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442 <strong>EAPC</strong> Abstracts<br />

142 Oral Presentation<br />

Assessment and measurement of quality of life and other<br />

symptoms<br />

Developing a Measure of Quality of Death and Dying (QODD) in<br />

the Pediatric Intensive Care Unit (PICU)<br />

Authors: Mildred Solomon Center for Applied Ethics Education<br />

Development Center U. STATES<br />

Adena Cohen-Bearak Education Development Center Newton U. STATES<br />

Deborah Sellers Education Development Center Newton U. STATES<br />

Sarah McGraw New England Research Institutes Watertown U. STATES<br />

Robert Truog Education Development Center Newton U. STATES<br />

Background: End-of-life care in the PICU poses challenges distinct from<br />

those for adults. Relatively little information is available about the quality<br />

of dying and death in the PICU. We present the results from a qualitative<br />

study to develop a measure of QODD in the PICU. Our aims are to<br />

describe constructs and indicators through: 1) a systematic literature<br />

review and 2) focus groups with PICU providers. These findings, combined<br />

with interviews with bereaved family members, will inform the<br />

development of a PICU QODD instrument. Methods: A Medline search<br />

identified 99 relevant articles. A moderator conducted six focus groups<br />

about death and dying in the PICU with 65 PICU providers (physicians,<br />

nurses and psychosocial) from two teaching hospitals. The study team<br />

abstracted themes and specific indicators on decision-making, family and<br />

clinician concerns, and quality of care from the 99 articles. Using both<br />

inductive and deductive approaches, three coders first read the transcripts<br />

and coded for the domains identified in the literature and new domains<br />

emerging from the transcripts. Second, they identified sub-themes and topics<br />

within each domain. Results: Eight core domains with indicators were<br />

identified: 1) Decisions; 2) Conflict; 3) Communication; 4) Continuity of<br />

care; 5) Emotional and psychosocial needs of the family; 6) Pain and other<br />

symptoms; 7) Choices around the circumstances of death and;<br />

8) Bereavement. A meta-theme, underlying all of the focus group findings,<br />

was the notion of the uniqueness of each child, family, and the circumstances<br />

of death. Conclusions: Some domains and indicators are unique to<br />

the PICU; unlike for adults, autonomy is not a core domain.<br />

Accommodating the uniqueness of each circumstance presents methodological<br />

challenges for the development of a tool. Measures should address<br />

the subjective assessment of satisfaction with care and alignment with<br />

hopes and priorities.<br />

143 Oral Presentation<br />

Assessment and measurement of quality of life and other<br />

symptoms<br />

Evaluation of the Palliative Prognostic Score (PaP) and routinely<br />

collected clinical data in prognostication of survival for<br />

patients referred to a palliative care consultation service in an<br />

acute care hospital<br />

Authors: Yoko Tarumi Oncology/Palliative Care Medicine University of<br />

Alberta CANADA<br />

Francis Lau University of Victoria, Health Information Science Victoria<br />

CANADA<br />

Lorelei Sawchuk Royal Alexandra Hospital, Palliative Care Program<br />

Edmonton CANADA<br />

Hue Quan Capital Health Regional Palliative Care Program Edmonton<br />

CANADA<br />

Sharon Watanabe University of Alberta, Onclogy/Palliative Care Medicine<br />

Edmonton CANADA<br />

Background: The PaP is a validated tool for survival prognostication in palliative<br />

care patients. The purpose of this study is to further validate the PaP<br />

and examine the additional prognostic utility of routinely collected clinical<br />

data. Methods: Cancer and non-cancer patients referred to a palliative care<br />

consultation service at an acute care hospital were included. This was a<br />

prospective cohort study on survival prediction based on PaP and other routinely<br />

collected clinical data: Palliative Performance (PPS), Folstein Mini<br />

Mental State Examination Score (MMSE), Edmonton Symptom<br />

Assessment Scale. Data were collected at initial consultation, and again at<br />

the time of final decision making for discharge planning. Other predictor<br />

variables were obtained via routinely collected administrative data including<br />

age group, gender, primary diagnosis, problems at referral, location and<br />

date of discharge, and location and date of death. Statistical Analysis:<br />

1) Kaplan-Meier (KM) survival analysis for above listed variables;<br />

2) Hazard ratios for death with above variables; 3) Calculation of PaP using<br />

both PPS and KPS; 4) Survival rate (%) by above variables. Results: A total<br />

312 cases have been included in the preliminary data analysis. 95 cases<br />

have been censored due to unavailability of date of death (expected to be<br />

ready by the end of 2007). KM analysis for PaP showed 30 day survival<br />

rates that are consistent with previous studies in each risk category: A<br />

(>70%), B (30–70%), and C (

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