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Ambulatory and stationary healthcare use in survivors of ARDS during the first year after discharge from ICU: findings from the DACAPO cohort
Annals of Intensive Carevolume 9, Article number: 70 (2019)
For many survivors of acute respiratory distress syndrome (ARDS), the process from discharge from intensive care unit (ICU) to recovery is long and difficult. However, healthcare use after discharge from ICU has received only little attention by research. This study sets out to investigate the extent of ambulatory and stationary healthcare use among survivors of ARDS in Germany (multicenter DACAPO cohort) and to analyze predictors of stationary healthcare use.
A total of 396 survivors of ARDS provided data at 1 year after discharge from ICU. Fifty percent of 1-year survivors were hospitalized for 48 days or longer after discharge from ICU, with 10% spending more than six out of 12 months in stationary care. The duration of hospitalization increased significantly by the length of the initial ICU stay. All participants reported at least one outpatient visit (including visits to general practitioners), and 50% contacted four or more different medical specialties within the first year after discharge from ICU.
For most of the patients, the first year after ARDS is characterized by an extensive amount of healthcare utilization, especially with regard to stationary health care. These findings shed light on the substantial morbidity of patients after ARDS and contribute to a better understanding of the situation of patients following discharge from ICU.
Acute respiratory distress syndrome (ARDS) is a severe life-threatening condition which requires intensive care treatment and in the majority of patients mechanical ventilation. Hospital mortality varies—depending on the severity of ARDS—between 35 and 46% . For some survivors of ARDS, the process to full recovery and return-to-work is long and difficult: Following discharge from the intensive care unit (ICU), limitations in functioning and health-related quality of life are common [2, 3] and many patients suffer from psychological sequelae [4, 5]. Studies have also shown that impairments can persist over years [6, 7].
Against the background of long-term morbidity after ARDS, a better knowledge of healthcare use among survivors of ARDS seems crucial. Healthcare use represents a multilayered construct: It is not only a reflection of patients’ individual characteristics, such as health status and perceived need of treatment, but also of characteristics of the healthcare system, e.g., the availability of and the access to specific services . Information on healthcare use contributes to the estimation of healthcare expenditures and can be useful for revealing situations of regional practice variation as well as under- or over-supply . From a health services research perspective, healthcare use is also a relevant outcome in itself.
Only few previous studies from Canada and the USA have investigated healthcare use in survivors of ARDS [10,11,12]. Between 1998 and 2001, a Canadian cohort study included 109 ARDS survivors, 39% of which had been readmitted to hospital during the first 2 years following ARDS . Two more recent cohort studies from the USA report data for the first year after discharge from ICU: 40% out of 839  and 52% out of 138 ARDS survivors  reported at least any hospitalization, respectively.
It has to be noted, though, that all these cohort studies applied—in part strict—exclusion criteria, such as the diagnosis of psychiatric or neurological disorders or low predicted life expectancy due to comorbidity, and possibly underestimated the account of healthcare utilization following ARDS. In addition, it is well known that the organization of healthcare systems can affect healthcare use making it difficult to compare findings between studies from different countries.
Healthcare use after ARDS in Germany has not been investigated which is why we set out to address this research gap by (1) describing the extent to which survivors of ARDS use ambulatory and stationary healthcare services during the first year after discharge from ICU and by (2) analyzing socio-demographic and disease-related predictors of stationary healthcare utilization.
This study analyzes data on healthcare utilization among patients after ARDS from the DACAPO study (“Surviving ARDS: the influence of quality of care and individual patient characteristics on health-related quality of life”), a multicenter patient cohort study whose primary aim was to investigate the influence of quality of care on health-related quality of life and return-to-work in survivors of ARDS. The study procedures, baseline characteristics and profile of the cohort are described in more detail elsewhere [13,14,15]. Briefly, patients with ARDS were included in the study during their stay in the ICU of a participating clinic in Germany. After discharge from ICU, patients were recontacted at 3, 6 and 12 months and asked to complete comprehensive self-report questionnaires.
