (24.0)
138/487 (28.3)
1
1
25–29.9 kg/m2
716/1973 (36.3)
174/487 (35.7)
0.83 (0.65, 1.07)
0.96 (0.74, 1.25)
0.78
30–39.9 kg/m2
679/1973 (34.4)
144/487 (29.6)
0.73 (0.56, 0.94)
0.98 (0.74, 1.29)
0.89
≥40 kg/m2
105/1973 (5.3)
31/487 (6.4)
1.01 (0.65, 1.58)
1.63 (1.02, 2.60)
0.042
Diabetes duration (years)
1767
10 (4–18)
15 (8–23)
1.47 (1.27, 1.69)
1.20 (1.04, 1.39)
0.015
HbA1c (mmol/mol)a
1800
61.6 (50.8–76.0)
59.6 (50.8–69.4)
0.80 (0.70, 0.91)
0.90 (0.78, 1.04)
0.16
HbA1c (%)a
1800
7.8 (6.8–9.1)
7.6 (6.8–8.5)
0.80 (0.70, 0.91)
0.90 (0.78, 1.04)
0.16
Hypertension
2769
1644/2198 (74.8)
482/571 (84.4)
1.83 (1.43, 2.33)
1.25 (0.97, 1.62)
0.090
Dyslipidaemia
2710
981/2157 (45.5)
286/553 (51.7)
1.28 (1.06, 1.55)
1.15 (0.95, 1.40)
0.16
Current tobacco use
2288
109/1855 (5.9)
22/433 (5.1)
0.86 (0.54, 1.37)
1.00 (0.61, 1.62)
0.99
Long-term diabetes complications
Microvascular complicationsb
1966
604/1591 (38.0)
265/375 (70.7)
3.94 (3.08, 5.03)
2.63 (2.03, 3.40)
<0.001
Macrovascular complicationsc
2627
725/2089 (34.7)
289/538 (53.7)
2.18 (1.80, 2.65)
1.60 (1.30, 1.95)
<0.001
Comorbidities
Heart failure
2651
200/2121 (9.4)
102/530 (19.2)
2.29 (1.76, 2.97)
1.59 (1.21, 2.10)
0.001
NAFLD or liver cirrhosis
2640
178/2098 (8.5)
40/542 (7.4)
0.86 (0.60, 1.23)
1.10 (0.76, 1.59)
0.63
Active cancer
2742
194/2175 (8.9)
59/567 (10.4)
1.19 (0.87, 1.61)
0.89 (0.65, 1.22)
0.47
COPD
2732
180/2168 (8.3)
83/564 (14.7)
1.91 (1.44, 2.52)
1.58 (1.18, 2.10)
0.002
Treated OSA
2593
211/2049 (10.3)
62/544 (11.4)
1.12 (0.83, 1.51)
1.22 (0.89, 1.67)
0.21
Routine treatment before admission
Metformin
2794
1306/2217 (58.9)
247/577 (42.8)
0.52 (0.43, 0.63)
0.63 (0.52, 0.77)
<0.001
Sulfonylurea/glinides
2794
633/2217 (28.6)
149/577 (25.8)
0.87 (0.71, 1.07)
0.83 (0.67, 1.03)
0.093
DPP4-inhibitors
2794
502/2217 (22.6)
113/577 (19.6)
0.83 (0.66, 1.05)
0.83 (0.65, 1.05)
0.12
GLP-1RA
2794
221/2217 (10.0)
33/577 (5.7)
0.55 (0.38, 0.80)
0.78 (0.53, 1.15)
0.21
Insulin
2796
762/2219 (34.3)
277/577 (48.0)
1.77 (1.47, 2.12)
1.72 (1.41, 2.08)
<0.001
Diureticsd
2794
768/2217 (34.6)
290/577 (50.3)
1.91 (1.58, 2.29)
1.48 (1.22, 1.80)
<0.001
β-Blockers
2794
732/2217 (33.0)
256/577 (44.4)
1.62 (1.34, 1.95)
1.27 (1.04, 1.54)
0.017
CCB
2794
710/2217 (32.0)
214/577 (37.1)
1.25 (1.03, 1.51)
1.17 (0.96, 1.43)
0.12
ARBs and/or ACE inhibitors and/or MRAe
2794
1219/2217 (55.0)
351/577 (60.8)
1.27 (1.05, 1.53)
1.15 (0.94, 1.40)
0.17
Statins
2794
983/2217 (44.3)
299/577 (51.8)
1.35 (1.12, 1.62)
1.27 (1.05, 1.54)
0.015
Anti-platelet therapy
2794
834/2217 (37.6)
291/577 (50.4)
1.69 (1.40, 2.03)
1.34 (1.11, 1.63)
0.003
Anticoagulation therapy
2794
352/2217 (15.9)
149/577 (25.8)
1.84 (1.48, 2.29)
1.25 (0.99, 1.58)
0.057
Population size was N = 2796. Data shown are n (%), and mean ± SD or median (25th–75th percentile) if not normally distributed
p values are calculated using Wald test (unadjusted and age-adjusted logistic regression, except for ‘age’ and ‘age class’, which were not adjusted). ORs correspond to an increase of 1 SD after natural-log transformation and standardisation for BMI, diabetes duration and HbA1c
aHbA1c determined in the 6 months prior to or in the first 7 days following hospital admission
