Literature DB >> 34636804

Differences and Similarities Among COVID-19 Patients Treated in Seven ICUs in Three Countries Within One Region: An Observational Cohort Study.

Dieter Mesotten1,2, Daniek A M Meijs3,4, Bas C T van Bussel3,5, Björn Stessel2,6, Jannet Mehagnoul-Schipper7, Anisa Hana4, Clarissa I E Scheeren8, Ulrich Strauch3, Marcel C G van de Poll3,9,10, Chahinda Ghossein-Doha3,11, Wolfgang F F A Buhre12, Johannes Bickenbach13, Margot Vander Laenen1, Gernot Marx13, Iwan C C van der Horst3,11.   

Abstract

OBJECTIVES: To investigate healthcare system-driven variation in general characteristics, interventions, and outcomes in coronavirus disease 2019 (COVID-19) patients admitted to the ICU within one Western European region across three countries.
DESIGN: Multicenter observational cohort study.
SETTING: Seven ICUs in the Euregio Meuse-Rhine, one region across Belgium, The Netherlands, and Germany. PATIENTS: Consecutive COVID-19 patients supported in the ICU during the first pandemic wave.
INTERVENTIONS: None.
MEASUREMENTS AND MAIN RESULTS: Baseline demographic and clinical characteristics, laboratory values, and outcome data were retrieved after ethical approval and data-sharing agreements. Descriptive statistics were performed to investigate country-related practice variation. From March 2, 2020, to August 12, 2020, 551 patients were admitted. Mean age was 65.4 ± 11.2 years, and 29% were female. At admission, Acute Physiology and Chronic Health Evaluation II scores were 15.0 ± 5.5, 16.8 ± 5.5, and 15.8 ± 5.3 (p = 0.002), and Sequential Organ Failure Assessment scores were 4.4 ± 2.7, 7.4 ± 2.2, and 7.7 ± 3.2 (p < 0.001) in the Belgian, Dutch, and German parts of Euregio, respectively. The ICU mortality rate was 22%, 42%, and 44%, respectively (p < 0.001). Large differences were observed in the frequency of organ support, antimicrobial/inflammatory therapy application, and ICU capacity. Mixed-multivariable logistic regression analyses showed that differences in ICU mortality were independent of age, sex, disease severity, comorbidities, support strategies, therapies, and complications.
CONCLUSIONS: COVID-19 patients admitted to ICUs within one region, the Euregio Meuse-Rhine, differed significantly in general characteristics, applied interventions, and outcomes despite presumed genetic and socioeconomic background, admission diagnosis, access to international literature, and data collection are similar. Variances in healthcare systems' organization, particularly ICU capacity and admission criteria, combined with a rapidly spreading pandemic might be important drivers for the observed differences. Heterogeneity between patient groups but also healthcare systems should be presumed to interfere with outcomes in coronavirus disease 2019.
Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine and Wolters Kluwer Health, Inc.

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Mesh:

Year:  2022        PMID: 34636804      PMCID: PMC8923276          DOI: 10.1097/CCM.0000000000005314

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   9.296


The coronavirus disease 2019 (COVID-19) pandemic spread over the world in 2020. In many countries, a quick rise in infection rate was identified. Many patients were admitted to hospitals with an important proportion requiring supportive treatment in an ICU, stretching ICU capacity to its limits, even in many developed countries (1, 2). Scarce ICU resources should be optimally used during a pandemic, ideally in close agreement with regular care, which inevitably affects physicians’ decisions. Consequently, it may be conceivable that admission criteria and treatment choices also vary throughout countries. Previous (multi)national studies have been performed in COVID-19 patients requiring ICU support (3–10), mostly presented per country (Supplementary Digital Content 1, http://links.lww.com/CCM/G799). However, these studies often comprised intervention studies in selected patients or cohort studies characterized by heterogeneity concerning population characteristics, such as race/ethnicity, genetic background, and socioeconomic status, reflecting differences in the population at risk. Furthermore, large interhospital variations in patient characteristics and outcomes have been reported, which might indicate different degrees of stress on healthcare systems (11, 12). These differences hamper direct comparison of healthcare systems and their responses to the pandemic. The Euregio Meuse-Rhine, a region covering parts of Belgium, The Netherlands, and Germany, is characterized by a high population density (3,900,000 inhabitants at 11,000 km2) and intense cross-border passage (13). Over 10% of inhabitants were positively tested for COVID-19 infection during the first pandemic wave (www.sanquin.nl-sanquin/nieuws/2020/11/antistoffen-bij-donors-meting-november). When comparing healthcare systems’ variation, the Euregio has the advantage that the population at risk is assumed to be somewhat homogeneous as they share a genetic background and have a comparable socioeconomic status (13). Furthermore, heterogeneity due to different ICU admission diagnoses was absent since the majority of patients were admitted for COVID-19 pneumonia. In addition, healthcare professionals’ vocational training, access to literature, and international guidelines for ICU practice are similar (14). ICU bed availability is an important difference between countries in general. For the Euregio, the availability of ICU beds in The Netherlands is 6.4, compared with 15.9 and 29.2 per 100,000 inhabitants for Belgium and Germany, respectively (15). Spatial ICU accessibility also varies across numerous European countries (16). Another potential difference is heterogeneity of COVID-19 disease itself. Although severe acute respiratory syndrome coronavirus 2 is a virus that causes one disease in name, heterogeneity in the course of COVID-19 infection exists (17), which might be amplified since no specific treatment for COVID-19 exists. Experimental off-label therapies, such as (hydroxy)chloroquine, antiviral drugs, and steroids, were used at the time without substantial evidence (18, 19). Thus, the interaction between varying healthcare systems and uncertainty and heterogeneity within COVID-19 disease and treatment may have led to practice variation. We, therefore, hypothesize that variable healthcare system responses to a pandemic drive variability in patient characteristics and disease severity, support strategies, therapies, and complications and, independent of these factors, determine outcome within a cohort of COVID-19 patients admitted to seven ICUs within the Euregio, one region across Belgium, The Netherlands, and Germany.

