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Association of Receipt of Palliative Care Interventions With Health Care Use, Quality of Life, and Symptom Burden Among Adults With Chronic Noncancer Illness: A Systematic Review and Meta-analysis

IMPORTANCE: The evidence for palliative care exists predominantly for patients with cancer. The effect of palliative care on important end-of-life outcomes in patients with noncancer illness is unclear. OBJECTIVE: To measure the association between palliative care and acute health care use, quality...

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Published in:JAMA : the journal of the American Medical Association 2020-10, Vol.324 (14), p.1439-1450
Main Authors: Quinn, Kieran L, Shurrab, Mohammed, Gitau, Kevin, Kavalieratos, Dio, Isenberg, Sarina R, Stall, Nathan M, Stukel, Therese A, Goldman, Russell, Horn, Daphne, Cram, Peter, Detsky, Allan S, Bell, Chaim M
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container_end_page 1450
container_issue 14
container_start_page 1439
container_title JAMA : the journal of the American Medical Association
container_volume 324
creator Quinn, Kieran L
Shurrab, Mohammed
Gitau, Kevin
Kavalieratos, Dio
Isenberg, Sarina R
Stall, Nathan M
Stukel, Therese A
Goldman, Russell
Horn, Daphne
Cram, Peter
Detsky, Allan S
Bell, Chaim M
description IMPORTANCE: The evidence for palliative care exists predominantly for patients with cancer. The effect of palliative care on important end-of-life outcomes in patients with noncancer illness is unclear. OBJECTIVE: To measure the association between palliative care and acute health care use, quality of life (QOL), and symptom burden in adults with chronic noncancer illnesses. DATA SOURCES: MEDLINE, Embase, CINAHL, PsycINFO, and PubMed from inception to April 18, 2020. STUDY SELECTION: Randomized clinical trials of palliative care interventions in adults with chronic noncancer illness. Studies involving at least 50% of patients with cancer were excluded. DATA EXTRACTION AND SYNTHESIS: Two reviewers independently screened, selected, and extracted data from studies. Narrative synthesis was conducted for all trials. All outcomes were analyzed using random-effects meta-analysis. MAIN OUTCOMES AND MEASURES: Acute health care use (hospitalizations and emergency department use), disease-generic and disease-specific quality of life (QOL), and symptoms, with estimates of QOL translated to units of the Functional Assessment of Chronic Illness Therapy-Palliative Care scale (range, 0 [worst] to 184 [best]; minimal clinically important difference, 9 points) and symptoms translated to units of the Edmonton Symptom Assessment Scale global distress score (range, 0 [best] to 90 [worst]; minimal clinically important difference, 5.7 points). RESULTS: Twenty-eight trials provided data on 13 664 patients (mean age, 74 years; 46% were women). Ten trials were of heart failure (n = 4068 patients), 11 of mixed disease (n = 8119), 4 of dementia (n = 1036), and 3 of chronic obstructive pulmonary disease (n = 441). Palliative care, compared with usual care, was statistically significantly associated with less emergency department use (9 trials [n = 2712]; 20% vs 24%; odds ratio, 0.82 [95% CI, 0.68-1.00]; I2 = 3%), less hospitalization (14 trials [n = 3706]; 38% vs 42%; odds ratio, 0.80 [95% CI, 0.65-0.99]; I2 = 41%), and modestly lower symptom burden (11 trials [n = 2598]; pooled standardized mean difference (SMD), −0.12; [95% CI, −0.20 to −0.03]; I2 = 0%; Edmonton Symptom Assessment Scale score mean difference, −1.6 [95% CI, −2.6 to −0.4]). Palliative care was not significantly associated with disease-generic QOL (6 trials [n = 1334]; SMD, 0.18 [95% CI, −0.24 to 0.61]; I2 = 87%; Functional Assessment of Chronic Illness Therapy-Palliative Care score mean difference, 4.7 [95% CI, −6.3 t
doi_str_mv 10.1001/jama.2020.14205
