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. 2022 Jan 21;36(2):230–238. doi: 10.1007/s00540-022-03036-9

Quality of life and mortality among survivors of acute respiratory distress syndrome in South Korea: a nationwide cohort study

Hey-ran Choi 1,#, In-Ae Song 2,#, Tak Kyu Oh 2,3,
PMCID: PMC8777182  PMID: 35061069

Abstract

Purpose

Worsening quality of life (QOL) is an important health issue in acute respiratory distress syndrome (ARDS) survivors. We aimed to investigate the prevalence of worsening QOL among ARDS survivors and their association with mortality.

Methods

South Korean National Health Insurance database information for all adults admitted to intensive care units for ARDS from January 1, 2010 to December 31, 2018 who survived ≥ 365 days were included in this study.

Results

A total of 4452 ARDS survivors were included in the final analysis. Total QOL had worsened in 1667 (37.4%) of the survivors at the follow-up 1 year after being diagnosed with the syndrome. Specifically, 1298 patients (29.2%) experienced decreased income, 334 (7.5%) lost their jobs, and 327 (7.3%) had newly acquired disabilities. In the multivariable Cox regression analysis, worsening QOL was not associated with 2-year all-cause mortality among survivors (P = 0.140). However, newly acquired disability was associated with 1.74-fold (hazard ratio [HR]: 1.74, 95% confidence interval [CI] 1.31–2.33; P < 0.001) higher 2-year all-cause mortality, while decreased income (P = 0.571) and unemployment (P = 0.952) were not associated with it. In addition, newly acquired respiratory disability was associated with a 6.61-fold higher risk of 2-year respiratory mortality (HR: 6.61, 95% CI 3.14–13.90; P < 0.001).

Conclusions

At the 1-year follow-up period, one-third of ARDS survivors experienced worsening QOL in South Korea. Specifically, newly acquired disability was associated with a higher risk of 2-year all-cause and respiratory mortality among patients who survived ARDS.

Supplementary Information

The online version contains supplementary material available at 10.1007/s00540-022-03036-9.

Keywords: Critical care, Intensive care units, Quality of life, Mortality, Respiratory distress syndrome

Introduction

Acute respiratory distress syndrome (ARDS) is a clinical syndrome characterized by acute hypoxemia with bilateral pulmonary infiltration and decreased lung compliance [1]. The prevalence of ARDS in the intensive care unit (ICU) was reported as 10.4% among ICUs in 50 countries [2]. As the mortality rate among ARDS patients varies from 11 to 87% globally [3], there might be many survivors of ARDS worldwide. Therefore, quality of life (QOL) among survivors of ARDS is a significant public health issue [4].

Previous studies reported that ARDS survivors experienced reduced QOL [58], and most studies evaluated the QOL of ARDS survivors using surveys [4]. Recent studies have focused on the QOL of ARDS survivors from various perspectives [913], and some researchers have reported that ARDS survivors experienced unemployment, lost earnings, an increased burden of healthcare utilization, and functional disabilities in daily life [1014]. Although there have been advances in understanding worsening QOL among ARDS survivors, its impact on further prognosis has not yet been identified.

Therefore, we aimed to examine the prevalence of worsening QOL among ARDS survivors as of the 1-year follow-up period after diagnosis of ARDS. In addition, we also examined whether worsening QOL was associated with mortality among the survivors. We hypothesized that ARDS survivors might experience worsening QOL and that it might be associated with poorer long-term survival.

Methods

Study design, setting, and ethical statement

The Reporting of Observational Studies in Epidemiology guidelines was followed in this study as a nationwide population-based cohort study in South Korea [15]. The Institutional Review Board (IRB) of Seoul National University Bundang Hospital approved the protocol of this study (Approval Number: X-2008-630-903), and national health insurance service (NHIS) approved data sharing after approval of the study protocol (Approval Number: NHIS-2021-1-424). The IRB waived the need for informed consent because we used data that were anonymized and had been extracted retrospectively for analysis in this study.