MATERIALS AND METHODS

The Euregio intensive care COVID cohort, part of the Euregio COVID Data Platform (CoDaP) project, was initiated at the beginning of the pandemic in early March 2020. With the opportunity of disease homogeneity of patients admitted to Euregio ICUs within a short period, provided by the COVID-19 pandemic, we aimed to investigate potential cross-border differences, including baseline demographics (20), disease course over time (17), sex (21), outcomes (22), and treatment (23, 24), and unravel potential healthcare systems’ and strategies’ variances (11, 25, 26) that could contribute to future collaboration and optimization of cross-border patient care. Investigators at the departments of Intensive Care Medicine of seven Euregio hospitals (two Belgian; four Dutch, including one academic hospital; and one German academic hospital), situated within a 50 km radius (Fig. 1), shared their plans selecting variables for data-sharing and collaboration on COVID-19. ICU resources and care were dictated mainly by individual countries. However, pandemic stress drove some international transportation of patients within the Euregio Meuse-Rhine (Fig. 2A), suggesting that cross-border collaboration, for example, delivering care under a joint healthcare mandate (e.g., European Union), would be helpful.
Figure 1.

Flow chart. COVID = coronavirus disease, Maastricht UMC+ = Maastricht University Medical Center +, RWTH = Rheinisch Westfälische Hochschule.

Figure 2.

Patient transportation (A) and ICU capacity before and during the pandemic wave (B). A, The arrows represent the transportation of patients (exact amount displayed as number) between ICUs (displayed as dots) inside and outside the Euregio Meuse-Rhine (displayed as arrows from outside circle to inside and inversely). B, General ICU capacity compared with maximum ICU capacity during first coronavirus disease 2019 wave reported in total number of ICU beds per center (i.e.16 to 32 means that VieCuri Hospital Venlo had 16 operational ICU beds before the pandemic, which was upgraded to 32 ICU beds due to pandemic needs). For Jessa and ZOL Hospital, the total number of beds comprises ICUs and cardiovascular care units. RWTH = Rheinisch Westfälische Hochschule, ZOL = Ziekenhuis Oost-Limburg.

Flow chart. COVID = coronavirus disease, Maastricht UMC+ = Maastricht University Medical Center +, RWTH = Rheinisch Westfälische Hochschule. Patient transportation (A) and ICU capacity before and during the pandemic wave (B). A, The arrows represent the transportation of patients (exact amount displayed as number) between ICUs (displayed as dots) inside and outside the Euregio Meuse-Rhine (displayed as arrows from outside circle to inside and inversely). B, General ICU capacity compared with maximum ICU capacity during first coronavirus disease 2019 wave reported in total number of ICU beds per center (i.e.16 to 32 means that VieCuri Hospital Venlo had 16 operational ICU beds before the pandemic, which was upgraded to 32 ICU beds due to pandemic needs). For Jessa and ZOL Hospital, the total number of beds comprises ICUs and cardiovascular care units. RWTH = Rheinisch Westfälische Hochschule, ZOL = Ziekenhuis Oost-Limburg. Extensive information regarding participating hospitals, inclusion criteria (27), patient admission and transfer (Fig. 2A) (28), collected variables, project aims (22, 29), and data collection, sharing, and cleaning (30) are described in Supplementary Digital Content 2 (http://links.lww.com/CCM/G800). Briefly, using a predefined study protocol, we collected demographic and clinical characteristics (i.e., comorbidities, hemodynamic and laboratory variables, and scores to assess disease severity), ventilation, circulatory and renal support, antimicrobial/inflammatory therapies, complications (i.e., thromboembolic events), and outcome variables (i.e., duration ICU stay, mortality). The majority of selected variables were routinely collected and available in regular Western European Intensive Care practice, such as in the Euregio Meuse-Rhine. In this retrospective study, data were pulled from electronic medical records and collected using the study protocol, depending on the available data infrastructure of each hospital. Ethical approval was obtained from the medical ethics committee (Medisch Ethische Toetsingscommissie 2020-1565/3 00 523) of Maastricht University Medical Center + (Maastricht UMC+). The study was performed in accordance with the General Data Protection Regulation and national data privacy laws. Based on the study protocol and ethical approval, data-sharing agreements between Maastricht UMC+ and other hospitals were drawn up by legal officers of Maastricht UMC+ and Clinical Trial Center Maastricht. Subsequently, these data-sharing agreements were judged by each participating hospital’s legal department and tailored to each hospital. Investigators, heads of ICU departments, and the hospital board of directors of Maastricht UMC+ and the other hospitals then signed the final agreed data-sharing agreement. IBM SPSS Statistics Version 25 (IBM Corporation, Armonk, NY) was used for analyses. Data are presented as mean ± sd, median (interquartile range), or percentages. The full cohort was categorized in a Belgian, Dutch, and German part of Euregio. Differences between countries were tested using one-way analysis of variance for means, Kruskal-Wallis test for medians, and chi-square for percentages, whereas Fisher exact test was used when observations within categories were low (< 5). With a random intercept for a center, mixed-effects logistic regression was used to investigate the association between Euregio country parts and ICU survival (52). To extensively challenge our hypothesis that variable healthcare system responses to a pandemic, but not disease severity, comorbidities, ICU support, therapies, and complications, determine outcome, we show six models extensively described in Supplementary Digital Content 2 (http://links.lww.com/CCM/G800). We report odds ratio (OR) with 95% CI. A two-sided p value of less than 0.05 was considered statistically significant.