The study was approved by the Ethics Committee of the University of Regensburg (file number: 13-101-0262) and (if required) additionally by the Ethics Committees of the participating hospitals.
Between September 2014 and April 2016, 1225 patients with ARDS from 61 hospitals all over Germany were included in the study. Inclusion criteria were the presence of ARDS (according to the criteria of the Berlin definition ) and being at least 18 years old. In order to ensure generalizability of the results, no exclusion criteria were applied. Patients or their caregivers/legal guardians were approached during the ICU stay and asked to provide written informed consent. In cases where caregivers/legal guardians consented to the participation in the study, patients had to confirm this preliminary consent after discharge from ICU.
Out of 877 ICU survivors, 396 (45%) returned the questionnaire at 1 year after discharge from ICU. Figure 1 depicts the patient flow over the course of the study and gives an overview of the sample size at different time points. The most frequent reason for study drop out was death during the period after discharge from ICU (N = 161). Other reasons included the inability to complete the questionnaire (insufficient knowledge of German, incapable due to morbidity), the lack of a person who could provide proxy reports, withdrawal of consent or invalid addresses.
Data sources and data collection
This study uses data from two data sources:
Patients’ sociodemographic, disease and treatment-related characteristics as well as information on referral to and discharge from ICU were reported by study physicians/nurses from the individual ICUs using the electronic data entry system OpenClinica (OpenClinica, LLC; https://www.openclinica.com/).
Information on healthcare utilization (comprising inpatient stays following ICU discharge and outpatient physician visits) was assessed by self-report questionnaires at 6 months and at 1 year after discharge from ICU.
Plausibility checks of self-report data were performed and comprised the following procedures: Data which was reported both by study participants and by study personnel from the participating ICUs were compared, in case of non-concordance information provided by study personnel was considered valid. If participants completed questionnaires both at 6 months and at 1 year, information of these two questionnaires was compared with each other. In cases of non-concordance, the information which was provided earlier was considered valid. Further, it was checked whether time spans of inpatient stays were overlapping or whether the reported events followed the expected order (ICU, inclusion in the study, referral from ICU, etc.). Implausible information was handled as missing values. If the duration of single inpatients stays was implausible, the overall duration of inpatient stays was not calculated.
Sociodemographic, disease and treatment-related characteristics
Sociodemographic data comprise age, sex, education, living situation, employment situation before ICU and health insurance. Disease- and treatment-related characteristics include cause of ARDS (pulmonary, extrapulmonary, other), severity of ARDS (mild, moderate, severe ), diagnosis of ARDS (in a participating hospital, in a transferring hospital), scores indicating disease severity and morbidity at admission to ICU (SOFA , SAPS-II ), length of stay in the hospital and the ICU (days) and mechanical ventilation at discharge from ICU.
The German healthcare system is mainly separated into three broad sectors: ambulatory medical treatment carried out by hospitals or by physicians in private practice, inpatient treatment provided by hospitals and rehabilitative treatment provided by rehabilitation facilities. This separation goes along with differences in underlying legislation and funding agencies . Albeit the healthcare sectors have different tasks and pursue different objectives, there is also overlap in the services provided and for someone utilizing a certain healthcare service this differentiation might not be obvious. As we use self-report data of healthcare use for the purpose of our analyses, we refer to the following categorization of healthcare use.
Inpatient stays/stationary care Patients were asked to provide information on all inpatient stays following discharge from ICU in chronological order. Dates of the stays as well as name and place of the institution were assessed. This information was used to calculate the number of inpatient stays and the sum of days patients spent in stationary care. A hospital stay was considered an inpatient stay if the patient spent at least one night in the hospital. Stays in rehabilitation units were also considered inpatient stays.
Outpatient physician visits/ambulatory care Patients were asked to report whether and how often they had visited primary care and specialized physicians since discharge from ICU. This included both physicians in private practice and hospitals offering ambulatory care. The specialty types considered in the questionnaire comprised general practitioners, internists, obstetricians/gynecologists, ophthalmologists, orthopedists, otolaryngologists, neurologists/psychiatrists, psychotherapists, surgeons, dermatologists, radiologists, dentists and a category for “other specialty.” Data were analyzed regarding the number of different specialties which have been contacted and to the total number of outpatient visits, separately for all visits and for all visits excluding general practitioner visits.