Data source

The data were extracted from the NHIS database and Statistics Korea for this study. First, information regarding disease diagnosis and prescription of drugs and/or procedures was extracted from the NHIS database. As a public health insurance system in South Korea, the NHIS contains all disease diagnoses using the International Statistical Classification of Diseases and Related Health Problems-tenth revision (ICD-10) codes and prescription information for patients to receive financial coverage of treatment expenses by the government. We extracted data regarding death from the database of Statistics Korea. As a central government organization, Statistics Korea records national statistics and data regarding accurate dates and causes of death of all individuals in South Korea. Physicians register the principal cause of death for all individuals in the database. All dates and causes of death were collected by December 31, 2020, for this study.

ARDS survivor

Adult (≥ 18 years old) critically ill patients who were admitted to the ICU between January 1, 2010, and December 31, 2018, and diagnosed with ARDS using ICD-10 codes of J80 were initially screened in this study. As ARDS is a syndrome that can occur with other pathologic conditions [16], we included both the main diagnosis cases and secondary diagnosis cases of ARDS. Therefore, patients with a primary diagnosis of pneumonia and a secondary diagnosis of ARDS were included in this study. The main diagnosis was defined by the NHIS after the end of hospitalization as a certain disease in which the patient’s demand for treatment or examination was the greatest during hospitalization. If a patient was admitted to the ICU with a diagnosis of ARDS two times or more during the study period, only the first episode of admission was considered in this study. Those who were alive ≥ 365 days after their ARDS diagnosis were considered ARDS “survivors”.

Quality of life among ARDS survivors

The QOL of ARDS survivors was evaluated using three methods. First, the household income level at ICU admission for ARDS was compared to the level 1 year later. The NHIS database contains the household income levels of subscribers to determine their insurance premiums. The household income level of all subscribers was determined according to income, living standards, property, and rate of participation in economic activities, and divided into four groups using the quartile ratio. Second, we evaluated unemployment after ARDS treatment. We examined the employment status before and after admission for ARDS treatment among survivors (employment status is registered in the NHIS database; self-employment was not considered). Third, new disabilities acquired within a year of ARDS diagnosis were evaluated. All individuals with any disability must be registered in the NHIS database to receive various benefits from the social welfare system in South Korea. There are 15 types of disabilities, including physical disability, brain lesion disability, visual disturbance, hearing disability, speech disability, intellectual disorder, autism, mental disorders, renal disorders, heart disorders, respiratory disabilities, hepatopathy, facial disfigurement, intestinal and urinary fistulae, and epilepsy. Each disability is determined strictly depending on the law by the specialist physician in each field. Regarding patients’ disabilities, each is assigned one of six grades according to severity (1st = most severe; 6th = most mild). In this study, the 1st–3rd grades of disability were considered “severe”; 4th–6th grades were considered “mild to moderate.” The criteria for the respiratory disability grading in South Korea are based on the symptoms of dyspnea, chest X-ray imaging, pulmonary function testing, and arterial blood gas analysis [17]; grading criteria are presented in Table S1.

Study endpoints

The primary endpoint in this study was worsening QOL (decreased household income, unemployment, and newly acquired disability) within 1 year after diagnosis of ARDS among survivors. The secondary endpoint was 2-year all-cause mortality among survivors of ARDS. If the main cause of death was respiratory disease (J00–J99), it was classified as “respiratory mortality”; all mortality not due to respiratory disease was classified as “other mortality.”

Covariates

Physical variables considered included age and sex; ARDS treatment results variables for survivors were divided into three types: (1) discharge and follow-up at the same hospital, (2) transfer to other long-term facility centers, and (3) discharge and outpatient clinic follow-up. Admitting departments were divided into internal medicine (IM) and non-IM. Length of hospitalization (days) and total cost of hospitalization (USD) were used as covariates. The type of hospital admission was also considered a covariate, and patients were divided into (1) transfer from another hospital, (2) admission through emergency room, or (3) admission through outpatient clinic. As high case volume centers were associated with improved hospital survival outcomes in patients with ARDS [18], we calculated the annual case volume of ARDS treatment in each hospital as a covariate.

The patients were assigned into four groups using quartile ratio, based on the hospital to which patients with ARDS were admitted, such as Q1 ≤ 4, Q2: 5–14, Q3: 15–28, and Q4 ≥ 29. The main diagnosis of ARDS, diagnoses of shock (R57), and sepsis (A40, A41, and R65.2) were considered covariates. If a patient with ARDS was diagnosed with sepsis as the primary diagnosis, it was considered “sepsis-associated ARDS.” Extracorporeal membrane oxygenation (ECMO), neuromuscular blockade (NMB) use, continuous renal replacement therapy (CRRT) use, and experience of cardiopulmonary resuscitation (CPR) were also considered covariates. The Charlson Comorbidity Index (CCI) was also calculated using registered ICD-10 codes of individual underlying diseases within 1 year before admission for ARDS, as shown in Table S2. The CCI was divided into four groups as categorical variables (0–1, 2–3, 4–5, and ≥ 6).

