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40
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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
February 2021 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
February 2021 List
URL Address
<a href="http://doi.org/10.1097/mlr.0000000000001388" target="_blank" rel="noreferrer noopener">http://doi.org/10.1097/mlr.0000000000001388</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
A Tertiary Care-based Complex Care Program: Improving Care for Children With Medical Complexity
Publisher
An entity responsible for making the resource available
Medical Care
Date
A point or period of time associated with an event in the lifecycle of the resource
2020
Subject
The topic of the resource
Infant; Child; Humans; Child Preschool; Infant Newborn; Length of Stay; Caregivers/psychology; Patient Care Team/organization & administration; Patient Acceptance of Health Care/statistics & numerical data; Hospitalization/statistics & numerical data; Emergency Service Hospital/statistics & numerical data; Patient Satisfaction; Quality Improvement/organization & administration; Case Management/organization & administration; Multiple Chronic Conditions/therapy; Tertiary Healthcare/economics/organization & administration
Creator
An entity primarily responsible for making the resource
Hogan AK; Galligan MM; Stack NJ; Leach KF; Aredas BL; English R; Dye M; Rubin D
Description
An account of the resource
OBJECTIVE: Children with medical complexity (CMC) have significant health care costs, but they also experience substantial unmet health care needs, hospitalizations, and medical errors. Their parents often report psychosocial stressors and poor care satisfaction. Complex care programs can improve the care for CMC. At our tertiary care institution, we developed a consultative complex care program to improve the quality and cost of care for CMC and to improve the experience of care for patients and families. METHODS: To address the needs of CMC at our institution, we developed the Compass Care Program, a consultative complex care program across inpatient and outpatient settings. Utilization data [hospital admissions per patient month; length of stay per admission; hospital days per patient month; emergency department (ED) visits per patient month; and institutional charges per patient month] and caregiver satisfaction data (obtained via paper survey at outpatient visits) were tracked over the period of participation in the program and compared preenrollment and postenrollment for program participants. RESULTS: Participants had significant decreases in hospital admissions per patient month, length of stay per admission, hospital days per patient month, and charges per patient month following enrollment (P<0.01) without a tandem increase in readmissions within 7 days of discharge. There was no statistically significant difference in ED visits. Caregiver satisfaction scores improved in all domains. CONCLUSION: Participation in a consultative complex care program can improve utilization patterns and cost of care for CMC, as well as experience of care for patients and families.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1097/mlr.0000000000001388" target="_blank" rel="noreferrer noopener">10.1097/mlr.0000000000001388</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2020
Aredas BL
Caregivers/psychology
Case Management/organization & administration
Child
Child Preschool
Dye M
Emergency Service Hospital/statistics & numerical data
English R
February 2021 List
Galligan MM
Hogan AK
Hospitalization/statistics & numerical data
Humans
Infant
Infant Newborn
Leach KF
Length Of Stay
Medical Care
Multiple Chronic Conditions/therapy
Patient Acceptance Of Health Care/statistics & Numerical Data
Patient Care Team/organization & administration
Patient Satisfaction
Quality Improvement/organization & administration
Rubin D
Stack NJ
Tertiary Healthcare/economics/organization & administration
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Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1016/j.casemgr.2004.11.005" target="_blank" rel="noreferrer">http://doi.org/10.1016/j.casemgr.2004.11.005</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Enabling the transition to hospice through effective palliative care
Publisher
An entity responsible for making the resource available
The Case Manager
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Humans; Prognosis; Needs Assessment; Organizational Objectives; quality of life; Models; Chronic disease; Life Expectancy; Attitude to Death/ethnology; Case Management/organization & administration; Continuity of Patient Care/organization & Disease Progression; Hospice Care/organization & administration/psychology; Organizational; Palliative Care/organization & Professional Role; Referral and Consultation/organization & United States
Creator
An entity primarily responsible for making the resource
Bomba PA
Description
An account of the resource
The end of life has changed dramatically in recent years as life expectancies have increased, chronic disease rates have risen, and families, health care systems, and society have changed. As technology has advanced, death too often has become viewed by society as "failure" and even "optional." Too often, referral to hospice has come too late to be sufficiently effective. While expertise in palliation of pain and symptoms at the end of life has been developed, palliative care has not been well integrated with management of chronic diseases or incorporated into the continuum of medical management from health and wellness to the end of life. We can, and must, do better.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1016/j.casemgr.2004.11.005" target="_blank" rel="noreferrer">10.1016/j.casemgr.2004.11.005</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Attitude To Death/ethnology
Backlog
Bomba PA
Case Management/organization & administration
Chronic Disease
Continuity of Patient Care/organization & Disease Progression
Hospice Care/organization & administration/psychology
Humans
Journal Article
Life Expectancy
Models
Needs Assessment
Organizational
Organizational Objectives
Palliative Care/organization & Professional Role
Prognosis
Quality Of Life
Referral and Consultation/organization & United States
The Case Manager
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1089/jpm.2005.8.26" target="_blank" rel="noreferrer">http://doi.org/10.1089/jpm.2005.8.26</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Impact of palliative care case management on resource use by patients dying of cancer at a Veterans Affairs medical center
Publisher
An entity responsible for making the resource available
Journal Of Palliative Medicine
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
The topic of the resource
Female; Humans; Male; Terminal Care; Logistic Models; Aged; Middle Aged; Comorbidity; Length of Stay; Hospitals; Comparative Study; retrospective studies; Case Management/organization & administration; Neoplasms/mortality/therapy; Palliative Care/statistics & numerical data/utilization; Veterans
Creator
An entity primarily responsible for making the resource
Back AL; Li YF; Sales AE
Description
An account of the resource
BACKGROUND: The VA Puget Sound Health Care System (VAPSHCS) started a palliative care service (PCS) in October 2001 to provide case management for patients with advanced cancer. OBJECTIVE: To examine resource use during the last 60 days of life for patients dying of cancer who received PCS compared to patients receiving usual care (non-PCS) during the same time period. DESIGN: Retrospective nonrandomized comparison of resource use using administrative data. SETTING: Tertiary care Veterans Affairs medical center. PARTICIPANTS: All patients who died of cancer between October 1, 2001 and October 31, 2002 at VAPSHCS. RESULTS: Two hundred sixty-five patients died of cancer during the specified time period, including 82 PCS and 183 non-PCS patients. PCS patients received case management for a mean of 79 days, and were younger, had more comorbid conditions, and were more likely to have had chemotherapy in the last 60 days of life than non-PCS patients. Variables associated with more acute care bed days in the last 60 days of life included: chemotherapy in the last 60 days of life, and a length of stay on PCS less than 60 days. Variables associated with fewer acute care bed days within the last 60 days of life included: being married, and a length of stay on PCS 60 days or more. Compared to non-PCS patients, the place of death for PCS patients was less likely to be acute care. CONCLUSION: PCS for 60 or more days prior to death was associated with decreased use of acute care hospital resources for patients dying of cancer.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1089/jpm.2005.8.26" target="_blank" rel="noreferrer">10.1089/jpm.2005.8.26</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Aged
Back AL
Backlog
Case Management/organization & administration
Comorbidity
Comparative Study
Female
Hospitals
Humans
Journal Article
Journal of Palliative Medicine
Length Of Stay
Li YF
Logistic Models
Male
Middle Aged
Neoplasms/mortality/therapy
Palliative Care/statistics & numerical data/utilization
Retrospective Studies
Sales AE
Terminal Care
Veterans