RESULTS

From March 2, 2020, to August 12, 2020, 551 patients with COVID-19 pneumonia were admitted to seven ICUs in Western Europe (Fig. 1). Eighteen patients (3%) were transferred between two or three Euregio ICUs (Fig. 2A). ICU capacity in the German part was not increased during COVID-19, in contrast to the Dutch and, to a lesser extent, the Belgian part (Fig. 2B).

Demographics, Disease Severity, and Comorbidities

Mean age was 65.4 ± 11.2 years, and 29% were female. Mean body mass index was 29.0 ± 5.3 kg/m2 (Table 1). At admission, disease severity, as defined by Acute Physiology and Chronic Health Evaluation (APACHE) II and Sequential Organ Failure Assessment (SOFA) scores, was 16.1 ± 5.5 and 6.2 ± 3.0.
TABLE 1.

Characteristics for the Full Euregio Intensive Care Cohort and Compared Between National Euregio Parts

CharacteristicsFull Cohort (n = 551)Belgian Part (n = 178)Dutch Part (n = 310)German Part (n = 63) p
Age, yr, mean ± sd65.4 ± 11.266.4 ± 12.065.2 ± 10.864.1 ± 10.60.302
Female, %293425350.061
Height, m, mean ± sd1.73 ± 0.11.71 ± 0.101.75 ± 0.101.74 ± 0.10< 0.001
Weight, kg, mean ± sd87.3 ± 17.184.3 ± 14.888.0 ± 17.791.7 ± 18.80.008
Body mass index, kg/m2, mean ± sd29.0 ± 5.329.0 ± 5.328.8 ± 5.030.3 ± 6.20.096
Obesity, %323229440.049
Dyslipidemia, %272924350.258
Diabetes mellitus, %263024220.287
Hypertension, %47514070< 0.001
Smoking, %202518210.165
Chronic liver disease, %11120.571a
Chronic lung disease, %18201341< 0.001
Chronic renal disease, %1225322< 0.001
Acute Physiology and Chronic Health Evaluation II score, mean ± sd16.1 ± 5.515.0 ± 5.516.8 ± 5.515.8 ± 5.30.002
Sequential Organ Failure Assessment score, mean ± sd6.2 ± 3.04.4 ± 2.77.4 ± 2.27.7 ± 3.2< 0.001
Admission location, %< 0.001
 Emergency department333931NA
 Hospital ward504961NA
 Other ICU1612868

NA = not available.

aFisher exact test.

Differences between national parts of Euregio were tested using the one-way analysis of variance for means, Kruskal-Wallis test for medians, and χ2 for percentages unless otherwise specified. Scores were based on data of first 24 hr of ICU stay. In the German part, data at admission from the hospital ward were unavailable. The comprehensive data for the full cohort were complete, except missings for height (n = 27), weight (n = 33), body mass index (n = 37), obesity (n = 20), dyslipidemia (n = 108), hypertension (n = 1), smoking (n = 96), and Sequential Organ Failure Assessment score (n = 112).