Descriptive statistics were computed. Patients’ characteristics are presented as frequencies and percentages for categorical or medians and interquartile ranges for continuous variables, respectively. Data on duration or frequency of health service utilization are provided as median and interquartile ranges.
This study describes healthcare utilization by different parameters. Duration of hospitalization was considered the most important outcome given the amount of healthcare costs and the severity of limitations for the patient’s life associated with hospitalization. Accordingly, the analysis of determinants of healthcare utilization was restricted to this outcome. In order to account for the extreme overdispersion of count data on duration of hospitalization, a multivariable negative binomial regression model was computed for analyzing the association between sociodemographic and disease-related variables with duration of hospitalization. We applied a two-step approach for the selection of independent variables: First, socio-demographic and disease-related variables were selected. Second, these variables were tested using an empirical criterion. All variables which were significantly associated (p < 0.05) with the outcome in univariable models were included in the final multivariable model. Incidence rate ratios (IRRs) and 95% confidence intervals (CIs) are provided.
All analyses were computed using Stata 14.1.
Sociodemographic as well as disease- and treatment-related characteristics of study participants who returned the self-report questionnaire at 1 year after discharge from ICU are displayed in Table 1. Two-thirds of persons were male. Median age at admission to ICU was 56 years (IQR 47–65). The vast majority had a moderate (46%) or severe form (43%) of ARDS (according to the classification provided by the Berlin definition ).
Discharge from ICU When discharged from ICU, most patients (59%) were referred within the same hospital, 41% to another hospital or to a rehabilitation unit. Only one person was discharged home.
Inpatient stays The number of patients’ individual hospital stays is depicted in Fig. 2a. Including the initial hospital stay for the treatment of ARDS, the median number of inpatient stays within 1 year after discharge from ICU was 3 (IQR 2–4). These stays comprised re-admissions to both ICUs and normal wards, admissions for medical problems not related to the initial ICU stay and rehabilitative measures. Only 10% of patients had no additional hospital stay after discharge from the clinic where they had been treated for ARDS.
Within the first year after discharge from ICU, the median number of days of hospitalization was 48 (IQR 31–76) (see Fig. 2b). The variability was high: Nearly 10% of patients were hospitalized for a period longer than 6 months.
Outpatient visits All study participants reported at least one outpatient visit to a general practitioner or any other physician during the first year after discharge from ICU. Most participants contacted physicians from various specialties: The median number of different medical specialties visited was 4 (IQR 3–6) including general practitioners and 3 (IQR 2–5) without general practitioners.
Table 2 provides an overview on which percentage of study participants utilized the different medical specialties. The most frequently contacted medical specialties were general practitioners with 93% of study participants reporting a visit, followed by internists with 56%. 37% of study participants had at least one visit to a neurologist, psychiatrist or psychotherapist.
Overall, the median number of outpatient visits during the first year after discharge from ICU was 15, with a high variability between participants (IQR 8–25). The median number of outpatient visits to a general practitioner was 7 (IQR 4–12), and the median number for visits to physicians from any other specialty was 8 (IQR 4–14).
In univariable analyses, indicators of disease severity (SOFA score, SAPS-II score), transferral from another hospital to the study hospital, length of ICU stay, overall length of hospital stay until discharge from ICU (including ICU stay) and mechanical ventilation at discharge from ICU were significantly associated with the number of days hospitalized during the first year after ICU (Table 3). There was no significant association with any of the sociodemographic variables.
Table 4 presents the results of the multivariable analysis. Since the predictor variables “length of hospital stay” and “length of ICU stay” were highly correlated (r = 0.9), only length of ICU stay was included in the multivariable model. Duration of hospitalization after discharge from ICU was significantly associated with length of ICU stay (incidence rate ratio (IRR): 1.10, 95% CI 1.05–1.15), with each 10 days of ICU stay prolonging the duration of hospitalization after discharge from ICU by 10%. All other associations were attenuated in the multivariable model and did not reach statistical significance.