Statistical analysis

The clinicopathological characteristics of total ARDS survivors are presented as numbers with percentages for categorical variables and mean values with standard deviation (SD) for continuous variables. First, QOL before and after ARDS treatment among survivors were examined. Second, QOL worsening according to age, the CCI, the number of days of total mechanical ventilatory support, duration of hospitalization, use of ECMO support, sepsis-associated ARDS, and the experience of CPR among ARDS survivors were examined. For continuous variables (age, CCI, day of total mechanical ventilatory support, and duration of hospitalization), median values were used as cutoffs to categorize the subgroups. Third, we examined worsening QOL among hospital survivors who were discharged after hospitalization for ARDS treatment, because the survivors who were discharged but died within a year after being diagnosed with ARDS, might affect the results. Following this, we performed a multivariable logistic regression analysis for QOL worsening among ARDS survivors. All covariates were included in the multivariate adjustment model. The Hosmer–Lemeshow test was used to confirm the model’s goodness of fit, and the results were presented as odds ratios (ORs) with 95% confidence intervals (CIs).

Next, we constructed multivariable Cox regression models for 2-year all-cause mortality after diagnosis of ARDS among survivors. Three separate models were constructed to avoid multicollinearity. Model 1 examined the association between worsening QOL and the risk of 2-year all-cause mortality. Model 2 examined the association between worsening QOL in detail (decreased income, unemployment, and newly acquired disability) and the risk of 2-year all-cause mortality. Model 3 examined the effect of newly acquired respiratory disability among total disability on the risk of 2-year all-cause mortality.

We performed multivariable Cox regression modeling for 2-year respiratory and other mortality after ARDS diagnosis among survivors. The results of Cox regression analyses were presented as hazard ratios (HRs) with 95% CIs, and log–log plots were used to confirm satisfaction of the central assumption of Cox proportional hazard models. Variance inflation factors (< 2.0) confirmed there was no issue of multicollinearity between variables in the model. All statistical analyses were performed using R software (version 4.0.3, R packages, R Project for Statistical Computing, Vienna, Austria), and statistical significance was set at P < 0.05.

Results

From January 1, 2010, to December 31, 2018, there were 23,280 cases in ICUs for ARDS treatment. After excluding 7407 patients, who were admitted to the ICU with a diagnosis of ARDS from 2010 to 2018 twice or more, 365 pediatric cases (< 18 years old), 15,508 adult patients with ARDS were initially screened. Among them, 11,056 patients died within a year of ARDS diagnosis, so 4452 ARDS survivors were included in the final analysis. The 2-year all-cause mortality occurred in 549 (12.3%) patients, and 138 (3.1%) died within 2 years due to respiratory disease, while 411 (9.2%) patients died due to other causes (Fig. 1). Clinicopathological characteristics are shown in Table 1. The mean age of survivors was 62.9 years (SD: 17.4 years old); 2657 (59.7%) were male. Among survivors, the mean length of hospitalization was 18.6 days (SD: 15.3 days) and the mean value of total cost for hospitalization was 9714.1 USD (SD: 12,266.7 USD).

Fig. 1.

Fig. 1

Flow chart depicting ARDS survivors. ARDS, acute respiratory distress syndrome

Table 1.