Characteristics for the Full Euregio Intensive Care Cohort and Compared Between National Euregio Parts NA = not available. aFisher exact test. Differences between national parts of Euregio were tested using the one-way analysis of variance for means, Kruskal-Wallis test for medians, and χ2 for percentages unless otherwise specified. Scores were based on data of first 24 hr of ICU stay. In the German part, data at admission from the hospital ward were unavailable. The comprehensive data for the full cohort were complete, except missings for height (n = 27), weight (n = 33), body mass index (n = 37), obesity (n = 20), dyslipidemia (n = 108), hypertension (n = 1), smoking (n = 96), and Sequential Organ Failure Assessment score (n = 112). Patients in the German part had more comorbidities, except for diabetes mellitus. Compared with the Belgian and German parts, fewer patients suffered from obesity, dyslipidemia, hypertension, chronic lung disease, and chronic renal disease in the Dutch part, and fewer patients smoked. APACHE II and SOFA scores were lower in the Belgian part than the Dutch and German parts. These differences remained for the subgroup of mechanically ventilated patients (Supplementary Digital Content 3, http://links.lww.com/CCM/G801).

Critical Care Supportive Strategies

Ventilation Support.

Seventy-nine percent of patients were supported by mechanical ventilation during ICU stay. We observed less mechanical ventilation in the Belgian part (53%) compared with the Dutch and German parts (89% and 100%, respectively) (Table 2). Pressure-controlled ventilation was the most applied modality in the Dutch and German parts, whereas volume-controlled ventilation was more frequently used in the Belgian part. The application of high-flow nasal oxygen was the highest in the Belgian part.
TABLE 2.

Intensive Care Supportive Treatments and Outcomes for the Full Euregio Intensive Care Cohort and Compared Between National Euregio Parts

VariablesFull Cohort (n = 551)Belgian Part (n = 178)Dutch Part (n = 310)German Part (n = 63) p
Ventilation support
 Invasive mechanical ventilation during ICU stay, %795389100< 0.001
 Reintubation, %8109NA0.042
 Duration of invasive mechanical ventilation, d, median (interquartile range)11 (2–23)4 (0–16)12 (5–23)32 (18–52)< 0.001
 Admission mode of ventilation support, %< 0.001
  Pressure control5477968
  Volume control82600
  Pressure support30122
  Continuous positive airway pressure1100
  Noninvasive mask ventilation2500
  High-flow nasal O22547170
  Spontaneous/nasal O2/other613210
  Unknown/missing data1110
Circulatory support
 Admission vasopressor use, %65397497< 0.001
 Admission dose of norepinephrine, µg/kg/min, median (interquartile range)0.13 (0.08–0.24)0.12 (0.07–0.20)0.11 (0.07–0.18)0.33 (0.14–0.53)< 0.001
 Mechanical circulatory support, %a64325< 0.001
Renal support
 Renal replacement therapy including chronic dialysis, %26301664< 0.001
Anti-infection/inflammation therapy
 Antibacterial therapy, %959496920.355b
 Antiviral medication, %0.009b
  Oseltamivir3042
  Lopinavir/ritonavir3432
  Remdesivir0.40.6020.087b
  (Hydroxy)chloroquine5736805< 0.001
  Antifungal medication9613NA0.304
  Steroids313830180.011
  Interleukin inhibitors41600.004b
Imaging diagnosis during ICU stay, %
 Pulmonary embolism1532311< 0.001
 Deep venous thrombosis10254NA< 0.001
ICU outcome
 ICU mortality, %36224244< 0.001
 Length of ICU stay, d, median (interquartile range)15 (6–30)10 (5–27)14 (7–24)33 (20–57)< 0.001

NA = not available.

aMortality rate in extracorporeal membrane oxygenation patients was 44% for the full cohort. Differences were tested by the Kruskal-Wallis test for medians and the χ2 for percentages unless otherwise specified. Admission corresponds to the first 24 hr of ICU stay. All patients were taken into account, implicating that treatments not received were calculated as zero. The comprehensive data for the full cohort were complete, except missings for reintubation (n = 65), mode of ventilation support (n = 5), duration of invasive mechanical ventilation (n = 4), admission vasopressor use (n = 4), admission dose of norepinephrine (n = 61), steroids (n = 3), antiviral medication (n = 3), interleukin inhibitors (n = 1), antifungal medication (n = 185), renal replacement therapy including chronic dialysis (n = 4), pulmonary embolism (n = 3), deep venous thrombosis (n = 66), and length of ICU stay (n = 1).

bFisher exact test.

Intensive Care Supportive Treatments and Outcomes for the Full Euregio Intensive Care Cohort and Compared Between National Euregio Parts NA = not available. aMortality rate in extracorporeal membrane oxygenation patients was 44% for the full cohort. Differences were tested by the Kruskal-Wallis test for medians and the χ2 for percentages unless otherwise specified. Admission corresponds to the first 24 hr of ICU stay. All patients were taken into account, implicating that treatments not received were calculated as zero. The comprehensive data for the full cohort were complete, except missings for reintubation (n = 65), mode of ventilation support (n = 5), duration of invasive mechanical ventilation (n = 4), admission vasopressor use (n = 4), admission dose of norepinephrine (n = 61), steroids (n = 3), antiviral medication (n = 3), interleukin inhibitors (n = 1), antifungal medication (n = 185), renal replacement therapy including chronic dialysis (n = 4), pulmonary embolism (n = 3), deep venous thrombosis (n = 66), and length of ICU stay (n = 1). bFisher exact test.