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The effect of palliative care on important end-of-life outcomes in patients with noncancer illness is unclear. OBJECTIVE: To measure the association between palliative care and acute health care use, quality of life (QOL), and symptom burden in adults with chronic noncancer illnesses. DATA SOURCES: MEDLINE, Embase, CINAHL, PsycINFO, and PubMed from inception to April 18, 2020. STUDY SELECTION: Randomized clinical trials of palliative care interventions in adults with chronic noncancer illness. Studies involving at least 50% of patients with cancer were excluded. DATA EXTRACTION AND SYNTHESIS: Two reviewers independently screened, selected, and extracted data from studies. Narrative synthesis was conducted for all trials. All outcomes were analyzed using random-effects meta-analysis. MAIN OUTCOMES AND MEASURES: Acute health care use (hospitalizations and emergency department use), disease-generic and disease-specific quality of life (QOL), and symptoms, with estimates of QOL translated to units of the Functional Assessment of Chronic Illness Therapy-Palliative Care scale (range, 0 [worst] to 184 [best]; minimal clinically important difference, 9 points) and symptoms translated to units of the Edmonton Symptom Assessment Scale global distress score (range, 0 [best] to 90 [worst]; minimal clinically important difference, 5.7 points). RESULTS: Twenty-eight trials provided data on 13 664 patients (mean age, 74 years; 46% were women). Ten trials were of heart failure (n = 4068 patients), 11 of mixed disease (n = 8119), 4 of dementia (n = 1036), and 3 of chronic obstructive pulmonary disease (n = 441). Palliative care, compared with usual care, was statistically significantly associated with less emergency department use (9 trials [n = 2712]; 20% vs 24%; odds ratio, 0.82 [95% CI, 0.68-1.00]; I2 = 3%), less hospitalization (14 trials [n = 3706]; 38% vs 42%; odds ratio, 0.80 [95% CI, 0.65-0.99]; I2 = 41%), and modestly lower symptom burden (11 trials [n = 2598]; pooled standardized mean difference (SMD), −0.12; [95% CI, −0.20 to −0.03]; I2 = 0%; Edmonton Symptom Assessment Scale score mean difference, −1.6 [95% CI, −2.6 to −0.4]). Palliative care was not significantly associated with disease-generic QOL (6 trials [n = 1334]; SMD, 0.18 [95% CI, −0.24 to 0.61]; I2 = 87%; Functional Assessment of Chronic Illness Therapy-Palliative Care score mean difference, 4.7 [95% CI, −6.3 to 15.9]) or disease-specific measures of QOL (11 trials [n = 2204]; SMD, 0.07 [95% CI, −0.09 to 0.23]; I2 = 68%). CONCLUSIONS AND RELEVANCE: In this systematic review and meta-analysis of randomized clinical trials of patients with primarily noncancer illness, palliative care, compared with usual care, was statistically significantly associated with less acute health care use and modestly lower symptom burden, but there was no significant difference in quality of life. Analyses for some outcomes were based predominantly on studies of patients with heart failure, which may limit generalizability to other chronic illnesses.</description><identifier>ISSN: 0098-7484</identifier><identifier>EISSN: 1538-3598</identifier><identifier>DOI: 10.1001/jama.2020.14205</identifier><identifier>PMID: 33048152</identifier><language>eng</language><publisher>United States: American Medical Association</publisher><subject><![CDATA[Adults ; Aged ; Bias ; Cancer ; Chronic Disease ; Chronic illnesses ; Chronic obstructive pulmonary disease ; Clinical trials ; Congestive heart failure ; Dementia - epidemiology ; Dementia - therapy ; Dementia disorders ; Emergency medical care ; Emergency medical services ; Emergency Service, Hospital - statistics & numerical data ; End of life ; Female ; Health care ; Health Services Needs and Demand - statistics & numerical data ; Heart failure ; Heart Failure - epidemiology ; Heart Failure - therapy ; Hospitalization - statistics & numerical data ; Humans ; Illnesses ; Lung diseases ; Male ; Meta-analysis ; Obstructive lung disease ; Odds Ratio ; Original Investigation ; Palliation ; Palliative care ; Palliative Care - statistics & numerical data ; Patients ; Pulmonary Disease, Chronic Obstructive - epidemiology ; Pulmonary Disease, Chronic Obstructive - therapy ; Quality of Life ; Randomized Controlled Trials as Topic - statistics & numerical data ; Signs and symptoms ; Symptom Assessment - statistics & numerical data ; Synthesis ; Systematic review]]></subject><ispartof>JAMA : the journal of the American Medical Association, 2020-10, Vol.324 (14), p.1439-1450</ispartof><rights>Copyright American Medical Association Oct 13, 2020</rights><rights>Copyright 2020 American Medical Association. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a353t-38ffbedbf3201d8c37ae3e83f8863e7c1b9692a90e9879f6559f993493c986703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33048152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quinn, Kieran L</creatorcontrib><creatorcontrib>Shurrab, Mohammed</creatorcontrib><creatorcontrib>Gitau, Kevin</creatorcontrib><creatorcontrib>Kavalieratos, Dio</creatorcontrib><creatorcontrib>Isenberg, Sarina R</creatorcontrib><creatorcontrib>Stall, Nathan M</creatorcontrib><creatorcontrib>Stukel, Therese A</creatorcontrib><creatorcontrib>Goldman, Russell</creatorcontrib><creatorcontrib>Horn, Daphne</creatorcontrib><creatorcontrib>Cram, Peter</creatorcontrib><creatorcontrib>Detsky, Allan S</creatorcontrib><creatorcontrib>Bell, Chaim M</creatorcontrib><title>Association of Receipt of Palliative Care Interventions With Health Care Use, Quality of Life, and Symptom Burden Among Adults With Chronic Noncancer Illness: A Systematic Review and Meta-analysis</title><title>JAMA : the journal of the American Medical Association</title><addtitle>JAMA</addtitle><description>IMPORTANCE: The evidence for palliative care exists predominantly for patients with cancer. The effect of palliative care on important end-of-life outcomes in patients with noncancer illness is unclear. OBJECTIVE: To measure the association between palliative care and acute health care use, quality of life (QOL), and symptom burden in adults with chronic noncancer illnesses. DATA SOURCES: MEDLINE, Embase, CINAHL, PsycINFO, and PubMed from inception to April 18, 2020. STUDY SELECTION: Randomized clinical trials of palliative care interventions in adults with chronic noncancer illness. Studies involving at least 50% of patients with cancer were excluded. DATA EXTRACTION AND SYNTHESIS: Two reviewers independently screened, selected, and extracted data from studies. Narrative synthesis was conducted for all trials. All outcomes were analyzed using random-effects meta-analysis. MAIN OUTCOMES AND MEASURES: Acute health care use (hospitalizations and emergency department use), disease-generic and disease-specific quality of life (QOL), and symptoms, with estimates of QOL translated to units of the Functional Assessment of Chronic Illness Therapy-Palliative Care scale (range, 0 [worst] to 184 [best]; minimal clinically important difference, 9 points) and symptoms translated to units of the Edmonton Symptom Assessment Scale global distress score (range, 0 [best] to 90 [worst]; minimal clinically important difference, 5.7 points). RESULTS: Twenty-eight trials provided data on 13 664 patients (mean age, 74 years; 46% were women). Ten trials were of heart failure (n = 4068 patients), 11 of mixed disease (n = 8119), 4 of dementia (n = 1036), and 3 of chronic obstructive pulmonary disease (n = 441). Palliative care, compared with usual care, was statistically significantly associated with less emergency department use (9 trials [n = 2712]; 20% vs 24%; odds ratio, 0.82 [95% CI, 0.68-1.00]; I2 = 3%), less hospitalization (14 trials [n = 3706]; 38% vs 42%; odds