Clinicopathological characteristics

Variable Mean (SD) or N (%)
Age, year 62.9 (17.4)
Sex, male 2657 (59.7)
Treatment result
 Discharge, and follow-up in same hospital 1691 (38.0)
 Transfer to other long-term facility center 366 (8.2)
 Discharge, and outpatient clinic follow-up 2395 (53.8)
Admitting department
 IM 3602 (80.9)
 Non-IM 850 (19.1)
Length of hospitalization, day 18.6 (15.3)
Total cost for hospitalization, USD 9714.1 (12,266.7)
Insurance coverage for hospitalization, USD 8161.4 (10,585.2)
Hospital admission
 Transfer from another hospital 264 (5.9)
 Admission through Emergency Room 2714 (61.0)
 Admission through outpatient clinic 1474 (33.1)
Annual case volume of ARDS admission
 Q1 ≤ 4 1070 (24.0)
 Q2: 5–14 907 (20.4)
 Q3: 15–28 1289 (29.0)
 Q4 ≥ 28 1186 (26.6)
Main diagnosis of ARDS 2246 (50.4)
Sepsis-associated ARDS 526 (11.8)
Diagnosis of shock during hospitalization 236 (5.3)
CCI at hospital admission for ARDS 3.3 (2.5)
 0–1 1180 (26.5)
 2–3 1536 (34.5)
 4–5 943 (21.2)
  ≥ 6 793 (17.8)
ECMO support 215 (4.8)
NMB use 1520 (34.1)
CRRT use 184 (4.1)
Duration of mechanical ventilator use, day 5.3 (8.1)
Experience of CPR during hospitalization 116 (2.6)
Year of admission for ARDS
 2010 602 (13.5)
 2011 470 (10.6)
 2012 430 (9.7)
 2013 361 (8.1)
 2014 465 (10.4)
 2015 443 (10.0)
 2016 613 (13.8)
 2017 523 (11.7)
 2018 545 (12.2)

SD, standard deviation; IM, internal medicine; ARDS, acute respiratory distress syndrome; CCI, Charlson comorbidity index; ECMO, extracorporeal membrane oxygenation; NMB, neuromuscular blockade; CPR, cardiopulmonary resuscitation

QOL among ARDS survivors

Table 2 shows the QOL before and after ARDS treatment among survivors. Among survivors, 1298 (29.2%) patients experienced decreased income, 334 patients (7.5%) lost their jobs, and 327 (7.3%) had newly acquired disabilities. Among the newly acquired disabilities, 66 (1.5%) had newly acquired respiratory disabilities. In addition, the mild to moderate and severe disability groups increased to 86 (1.9%) and 221 (4.9%), respectively, after ARDS treatment. Eventually, total QOL worsened in 1667 (37.4%) ARDS survivors 1 year after their ARDS diagnosis. Table 3 shows the results of the multivariable logistic regression model for QOL worsening among ARDS survivors. Younger age (OR: 0.99, 95% CI 0.99–0.99; P < 0.001), male sex (vs. female; OR: 1.17, 95% CI 1.03–1.32; P = 0.018), and total cost of hospitalization (1000 USD increase; OR, 1.01, 95% CI 1.01–1.02; P = 0.022) were associated with worsening QOL. In addition, survivors who were transferred to other long-term facility centers (OR: 0.74, 95% CI 0.70–0.91; P = 0.017) or discharged and with follow-ups in outpatient clinics (OR: 0.80, 95% CI 0.70–0.91; P = 0.001) were associated with a lower incidence of worsening QOL. Table 4 shows the QOL worsening according to age, the CCI, the number of days of total mechanical ventilatory support, duration of hospitalization, use of ECMO support, sepsis-associated ARDS, and experience of CPR among ARDS survivors. Of the ARDS survivors, 43% (945/2,200) of age < 66-year-old group experienced QOL worsening, while 32.1% of age ≥ 66-year-old experienced QOL worsening among ARDS survivors. Table S3 also shows the QOL before and after ARDS treatment among hospital survivors who were discharged alive after hospitalization for ARDS treatment. Of the survivors, 1310 (14.5%) experienced decreased income, 287 (3.2%) lost their job, and 178 (2.0%) newly acquired a disability. Thus, the QOL worsened in 1608 (17.8%) ARDS survivors. However, QOL of 3621 survivors (40.2%) had not been evaluated after discharge because data could not be obtained regarding their income level, job, or disability due to death within a year after being diagnosed with ARDS.

Table 2.