Until now, healthcare utilization following ARDS has received only little attention by research and healthcare providers. Our study contributes to a better understanding of the situation of patients after ARDS by providing a comprehensive description of both stationary and ambulatory healthcare use during the first 12 months after discharge from ICU in a large German cohort of 1-year survivors of ARDS: We found that 50% of 1-year survivors were hospitalized for 48 days or longer after discharge from ICU. Ten percent spent even more than six out of 12 months in stationary care. The duration of hospitalization increased significantly by the length of the initial ICU stay. Remarkably, none of the other investigated variables were associated with the duration of hospitalization. Study participants reported also a substantial amount of outpatient physician visits, with 50% of former ARDS patients having contact to four or more different medical specialties (including general practitioners) within a 1-year period.
The extent of healthcare utilization in 1-year survivors of ARDS
Findings on healthcare utilization have to be discussed in view of the respective healthcare system as comparability across countries is severely impeded due to structural differences between systems : The German healthcare system is characterized by a separation between the hospital and the outpatient sector as well as between acute care and rehabilitative treatment. The number of hospital beds per inhabitant is larger than that in most of the other European countries  and also the duration of hospital stays is longer . Health insurance is mandatory, and the access to and the reimbursement of services are comprehensive . With regard to patients after ARDS, their situation is characterized by the following specific circumstances in Germany: Albeit the rehabilitation system is elaborated , there are no follow-up clinics or rehabilitation units that are specialized in the care of former ARDS patients. Thus, the choice of a clinic or a rehabilitation unit is informed by the underlying disease which has caused ARDS or it follows practical considerations such as whether an institution is able to deal with a patient’s health status and need of care as well as the currently available capacities.
Acknowledging these specifics of the German healthcare system which are related to the extent of healthcare utilization, we refer to a sample of sepsis survivors and to a representative sample from the general population in Germany which might help to interpret the data on healthcare use of patients after ARDS:
The SMOOTH study included 291 survivors of sepsis and investigated the effects of a primary-care-based intervention . A variety of secondary outcomes were assessed, among others measures of healthcare utilization. With respect to stationary healthcare utilization, participants from that study had values far below these of our study among ARDS survivors. During the first 6 months after discharge from ICU, former sepsis patients from the control group (care as usual) spent a median time of 8 days (IQR 0–32) in a hospital and of 0 days (IQR 0–21) in a rehabilitation clinic. During the months seven to 12 after discharge, the median number of days of both hospital and rehabilitation stay was 0 . However, the number of outpatient visits was comparable to our study.
The representative German Health Interview and Examination Survey for Adults (DEGS1) found that 16% of the general population was hospitalized at least once during a 1-year period for on average 9.7 nights. Not unexpectedly, this is in stark contrast to the findings from our sample: 90% of participants had one or more additional hospital stays (including rehabilitation) within the first year after discharge from ICU. With respect to healthcare use in the outpatient sector, the DEGS1 survey found that the mean number of outpatient visits (including visits to general practitioners) per year was 9.2 in the general population. However, persons over the age of 70 years and people with poor self-rated health had a mean number of 11.5 and 15.0 visits, respectively . The latter corresponds to the finding obtained from our cohort and reflects a substantial morbidity among survivors of ARDS.
Concurrent treatment by different healthcare providers
The majority of patients in our sample had several inpatient stays and visited also physicians from a variety of disciplines. The number of different contacted medical specialist groups is elevated in our cohort as compared to the general population . This finding may reflect many comorbidities or ARDS sequelae which compromise different organ systems and impair patients’ functioning at various levels. For the latter, in the last decade, the term post-intensive care syndrome (PICS) has been proposed . PICS summarizes new or worsening impairments in physical, mental and cognitive functioning which can occur after prolonged treatments in the ICU and are often not sufficiently covered by healthcare.
But the relatively high number of different contacted medical specialties may also be read as frequent referrals between specialties pointing out the need for other or additional treatments tailored to the needs of former critically ill patients. Whichever way, concurrent treatment provided by different physicians is likely to make the flow of information more difficult and is a challenge for both the involved healthcare providers and the patients.