Circulatory Support.

At admission, 65% of patients were supported by vasopressors. We observed less vasopressor use (39%) in the Belgian part when compared with the Dutch (74%) and German parts (97%). Accordingly, the median dose of norepinephrine was highest in the German part (0.33 µg/kg/min [0.14–0.53 µg/kg/min]). Mechanical circulatory support was highest in the German part (25%).

Renal Support.

Renal replacement therapy was highest in the German part (64%) compared with the Dutch (16%) and Belgian parts (30%). Approximately half of the population on renal replacement therapy in the Belgian part was on chronic dialysis (before ICU admission), which was not present in the Dutch and German parts.

Antimicrobial/Inflammation Therapies.

Almost every patient received antibacterial therapy during ICU stay (94%, 96%, and 92% for the Belgian, the Dutch, and the German parts, respectively). (Hydroxy)chloroquine was most often used in the Dutch part, with 80% of patients receiving this therapy (Table 2). In the German part, steroids were used the least (18%).

Complications.

Diagnosis of pulmonary embolism during ICU stay was highest in the Dutch part (23%), whereas an imaging diagnosis of deep vein thrombosis during ICU stay was higher in the Belgian (25%) than the Dutch Euregio part.

Outcomes.

In the Belgian part, the length of stay and mortality in the ICU were the lowest, compared with both Dutch and German parts (10 d [5–27 d], 14 d [7–24 d], and 33 d [20–57 d], and 22%, 42%, and 44%, respectively [both p < 0.001]) (Table 2), with similar results in the subgroup of mechanically ventilated patients (Supplementary Digital Content 4, http://links.lww.com/CCM/G802). In crude models and after adjustment for age, sex, and APACHE II score, with a random center effect, patients in the Dutch Euregio part had an OR (95% CI) of 2.5 (1.7–3.9), and patients in the German Euregio part had an OR (95% CI) of 2.8 (1.5–5.2) for mortality, compared with patients in the Belgian Euregio part (Table 3, models 1 and 2). Additional adjustment for comorbidities (model 3), supportive strategies (model 4), therapies (model 5), and complications (model 6) showed a similarly higher OR for mortality in the Dutch and German parts. This observation was similar when analyses were repeated for mechanically ventilated patients only (Table 3).
TABLE 3.

The Association Between Euregio Country Parts and ICU Death by Mixed-Logistic Regression Analyses

ModelsFull Cohort, n = 551Mechanically Ventilated Subcohort, n = 434
OR95% CI p OR95% CI p
Model 1: crude, with random intercept for center
 Belgian part
 Dutch part2.51.7–3.9< 0.0012.01.2–3.50.008
 German part2.81.5–5.20.0012.01.0–4.00.055
Model 2: model 1 + age, sex, Acute Physiology and Chronic Health Evaluation II score
 Belgian part
 Dutch part2.81.6–4.8< 0.0011.91.1–3.30.019
 German part3.91.7–8.70.0012.41.1–4.90.020
Model 3: model 2 + obesity, dyslipidemia, diabetes, hypertension, smoking, chronic lung, liver, and renal disease
 Belgian part
 Dutch part3.71.6–8.60.0022.11.1–3.90.023
 German part3.71.2–11.70.0262.20.9–5.10.075
Model 4: model 2 + mechanical ventilation during ICU staya, vasopressor use at admission, mechanical circulatory support, renal replacement therapy including chronic dialysis
 Belgian part
 Dutch part2.31.3–4.00.0033.31.3–8.10.011
 German part1.60.7–3.40.2513.71.1–13.30.042
Model 5: model 2 + antibacterial therapy, steroids, (hydroxy)chloroquine, remdesivir, antiviral medication, interleukin inhibitors, antifungal medication
 Belgian part
 Dutch part3.31.7–6.10.0012.81.3–5.80.007
 German part4.11.8–9.3< 0.0013.11.3–7.50.012
Model 6: model 2 + pulmonary embolism, deep vein thrombosis
 Belgian part
 Dutch part2.51.5–4.40.0011.60.8–3.00.181
 German part3.91.8–8.60.0012.10.9–4.80.069

OR = odds ratio.

aModel 4 for mechanically ventilated patients only (n = 434): the variable mechanical ventilation during ICU stay was replaced by the variable invasive ventilation duration.

p values estimated by mixed-effect logistic regression. A higher OR indicates a higher odds of ICU death between parts of Euregio, with the Belgian part as reference.

Dashes indicate the Belgian part is the reference group.