QOL before and after ARDS treatment

Variable Before ARDS After ARDS
Presence of joba 2239 (49.7) 2294 (51.5)
Annual income levelb
 Q1 (lowest) 1321 (29.7) 1380 (31.0)
 Q2 755 (17.0) 682 (15.3)
 Q3 903 (20.3) 882 (19.8)
 Q4 (highest) 1380 (31.0) 1354 (30.4)
 Unknown 93 (2.1) 154 (3.5)
Disabilityc
 Mild to moderate 454 (10.2) 540 (12.1)
 Severe 568 (12.8) 789 (17.7)
Disability type
 Physical disability 402 (9.0) 435 (9.8)
 Brain lesion disability 210 (4.7) 346 (7.8)
 Visual disturbance 82 (1.8) 92 (2.1)
 Hearing disability 98 (2.2) 114 (2.6)
 Speech disability 3 (0.1) 5 (0.1)
 Intellectual disorder 55 (1.2) 60 (1.3)
 Autism 1 (0.0) 1 (0.0)
 Mental disorder 38 (0.9) 37 (0.8)
 Renal disorder 59 (1.3) 99 (2.2)
 Heart disorder 5 (0.1) 9 (0.2)
 Respiratory disability 51 (1.1) 117 (2.6)
 Hepatopathy 3 (0.1) 4 (0.1)
 Facial disfigurement 0 (0.0) 0 (0.0)
 Intestinal and urinary fistulae 9 (0.2) 12 (0.3)
 Epilepsy 6 (0.1) 6 (0.1)

1298 (29.2%) experienced decreased income, 334 (7.5%) lost job, and 327 (7.3%) had newly acquired disability. 66 (1.5%) have newly acquired respiratory disability

Total QOL worsening occurred in 1667 (37.4%) among ARDS survivors

QOL, quality of life; ARDS, acute respiratory distress syndrome

Table 3.

Multivariable logistic regression model for QOL worsening among ARDS survivors

Variable OR (95% CI) P value
Age, year 0.99 (0.99, 0.99)  < 0.001
Sex, male 1.17 (1.03, 1.32) 0.018
Admitting department: IM (vs non-IM) 0.91 (0.78, 1.07) 0.261
Total cost for hospitalization, USD, per 1000 USD 1.01 (1.01, 1.02) 0.022
Hospital admission
 Transfer from another hospital 1
 Admission through Emergency Room 1.00 (0.77, 1.31) 0.984
 Admission through outpatient clinic 0.90 (0.68, 1.18) 0.434
Annual case volume of ARDS admission
 Q2: 5–14 (vs Q1 ≤ 4) 1.04 (0.85, 1.26) 0.728
 Q3: 15–28 (vs Q1 ≤ 4) 0.95 (0.79, 1.14) 0.579
 Q4 ≥ 28 (vs Q1 ≤ 4) 1.11 (0.91, 1.34) 0.296
Treatment result
 Discharge, and follow-up in same hospital 1
 Transfer to other long-term facility center 0.74 (0.58, 0.95) 0.017
 Discharge, and outpatient clinic follow-up 0.80 (0.70, 0.91) 0.001
Main diagnosis of ARDS (vs secondary diagnosis of ARDS) 0.92 (0.81, 1.04) 0.184
Sepsis-associated ARDS 1.03 (0.85, 1.26) 0.742
Diagnosis of shock during hospitalization 0.79 (0.60, 1.05) 0.110
CCI at hospital admission for ARDS treatment
 2–3 (vs 0–1) 0.94 (0.80, 1.11) 0.466
 4–5 (vs 0–1) 0.92 (0.76, 1.10) 0.355
  ≥ 6 (vs 0–1) 1.12 (0.92, 1.36) 0.249
ECMO support 0.89 (0.63, 1.24) 0.473
NMBA use 0.98 (0.84, 1.15) 0.815
CRRT use 1.13 (0.81, 1.57) 0.469
Duration of mechanical ventilator use, day 1.00 (0.99, 1.01) 0.428
Experience of CPR during hospitalization 1.05 (0.71, 1.54) 0.817
Year of admission for ARDS
 2011 (vs 2010) 1.00 (0.77, 1.30) 0.998
 2012 (vs 2010) 1.34 (1.03, 1.74) 0.027
 2013 (vs 2010) 1.06 (0.80, 1.40) 0.706
 2014 (vs 2010) 1.04 (0.81, 1.36) 0.744
 2015 (vs 2010) 1.20 (0.93, 1.56) 0.165
 2016 (vs 2010) 1.20 (0.94, 1.53) 0.139
 2017 (vs 2010) 1.08 (0.84, 1.39) 0.546
 2018 (vs 2010) 1.46 (1.13, 1.87) 0.003

Hosmer Lemeshow test, Chi-square: 4.54, df = 8, P = 0.806

QOL, quality of life; OR, Odds ratio; CI, confidence interval; ARDS, acute respiratory distress syndrome; IM, internal medicine; CCI, Charlson comorbidity index; ECMO, extracorporeal membrane oxygenation; NMB, neuromuscular blockade; CPR, cardiopulmonary resuscitation

Table 4.

