Translating clinical trial results into personalized recommendations by considering multiple outcomes and subjective views
Currently, clinicians rely mostly on population-level treatment effects from RCTs, usually considering the treatment's benefits. This study proposes a process, focused on practical usability, for translating RCT data into personalized treatment recommendations that weighs benefits against harms...
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| Published in: | NPJ digital medicine Vol. 2; no. 1; p. 81 |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Nature Publishing Group UK
21.08.2019
Nature Publishing Group |
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| ISSN: | 2398-6352, 2398-6352 |
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| Abstract | Currently, clinicians rely mostly on population-level treatment effects from RCTs, usually considering the treatment's benefits. This study proposes a process, focused on practical usability, for translating RCT data into personalized treatment recommendations that weighs benefits against harms and integrates subjective perceptions of relative severity. Intensive blood pressure treatment (IBPT) was selected as the test case to demonstrate the suggested process, which was divided into three phases: (1) Prediction models were developed using the Systolic Blood-Pressure Intervention Trial (SPRINT) data for benefits and adverse events of IBPT. The models were externally validated using retrospective Clalit Health Services (CHS) data; (2) Predicted risk reductions and increases from these models were used to create a yes/no IBPT recommendation by calculating a severity-weighted benefit-to-harm ratio; (3) Analysis outputs were summarized in a decision support tool. Based on the individual benefit-to-harm ratios, 62 and 84% of the SPRINT and CHS populations, respectively, would theoretically be recommended IBPT. The original SPRINT trial results of significant decrease in cardiovascular outcomes following IBPT persisted only in the group that received a “yes-treatment” recommendation by the suggested process, while the rate of serious adverse events was slightly higher in the "no-treatment" recommendation group. This process can be used to translate RCT data into individualized recommendations by identifying patients for whom the treatment’s benefits outweigh the harms, while considering subjective views of perceived severity of the different outcomes. The proposed approach emphasizes clinical practicality by mimicking physicians’ clinical decision-making process and integrating all recommendation outputs into a usable decision support tool. |
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| AbstractList | Currently, clinicians rely mostly on population-level treatment effects from RCTs, usually considering the treatment's benefits. This study proposes a process, focused on practical usability, for translating RCT data into personalized treatment recommendations that weighs benefits against harms and integrates subjective perceptions of relative severity. Intensive blood pressure treatment (IBPT) was selected as the test case to demonstrate the suggested process, which was divided into three phases: (1) Prediction models were developed using the Systolic Blood-Pressure Intervention Trial (SPRINT) data for benefits and adverse events of IBPT. The models were externally validated using retrospective Clalit Health Services (CHS) data; (2) Predicted risk reductions and increases from these models were used to create a yes/no IBPT recommendation by calculating a severity-weighted benefit-to-harm ratio; (3) Analysis outputs were summarized in a decision support tool. Based on the individual benefit-to-harm ratios, 62 and 84% of the SPRINT and CHS populations, respectively, would theoretically be recommended IBPT. The original SPRINT trial results of significant decrease in cardiovascular outcomes following IBPT persisted only in the group that received a “yes-treatment” recommendation by the suggested process, while the rate of serious adverse events was slightly higher in the "no-treatment" recommendation group. This process can be used to translate RCT data into individualized recommendations by identifying patients for whom the treatment’s benefits outweigh the harms, while considering subjective views of perceived severity of the different outcomes. The proposed approach emphasizes clinical practicality by mimicking physicians’ clinical decision-making process and integrating all recommendation outputs into a usable decision support tool. Currently, clinicians rely mostly on population-level treatment effects from RCTs, usually considering the treatment's benefits. This study proposes a process, focused on practical usability, for translating RCT data into personalized treatment recommendations that weighs benefits against harms and integrates subjective perceptions of relative severity. Intensive blood pressure treatment (IBPT) was selected as the test case to demonstrate the suggested process, which was divided into three phases: (1) Prediction models were developed using the Systolic Blood-Pressure Intervention Trial (SPRINT) data for benefits and adverse events of IBPT. The models were externally validated using retrospective Clalit Health Services (CHS) data; (2) Predicted