ratio, 0.80 [95% CI, 0.65-0.99]; I2 = 41%), and modestly lower symptom burden (11 trials [n = 2598]; pooled standardized mean difference (SMD), −0.12; [95% CI, −0.20 to −0.03]; I2 = 0%; Edmonton Symptom Assessment Scale score mean difference, −1.6 [95% CI, −2.6 to −0.4]). Palliative care was not significantly associated with disease-generic QOL (6 trials [n = 1334]; SMD, 0.18 [95% CI, −0.24 to 0.61]; I2 = 87%; Functional Assessment of Chronic Illness Therapy-Palliative Care score mean difference, 4.7 [95% CI, −6.3 to 15.9]) or disease-specific measures of QOL (11 trials [n = 2204]; SMD, 0.07 [95% CI, −0.09 to 0.23]; I2 = 68%). CONCLUSIONS AND RELEVANCE: In this systematic review and meta-analysis of randomized clinical trials of patients with primarily noncancer illness, palliative care, compared with usual care, was statistically significantly associated with less acute health care use and modestly lower symptom burden, but there was no significant difference in quality of life. Analyses for some outcomes were based predominantly on studies of patients with heart failure, which may limit generalizability to other chronic illnesses.</description><subject>Adults</subject><subject>Aged</subject><subject>Bias</subject><subject>Cancer</subject><subject>Chronic Disease</subject><subject>Chronic illnesses</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Clinical trials</subject><subject>Congestive heart failure</subject><subject>Dementia - epidemiology</subject><subject>Dementia - therapy</subject><subject>Dementia disorders</subject><subject>Emergency medical care</subject><subject>Emergency medical services</subject><subject>Emergency Service, Hospital - statistics &amp; numerical data</subject><subject>End of life</subject><subject>Female</subject><subject>Health care</subject><subject>Health Services Needs and Demand - statistics &amp; numerical data</subject><subject>Heart failure</subject><subject>Heart Failure - epidemiology</subject><subject>Heart Failure - therapy</subject><subject>Hospitalization - statistics &amp; numerical data</subject><subject>Humans</subject><subject>Illnesses</subject><subject>Lung diseases</subject><subject>Male</subject><subject>Meta-analysis</subject><subject>Obstructive lung disease</subject><subject>Odds Ratio</subject><subject>Original Investigation</subject><subject>Palliation</subject><subject>Palliative care</subject><subject>Palliative Care - statistics &amp; numerical data</subject><subject>Patients</subject><subject>Pulmonary Disease, Chronic Obstructive - epidemiology</subject><subject>Pulmonary Disease, Chronic Obstructive - therapy</subject><subject>Quality of Life</subject><subject>Randomized Controlled Trials as Topic - statistics &amp; numerical data</subject><subject>Signs and symptoms</subject><subject>Symptom Assessment - statistics &amp; numerical data</subject><subject>Synthesis</subject><subject>Systematic review</subject><issn>0098-7484</issn><issn>1538-3598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpdUk1vEzEUXCEQTQtnJA7IEpce2NZe74fdA1KIgEYK31QcLcf7tnHktYPtDcr_44fhTdIK8OXZfjOjefZk2TOCLwjG5HIte3lR4CIdywJXD7IJqSjLacXZw2yCMWd5U7LyJDsNYY3TIrR5nJ1QiktGqmKS_Z6G4JSWUTuLXIe-ggK9ieP2szRmbGwBzaQHNLcR_BbsCA3oh44rdA3SpLJv3wR4hb4M0ui4G-kL3aULaVv0bddvouvRm8G3YNG0d_YWTdvBxKPMbOWd1Qp9dFZJq8CjuTEWQrhC08QOEfrkQyVzWw2_9pofIMpcWml2QYcn2aNOmgBPj_Usu3n39vvsOl98ej-fTRe5pBWNOWVdt4R22dECk5Yp2kigwGjHWE2hUWTJa15IjoGzhnd1VfGOc1pyqjirG0zPstcH3c2w7KFV6S28NGLjdS_9Tjipxb8dq1fi1m0Fw7wsizoJnB8FvPs5QIii10GBMdKCG4IoygrX6b84TdCX_0HXbvBp4D2qJLyqyOjo8oBS3oXgobs3Q7AYEyLGhIgxIWKfkMR48fcM9_i7SCTA8wNgJN51i6YhNa7pH9Zjwjs</recordid><startdate>20201013</startdate><enddate>20201013</enddate><creator>Quinn, Kieran L</creator><creator>Shurrab, Mohammed</creator><creator>Gitau, Kevin</creator><creator>Kavalieratos, Dio</creator><creator>Isenberg, Sarina R</creator><creator>Stall, Nathan