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Characteristics and outcomes of frail patients with suspected infection in intensive care units: a descriptive analysis from a multicenter cohort study
BMC Geriatrics volume 20, Article number: 485 (2020)
Abstract
Background
Frailty is associated with morbidity and mortality in patients admitted to intensive care units (ICUs). However, the characteristics of frail patients with suspected infection remain unclear. We aimed to investigate the characteristics and outcomes of frail patients with suspected infection in ICUs.
Methods
This is a secondary analysis of a multicenter cohort study, including 22 ICUs in Japan. Adult patients (aged ≥16 years) with newly suspected infection from December 2017 to May 2018 were included. We compared baseline patient characteristics and outcomes among three frailty groups based on the Clinical Frailty Scale (CFS) score: fit (score, 1–3), vulnerable (score, 4), and frail (score, 5–9). We conducted subgroup analysis of patients with sepsis defined as per Sepsis-3 criteria. We also produced Kaplan–Meier survival curves for 90-day survival.
Results
We enrolled 650 patients with suspected infection, including 599 (92.2%) patients with sepsis. Patients with a median CFS score of 3 (interquartile range [IQR] 3–5) were included: 337 (51.8%) were fit, 109 (16.8%) were vulnerable, and 204 (31.4%) were frail. The median patient age was 72 years (IQR 60–81). The Sequential Organ Failure Assessment scores for fit, vulnerable, and frail patients were 7 (IQR 4–10), 8 (IQR 5–11), and 7 (IQR 5–10), respectively (p = 0.59). The median body temperatures of fit, vulnerable, and frail patients were 37.5 °C (IQR 36.5 °C–38.5 °C), 37.5 °C (IQR 36.4 °C–38.6 °C), and 37.0 °C (IQR 36.3 °C–38.1 °C), respectively (p < 0.01). The median C-reactive protein levels of fit, vulnerable, and frail patients were 13.6 (IQR 4.6–24.5), 12.1 (IQR 3.9–24.9), 10.5 (IQR 3.0–21.0) mg/dL, respectively (p < 0.01). In-hospital mortality did not statistically differ among the patients according to frailty (p = 0.19). Kaplan–Meier survival curves showed little difference in the mortality rate during short-term follow-up. However, more vulnerable and frail patients died after 30-day than fit patients; this difference was not statistically significant (p = 0.25). Compared with the fit and vulnerable groups, the rate of home discharge was lower in the frail group.
Conclusion
Frail and vulnerable patients with suspected infection tend to have poor disease outcomes. However, they did not show a statistically significant increase in the 90-day mortality risk.
Background
Frailty is a clinical status and a multidimensional syndrome characterized by the loss of physiologic and cognitive reserves [1, 2]. There are two major approaches to its measurement: the phenotypic frailty model and the frailty index of deficit accumulation [3]. The phenotypic frailty model focuses predominantly on physical symptoms, such as weight loss, exhaustion, weakness, slowness, and reduced physical activity. The frailty index of deficit accumulation focuses on comorbidities, illness, laboratory abnormalities, and functional impairments. Although majority of frailty assessment tools fall into either approach [4, 5], agreement between these tools has been shown to greatly vary [6, 7]. Clinical Frailty Scale (CFS) [1] has been developed as a simple screening tool to assess frailty and has been validated in critical care settings [8, 9].
There is a growing interest in the impact of frailty on patients with critical illness due in part to the increased risk of morbidity and mortality in patients with critical illnesses in intensive care units (ICUs) [8]. Infection in critically ill older adult patients have unique features compared with young patients, wherein the older adults have higher susceptibility to infection [10, 11] and exhibit atypical signs of infection [12, 13]. Moreover, indications for ICU admission of older adult patients remain controversial [14]. However, most previous studies have described the clinical features of frailty in the older adult [15,16,17] or patients with heterogeneous diseases in ICUs [18,19,20,21]. The specific clinical characteristics of frail patients with suspected infection, including sepsis, which is one of the major causes of admission to ICUs, are unknown [22].
