Literature DB >> 15471649

Measuring hospice care: the National Hospice and Palliative Care Organization National Hospice Data Set.

Stephen R Connor1, Martha Tecca, Judi LundPerson, Joan Teno.   

Abstract

Hospice has seen rapid growth in recent years, but there is a lack of consistency among hospices when it comes to compliance with standards of care. Consequently, hospices vary in performance and in services they provide. With state hospice organizations, the NHPCO developed a National Data Set (NDS) intended to understand demographics, practices, and outcomes; illustrate industry effectiveness; facilitate communication of industry legislative needs; and to support agency performance and improvement. Our paper describes development of the NDS and data that are being collected, and summarizes key findings from the 2000, 2001, and 2002 NDS. The data collection process, which began in 1999, has evolved substantially over a 4-year period to the point that we believe the 2002 NDS represents a well-designed core that will receive only minor modifications annually. This database will be invaluable for comparative audit, clinical practice and managing services because only that which is measured can be improved.

Mesh:

Year:  2004        PMID: 15471649     DOI: 10.1016/j.jpainsymman.2004.07.003

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  10 in total

1.  Association between the duration of palliative care service and survival in terminal cancer patients.

Authors:  Yong Joo Lee; Jung-Hwa Yang; Jung-Wook Lee; Johi Yoon; Jung-Ran Nah; Whan-Seok Choi; Chul-Min Kim
Journal:  Support Care Cancer       Date:  2014-10-04       Impact factor: 3.603

2.  Variations in process and outcome in inpatient palliative care services in Korea.

Authors:  Jin Young Choi; Dong Wook Shin; Jina Kang; Young Ji Baek; Ha Na Mo; Byung-Ho Nam; Won Seok Seo; Jong Hyock Park; Jung Hoe Kim; Kee Taig Jung
Journal:  Support Care Cancer       Date:  2011-02-24       Impact factor: 3.603

Review 3.  African American elders' psychological-social-spiritual cultural experiences across serious illness: an integrative literature review through a palliative care lens.

Authors:  Heather Lea Coats
Journal:  Ann Palliat Med       Date:  2017-04-17

4.  Providing hospice care to children and young adults: A descriptive study of end-of-life organizations.

Authors:  Lisa Lindley; Barbara Mark; Shoou-Yih Daniel Lee
Journal:  J Hosp Palliat Nurs       Date:  2009-11       Impact factor: 1.918

5.  Factors that influence the presence of a hospice in a rural community.

Authors:  Cathy L Campbell; Elizabeth Merwin; Guofen Yan
Journal:  J Nurs Scholarsh       Date:  2009       Impact factor: 3.176

6.  Hospice Care Experiences Among Cancer Patients and Their Caregivers.

Authors:  Layla Parast; Anagha A Tolpadi; Joan M Teno; Marc N Elliott; Rebecca Anhang Price
Journal:  J Gen Intern Med       Date:  2021-01-19       Impact factor: 5.128

7.  Factors Associated with Quality of Dying and Death in Korean Intensive Care Units: Perceptions of Nurses.

Authors:  Haeyoung Lee; Seung-Hye Choi
Journal:  Healthcare (Basel)       Date:  2021-01-05

Review 8.  Death and dying in the US: the barriers to the benefits of palliative and hospice care.

Authors:  Albert J Finestone; Gail Inderwies
Journal:  Clin Interv Aging       Date:  2008       Impact factor: 4.458

9.  A comparative analysis of computer based hospice palliative care datasets in Canada.

Authors:  Craig E Kuziemsky; Francis Lau
Journal:  BMC Palliat Care       Date:  2008-05-12       Impact factor: 3.234

10.  Creation of Minimum Standard Tool for Palliative Care in India and Self-evaluation of Palliative Care Programs Using It.

Authors:  Mr Rajagopal; Anjum Khan Joad; Maryann Muckaden; Reena George; Harmala Gupta; Mhoira Ef Leng; Gayatri Palat; Firuza Patel; Biju Raghavan; Suresh K Reddy; Mm Sunilkumar; Mallika Tiruvadanan; Stephen R Connor
Journal:  Indian J Palliat Care       Date:  2014-09
  10 in total

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