The Association Between Euregio Country Parts and ICU Death by Mixed-Logistic Regression Analyses OR = odds ratio. aModel 4 for mechanically ventilated patients only (n = 434): the variable mechanical ventilation during ICU stay was replaced by the variable invasive ventilation duration. p values estimated by mixed-effect logistic regression. A higher OR indicates a higher odds of ICU death between parts of Euregio, with the Belgian part as reference. Dashes indicate the Belgian part is the reference group.

DISCUSSION

In this multinational observational cohort study of COVID-19 patients admitted to seven neighboring ICUs in the Euregio Meuse-Rhine, one region across Belgium, The Netherlands, and Germany, during the first pandemic wave, we demonstrated many similarities, but also remarkable differences in general characteristics, applied interventions, and outcomes. The Euregio Meuse-Rhine has many similarities. In addition to similar international guidelines, healthcare standards, access to literature, and vocational training of ICU healthcare professionals (31), the general population’s presumed genetic and socioeconomic background is comparable (13). We found similarities among patients (e.g., age over 60 yr, the predominance of male patients, the majority of comorbidities, and the use of antibiotics). The differences were surprisingly more prominent. First, at baseline, patients in the German part of Euregio had more often obesity, hypertension, and chronic lung disease than patients in the Belgian and Dutch parts. In the Dutch part of Euregio, fewer patients suffered from chronic renal disease than patients in the Belgian and German parts. Second, the APACHE II and SOFA scores at admission in the Belgian part were lower, indicating a lower disease severity than in the Dutch and German parts. Third, interventions to support respiration, circulation, and renal function showed notable differences between countries. Fourth, the length of stay and ICU mortality were higher in the Dutch and German parts than in the Belgian part, and multivariable analyses for ICU mortality showed independence of age, sex, disease severity, comorbidities, support strategies, therapies, and complications. These differences between Euregio country parts, like others (11), suggest variances in practice, referrals, and healthcare system organization, while under stress responding to a pandemic. Fifth, standard ICU capacity in the German part was sufficient, in contrast to the Dutch and Belgian parts that required expansion of ICU beds. We speculate that this has influenced care, as, for example, resource-consuming therapy such as extracorporeal membrane oxygenation was applied in the German part more often. The relatively lower use of mechanical ventilation in the Belgian part was likely driven by admitting patients to the ICU earlier in the disease course compared with the Dutch part of Euregio. At the beginning of the pandemic, COVID-19 patients admitted to the ICU in the Dutch part were usually intubated at admission, as the potential spreading of contagious aerosols by high-flow nasal oxygen was an issue of discussion (32). For mechanical ventilation, a striking difference in ventilator settings was shown. Volume-controlled mechanical ventilation was mostly used in the Belgian part. In contrast, pressure-controlled ventilation was the number one ventilation modality in The Netherlands, as observed in our study and a ventilation study in ICUs in The Netherlands (33) and the German part of Euregio. Using a specific setting might result from specialty training interacting within a specific healthcare system. However, whether a specific ventilator setting is associated with different outcomes is unknown (34). Furthermore, steroids were prescribed in 38% in the Belgian, 30% in the Dutch, and 18% in the German part. (Hydroxy)chloroquine was prescribed in 57% of the cohort, mainly driven by the 80% usage in the Dutch part of Euregio (35). The differences in the use of these antimicrobial/inflammation therapies showed that in the Dutch part, more therapies that were still under investigation were used compared, in particular, with the German part. For some of these therapies, more recent evidence shows a lack of benefit (4, 36). In individual hospitals, ICU protocols vary, in particular those created during the first weeks of the pandemic based on both international and national guidelines (23, 35). For example, diagnostics on thrombotic events differ, as the Belgian part of Euregio used leg ultrasound, and the Dutch part used CT pulmonary angiography. Each healthcare system might have interacted differently with the fast-growing number of published studies and the rapidly succeeding disease insights (3, 4, 7, 29, 37). The similarities in treatment protocols between countries might grow as evidence from more extensive studies is implemented and recommended by international guidelines. Furthermore, heterogeneity is partly explained by the different settings. In the German part of Euregio, only one hospital joined, and as a university hospital, the severity of patients’ disease and the need for mechanical support might hamper generalizability to other German hospitals. In the Belgian part, two general hospitals were included, whereas the Dutch part included three general hospitals and a university hospital. Nevertheless, as we included all COVID-19 ICU patients admitted to our seven hospitals within a short period, had a prespecified data collection protocol using readily available data in Western European ICUs, and performed multivariable analyses, our results have a high internal validity and generalizability for Euregio. However, when comparing countries, external validity cannot be assumed, as the seven hospitals cannot represent each of their countries as a whole. Briefly, reported data of Euregio country parts on sex, age, disease severity, comorbidities, support strategies, therapies, complications, and outcomes reveal some differences but appear largely comparable with each parent nation (8, 33, 38) (www.stichting-nice.nl) and other nations (5, 6, 11, 19, 37, 39) (for extensive information, see Supplementary Digital Content 1, http://links.lww.com/CCM/G799). Despite numerous studies among countries on the organization of Intensive Care Medicine during the COVID-19 pandemic were published (3–10), healthcare systems could not be compared directly based on their results. Our study underscores previous evidence that regional population variation might be unnoticed when evaluating data on a national level only (25, 40–42), whereas drivers of regional variation affect the risk and outcome of patients, independent of age, sex, disease severity, comorbidities, critical care support strategies, therapies, and complications (43–45). The differences observed in our cohort foster discussion about admission criteria and the interpretation of available evidence as resembled in the differences in organ support therapy. Our study has several limitations. First, our study was not designed to compare ICU COVID-19 care outcomes between nations (5–7), although our Euregio has the unique advantage to compare healthcare systems within one region, the hospitals included in this study are only a proxy for their national healthcare system, which hampers generalizability to other hospitals in that individual country. However, this is instead more a source of heterogeneity than a limitation. Second, the number of variables for the current study is limited, as we aimed to collect mainly routinely available patient data. In particular, more extensive data on the population (e.g., race and ethnicity) were not available, which is a limitation. Third, the included patients are a selection of patients admitted to the hospital. We have no data on whether certain patients were not referred for care to the ICU and whether decisions to forgo life-sustaining treatment during ICU admission were installed (46). Nevertheless, our multivariable analyses taking dependency within centers into account show that differences in ICU outcome between Euregio parts remain after adjustments for age, sex, disease severity, comorbidities, support strategies, therapies, and complications. This suggests that other healthcare system factors (among them ICU admission criteria or end-of-life practices, for example) play a role.