bMicrovascular complication was defined as history of one or more of the following: diabetic kidney disease and/or severe diabetic retinopathy and/or diabetic foot ulcer
cMacrovascular complication was defined as history of one or more of the following comorbidities: ischaemic heart disease (acute coronary syndrome and/or coronary artery revascularisation) and/or cerebrovascular disease (stroke and/or transient ischaemic attack) and/or peripheral artery disease (amputation owing to ischaemic disease and/or lower limb artery revascularisation)
dDiuretics stands here for loop diuretics, thiazide diuretics, and potassium-sparing diuretics
eMRAs include spironolactone and eplerenone
Abbreviations: EU, Europid; MENA, Middle East North Africa; AC, African or Caribbean; AS, Asian; NAFLD, non-alcoholic fatty liver disease; GLP-1RA, glucagon-like peptide 1-receptor agonist
When considering the characteristics on admission, COVID-19 symptoms, fever and dyspnoea were positively associated with death within 28 days after adjustment for age (Table 4). Nearly all biological covariates reflecting COVID-19 severity were associated with death, including admission plasma glucose, plasma creatinine, AST, white cells, lymphocyte and platelet counts and CRP level.
Table 4
Characteristics on admission in CORONADO participants, according to death within 28 days
Death within 28 days
Variable
Available data
No (n = 2219)
Yes (n = 577)
Unadjusted OR (95% CI)a
Age-adjusted OR (95% CI)a
Age-adjusted p value
Time from symptom onset to hospital admission (days)
2743
6 (3–9)
4 (1–7)
0.94 (0.92, 0.96)
0.97 (0.95, 0.98)
<0.001
Clinical presentation
Fever
2755
1647/2190 (75.2)
430/565 (76.1)
1.05 (0.85, 1.30)
1.28 (1.02, 1.60)
0.034
Dyspnoea
2754
1338/2188 (61.2)
433/566 (76.5)
2.07 (1.67, 2.56)
2.34 (1.87, 2.92)
<0.001
Abnormal chest CT scan
1982
1560/1615 (96.6)
359/367 (97.8)
1.58 (0.75, 3.35)
2.05 (0.95, 4.46)
0.069
Biological findings
Positive SARS-CoV-2 PCR
2705
2018/2155 (93.6)
529/550 (96.2)
1.71 (1.07, 2.73)
1.92 (1.18, 3.12)
0.008
Admission plasma glucose (mmol/l)
1551
9.2 (7.0–13.2)
10.2 (7.1–14.5)
1.07 (0.94, 1.21)
1.21 (1.06, 1.38)
0.005
Plasma creatinine (μmol/l)
2602
87 (66–121)
121 (85–185)
1.69 (1.54, 1.85)
1.65 (1.49, 1.81)
<0.001
eGFR (ml min−1 [1.73 m]−2)a
2602
74.8 (47.6–93.1)
45.7 (27.2–70.1)
0.56 (0.51, 0.61)
0.62 (0.56, 0.68)
<0.001
ALT (%ULN)
2478
0.63 (0.43–1.00)
0.59 (0.39–0.98)
1.01 (0.92, 1.12)
1.15 (1.05, 1.27)
0.004
AST (%ULN)
2444
1.03 (0.72–1.50)
1.33 (0.87–2.03)
1.46 (1.33, 1.60)
1.58 (1.43, 1.75)
<0.001
GGT (%ULN)
2317
0.95 (0.56–1.75)
0.95 (0.54–1.83)
1.04 (0.94, 1.16)
1.10 (0.99, 1.22)
0.067
Haemoglobin (g/l)
2728
128 (115–142)
124 (109–139)
0.81 (0.74, 0.89)
0.86 (0.78, 0.95)
0.003
White cell count (103/mm3)
2726
6450 (4900–8510)
7260 (5420–10,100)
1.35 (1.23, 1.48)
1.34 (1.22, 1.48)
<0.001
Lymphocyte count (103/mm3)
2646
1015 (710–1430)
845 (550–1200)
0.74 (0.66, 0.82)
0.80 (0.72, 0.89)
<0.001
Platelet count (103/mm3)
2725
205 (159–263)
186 (142–241)
0.77 (0.70, 0.84)
0.79 (0.72, 0.87)
<0.001
CRP (mg/l)
2612
80 (36–140)
111 (59–181)
1.49 (1.33, 1.66)