Therefore, we aimed to investigate the association between frailty and patient characteristics, clinical features, and outcomes among adult patients with suspected infection in ICUs.
Methods
Design and participants
This is a secondary analysis of data from the Japanese Association for Acute Medicine (JAAM) Sepsis Prognostication in Intensive Care Unit and Emergency Room (SPICE) study, a multicenter study of patients with sepsis. The JAAM SPICE study was composed of a SPICE emergency room cohort and a SPICE ICU cohort. We used the SPICE ICU cohort. The SPICE ICU cohort included adult patients (aged ≥16 years) admitted to a participating ICU with a suspected infection. We excluded patients who had missing data on frailty.
Data collection
Data were collected by the SPICU ICU investigators as part of the routine clinical workup. Data collection methods have been described in a previous study [23]; the investigators entered data into an online standardized template. Patient information included demographic characteristics, admission source, comorbidities, frailty, sites of infection, sepsis-related severity scores including the Sequential Organ Failure Assessment (SOFA) score and the Acute Physiology and Chronic Health Evaluation II score, and laboratory data. In addition, we collected data regarding in-hospital mortality, place after discharge, ventilator-free days (VFDs), ICU-free days (IFDs), and length of hospital stay (LOS).
Definitions
Suspected infection was defined as the administration of antibiotics and the sampling of any bacterial culture or imaging test undertaken for the purpose of investigating the source of infection. Sepsis and septic shock were defined on the basis of Sepsis-3 criteria [24]. Frailty was evaluated using CFS scores [1]. The CFS score is a 9-point assessment tool used to quantify frailty. Clinicians determined patients’ CFS scores by interviewing them or their surrogates and reviewing their medical records upon admission to the hospital. No training on the use of the CFS score was provided as the score was deemed to be easily understandable by clinicians. Moreover, VFDs were defined as the number of days within the first 28 days after enrollment during which a patient was able to breathe without a ventilator. Patients who died during the study period were assigned a VFD score of 0. IFDs were calculated in a similar manner to the VFDs.
Analysis
We compared baseline patient characteristics and outcomes, including in-hospital, 30-day, and 90-day mortality, among the three frailty groups based on the CFS score, i.e., fit (score 1–3), vulnerable (score 4), and frail (score 5–9), and evaluated the findings in light of previous reports [15, 25]. The 90-day survival as an outcome was chosen to evaluate differences in survival rates among the groups based on previous studies reporting that frailty might affect long-term survival [18, 21]. Continuous variables were summarized using the median and interquartile range (IQR) and compared using the Kruskal-Wallis test. Categorical variables were summarized using numbers and percentages and compared using the chi-squared test or Fisher exact test, where appropriate. Kaplan–Meier survival curves for 90-day survival were produced and compared using a log-rank test. We conducted a Cox proportional hazards regression analysis to assess the impact of frailty on 90-day survival. Adjusted variables in the analysis included age, sex, the Charlson comorbidity index, and the SOFA score, which were selected on the basis of clinical relevance and previous reports [15, 18]. We tested for interactions between frailty and age, frailty and the Charlson comorbidity index, and age and the Charlson comorbidity index. We also conducted a subgroup analysis of patients diagnosed with sepsis based on Sepsis-3 criteria. A p-value of < 0.05 was considered to indicate statistical significance. All statistical analyses were performed with EZR (version 1.38; Saitama Medical Center, Jichi Medical University, Saitama, Japan), a graphical user interface for R (version 3.5.0; The R Foundation for Statistical Computing, Vienna, Austria) [26]. EZR is a modified version of the R commander designed to apply statistical functions that are frequently used in biostatistics.