QOL worsening according to age, CCI, day of total mechanical ventilatory support, duration of hospitalization, use of ECMO support, sepsis-associated ARDS, and experience of CPR among ARDS survivors

Subgroups QOL worsening after ARDS treatment n (%)
Age
 Age ≥ 66-year-old 722 of 2252 (32.1)
 Age < 66-year-old 945 of 2200 (43.0)
CCI at ARDS
  > 3 points 652 of 1736 (37.6)
  ≤ 3 points 1015 of 2716 (37.4)
Day of total mechanical ventilator support
  ≥ 2 days 662 of 1682 (39.4)
  < 2 days 1005 of 2770 (36.3)
Duration of hospitalization at ARDS treatment
  ≥ 15 days 908 of 2367 (38.4)
  < 15 days 759 of 2085 (36.4)
Use of ECMO support
 ECMO support 101 of 215 (47.0)
 No ECMO support 1566 of 4237 (37.0)
Sepsis
 Sepsis-associated ARDS 1566 of 4237 (37.0)
 Non-sepsis-associated ARDS 1456 of 3926 (37.1)
CPR
 Experience of CPR 52 of 116 (44.8)
 No experience of CPR 1615 of 4336 (37.2)

QOL, quality of life; CCI, Charlson comorbidity index; ARDS, acute respiratory distress syndrome; ECMO, extracorporeal membrane oxygenation; CPR, cardiopulmonary resuscitation

Survival analysis

Table 5 shows the results of the multivariable Cox regression model for 2-year all-cause mortality after the diagnosis of ARDS. In model 1, worsening of QOL was not associated with 2-year all-cause mortality among survivors (HR: 1.10, 95% CI 0.92–1.78; P = 0.140). All HRs with 95% CIs of the covariates in Model 1 are presented in Table S4. In model 2, newly acquired disability was associated with 1.74-fold (HR: 1.74, 95% CI 1.31–2.33; P < 0.001) higher 2-year all-cause mortality, but decreased income (P = 0.571) and unemployment (P = 0.952) were not.

Table 5.

Multivariable Cox regression model for 2-year mortality after diagnosis of ARDS

Variable HR (95% CI) P value
QOL worsening (model 1) 1.10 (0.92, 1.78) 0.140
QOL worsening in detail (model 2)
 Decreased income 0.95 (0.78, 1.15) 0.571
 Loss of job 1.01 (0.71, 1.43) 0.952
 Newly acquired disability 1.74 (1.31, 2.33)  < 0.001
QOL worsening in detail (model 3)
 Decreased income 0.94 (0.75, 1.10) 0.482
 Loss of job 1.00 (0.70, 1.43) 0.948
 Newly acquired respiratory disability 3.15 (1.89, 5.24)  < 0.001

ARDS, acute respiratory distress syndrome; HR, hazard ratio; CI, confidence interval; QOL, quality of life

In model 3, newly acquired respiratory disability was associated with a 3.15-fold higher 2-year all-cause mortality (HR: 3.15, 95% CI 1.89–5.24; P < 0.001). Table S5 shows the results of multivariable Cox regression models for 2-year respiratory and other mortality rates after ARDS diagnosis among survivors. The newly acquired disability was not associated with 2-year respiratory mortality (P = 0.163), but newly acquired respiratory disability was associated with a 6.61-fold higher risk of 2-year respiratory mortality (HR: 6.61, 95% CI 3.14–13.90; P < 0.001). In addition, newly acquired disability and respiratory disability were associated with 1.80-fold (HR: 1.80, 95% CI 1.30–2.49; P < 0.001) and 2.09-fold (HR: 2.09, 95% CI 1.03–4.26; P = 0.042) higher risk of 2-year mortality, respectively. Figures S1 and S2 show the survival plots that were derived from the multivariable Cox regression model for 2-year all-cause mortality among ARDS survivors (Fig. S1: newly acquired disability group vs. others; Fig. S2: newly acquired respiratory disability group vs. others).