1.62 (1.44, 1.82)
<0.001
LDH (U/l)
1427
338 (257–464)
436 (311–620)
1.97 (1.61, 2.42)
2.20 (1.78, 2.72)
<0.001
CPK (U/l)
1385
120 (63–265)
202 (82–485)
1.45 (1.28, 1.65)
1.52 (1.33, 1.74)
<0.001
Fibrinogen (g/l)
1424
6.3 (5.0–7.4)
6.3 (4.9–7.5)
1.04 (0.92, 1.18)
1.10 (0.97, 1.24)
0.13
Population size was N = 2796. Data shown are n (%) and or median (25th–75th percentile)
p values are calculated using Wald test (unadjusted and age-adjusted logistic regression). Quantitative variables were natural-log transformed and associated ORs correspond to an increase of 1 SD after standardisation, except for time from symptoms onset to hospital admission (1 day increase)
Multivariable models for death within 28 days are presented in Fig. 2. After multiple adjustment, older age, history of microvascular complications, insulin and statin routine medication, dyspnoea on admission, higher AST, higher white cell count, lower platelet count and higher CRP level were associated with a greater risk of death when routine metformin therapy and a longer time between symptom onset and hospital admission were negatively associated with death. In a sensitivity analysis restricted to participants with positive SARS-CoV-2 PCR or those with available admission plasma glucose, the results were similar (ESM Table 8).
Outcomes within 7 days
In the first 7 days following hospital admission, the prespecified primary outcome (tracheal intubation for mechanical ventilation and/or death) occurred in 800 (28.6%) participants and death in 312 (11.2%). The phenotypic characteristics of CORONADO participants according to the primary outcome are described in ESM Table 2 (features prior to admission) and ESM Table 3 (features on admission). Multivariable analysis (n = 1335, ESM Table 4) identified dyspnoea on admission, higher AST, higher white cell count, lower platelet count and higher CRP level as positively associated and metformin use as negatively associated with the primary outcome. The same results were observed in a sensitivity analysis on the complete-case population restricted to patients with positive PCR (n = 1249) or with available plasma glucose on admission (n = 761) (ESM Table 4).
Discussion
CORONADO is the first registered study that specifically aimed to describe the phenotypic characteristics and to identify prognostic factors in patients with diabetes hospitalised for COVID-19. The present analysis reports the results of the complete CORONADO study totalling 2796 participants from 68 centres with complete follow-up up to day 28. We noted that one out of two CORONADO participants returned home by day 28. Younger age, routine metformin therapy and a longer duration of symptoms before admission were independently associated with such a favourable outcome, while a history of microvascular complications, routine anticoagulant therapy, dyspnoea and biological markers of COVID-19 severity were associated with a reduced chance of discharge by day 28. In contrast, BMI, HbA1c and other comorbidities were not associated with this outcome. Results for death within 28 days mirrored the factors found for hospital discharge in an opposite way.