Results
We enrolled 650/652 patients with suspected infection from the SPICE ICU database, after excluding 2 patients who had missing data on frailty. The median age of the patients was 72 years (IQR 60–81), and 369 (56.8%) were men. The median CFS score was 3 (IQR 3–5). There were 337 (51.8%) fit patients, 109 (16.8%) vulnerable patients, and 204 (31.4%) frail patients (Table 1 and Fig. 1). The age of patients increased with increasing frailty: fit 67 years (IQR 54–78); vulnerable 73 years (IQR 64–81); and frail 77 years (IQR 69–84), p < 0.01. Comorbidities including congestive heart failure, cerebrovascular diseases, dementia, and chronic obstructive pulmonary disease (COPD) were more common in vulnerable and frail patients than in fit patients (p < 0.01). The SOFA scores of fit, vulnerable, and frail patients were 7 (IQR 4–10), 8 (IQR 5–11), and 7 (IQR 5–10), respectively (p = 0.59). The patients’ median body temperatures were as follows: fit 37.5 °C (IQR 36.5 °C–38.5 °C); vulnerable 37.5 °C (IQR 36.4 °C–38.6 °C); and frail 37.0 °C (IQR 36.3 °C–38.1 °C), p < 0.01. C-reactive protein levels in fit, vulnerable, and frail patients were 13.6 (IQR 4.6–24.5) mg/dL, 12.1 (IQR 3.9–24.9) mg/dL, 10.5 (IQR 3.0–21.0) mg/dL, respectively (p = 0.04).
Table 2 shows the outcomes among fit, vulnerable, and frail patients. There was no statistically significant difference in in-hospital mortality between the three frailty groups: fit 55/335 (16.4%); vulnerable 23/107 (21.5%); and frail 45/203 (22.2%), p = 0.19. Likewise, frailty was not associated with 30-day or 90-day mortality. There were no significant differences in IFDs, VFDs, or LOS between the three frailty groups. Frailty was associated with disposition after discharge (discharge to home: fit 125/280 [44.6%]; vulnerable 36/84 [42.9%]; and frail 40/158 [25.3%], p < 0.01).
Figure 2 shows the Kaplan–Meier survival curves stratified by the three groups. There was little difference in in-hospital mortality between the groups during 30-day. However, more vulnerable and frail patients died after 30-day phase than did fit patients, although this difference was not statistically significant (p = 0.25). Cox proportional hazards regression analysis did not demonstrate an association between in-hospital mortality and frailty (vulnerable vs. fit: adjusted hazard ratio 1.16 [95% confidential interval, 0.70–1.92], p = 0.57, frail vs. fit: adjusted hazard ratio 1.13 [95% confidential interval 0.75–1.72], p = 0.56), and there were no interactions between frailty and age, frailty and the Charlson comorbidity index, and age and the Charlson comorbidity index (Table 3).
Among patients with suspected infection, 599 (92.2%) patients were diagnosed with sepsis. The subgroup analysis of patients with sepsis gave similar results to the primary analysis (Tables 4 and 5). Similarly, there was no association between in-hospital mortality and frailty in patients with sepsis (vulnerable vs. fit: adjusted hazard ratio 1.22 [95% confidential interval, 0.73–2.04], p = 0.45, frail vs. fit: adjusted hazard ratio 1.26 [95% confidential interval 0.82–1.93], p = 0.29; Table 6).
Discussion
We investigated the association between frailty and clinical characteristics and outcomes among patients with suspected infection in ICUs. One strength of the present study is the focus on older adult patients with suspected infection in Japan, one of the leading aging countries. The results of our study provide insights for use by societies with impending aging populations. Approximately one-third of the patients were classified as frail according to the CFS score. Frail patients were more likely to be older and had more comorbidities; they were also less likely to be discharged home and had lower temperature and C-reactive protein levels. Vulnerable and frail patients appeared to have poor 30-day outcomes compared with fit patients, although they did not appear to have a statistically significant increased 90-day mortality risk.