Utilization of mental health care
The percentage of patients who visited a neurologist/psychiatrist or psychotherapist is of special interest. The still-existing stigma associated with mental illness , low rates of help seeking for mental health problems  and concerns regarding the availability of mental health care  suggest that patients’ access to these specialties might be more difficult as compared to others. However, the percentages of 32% and 14% in our study are quite high as compared to 8% and 4% of people from the general population in Germany who had contact to a psychiatrist/neurologist or psychotherapist within a 1-year period, respectively . As help seeking for mental disorders can be difficult for some people, these high percentages of patients after ARDS who utilized mental health care are likely to reflect a special need of this population. A systematic review found that mental disorders are common in people after ARDS: The prevalences for depression, anxiety and post-traumatic stress disorder (PTSD) approximately range between 20 and 40% . A more recent study reported that even two-thirds of patients after ARDS are experiencing symptoms of mental disease .
Strengths and limitations
To the best of our knowledge, this is the first study on healthcare utilization in survivors of ARDS in Germany. It used primary data and investigated patients’ healthcare utilization both in the inpatient and the outpatient sectors.
In contrast to other cohorts of ARDS survivors, no exclusion criteria (e.g., with regard to comorbidity or to estimated life expectancy) were applied. Our study sample corresponded to the characteristics expected for ARDS cohorts with regard to the distribution of sex and age . However, the liberal inclusion criteria might have led to a higher proportion of severely ill patients—as can be seen by 40% of persons in our study sample which had a severe form of ARDS—and to high extents of healthcare utilization following the ICU stay.
Information on healthcare utilization after discharge from ICU was gathered through self-report questionnaires. Extensive plausibility checks were conducted, and the majority of patients were found to provide apparently comprehensive and detailed accounts on their contacts with healthcare providers. Nevertheless, we cannot exclude that data on healthcare utilization are incomplete or imprecise and by using self-report data on inpatient stays we were not able to differentiate between different types of hospitals and rehabilitation units. With regard to the findings obtained in our study, this limitation of self-report data could have led to an underestimation of the extent of healthcare utilization. It seems unlikely that persons reported non-existent hospital stays or contacts to a physician; but contacts with the healthcare system might have been omitted or not been correctly recalled—particularly with regard to ambulatory health care and in people who used healthcare services extensively [31, 32].
Our study focused on two major aspects of healthcare use (inpatient stays and ambulatory visits); however, the use of other health services (such as medication, medical aids and remedies, nursing care, etc.) was not considered.
In addition, we were not able to depict the mutual referrals of patients (e.g., between stationary and outpatient care or between different specialties), whether and how the various contacts with the healthcare system were interrelated and which were the reasons for the use of the various services. Our study does not allow for the differentiation between healthcare uses due to sequelae of ARDS or the ICU stay and due to any other complaints.
It should be noted that the sample for this study was people who survived the first year after ARDS and responded to the questionnaire. Thus, our study gives important insights into the health and living situation of long-term survivors of ARDS, but conclusions about healthcare utilization caused by ARDS cannot be drawn as we lack information on persons who have died during the first year after ARDS. However, one might speculate that these persons utilized health services even more often. Further, a considerable proportion of study participants were lost to follow-up. Unfortunately, loss to follow-up is a problem in many studies investigating long-term survivors [e.g., 33–35], and compromises the external validity of our findings.
In terms of clinical implications, clinicians should be aware that longer ICU stays entail the need to utilize many further health services in patients who survive ARDS. Future studies should additionally supplement self-report data with routine data provided by administrations or health insurances. This would allow for a more detailed description of healthcare use (e.g., the type and specialization of an institution) and an assessment of underlying reasons (e.g., main diagnosis).
For many patients, the first year after ARDS is characterized by an extensive amount of healthcare utilization, especially with regard to stationary health care. The length of the initial ICU stay was associated with the duration of hospitalization during the first year after ARDS.