CONCLUSIONS

Despite many similarities, this observational cohort study shows that admission (20, 21, 47), organ support, treatment (23, 24, 48), and outcomes (17, 22) of COVID-19 patients at the ICU strikingly differ within the Euregio Meuse-Rhine. These differences are likely related to variances in healthcare systems, particularly ICU capacity, with each country responding differently to the rapidly evolving pandemic (11, 25, 26). To compare study outcomes and generalize these results to individual hospitals, caregivers should be aware of the possible differences. In-depth studies of the differences in protocol alignment, healthcare practice, guidelines (14), and trust in regional collaboration between healthcare systems (49, 50) are necessary to improve care for critically ill patients, also beyond COVID-19 (51).
  47 in total

1.  Is Mortality Rate of Ventilated Patients With Coronavirus Disease 2019 So High?

Authors:  Bernard Lambermont; Justine Huart; J Geoffrey Chase; Pierre Delanaye
Journal:  Crit Care Med       Date:  2021-07-01       Impact factor: 7.598

Review 2.  Pathophysiology, Transmission, Diagnosis, and Treatment of Coronavirus Disease 2019 (COVID-19): A Review.

Authors:  W Joost Wiersinga; Andrew Rhodes; Allen C Cheng; Sharon J Peacock; Hallie C Prescott
Journal:  JAMA       Date:  2020-08-25       Impact factor: 56.272

3.  Clinical trials of disease stages in COVID 19: complicated and often misinterpreted.

Authors:  Jay J H Park; Eric H Decloedt; Craig R Rayner; Mark Cotton; Edward J Mills
Journal:  Lancet Glob Health       Date:  2020-08-20       Impact factor: 26.763

4.  Interventions for treatment of COVID-19: A living systematic review with meta-analyses and trial sequential analyses (The LIVING Project).

Authors:  Sophie Juul; Emil Eik Nielsen; Joshua Feinberg; Faiza Siddiqui; Caroline Kamp Jørgensen; Emily Barot; Niklas Nielsen; Peter Bentzer; Areti Angeliki Veroniki; Lehana Thabane; Fanlong Bu; Sarah Klingenberg; Christian Gluud; Janus Christian Jakobsen
Journal:  PLoS Med       Date:  2020-09-17       Impact factor: 11.069

5.  Large-scale ICU data sharing for global collaboration: the first 1633 critically ill COVID-19 patients in the Dutch Data Warehouse.

Authors:  Lucas M Fleuren; Daan P de Bruin; Michele Tonutti; Robbert C A Lalisang; Paul W G Elbers
Journal:  Intensive Care Med       Date:  2021-02-17       Impact factor: 17.440

6.  COVID-19 pneumonia and the appropriate use of antibiotics.

Authors:  Amy Sarah Ginsburg; Keith P Klugman
Journal:  Lancet Glob Health       Date:  2020-11-11       Impact factor: 26.763

7.  The role of organizational characteristics on the outcome of COVID-19 patients admitted to the ICU in Belgium.

Authors:  Fabio Silvio Taccone; Nina Van Goethem; Robby De Pauw; Xavier Wittebole; Koen Blot; Herman Van Oyen; Tinne Lernout; Marion Montourcy; Geert Meyfroidt; Dominique Van Beckhoven
Journal:  Lancet Reg Health Eur       Date:  2020-12-23

8.  Surviving Sepsis Campaign: guidelines on the management of critically ill adults with Coronavirus Disease 2019 (COVID-19).