Regarding death, we reported a mortality rate of 11.2% within 7 days which reached 20.6% within 28 days. These findings can be compared to international reports. In a meta-analysis considering a majority of Chinese studies, in-hospital mortality was encountered in 299/2571 (11.6%) but the severity of illness in those patients is questionable since they were admitted early in the pandemic [15]. In contrast, in a retrospective cohort analysis of 1126 patients with diabetes hospitalised with COVID-19 at a large academic medical centre in New York City, the mortality rate was 33.1%, much higher than our findings. The higher prevalence of cardiovascular and chronic kidney disease, both independently associated with mortality, could explain this discrepancy [16]. In the UK, Docherty et al reported data on 20,133 hospitalised COVID-19 patients including 4949 with diabetes (1299 with and 3650 without diabetes complications) [17]. This study is consistent with our findings, with a population of similar age (mean age: 73 years in the UK study vs 70 years in CORONADO). In-hospital death occurred in 1080/3650 patients with uncomplicated diabetes (29.6%) and in 389/1299 (29.9%) with complicated diabetes, although the observational period is not directly mentioned. We therefore believe that our data are generalisable, at least to people living with diabetes in Europe.
With regard to prognostic factors of death, our results are in accordance with three nationwide studies from the UK. Holman et al evidenced that death was associated with age and male sex, but also with deprivation, which is not available in our report, while a U-shaped relationship was found for HbA1c [18]. OpenSAFELY was able to examine, through electronic health record analysis, a population of more than 17 million people linked to more than 10,000 COVID-related deaths and showed that death was associated with male sex, age, BMI, and a clearly graded effect of HbA1c: the higher the HbA1c the greater the risk of death [19], while we could not show this for HbA1c in our more limited dataset. More recently Knight et al computed a prognostic score of in-hospital death considering a population with over 20% of people affected by diabetes. In accordance with our findings, they also identified age, sex and CRP as prognostic factors while other factors were not directly available in our study [20].
However, these papers did not mention hospital discharge and consider general populations and mostly ambulatory patients, which is at variance with what was performed in the CORONADO study.
It should be noted that the numbers of patients who died during follow-up were close to being equally distributed within the first 7 days (11.2%) and day 8 to day 28 (9.5%), while tracheal intubation for mechanical ventilation occurred, as expected, predominantly within 7 days after admission (532/556, 95.6%). These findings are in line with the previously described clinical course of the disease. Thus, in 54 non-survivors of COVID-19 from Wuhan, China, the median hospital length of stay was of 7.5 days [2]. Moreover, Argenziano et al found that 71.6% of 225 patients were intubated within the first 3 days following admission to the emergency room [7].
In addition to data on in-hospital death, we believe data on home discharge within 28 days should be reported since it is a positive result of value for both patients and physicians and it provides another perspective on COVID-19. Our data support the reasonable opinion that factors associated with home discharge mirror, as expected, those associated with the severity of the disease. This turned out to be true with biological covariates on admission such as plasma creatinine, AST and CRP, with a particular importance for admission blood glucose.
While our multivariable analyses were performed on a limited number of participants, owing to missing data, the current study helped to establish the relative contribution of admission blood glucose on the risk of death and on the chance of discharge. We found that chronic glycaemic control assessed with pre-admission or admission HbA1c did not impact on the fate of COVID-19 patients, with no significant association with death or with discharge within 28 days. In contrast, increased admission plasma glucose concentration was a strong predictor of death and, consistently, of a lower chance of discharge. We have recently commented on two interesting studies reporting on the question of admission plasma glucose in COVID-19 and community-acquired pneumonia [21, 22]. This association between blood glucose control and prognosis in hospitalised COVID-19 patients has also been observed in patients without previously diagnosed diabetes [23‐25]. Furthermore, other studies suggest that blood glucose control during hospitalisation is associated with COVID-19 outcomes [26, 27]. However, due to the observational design of our study and others, no conclusion regarding causality can be drawn. The relationship between admission plasma glucose and severe conditions was previously established in many clinical situations, including, for instance, heart failure, stroke or myocardial infarction [28‐31]. In none of these situations did strict metabolic control consistently decrease mortality.
