Using electronic health records for quality measurement and accountability in care of the seriously ill : opportunities and challenges

Article

CURTIS, J. Randall | SATHITRATANACHEEWIN, Seelwan | STARKS, Helene | LEE, Robert Y. | KROSS, Erin K. | DOWNEY, Lois | SIBLEY, James | LOBER, William | LOGGERS, Elizabeth T. | FAUSTO, James A. | LINDVALL, Charlotta | ENGELBERG, Ruth A.

BACKGROUND: As our population ages and the burden of chronic illness rises, there is increasing need to implement quality metrics that measure and benchmark care of the seriously ill, including the delivery of both primary care and specialty palliative care. Such metrics can be used to drive quality improvement, value-based payment, and accountability for population-based outcomes. METHODS: In this article, we examine use of the electronic health record (EHR) as a tool to assess quality of serious illness care through narrative review and description of a palliative care quality metrics program in a large healthcare system. RESULTS: In the search for feasible, reliable, and valid palliative care quality metrics, the EHR is an attractive option for collecting quality data on large numbers of seriously ill patients. However, important challenges to using EHR data for quality improvement and accountability exist, including understanding the validity, reliability, and completeness of the data, as well as acknowledging the difference between care documented and care delivered. Challenges also include developing achievable metrics that are clearly linked to patient and family outcomes and addressing data interoperability across sites as well as EHR platforms and vendors. This article summarizes the strengths and weakness of the EHR as a data source for accountability of community- and population-based programs for serious illness, describes the implementation of EHR data in the palliative care quality metrics program at the University of Washington, and, based on that experience, discusses opportunities and challenges. Our palliative care metrics program was designed to serve as a resource for other healthcare systems. DISCUSSION: Although the EHR offers great promise for enhancing quality of care provided for the seriously ill, significant challenges remain to operationalizing this promise on a national scale and using EHR data for population-based quality and accountability.

https://www.liebertpub.com/doi/pdf/10.1089/jpm.2017.0542

Voir la revue «JOURNAL OF PALLIATIVE MEDICINE, 21»

Autres numéros de la revue «JOURNAL OF PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

Using electronic health records for quality m...

Article indépendant | CURTIS, J. Randall | JOURNAL OF PALLIATIVE MEDICINE | n°S2 | vol.21

BACKGROUND: As our population ages and the burden of chronic illness rises, there is increasing need to implement quality metrics that measure and benchmark care of the seriously ill, including the delivery of both primary care an...

Temporal trends between 2010 and 2015 in inte...

Article indépendant | SATHITRATANACHEEWIN, Seelwan | JOURNAL OF PAIN AND SYMPTOM MANAGEMENT | n°1 | vol.55

Context: Recent analyses of Medicare data show decreases over time in intensity of end-of-life care. Few studies exist regarding trends in intensity of end-of-life care for those under 65 years of age. Objectives: To examine recen...

Temporal trends between 2010 and 2015 in inte...

Article indépendant | SATHITRATANACHEEWIN, Seelwan | JOURNAL OF PAIN AND SYMPTOM MANAGEMENT | n°1 | vol.55

Context: Recent analyses of Medicare data show decreases over time in intensity of end-of-life care. Few studies exist regarding trends in intensity of end-of-life care for those under 65 years of age. Objectives: To examine recen...

De la même série

Feasibility of a palliative care intervention...

Article | VERMA, Manisha | JOURNAL OF PALLIATIVE MEDICINE | n°3 | vol.36

Background: Patients with hepatocellular cancer (HCC) are at risk for poor quality of life (QoL) and high symptom burden, coupled with limited treatment options. Palliative care (PC) can play an important role in reducing the suff...

"You suffer from being interested" : a tribut...

Article | MILLER, Pringl | JOURNAL OF PALLIATIVE MEDICINE | n°12 | vol.31

I met Hank during my palliative medicine fellowship after his nurse Cynthia paged me to request a consult for existential suffering. When reviewing Hank's electronic medical record, it became evident he was dying and averse to spe...

Evaluating a pediatric palliative care electi...

Article | CRAWFORD, Claire | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

Background: Hospice and palliative medicine is important in the education of pediatric residents. Little is known about if and how residents' learnings during a pediatric palliative care elective fulfill core competencies and Pedi...

Associations between measures of disability a...

Article | CHANG, Victoria A. | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

Background: The modified Rankin Scale (mRS), which measures degree of disability in daily activities, is the most common outcome measure in stroke research. Quality of life (QoL), however, is impacted by factors other than disabil...

Preliminary findings of an adapted nurse-led ...

Article | LAYNE, Diana | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

Context: Despite the increased number of people living with Alzheimer's disease and related dementias (PLWD), limited early palliative care interventions exist for this population. Adapting promising interventions for other progre...

Chargement des enrichissements...