Availability of data and materials
Data are available upon request from the original data holders (the two principal investigators (PIs) TB and CA).
acute respiratory distress syndrome
intensive care unit
incidence rate ratio
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We are indebted to all the intensive care specialists and study nurses throughout Germany, who, with great commitment, recruited patients for the DACAPO study: Aachen, Aachen University Hospital RWTH Aachen, Department of Anesthesiology (PD Dr. Johannes Bickenbach, Dr. Thorben Beeker, PD Dr. Tobias Schürholz, Jessica Pezechk); Amberg, Klinikum Amberg, Department for Anaesthesiology (Dr. Jens Schloer); Augsburg, Klinikum Augsburg (Dr. Ulrich Jaschinski, Ilse Kummer); Bamberg, Sozialstiftung Bamberg Hospital, Department for Anaesthesiology (Dr. Oliver Kuckein); Berlin, Charité - University Medicine Berlin, Department of Anaesthesiology and Intensive Care Medicine (PD Dr. Steffen Weber-Carstens, Dr. Anton Goldmann, Dr. Stefan Angermair, Krista Stoycheva); Berlin, HELIOS Klinikum Berlin-Buch, Department of Intensive Care Medicine (Prof. Dr. Jörg Brederlau, Nadja Rieckehr, Gabriele Schreiber, Henriette Haennicke); Bielefeld, Ev. Krankenhaus Bielefeld. Department of Anesthesiology, Intensive Care Medicine, Emergency Medicine and Pain Therapy (Dr. Friedhelm Bach, Dr. Immo Gummelt, Dr. Silke Haas, Catharina Middeke, Dr. Ina Vedder, Marion Klaproth); Bochum, Ruhr University Bochum, Department of Anaesthesiology (Prof. Dr. Michael Adamzik, Dr. Jan Karlik, Dr. Stefan Martini, Luisa Robitzky); Bonn, University Hospital Bonn, Department of Anesthesiology and Intensive Care Medicine (Prof. Dr. Christian Putensen, Dr. Thomas Muders, Ute Lohmer); Bremen, Klinikum Bremen-Mitte, Department of Anesthesiology (Prof. Dr. Rolf Dembinski); Deggendorf, Medical Center, Department of Anaesthesiology and Intensive Care Medicine (Dr. Petra Schäffner, Dr. Petra Wulff-Werner); Dortmund, Klinikum Dortmund, Department of Critical Care Medicine (Elke Landsiedel-Mechenbier, Daniela Nickoleit-Bitzenberger, Ann-Kathrin Silber); Dresden, University Hospital Dresden Carl Gustav Carus, Department of Anesthesiology and Intensive Care Medicine (Prof. Dr. Maximilian Ragaller, Prof. Dr. Marcello Gama de Abreu, Alin Ulbricht, Linda Reisbach); Frankfurt am Main, University Hospital Frankfurt, Department of Anaethesiology, Intensive Care Medicine and Pain Therapy (Prof. Dr. Kai Zacharowski, Prof. Dr. Patrick Meybohm, Simone Lindau, Haitham Mutlak); Freiburg, University Medical Center Freiburg, Department of Anaesthesiology and Critical Care Medicine Freiburg (Prof. Dr. Alexander Hötzel, Dr. Johannes Kalbhenn); Freising, Klinikum Freising, Department of Anaesthesiology (Dr. Christoph Metz, Dr. Stefan Haschka); Göppingen, Klinik am Eichert, ALB FILS Kliniken, Department of Anaesthesiology and Intensive Care (Dr. Stefan Rauch); Göttingen, University Medical Center, Department of Anaesthesiology, Emergency and Intensive Care Medicine (Prof. Dr. Michael Quintel, Dr. Lars-Olav Harnisch, Dr. Sophie Baumann, Andrea Kernchen); Greifswald, University Medicine Greifswald, Department of Internal Medicine B (Dr. Sigrun Friesecke, Sebastian Maletzki); Hamburg, University Hospital Hamburg-Eppendorf, Department of Intensive Care Medicine, Center of Anesthesiology and Intensive Care Medicine (Prof. Dr. Stefan Kluge, Dr. Olaf Boenisch, Dr. Daniel Frings, Birgit Füllekrug, Dr. Nils Jahn, Dr. Knut Kampe, Grit Ringeis, Brigitte Singer, Dr. Robin Wüstenberg); Hannover, Hannover Medical School, Department of Anaesthesiology and Intensive Care Medicine (Dr. Jörg Ahrens, Dr. Heiner Ruschulte, Dr. Andre Gerdes, Dr. Matthias Groß); Hannover, Hannover Medical School, Department of Respiratory Medicine (Dr. Olaf Wiesner, Aleksandra Bayat-Graw); Heidelberg, University of Heidelberg, Department of Anaesthesiology (Dr. Thorsten Brenner, Dr. Felix Schmitt, Anna Lipinski); Herford, Klinikum Herford, Clinic for Anaesthesiology, Surgical Intensive Care Medicine, Emergency Care Medicine, Pain Management (Prof. Dr. Dietrich Henzler, Dr. Klaas Eickmeyer, Dr. Juliane Krebs, Iris Rodenberg); Homburg, Homburg University Medical Centre, Department of Anaesthesiology, Intensive Care and Pain Medicine (Dr. Heinrich Groesdonk, Kathrin Meiers, Karen Salm, Prof. Dr. Thomas Volk); Ibbenbüren, Ibbenbüren General Hospital, Division of Thoracic Surgery and Lung Support (Prof. Dr. Stefan Fischer, Basam Redwan); Immenstadt, Kempten-Oberallgaeu Hospitals, Clinic for Pneumology, Thoracic Oncology, Sleep- and Respiratory Critical Care (Dr. Martin Schmölz, Dr. Kathrin Schumann-Stoiber, Simone Eberl); Ingolstadt, Klinikum Ingolstadt, Department of Anaesthesiology and Critical Care Medicine (Prof. Dr. Gunther Lenz, Thomas von Wernitz-Keibel, Monika Zackel); Jena, Jena University Hospital, Deptartment of Anesthesiology and Intensive Care Therapy (Dr. Frank Bloos, Dr. Petra Bloos, Anke Braune, Anja Haucke, Almut Noack, Steffi Kolanos, Heike Kuhnsch, Karina Knuhr-Kohlberg); Kassel, Klinikum Kassel, Department of Anaesthesiology (PD Dr. Markus Gehling); Kempten, Klinikum Kempten-Oberallgäu gGmbH, Department for Anesthesia and Operative Intensive Care (Prof. Dr. Mathias Haller, Dr. Anne Sturm, Dr. Jannik Rossenbach); Kiel, University Medical Center Schleswig–Holstein, Campus Kiel, Department of Anesthesiology and Intensive Care Medicine (Dr. Dirk Schädler, Stefanie D’Aria); Köln, Cologne-Merheim Hospital, Department of Pneumology and Critical Care Medicine (Prof. Dr. Christian Karagiannidis, Dr. Stephan Straßmann, Prof. Dr. Wolfram Windisch); Köln, University Hospital of Cologne, Department of Anaesthesiology and Intensive Care Medicine (Prof. Dr. Thorsten Annecke, PD Dr. Holger Herff); Langen, Asklepios Kliniken Langen-Seligenstadt, Department of Anesthesiology and Intensive Care Medicine (Dr. Michael Schütz); Leipzig, University of Leipzig, Department of Anesthesiology and Intensive Care Medicine (PD Dr. Sven Bercker, Hannah Reising, Mandy Dathe, Christian Schlegel); Ludwigsburg, Klinikum Ludwigsburg, Academic Teaching Hospital, University of Heidelberg, Department of Anaesthesiology (Katrin Lichy); Ludwigshafen, Klinikum Ludwigshafen, Department of Anesthesiology and Intensive Care Medicine (Prof. Dr. Wolfgang Zink, Dr. Jana Kötteritzsch); Mainz, University Medical Center Mainz, Department of Anaesthesiology (Dr. Marc Bodenstein, Susanne Mauff, Peter Straub); Magdeburg, Magdeburg University Medical Centre, Department of Anaesthesiology and Intensive Care Medicine (Dr. Christof Strang, Florian Prätsch, Prof. Dr. Thomas Hachenberg); Mannheim, University Medical Center Mannheim, Department of Anaesthesiology and Surgical Intensive Care