Discussion

In this population-based cohort study, we showed that almost one-third (37.4%) of ARDS survivors experienced worsening QOL at the 1-year follow-up period after diagnosis of ARDS. Among the QOL factors, acquired disability was an independent risk factor for poorer 2-year survival, while unemployment and decreased household income level were not significantly associated poorer 2-year survival. Interestingly, newly acquired respiratory disability was a more significant risk factor for poorer 2-year all-cause and respiratory mortality.

The newly acquired disability means that ARDS survivors had a persistent and functional disability in daily life due to ARDS after hospital discharge, as reported in a previous study [11]. We recently reported that newly acquired disability was a significant risk factor for poorer survival among survivors of sepsis [19] or ECMO therapy [20]. In addition to the previous reports [19, 20], our current results suggest that the newly acquired disability showed severe comorbid status and poor recovery from ARDS after hospital discharge. According to a study by Herridge et al., decreased QOL due to physical sequelae is a hallmark legacy in ARDS survivors [11]. We also showed that the decreased QOL due to newly acquired disability might worsen the long-term survival outcomes among ARDS survivors.

Interestingly, newly acquired respiratory disability was a significant risk factor for poorer 2-year all-cause and respiratory mortality. A pulmonologist in South Korea determined most respiratory disabilities, and we examined the criteria for determining respiratory disability (Table S1). According to the criteria, we can identify that the survivors with acquired disability suffered from severe restrictive patterns of respiratory disease with hypoxemia. Considering that chronic respiratory disease-related death is a substantial issue in Asian countries [21], the severe pattern of chronic respiratory diseases such as respiratory disability might affect poorer survival outcomes among South Korean ARDS survivors. In addition, we recently reported that newly developed chronic respiratory diseases were associated with higher 5-year mortality among survivors of ECMO therapy due to respiratory failure or ARDS [22]; thus, ARDS survivors who have a new respiratory disability might also be a high-risk group that needs special attention during healthcare utilization.

Regarding income level and unemployment, we found no significant association between these factors and mortality in this study. These results echo the associations between household income level and unemployment previously observed in survivors of sepsis and ECMO in South Korea [19, 20]. In South Korea, all individuals pay a fixed rate for health insurance premiums based on their income, with approximately 67% of their medical expenses being subsidized by the government [23]. However, those who cannot afford insurance premiums or have difficulty financially supporting themselves are included in the Medical Aid Program. In this program, the government covers almost all medical expenses to reduce the financial burden of medical costs [24]. Therefore, mortality was not influenced by unemployment or decreased household income levels among ARDS survivors in South Korea.

In the subgroup analysis, this study revealed that worsening QOL was more evident among ARDS survivors in the < 66-year-old age group, ≥ 2 days of total mechanical ventilator support group, and ≥ 15 days of hospitalization of the ARDS treatment group, ECMO support group, and survivors who experienced CPR during hospitalization. Joblessness and lost earnings were significantly reported among ARDS survivors in the United States [12]. As people younger than 66 years might enjoy higher levels of employment and household income than those older than 66 years, the deterioration of QOL might occur more frequently in relatively younger ARDS survivors. Recently, prolonged duration of invasive mechanical ventilation was associated with worsening QOL among Coronavirus disease-related ARDS survivors in Italy [25]. Although the prolonged duration of mechanical ventilatory support was not associated with the prevalence of worsening QOL in multivariable model (Table 3), it was observed that QOL worsened in the ≥ 2 days of total mechanical ventilator support group and ≥ 15 days of hospitalization in the ARDS treatment group of this study. Therefore, the impact of these factors on worsening QOL among ARDS survivors should be confirmed in future study.

This study has several limitations. First, there were some variables we could not include because the NHIS database does not record d them, such as body mass index, PaO2/FiO2 ratio, and Acute Physiologic Assessment and Chronic Health Evaluation II scores at admission for ARDS treatment. Second, we used registered ICD-10 codes for calculating CCI in this study, but the codes might differ from the actual underlying diseases. For example, some patients with mild liver disease could not be diagnosed using ICD-10 codes due to their lack of access to healthcare resources. Third, some treatment options, such as prone positioning, were not included in this study because they do not have prescription codes in South Korea [26]. Fourth, we did not assess the severity of ARDS; thus, the survival analysis in this study should be carefully interpreted. Lastly, the generalizability of our findings might be limited because the public health insurance system in South Korea cannot be applied to other countries.