M</creator><creator>Stukel, Therese A</creator><creator>Goldman, Russell</creator><creator>Horn, Daphne</creator><creator>Cram, Peter</creator><creator>Detsky, Allan S</creator><creator>Bell, Chaim M</creator><general>American Medical Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20201013</creationdate><title>Association of Receipt of Palliative Care Interventions With Health Care Use, Quality of Life, and Symptom Burden Among Adults With Chronic Noncancer Illness: A Systematic Review and Meta-analysis</title><author>Quinn, Kieran L ; Shurrab, Mohammed ; Gitau, Kevin ; Kavalieratos, Dio ; Isenberg, Sarina R ; Stall, Nathan M ; Stukel, Therese A ; Goldman, Russell ; Horn, Daphne ; Cram, Peter ; Detsky, Allan S ; Bell, Chaim M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a353t-38ffbedbf3201d8c37ae3e83f8863e7c1b9692a90e9879f6559f993493c986703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adults</topic><topic>Aged</topic><topic>Bias</topic><topic>Cancer</topic><topic>Chronic Disease</topic><topic>Chronic illnesses</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Clinical trials</topic><topic>Congestive heart failure</topic><topic>Dementia - epidemiology</topic><topic>Dementia - therapy</topic><topic>Dementia disorders</topic><topic>Emergency medical care</topic><topic>Emergency medical services</topic><topic>Emergency Service, Hospital - statistics &amp; numerical data</topic><topic>End of life</topic><topic>Female</topic><topic>Health care</topic><topic>Health Services Needs and Demand - statistics &amp; numerical data</topic><topic>Heart failure</topic><topic>Heart Failure - epidemiology</topic><topic>Heart Failure - therapy</topic><topic>Hospitalization - statistics &amp; numerical data</topic><topic>Humans</topic><topic>Illnesses</topic><topic>Lung diseases</topic><topic>Male</topic><topic>Meta-analysis</topic><topic>Obstructive lung disease</topic><topic>Odds Ratio</topic><topic>Original Investigation</topic><topic>Palliation</topic><topic>Palliative care</topic><topic>Palliative Care - statistics &amp; numerical data</topic><topic>Patients</topic><topic>Pulmonary Disease, Chronic Obstructive - epidemiology</topic><topic>Pulmonary Disease, Chronic Obstructive - therapy</topic><topic>Quality of Life</topic><topic>Randomized Controlled Trials as Topic - statistics &amp; numerical data</topic><topic>Signs and symptoms</topic><topic>Symptom Assessment - statistics &amp; numerical data</topic><topic>Synthesis</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quinn, Kieran L</creatorcontrib><creatorcontrib>Shurrab, Mohammed</creatorcontrib><creatorcontrib>Gitau, Kevin</creatorcontrib><creatorcontrib>Kavalieratos, Dio</creatorcontrib><creatorcontrib>Isenberg, Sarina R</creatorcontrib><creatorcontrib>Stall, Nathan M</creatorcontrib><creatorcontrib>Stukel, Therese A</creatorcontrib><creatorcontrib>Goldman, Russell</creatorcontrib><creatorcontrib>Horn, Daphne</creatorcontrib><creatorcontrib>Cram, Peter</creatorcontrib><creatorcontrib>Detsky, Allan S</creatorcontrib><creatorcontrib>Bell, Chaim M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; 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The effect of palliative care on important end-of-life outcomes in patients with noncancer illness is unclear. OBJECTIVE: To measure the association between palliative care and acute health care use, quality of life (QOL), and symptom burden in adults with chronic noncancer illnesses. DATA SOURCES: MEDLINE, Embase, CINAHL, PsycINFO, and PubMed from inception to April 18, 2020. STUDY SELECTION: Randomized clinical trials of palliative care interventions in adults with chronic noncancer illness. Studies involving at least 50% of patients with cancer were excluded. DATA EXTRACTION AND SYNTHESIS: Two reviewers independently screened, selected, and extracted data from studies. Narrative synthesis was conducted for all