Our results also establish an association between routine therapy and chance of discharge or risk of death. Interestingly, metformin was associated with favourable outcomes (both lower risk of death and greater chance of discharge within 28 days). Conversely, statin use was associated with higher risk of death and anticoagulation therapy with a reduced chance of discharge. The findings with statins are surprising since the in-hospital use of this drug class has been recently associated with a lower risk of 28-day mortality in 13,981 patients with COVID-19 from China [32]. Unexpectedly, we also found a higher risk of primary outcomes within 7 days (but not of other outcomes) in patients taking calcium channel blockers (CCBs) on admission. However, whether these findings reflect a significant negative effect or a mere indication bias would require more sophisticated adjustment methods such as specific propensity score, which is beyond the scope of the current paper.
Study limitations
Some limitations must be acknowledged here. First, we focused on hospitalised COVID-19 cases and our results cannot be generalised to all COVID-19 patients with diabetes, especially those with a less severe form of the disease. Second, we focused on those discharged to their home or to a long-term care facility. Since insufficient ascertainment was available from those transferred to another hospital or rehabilitation centre, our figures are conservative even if we believe that transfer is unlikely to lead to short-term discharge before day 28. Third, it can also be argued that the 28-day observation period was too short with 12.2% of admitted participants requiring more prolonged hospitalisation in the same hospital. Nonetheless, this 28-day mark is a well-established milestone, particularly in an ICU setting, and further outcomes probably reflect other medical issues. Fourth, for a non-negligible number of patients (249/2796, 8.9%), SARS-CoV-2 PCR was not available or negative. However, the main analyses were replicated in the subset with a positive SARS-CoV-2 PCR showing similar results. Fifth, due to the exploratory nature of the results, our work must be read as a post hoc analysis. The chosen multivariable approach infers, by design, obvious limitations: a lack of control of type 1 error; the transformation of quantitative variables, which was needed to comply with the statistical assumption of the model, at the expense of less natural clinical interpretation; and the adjustment set, based on background knowledge, which is associated with a risk of overfitting. Sixth, although specific treatment for COVID-19, such as corticosteroid, immunotherapy or antiviral agents could influence prognosis, data about such treatment given during hospitalisation were not available in our study. Ultimately, our results are hampered by missing data, such as HbA1c. Nevertheless, the CORONADO study is, to date, the most accurate study providing such information. The inclusion of additional studies of a similar nature would help to increase our confidence in observations with significant missing data.
The study strengths must also be acknowledged, such as the originality of the medical question leading to the CORONADO initiative and the inclusion of participants with a nationwide coverage, in any department of a participating hospital, including the ICU and medical units. We also recorded patients’ phenotypic characteristics in a structured manner and did not solely rely on medico-administrative databases.
In conclusion, the CORONADO study refined the phenotypes of hospitalised COVID-19 patients with diabetes. To summarise, younger age, routine metformin therapy and longer symptom duration on admission were positively associated with discharge. History of microvascular complications, anticoagulant routine therapy, dyspnoea on admission, and higher AST, white cell count and CRP levels were associated with a reduced chance of discharge. Deleterious and protective factors for discharge mirrored those for death by day 28, respectively. The identification of favourable variables associated with hospital discharge and deleterious variables associated with death can lead to patient reclassification and help to use resources adequately according to individual patient profile.
Acknowledgements
We thank the sponsor (Direction de la Recherche Clinique et de l’Innovation - DRCI CHU Nantes) clinical project manager (M. Saignes) and assistant (J. Saunier), clinical research associates (S. El Andaloussi, J. Martin-Gauthier, E. Rebouilleau) and data managers (B. Guyomarch, T. Roman); all at CHU Nantes. We are grateful to P. Tucker (Trets, France) for editing the manuscript. We acknowledge all medical staff involved in the diagnosis and treatment of patients with COVID-19 in participating centres. We thank all GPs, specialists, pharmacists and biological laboratories in charge of hospitalised patients for providing additional medical information to investigators. We thank the Société Francophone du Diabète (SFD) and Société Française d’Endocrinologie (SFE) for disseminating study design and organisation, the Fédération Française des Diabétiques (FFD) for participating in the study organisation.