As many previous studies have reported, our study showed an increase in frailty with aging. The proportion of older adult patients in our study was higher than that in previous studies regarding frailty; the median age of patients in our study was 72 years; in other studies, the median age was 62 [18] and 64 years [19]. The presence of higher proportion of older adult patients in our study could be because Japan has one of the world’s oldest populations [27]. Another explanation may be that our cohort included a large proportion of patients with sepsis [28]. Regarding the prevalence of frailty, our finding was comparable to previous studies [18, 21, 29] that included ICU populations. The prevalence of frailty varies widely across studies based on patient age [19, 20, 25]. Studies that include a large number of very old patients have a higher prevalence of frailty [15]. The diversity in study population, setting, and study design may have contributed to the different characteristics of frail populations.
We confirmed that frail and vulnerable patients had more comorbidities compared with fit patients. Comorbidities included congestive heart failure, cerebrovascular diseases, and COPD as well as those described in previous studies [30, 31]. Our results were very similar to previous reports that included heterogeneous diseases, although we selected patients with suspected infection only. There exists a controversy regarding the relationship between individual comorbidities and frailty [32]. The combination of individual comorbidities and frailty may not be related to the primary disease, although it is natural that more comorbidities lead to greater frailty.
Our findings with regard to body temperature and C-reactive protein levels suggest that frailty may be associated with a poor acute inflammatory response. The older adults often have an absent or diminished febrile response to infections [13]. Some studies have reported that frailty was associated with chronic changes in the immune response, including the imbalance of decline in immune function and increased inflammation [33, 34]. Other studies have reported that aging was related to changes in the acute immune response [13, 35], due to dysfunction of immune cells or decreased cytokines working as part of innate and adaptive immunity [35]. Both frailty and aging may be involved in weakening of the acute inflammatory response. However, a blunted response was not observed in white blood cell or platelet count in frail patients. Differences in pathophysiological mechanisms and kinetics might have contributed to the differences observed in white blood cell count and C-reactive protein level changes [36]. Further studies are needed to clarify the relationship between frailty, aging, and poor inflammatory responses.
Regarding mortality, we found that more vulnerable and frail patients died after 30-day, although this difference was not statistically significant. This tendency was consistent with some previous reports [1, 18]. In 30-day, disease severity may have had a greater impact on mortality than frailty. We did not observe the patients’ status after discharge, and frail patients who transferred to other institutions might have subsequently died. However, the short-term outcomes in our study were not in agreement with those reported by Fernando et al. [29] Several differences between the studies might explain this discordance. First, the overall mortality was higher (37.0%) and the median hospital stay was shorter (13 days in frail patients and 9 days in non-frail patients) in the study by Fernando et al., indicating that our study included patients with less severe clinical conditions. In addition, differences in the follow-up period might have affected the results. We did not follow patient outcomes after discharge, even those who were discharged to another facility in the early phase. Last observation carry-forward might have contributed to better outcomes. Moreover, the Japanese universal health care system might have contributed to lower mortality in frail patients [37]. Death with dignity for benign diseases has not yet been well understood in Japan. Frail patients tend to be treated at a lower cost if they are admitted to tertiary centers rather than chronic care hospitals, regardless of their quality of life after treatment. Alternatively, the relationship between the severity of frailty and mortality may not have been linear among patients with sepsis. Mortality from septic shock is very high [22]. Vulnerable and frail patients may have already been at risk of death. Further studies are needed to assess the association between the severity of frailty and mortality in patients with sepsis.
Limitations
This study had some limitations. First, fewer patients had CFS scores of 5 in our study compared with those in previous studies [15, 18, 21]. In addition, analysis for data reliability was not performed. Moreover, mild dementia is generally observed in patients with a CFS score of 5 according to the original study. However, 3.6% of fit patients had dementia according to the Charlson comorbidity index, and the possibility of misclassification remains. However, in the study that introduced CFS [1], 3.7% of patients with a CFS score of 1 had dementia, similar to that observed in our study. The CFS score is not widely used to assess frailty in Japan. Education in the use of the CFS score may have been necessary although CFS has been found to be a reliable tool even if the assessor is different [38]. Second, we did not have information about treatments that may have been related to the patients’ outcomes in this database. However, most patients should have received appropriate treatments according to guidelines such as the Surviving Sepsis Campaign Guideline, which is used in national certified ICUs [39]. Third, we did not have information on delirium. Because of the high association between frailty and delirium, this unreported factor might have introduced bias to a higher degree in this population.
