Ron D. Hays, Ph.D. UCLA Department of Medicine

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Presentation transcript:

Methodological Challenges in Studying Patient-Centered Communication in Cancer Care Ron D. Hays, Ph.D. UCLA Department of Medicine May 16, 2006, 1:15-1:30pm

Five M’s for Process and Outcomes 1) Measurement 2) Monitoring over time 3) Mediators 4) Moderators 5) Making Sense of Associations

Multiple Methods of Measuring Patient-Centered Communication (PCC) 6/19/2018 Multiple Methods of Measuring Patient-Centered Communication (PCC) Patient report Physician report Peer assessment Observational measures Videotape Audiotape Standardized patients Medical records Care diaries Different strengths and weaknesses. Patient report provides direct information from the perspective of the target of communication, but not a good source of technical quality of care. Physician report provides expert perspective from a direct participant but has limitation of biased from vested interest. Peers may have limited opportunities to observe patient care of colleagues. Observational measures contain rich detail from the frame of medium (what the camera sees, voice) but require skill in distilling the essential elements.

Measuring the PCC Functions Fostering healing relationships Exchanging information Eliciting and validating emotions Managing uncertainty Making decisions Navigating the system How is a “healing” relationship operationalized? What is the basis for determining when uncertainty has been managed optimally? How far do existing measures take us in measuring uncertainty—e.g., MUIS/Merle Mischel’s measures: 1) parents’ perception of uncertainty in illness scales; 2) adult uncertainty in illness scale What is a decision? What is an informed decision?

Monitoring over time In contrast to single physician and cross-sectional design Doctors nested within patients Multiple providers (physicians, nurses), multiple interactions over time, and multiple channels of communication (face-to-face, phone, email) EMRs and PHRs

6/19/2018 Evaluating Outcomes PCC should result in patients having more positive perceptions of care, better functioning and well-being, and increased survival Mediators and moderators not well understood

Quality of Care and Outcomes of Care Technical Quality Interpersonal Quality (including Communication) Clinical Outcomes Patient-reported Outcomes

Testing Mediators Pain (C) Patient Activation (A) Adherence (B) Oliver, Kravitz, Kaplan and Meyers (2001)

Evaluation of Mediation Model 1: A direct effect on C Model 2: A direct effect on B Model 3: B direct effect on C* Model 4: In multivariate model predicting C from A and B, A direct effect on C reduced compared to Model 1

Evaluating Moderators Moderator = significant interaction Education is a moderator of relationship between patient involvement in care and satisfaction with care if it has a positive effect for those with at least a high school degree but a non-significant effect for those without a high school degree Possible moderators (individual, group, organizational)? Coping style Family resilency

Making Sense of Associations Non-randomized study designs Self-selection of treatment Statistical Adjustments Casemix adjustment Age, education, prior health, etc. Propensity models Unmeasured burden of illness Sicker patients receive more intensive process of care. Standard regression analyses show that more intensive and higher quality care is associated with worse outcomes Instrumental variable models may help account for unmeasured burden of illness McClellan, McNeil, & Newhouse (1994)

Paths mentioned Continuity relationship -> better outcomes “Effect modifier” (Kurt Stange) or main effect Main effect PCC -> Treatment acceptance -> Outcomes (Ed Wagner) PCC -> Imagine disease experience -> Better decisions (Albert Mulley) Terror reduction -> Think clearly -> Better decisions (Tim Quill) Better decision is consistent with values (satisfied with decision) Nurse call -> self-efficacy/empowerment-> outcome (Merle Mischel) Structural differences NCI comprehensive care clinic (Terrance Albrecht) Health care team -> facilitate access to information (Steve Taplin) Medical home -> coordinate info (Ed Wagner)

Discussion