Authors’ relationships and activities
BC reports grants and personal fees from Amgen, AstraZeneca, Akcea, Genfit, Gilead, Eli Lilly, Novo Nordisk, and MSD, and grants and personal fees from Sanofi and Regeneron. PD reports personal fees from Novo Nordisk, Sanofi, Eli Lilly, MSD, Novartis, Abbott, AstraZeneca, Boehringer Ingelheim and Mundipharma. J-FG reports personal fees and non-financial support from Eli Lilly, Novo Nordisk and AstraZeneca, personal fees from Bristol-Myers Squibb, Gilead and Bayer; all disclosures above unrelated to this presentation. PG reports personal fees from Abbott, Amgen, AstraZeneca, Boehringer Ingelheim, Eli Lilly, MSD, Mundipharma, Sanofi and Servier, and grants and personal fees from Novo Nordisk. SH reports personal fees and non-financial support from AstraZeneca, grants and personal fees from Bayer, personal fees from Boehringer Ingelheim, grants from Dinno Santé, personal fees from Eli Lilly, non-financial support from LVL, personal fees and non-financial support from MSD, personal fees from Novartis, grants from Pierre Fabre Santé, personal fees and non-financial support from Sanofi, personal fees and non-financial support from Servier, and personal fees from Valbiotis. MP reports personal fees and non-financial support from Novo Nordisk, and non-financial support from Sanofi and Amgen. LP reports personal fees and non-financial support from Sanofi, Eli Lilly, Novo Nordisk and MSD. RRoussell reports grants, personal fees and non-financial support from Sanofi and Novo Nordisk, personal fees and non-financial support from Eli Lilly, personal fees from Mundipharma, Janssen, Servier, MSD, Medtronic, Abbott, Diabnext and Applied Therapeutics, and grants and personal fees from AstraZeneca. BV reports grants and personal fees from Amgen, and personal fees from Novo Nordisk, Amgen, AstraZeneca, Eli Lilly, Novo Nordisk, MSD and Sanofi. MW reports personal fees from Novo Nordisk. PW reports personal fees from Sanofi, Novo Nordisk, AstraZeneca, MSD and Novartis, and non-financial support from Novo Nordisk, Eli Lilly and MSD. All other authors declare that there are no relationships or activities that might bias, or be perceived to bias, their work.
Contribution statement
BC, SH and MW are the guarantors of this work and, as such, had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. LP and MW contributed to the work equally and should be regarded as joint first authors. BC and SH contributed to the work equally and should be regarded as joint senior authors.
Substantial contributions to conception and design
BC, J-FG, PG, SH, MP, LP, RRobert, RRoussel and MW designed the study, which was edited and validated by all members of the scientific committee of the study (the list of scientific committee members available in the ESM).
Substantial contributions to acquisition of data, or analysis and interpretation of data
PAG and MW performed the statistical analyses, LP, PG, MP, CA, P-YB, J-BB, LB, OB, CC, NC, PD, BD, DD, MD, OD, AF-F, J-FG, A-MG, NJ, EL, J-PLB, ML, NM, PM, FP, VR, DS-B, PS, SS, BT, CV, F-LV, BV, PW, AZ, RRoussel, BC and SH contributed to acquisition of data. BC, PG, SH and MP conducted the fundraising of the study, with additional help from B. Bauduceau (FFRD- Fondation Francophone de Recherche sur le Diabète).
Drafting the article or revising it critically for important intellectual content
BC, PAG, PG, SH, MP, LP, RRoussel and MW drafted the first version of the manuscript. All co-authors critically reviewed and edited the manuscript, and all authors gave final approval of the version to be published.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Mit e.Med Innere Medizin erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Innere Medizin, den Premium-Inhalten der internistischen Fachzeitschriften, inklusive einer gedruckten internistischen Zeitschrift Ihrer Wahl.
Mit e.Med Allgemeinmedizin erhalten Sie Zugang zu allen CME-Fortbildungen und Premium-Inhalten der allgemeinmedizinischen Zeitschriften, inklusive einer gedruckten Allgemeinmedizin-Zeitschrift Ihrer Wahl.
Bei Reizdarmsyndrom scheinen Diäten, wie etwa die FODMAP-arme oder die kohlenhydratreduzierte Ernährung, effektiver als eine medikamentöse Therapie zu sein. Das hat eine Studie aus Schweden ergeben, die die drei Therapieoptionen im direkten Vergleich analysierte.
Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.
Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.
Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.
Update Innere Medizin
Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.