Conclusions
Among patients admitted to ICUs with suspected infection, frail patients were more likely to be older and have more comorbidities; frail patients were also less likely to be discharged home and had lower temperature and C-reactive protein levels. However, frail patients did not have a statistically significant increased 90-day mortality risk.
Availability of data and materials
The datasets analyzed during the current study is available with the corresponding author on reasonable request.
Abbreviations
- CFS:
-
Clinical frailty scale
- COPD:
-
Chronic obstructive pulmonary disease
- ICUs:
-
Intensive care units
- IFDs:
-
ICU-free days
- IQR:
-
Interquartile range
- JAAM:
-
Japanese Association for Acute Medicine
- LOS:
-
Length of hospital stay
- SOFA:
-
Sequential organ failure assessment
- SPICE:
-
Sepsis Prognostication in Intensive Care Unit and Emergency Room
- VFDs:
-
Ventilator-free days
References
Rockwood K, Song X, MacKnight C, Bergman H, Hogan DB, McDowell I, et al. A global clinical measure of fitness and frailty in elderly people. CMAJ. 2005;173:489–95.
Clegg A, Young J, Iliffe S, Rikkert MO, Rockwood K. Frailty in elderly people. Lancet. 2013;381:752–62.
Walston JD, Bandeen-Roche K. Frailty: a tale of two concepts. BMC Med. 2015;13:185.
Walston J, Buta B, Xue QL. Frailty screening and interventions: considerations for clinical practice. Clin Geriatr Med. 2018;34:25–38.
Buckinx F, Rolland Y, Reginster JY, Ricour C, Petermans J, Bruyere O. Burden of frailty in the elderly population: perspectives for a public health challenge. Arch Public Health. 2015;73:19.
Aguayo GA, Donneau AF, Vaillant MT, Schritz A, Franco OH, Stranges S, et al. Agreement between 35 published frailty scores in the general population. Am J Epidemiol. 2017;186:420–34.
Pritchard JM, Kennedy CC, Karampatos S, Ioannidis G, Misiaszek B, Marr S, et al. Measuring frailty in clinical practice: a comparison of physical frailty assessment methods in a geriatric out-patient clinic. BMC Geriatr. 2017;17:264.
Muscedere J, Waters B, Varambally A, Bagshaw SM, Boyd JG, Maslove D, et al. The impact of frailty on intensive care unit outcomes: a systematic review and meta-analysis. Intensive Care Med. 2017;43:1105–22.
McDermid RC, Stelfox HT, Bagshaw SM. Frailty in the critically ill: a novel concept. Crit Care. 2011;15:301.
Kotfis K, Wittebole X, Jaschinski U, Solé-Violán J, Kashyap R, Leone M, et al. A worldwide perspective of sepsis epidemiology and survival according to age: observational data from the ICON audit. J Crit Care. 2019;51:122–32.
Martin GS, Mannino DM, Moss M. The effect of age on the development and outcome of adult sepsis. Crit Care Med. 2006;34:15–21.
Wester AL, Dunlop O, Melby KK, Dahle UR, Wyller TB. Age-related differences in symptoms, diagnosis and prognosis of bacteremia. BMC Infect Dis. 2013;13:346.
Norman DC. Clinical features of infection in older adults. Clin Geriatr Med. 2016;32:433–41.
Guidet B, Leblanc G, Simon T, Woimant M, Quenot JP, Ganansia O, et al. Effect of systematic intensive care unit triage on long-term mortality among critically ill elderly patients in France: a randomized clinical trial. JAMA. 2017;318:1450–9.