trials. All outcomes were analyzed using random-effects meta-analysis. MAIN OUTCOMES AND MEASURES: Acute health care use (hospitalizations and emergency department use), disease-generic and disease-specific quality of life (QOL), and symptoms, with estimates of QOL translated to units of the Functional Assessment of Chronic Illness Therapy-Palliative Care scale (range, 0 [worst] to 184 [best]; minimal clinically important difference, 9 points) and symptoms translated to units of the Edmonton Symptom Assessment Scale global distress score (range, 0 [best] to 90 [worst]; minimal clinically important difference, 5.7 points). RESULTS: Twenty-eight trials provided data on 13 664 patients (mean age, 74 years; 46% were women). Ten trials were of heart failure (n = 4068 patients), 11 of mixed disease (n = 8119), 4 of dementia (n = 1036), and 3 of chronic obstructive pulmonary disease (n = 441). Palliative care, compared with usual care, was statistically significantly associated with less emergency department use (9 trials [n = 2712]; 20% vs 24%; odds ratio, 0.82 [95% CI, 0.68-1.00]; I2 = 3%), less hospitalization (14 trials [n = 3706]; 38% vs 42%; odds ratio, 0.80 [95% CI, 0.65-0.99]; I2 = 41%), and modestly lower symptom burden (11 trials [n = 2598]; pooled standardized mean difference (SMD), −0.12; [95% CI, −0.20 to −0.03]; I2 = 0%; Edmonton Symptom Assessment Scale score mean difference, −1.6 [95% CI, −2.6 to −0.4]). Palliative care was not significantly associated with disease-generic QOL (6 trials [n = 1334]; SMD, 0.18 [95% CI, −0.24 to 0.61]; I2 = 87%; Functional Assessment of Chronic Illness Therapy-Palliative Care score mean difference, 4.7 [95% CI, −6.3 to 15.9]) or disease-specific measures of QOL (11 trials [n = 2204]; SMD, 0.07 [95% CI, −0.09 to 0.23]; I2 = 68%). CONCLUSIONS AND RELEVANCE: In this systematic review and meta-analysis of randomized clinical trials of patients with primarily noncancer illness, palliative care, compared with usual care, was statistically significantly associated with less acute health care use and modestly lower symptom burden, but there was no significant difference in quality of life. Analyses for some outcomes were based predominantly on studies of patients with heart failure, which may limit generalizability to other chronic illnesses.</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>33048152</pmid><doi>10.1001/jama.2020.14205</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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1538-3598
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8094426
source American Medical Association Current Titles
subjects Adults
Aged
Bias
Cancer
Chronic Disease
Chronic illnesses
Chronic obstructive pulmonary disease
Clinical trials
Congestive heart failure
Dementia - epidemiology
Dementia - therapy
Dementia disorders
Emergency medical care
Emergency medical services
Emergency Service, Hospital - statistics & numerical data
End of life
Female
Health care
Health Services Needs and Demand - statistics & numerical data
Heart failure
Heart Failure - epidemiology
Heart Failure - therapy
Hospitalization - statistics & numerical data
Humans
Illnesses
Lung diseases
Male
Meta-analysis
Obstructive lung disease
Odds Ratio
Original Investigation
Palliation
Palliative care
Palliative Care - statistics & numerical data
Patients
Pulmonary Disease, Chronic Obstructive - epidemiology
Pulmonary Disease, Chronic Obstructive - therapy
Quality of Life
Randomized Controlled Trials as Topic - statistics & numerical data
Signs and symptoms
Symptom Assessment - statistics & numerical data
Synthesis
Systematic review
title Association of Receipt of Palliative Care Interventions With Health Care Use, Quality of Life, and Symptom Burden Among Adults With Chronic Noncancer Illness: A Systematic Review and Meta-analysis
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