Authors:  Waleed Alhazzani; Morten Hylander Møller; Yaseen M Arabi; Mark Loeb; Michelle Ng Gong; Eddy Fan; Simon Oczkowski; Mitchell M Levy; Lennie Derde; Amy Dzierba; Bin Du; Michael Aboodi; Hannah Wunsch; Maurizio Cecconi; Younsuck Koh; Daniel S Chertow; Kathryn Maitland; Fayez Alshamsi; Emilie Belley-Cote; Massimiliano Greco; Matthew Laundy; Jill S Morgan; Jozef Kesecioglu; Allison McGeer; Leonard Mermel; Manoj J Mammen; Paul E Alexander; Amy Arrington; John E Centofanti; Giuseppe Citerio; Bandar Baw; Ziad A Memish; Naomi Hammond; Frederick G Hayden; Laura Evans; Andrew Rhodes
Journal:  Intensive Care Med       Date:  2020-03-28       Impact factor: 17.440

9.  Serial measurements in COVID-19-induced acute respiratory disease to unravel heterogeneity of the disease course: design of the Maastricht Intensive Care COVID cohort (MaastrICCht).

Authors:  Jeanette Tas; Rob J J van Gassel; Serge J H Heines; Mark M G Mulder; Nanon F L Heijnen; Melanie J Acampo-de Jong; Julia L M Bels; Frank C Bennis; Marcel Koelmann; Rald V M Groven; Moniek A Donkers; Frank van Rosmalen; Ben J M Hermans; Steven Jr Meex; Alma Mingels; Otto Bekers; Paul Savelkoul; Astrid M L Oude Lashof; Joachim Wildberger; Fabian H Tijssen; Wolfgang Buhre; Jan-Willem E M Sels; Chahinda Ghossein-Doha; Rob G H Driessen; Pieter L Kubben; Marcus L F Janssen; Gerry A F Nicolaes; Ulrich Strauch; Zafer Geyik; Thijs S R Delnoij; Kim H M Walraven; Coen DA Stehouwer; Jeanine A M C F Verbunt; Walther N K A Van Mook; Susanne van Santen; Ronny M Schnabel; Marcel J H Aries; Marcel C G van de Poll; Dennis Bergmans; Iwan C C van der Horst; Sander van Kuijk; Bas C T van Bussel
Journal:  BMJ Open       Date:  2020-09-29       Impact factor: 2.692

Review 10.  How the COVID-19 pandemic will change the future of critical care.

Authors:  Yaseen M Arabi; Elie Azoulay; Hasan M Al-Dorzi; Jason Phua; Jorge Salluh; Alexandra Binnie; Carol Hodgson; Derek C Angus; Maurizio Cecconi; Bin Du; Rob Fowler; Charles D Gomersall; Peter Horby; Nicole P Juffermans; Jozef Kesecioglu; Ruth M Kleinpell; Flavia R Machado; Greg S Martin; Geert Meyfroidt; Andrew Rhodes; Kathryn Rowan; Jean-François Timsit; Jean-Louis Vincent; Giuseppe Citerio
Journal:  Intensive Care Med       Date:  2021-02-22       Impact factor: 17.440

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  4 in total

Review 1.  COVID-19 Coagulopathy: From Pathogenesis to Treatment.

Authors:  Teba Alnima; Mark M G Mulder; Bas C T van Bussel; Hugo Ten Cate
Journal:  Acta Haematol       Date:  2022-02-08       Impact factor: 3.068

Review 2.  Temporary mechanical circulatory support for COVID-19 patients: A systematic review of literature.

Authors:  Silvia Mariani; Maria Elena De Piero; Justine M Ravaux; Alexander Saelmans; Michal J Kawczynski; Bas C T van Bussel; Michele Di Mauro; Anne Willers; Justyna Swol; Mariusz Kowalewski; Tong Li; Thijs S R Delnoij; Iwan C C van der Horst; Jos Maessen; Roberto Lorusso
Journal:  Artif Organs       Date:  2022-05-01       Impact factor: 2.663

3.  SepsEast Registry indicates high mortality associated with COVID-19 caused acute respiratory failure in Central-Eastern European intensive care units.

Authors:  Jan Benes; Miłosz Jankowski; Konstanty Szułdrzynski; Roman Zahorec; Mitja Lainscak; Zoltán Ruszkai; Matej Podbregar; Jan Zatloukal; Jakub Kletecka; Krzysztof Kusza; Jakub Szrama; Estera Ramic; Katarina Galkova; Stefan Krbila; Josef Valky; Jaka Ivanic; Marko Kurnik; Angéla Mikó; Tamás Kiss; Barbara Hetényi; Peter Hegyi; Alan Sustic; Zsolt Molnar
Journal:  Sci Rep       Date:  2022-09-01       Impact factor: 4.996

4.  Influence of Geopolitics on Severity and Outcome in COVID-19.

Authors:  Philippe R Bauer
Journal:  Crit Care Med       Date:  2022-04-01       Impact factor: 9.296

  4 in total

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