Medicine (Dr. Thomas Kirschning, Dr. Thomas Friedrich, Dr. Dennis Mangold); Marburg, University Hospital, Department of Anaesthesiology (Dr. Christian Arndt, Tilo Koch); Mönchengladbach, Kliniken Maria-Hilf GmbH, Department of Cardiology (Dr. Hendrik Haake, Katrin Offermanns); München, Bogenhausen Hospital, Department of Anaesthesiology (Prof. Dr. Patrick Friederich, Dr. Florian Bingold); München, Klinikum Großhadern, Department of Anaesthesiology (Dr. Michael Irlbeck, Prof. Dr. Bernhard Zwissler); München, Klinikum Neuperlach, Städtisches Klinikum München GmbH, Department of Anesthesiology, Critical Care and Pain Medicine (PD Dr. Ines Kaufmann); München, Klinikum rechts der Isar, Department for Anaesthesiology of the Technical University of Munich (Dr. Ralph Bogdanski, Dr. Barbara Kapfer, Dr. Markus Heim, PD Dr. Günther Edenharter); Münster, University Hospital Münster, Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy (Prof. Dr. Björn Ellger, Daniela Bause); Neumarkt, Kliniken des Landkreises Neumarkt i.d.OPf, Department for Anaesthesiology and Intensive Care Medicine (Dr. Götz Gerresheim); Nürnberg, General Hospital Nuremberg, Paracelsus Medical University, Department of Emergency Medicine and Intensive Care (Dr. Dorothea Muschner, Prof. Dr. Michael Christ, Arnim Geise); Osnabrück, Marienhospital Osnabrück, Department of Anaesthesiology (PD Dr. Martin Beiderlinden, Dr. Thorsten Heuter); Passau, Klinikum Passau, Department for Anaesthesiology (Dr. Alexander Wipfel); Regensburg, Caritas Krankenhaus St. Josef, Department for Anaesthesiology (Dr. Werner Kargl, Dr. Marion Harth, Dr. Christian Englmeier); Regensburg, Regensburg University Hospital, Department of Anaesthesiology, Operative Intensive Care (Prof. Dr. Thomas Bein, Dr. Sebastian Blecha, Dr. Kathrin Thomann-Hackner, Marius Zeder); Stuttgart, Katharinenhospital, Department of Anesthesiology (Dr. Markus Stephan); Traunstein, Klinikum Traunstein, Department of Anaesthesiology (Dr. Martin Glaser); Tübingen, Tübingen University Hospital, Eberhard-Karls University Tübingen, Department of Anaesthesiology and Intensive Care Medicine (PD Dr. Helene Häberle); Ulm, Ulm University, Department of Anesthesiology (Prof. Dr. Hendrik Bracht, Christian Heer, Theresa Mast); Würzburg, University of Würzburg, Department of Anaesthesia and Critical Care (PD Dr. Markus Kredel, PD Dr. Ralf Müllenbach).
Further, we are grateful to previous members of the Regensburg DACAPO study team (medical documentation: Phillip Sebök, study physician: Kathrin Thomann-Hackner), to the members of the Advisory Board of the DACAPO-Study (Prof. Dr. Julika Loss, Prof. Dr. Bernhard Graf, Prof. Dr. Michael Leitzmann, Prof. Dr. Michael Pfeifer, Regensburg, Germany) and to our student assistants (Simon Bein, Vreni Brunnthaler, Carina Forster, Stefanie Hertling, Sophie Höhne, Carolin Schimmele, Elisa Valletta, Philipp Drewitz and Chiara Eberle).
Ethics approval and consent to participate
The DACAPO study was approved by the Ethics Committee of the University of Regensburg (file number: 13-101-0262) and (if required) additionally by the Ethics Committees of the participating hospitals.
Consent for publication
TB received honoraria for lectures from Xenios Company, Germany. All other authors declare that they have no competing interests.
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