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Patient Perspectives: An Integral Part of Health Technology Assessment Methodology

Published online by Cambridge University Press:  16 December 2022

Jason Spangler
Affiliation:
Innovation and Value Initiative, Alexandria, VA, USA
Tiffany Huth
Affiliation:
Innovation and Value Initiative, Alexandria, VA, USA
Richard Xie*
Affiliation:
Innovation and Value Initiative, Alexandria, VA, USA
*
*Author for correspondence: Richard Xie, E-mail: richard.xie@thevalueinitiative.org
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Abstract

Type
Letter
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2022. Published by Cambridge University Press

Dear Editor:

The article Patient-centered health technology assessment: a perspective on engagement in health technology assessment by three patient organizations and a health technology assessment body (20 October 2022) brings forth important considerations of vital patient engagement during health technology assessment (HTA), and specifically, with the value assessment review by the Institute for Clinical and Economic Review (ICER) of two lupus therapies.

The Innovation and Value Initiative (IVI) commends some of the practical learnings and applauds the patient representatives’ and ICER’s commitment to engagement throughout this review.

However, this commitment needs to go beyond eliciting patient-important factors merely as inputs for “contextual considerations.” As one example, the authors noted the importance of factors such as “patients’ and caregivers’ career goals,” but our field does not currently have good approaches for measuring and incorporating these impacts into economic models. Existing HTA approaches fall short by not actively updating our methodology or data collection to truly incorporate lived experience into economic models.

Looking to different experiences with ICER reviews can provide additional insight. Sick Cells, an organization dedicated to elevating the voices of those with sickle cell disease, recently detailed their experience on a review in the white paper, Finding Equity in Value.(Reference Linthicum, Jalowsky, Valentine, Ahmed, Bright and Chapman1) As with the lupus review, ICER identified patient-important concerns, but merely considered these as contextual considerations rather than part of their base-case analysis. Sick Cells writes that “ICER, as the ultimate decision authority, chose to proceed with the evaluation despite known limitations in evidence and clear input from BIPOC stakeholders concerned about the equity implications of the decisions.”

This article also states that: “Although ICER’s methodology and consideration of cost would be standard in most countries with public HTA institutions, it is less known and accepted in the United States.” While ICER’s methodology indeed reflects the status quo for HTA, there is growing recognition that existing process and methods do not adequately capture patient perspectives. In our experience, decision makers, especially employers, health systems, and payors, understand the importance of patient experience as a driver of value. Nevertheless, we still lack consistent processes and methods to measure and incorporate this essential ingredient into HTA. Fundamental change is needed now – HTA organizations must invest in the hard work to ensure decision makers have a complete view of that value. Thus, more effort is needed to partner with patient communities to build patient perspectives and lived experience into core HTA methods.

It is essential to develop and test better processes and methods to achieve this, and it is being done. As one example, IVI is testing and improving systematic approaches to elicit qualitative and quantitative patient input that can then be incorporated into methods to inform HTA.(Reference Xie, Malik, Linthicum and Bright2;Reference dosReis, Bozzi, Butler, Xie, Chapman, Bright, Malik and Slejko3) We have actively changed our approach and scope of our value assessment models based on the extensive patient feedback we received.

We challenge the HTA community to continue advancing research to make patient perspectives an integral part of HTA methodology so that we no longer relegate this valuable input to “contextual considerations.”

Conflicts of Interest

The authors declare none.

References

Linthicum, M., Jalowsky, M., Valentine, A., Ahmed, R., Bright, J., & Chapman, R. Finding Equity in Value - Racial and Health Equity Implications of US HTA Processes. IVI Sick Cells Whitepaper. Published online 2022.Accessed December 12, 2022. https://www.thevalueinitiative.org/wp-content/uploads/2022/10/IVI_Sick-Cells_Equity-in-Value_2022.pdfGoogle Scholar
Xie, R. Z., Malik, E. D., Linthicum, M. T., & Bright, J. L. (2021). Putting stakeholder engagement at the center of health economic modeling for health technology assessment in the United States. Pharmacoeconomics, 39(6), 631638.CrossRefGoogle Scholar
dosReis, S., Bozzi, L. M., Butler, B., Xie, R. Z., Chapman, R. H., Bright, J., Malik, E., & Slejko, J. F. (2022). Preferences for Treatments for Major Depressive Disorder: Formative Qualitative Research Using the Patient Experience. The Patient-Patient-Centered Outcomes Research, 110.CrossRefGoogle Scholar