Flaatten H, De Lange DW, Morandi A, Andersen FH, Artigas A, Bertolini G, et al. The impact of frailty on ICU and 30-day mortality and the level of care in very elderly patients (>/= 80 years). Intensive Care Med. 2017;43:1820–8.
Silva-Obregon JA, Quintana-Diaz M, Saboya-Sanchez S, Marian-Crespo C, Romera-Ortega MÁ, Chamorro-Jambrina C, et al. Frailty as a predictor of short- and long-term mortality in critically ill older medical patients. J Crit Care. 2020;55:79–85.
Heyland DK, Garland A, Bagshaw SM, Cook D, Rockwood K, Stelfox HT, et al. Recovery after critical illness in patients aged 80 years or older: a multi-center prospective observational cohort study. Intensive Care Med. 2015;41:1911–20.
Brummel NE, Bell SP, Girard TD, Pandharipande PP, Jackson JC, Morandi A, et al. Frailty and subsequent disability and mortality among patients with critical illness. Am J Respir Crit Care Med. 2017;196:64–72.
De Geer L, Fredrikson M, Tibblin AO. Frailty predicts 30-day mortality in intensive care patients: a prospective prediction study. Eur J Anaesthesiol. 2020. https://doi.org/10.1097/EJA.0000000000001156.
Bagshaw M, Majumdar SR, Rolfson DB, Ibrahim Q, McDermid RC, Stelfox HT. A prospective multicenter cohort study of frailty in younger critically ill patients. Crit Care. 2016;20:175.
Bagshaw SM, Stelfox HT, McDermid RC, Rolfson DB, Tsuyuki RT, Baig N, et al. Association between frailty and short- and long-term outcomes among critically ill patients: a multicentre prospective cohort study. CMAJ. 2014;186:E95–102.
Vincent J-L, Marshall JC, Ñamendys-Silva SA, François B, Martin-Loeches I, Lipman J, et al. Assessment of the worldwide burden of critical illness: the intensive care over nations (ICON) audit. Lancet Respir Med. 2014;2:380–6.
Abe T, Yamakawa K, Ogura H, Kushimoto S, Saitoh D, Fujishima S, et al. Epidemiology of sepsis and septic shock in intensive care units between sepsis-2 and sepsis-3 populations: sepsis prognostication in intensive care unit and emergency room (SPICE-ICU). J Intensive Care. 2020;8:44.
Singer M, Deutschman CS, Seymour CW, Shankar-Hari M, Annane D, Bauer M, et al. The third international consensus definitions for sepsis and septic shock (Sepsis-3). JAMA. 2016;315:801–10.
Hope AA, Hsieh SJ, Petti A, Hurtado-Sbordoni M, Verghese J, Gong MN. Assessing the usefulness and validity of frailty markers in critically ill adults. Ann Am Thorac Soc. 2017;14:952–9.
Kanda Y. Investigation of the freely available easy-to-use software 'EZR' for medical statistics. Bone Marrow Transplant. 2013;48:452–8.
Chang AY, Skirbekk VF, Tyrovolas S, Kassebaum NJ, Dieleman JL. Measuring population ageing: an analysis of the global burden of disease study 2017. Lancet Public Health. 2019;4:e159–67.
Sakr Y, Jaschinski U, Wittebole X, Szakmany T, Lipman J, Ñamendys-Silva SA, et al. Sepsis in intensive care unit patients: worldwide data from the intensive care over nations audit. Open Forum Infect Dis. 2018;5:ofy313.
Fernando SM, McIsaac DI, Perry JJ, Rochwerg B, Bagshaw SM, Thavorn K, et al. Frailty and associated outcomes and resource utilization among older ICU patients with suspected infection. Crit Care Med. 2019;47:e669–76.
Hanlon P, Nicholl BI, Jani BD, Lee D, McQueenie R, Mair FS. Frailty and pre-frailty in middle-aged and older adults and its association with multimorbidity and mortality: a prospective analysis of 493 737 UK biobank participants. Lancet Public Health. 2018;3:e323–32.