In conclusion, at the 1-year follow-up, one-third of ARDS survivors in South Korea experienced worsening QOL. Specifically, newly acquired disability and respiratory disability were associated with a higher risk of 2-year all-cause and respiratory mortality among ARDS survivors. Our results suggest that worsening of QOL is a serious concern and public health issue among ARDS survivors, and QOL might negatively affect long-term survival.

Supplementary Information

Below is the link to the electronic supplementary material.

540_2022_3036_MOESM1_ESM.docx (13.6KB, docx)

Supplementary file1: Table S1. Criteria for decision for respiratory disability grading in South Korea (docx 14 KB).

540_2022_3036_MOESM2_ESM.docx (16.3KB, docx)

Supplementary file2: Table S2. The ICD-10 codes used by comorbidity to compute the Charlson Comorbidity Index (docx 17kB).

540_2022_3036_MOESM3_ESM.docx (16.3KB, docx)

Supplementary file3: Table S3. QOL before and after ARDS treatment among hospital survivors (docx 17 KB).

540_2022_3036_MOESM4_ESM.docx (17.2KB, docx)

Supplementary file4: Table S4. Table S4. All HRs with 95% CIs of the covariates in Model 1 (docx 18 KB).

540_2022_3036_MOESM5_ESM.docx (15.3KB, docx)

Supplementary file5: Table S5. Multivariable Cox regression models for 2-year respiratory and other mortality rates after ARDS diagnosis among survivors (docx 16 KB).

540_2022_3036_MOESM6_ESM.tif (1.4MB, tif)

Supplementary file6: Fig. S1. Survival plot that derived from multivariable Cox regression model for 2-year all-cause mortality among ARDS survivors (Newly acquired disability group vs others) (TIF 1461 KB).

540_2022_3036_MOESM7_ESM.tif (1.5MB, tif)

Supplementary file7: Fig. S2. Survival plot that derived from multivariable Cox regression model for 2-year all-cause mortality among ARDS survivors (Newly acquired respiratory disability group vs others) (TIF 1556 KB).

Acknowledgements

None.

Author contributions

TKO designed the study, analyzed, and interpreted the data, and drafted the manuscript; IAS and HRC contributed to the study conceptualization, acquisition of data, and review of the manuscript. All the authors have provided approval for the final version of the manuscript.

Funding

None.

Declarations

Conflict of interests

The authors have no conflicts of interest.

Footnotes

Publisher's Note

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

Hey-ran Choi and In-Ae Song have equal contribution as the co-first authors.

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Associated Data

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

Supplementary Materials

540_2022_3036_MOESM1_ESM.docx (13.6KB, docx)

Supplementary file1: Table S1. Criteria for decision for respiratory disability grading in South Korea (docx 14 KB).

540_2022_3036_MOESM2_ESM.docx (16.3KB, docx)

Supplementary file2: Table S2. The ICD-10 codes used by comorbidity to compute the Charlson Comorbidity Index (docx 17kB).

540_2022_3036_MOESM3_ESM.docx (16.3KB, docx)

Supplementary file3: Table S3. QOL before and after ARDS treatment among hospital survivors (docx 17 KB).

540_2022_3036_MOESM4_ESM.docx (17.2KB, docx)

Supplementary file4: Table S4. Table S4. All HRs with 95% CIs of the covariates in Model 1 (docx 18 KB).

540_2022_3036_MOESM5_ESM.docx (15.3KB, docx)

Supplementary file5: Table S5. Multivariable Cox regression models for 2-year respiratory and other mortality rates after ARDS diagnosis among survivors (docx 16 KB).

540_2022_3036_MOESM6_ESM.tif (1.4MB, tif)

Supplementary file6: Fig. S1. Survival plot that derived from multivariable Cox regression model for 2-year all-cause mortality among ARDS survivors (Newly acquired disability group vs others) (TIF 1461 KB).

540_2022_3036_MOESM7_ESM.tif (1.5MB, tif)

Supplementary file7: Fig. S2. Survival plot that derived from multivariable Cox regression model for 2-year all-cause mortality among ARDS survivors (Newly acquired respiratory disability group vs others) (TIF 1556 KB).


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