Denfeld QE, Winters-Stone K, Mudd JO, Gelow JM, Kurdi S, Lee CS. The prevalence of frailty in heart failure: a systematic review and meta-analysis. Int J Cardiol. 2017;236:283–9.
Fried LP, Ferrucci L, Darer J, Williamson JD, Anderson G. Untangling the concepts of disability, frailty, and comorbidity: implications for improved targeting and care. J Gerontol A Biol Sci Med Sci. 2004;59:255–63.
Pansarasa O, Pistono C, Davin A, Bordoni M, Mimmi MC, Guaita A, et al. Altered immune system in frailty: genetics and diet may influence inflammation. Ageing Res Rev. 2019;54:100935.
Van Epps P, Oswald D, Higgins PA, Hornick TR, Aung H, Banks RE, et al. Frailty has a stronger association with inflammation than age in older veterans. Immun Ageing. 2016;13:27.
Wessels I, Jansen J, Rink L, Uciechowski P. Immunosenescence of polymorphonuclear neutrophils. ScientificWorldJournal. 2010;10:145–60.
Peltola V, Toikka P, Irjala K, Mertsola J, Ruuskanen O. Discrepancy between total white blood cell counts and serum C-reactive protein levels in febrile children. Scand J Infect Dis. 2007;39:560–5.
Kuzuya M, Masuda Y, Hirakawa Y, Iwata M, Enoki H, Hasegawa J, et al. Day care service use is associated with lower mortality in community-dwelling frail older people. J Am Geriatr Soc. 2006;54:1364–71.
Shears M, Takaoka A, Rochwerg B, Bagshaw SM, Johnstone J, Holding A, et al. Assessing frailty in the intensive care unit: a reliability and validity study. J Crit Care. 2018;45:197–203.
Abe T, Ogura H, Shiraishi A, Kushimoto S, Saitoh D, Fujishima S, et al. Characteristics, management, and in-hospital mortality among patients with severe sepsis in intensive care units in Japan: the FORECAST study. Crit Care. 2018;22:322.
Acknowledgements
We thank the JAAM SPICE Study Group for its valuable contribution to this study. We thank Enago (https://www.enago.jp) for the final English language editing. We will present this research at 33nd annual congress European society of intensive care medicine (ESICM) 2020.
Funding
This study was supported by the Japanese Association for Acute Medicine (2014–01). The funding body did not contribute to the design of the study, collection, analysis, and interpretation of data, and in writing the manuscript.
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AK conceived of and designed this study, analyzed and interpreted patient data, and was a major contributor in writing the manuscript. TA contributed to the acquisition of data, conceived of and designed this study, interpreted the data, and revised the manuscript for important intellectual content. KY contributed to the acquisition of data, interpreted the data. HO, SK, DS, and SF contributed to the acquisition of data, and revised the manuscript for important intellectual content. YO, JK, YS1, JS, YS2, NT, TT, RT, TN1, and TH contributed to the acquisition of data. HI analyzed and interpreted the data. TN2 revised the manuscript for important intellectual content. SG contributed to the acquisition of data, interpreted the data, and revised the manuscript for important intellectual content. All authors read and approved the final manuscript. YS1 corresponds to Yuichiro Sakamoto and TN1 corresponds to Taka-aki Nakada.
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The study protocol was reviewed and approved by the Research Ethics Committee of all participating institutions at the Japanese Association for Acute Medicine (JAAM) SPICE study group. Given the retrospective and anonymized nature of this study in the routine care, the Ethics Committees waived the need for informed consent from the study participants. The Institutional Review Board of Hokkaido University, a leading institution in SPICE, approved this study (approval no. 016–0386).
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Komori, A., Abe, T., Yamakawa, K. et al. Characteristics and outcomes of frail patients with suspected infection in intensive care units: a descriptive analysis from a multicenter cohort study. BMC Geriatr 20, 485 (2020). https://doi.org/10.1186/s12877-020-01893-1
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DOI: https://doi.org/10.1186/s12877-020-01893-1