risk reductions and increases from these models were used to create a yes/no IBPT recommendation by calculating a severity-weighted benefit-to-harm ratio; (3) Analysis outputs were summarized in a decision support tool. Based on the individual benefit-to-harm ratios, 62 and 84% of the SPRINT and CHS populations, respectively, would theoretically be recommended IBPT. The original SPRINT trial results of significant decrease in cardiovascular outcomes following IBPT persisted only in the group that received a "yes-treatment" recommendation by the suggested process, while the rate of serious adverse events was slightly higher in the "no-treatment" recommendation group. This process can be used to translate RCT data into individualized recommendations by identifying patients for whom the treatment's benefits outweigh the harms, while considering subjective views of perceived severity of the different outcomes. The proposed approach emphasizes clinical practicality by mimicking physicians' clinical decision-making process and integrating all recommendation outputs into a usable decision support tool.Currently, clinicians rely mostly on population-level treatment effects from RCTs, usually considering the treatment's benefits. This study proposes a process, focused on practical usability, for translating RCT data into personalized treatment recommendations that weighs benefits against harms and integrates subjective perceptions of relative severity. Intensive blood pressure treatment (IBPT) was selected as the test case to demonstrate the suggested process, which was divided into three phases: (1) Prediction models were developed using the Systolic Blood-Pressure Intervention Trial (SPRINT) data for benefits and adverse events of IBPT. The models were externally validated using retrospective Clalit Health Services (CHS) data; (2) Predicted risk reductions and increases from these models were used to create a yes/no IBPT recommendation by calculating a severity-weighted benefit-to-harm ratio; (3) Analysis outputs were summarized in a decision support tool. Based on the individual benefit-to-harm ratios, 62 and 84% of the SPRINT and CHS populations, respectively, would theoretically be recommended IBPT. The original SPRINT trial results of significant decrease in cardiovascular outcomes following IBPT persisted only in the group that received a "yes-treatment" recommendation by the suggested process, while the rate of serious adverse events was slightly higher in the "no-treatment" recommendation group. This process can be used to translate RCT data into individualized recommendations by identifying patients for whom the treatment's benefits outweigh the harms, while considering subjective views of perceived severity of the different outcomes. The proposed approach emphasizes clinical practicality by mimicking physicians' clinical decision-making process and integrating all recommendation outputs into a usable decision support tool. |
| ArticleNumber | 81 |
| Author | Cohen-Stavi, Chandra J. Karpati, Tomas Dagan, Noa Hoshen, Moshe Balicer, Ran D. Gilutz, Harel Podjarny, Eduardo Bachmat, Eitan Akriv, Amichay Leibowitz, Morton Avgil Tsadok, Meytal Gofer, Ilan |
| Author_xml | – sequence: 1 givenname: Noa surname: Dagan fullname: Dagan, Noa email: noa.dgn@gmail.com organization: Clalit Research Institute, Clalit Health Services, Computer Science Department, Ben Gurion University of the Negev, Public Health Department, Ben Gurion University of the Negev – sequence: 2 givenname: Chandra J. surname: Cohen-Stavi fullname: Cohen-Stavi, Chandra J. organization: Clalit Research Institute, Clalit Health Services – sequence: 3 givenname: Meytal surname: Avgil Tsadok fullname: Avgil Tsadok, Meytal organization: Clalit Research Institute, Clalit Health Services – sequence: 4 givenname: Morton surname: Leibowitz fullname: Leibowitz, Morton organization: Clalit Research Institute, Clalit Health Services – sequence: 5 givenname: Moshe surname: Hoshen fullname: Hoshen, Moshe organization: Clalit Research Institute, Clalit Health Services – sequence: 6 givenname: Tomas orcidid: 0000-0003-2650-6192 surname: Karpati fullname: Karpati, Tomas organization: Clalit Research Institute, Clalit Health Services – sequence: 7 givenname: Amichay surname: Akriv fullname: Akriv, Amichay organization: Clalit Research Institute, Clalit Health Services – sequence: 8 givenname: Ilan surname: Gofer fullname: Gofer, Ilan organization: Clalit Research Institute, Clalit Health Services – sequence: 9 givenname: Harel surname: Gilutz fullname: Gilutz, Harel organization: Clalit Research Institute, Clalit Health Services – sequence: 10 givenname: Eduardo surname: Podjarny fullname: Podjarny, Eduardo organization: ADAM Institute of High Blood Pressure, Clalit Health Services – sequence: 11 givenname: Eitan surname: Bachmat fullname: Bachmat, Eitan organization: Clalit Research Institute, Clalit Health Services, Computer Science Department, Ben Gurion University of the Negev – sequence: 12 givenname: Ran D. surname: Balicer fullname: Balicer, Ran D. organization: Clalit Research Institute, Clalit Health Services, Public Health Department, Ben Gurion University of the Negev |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31453376$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_jacc_2021_02_058 crossref_primary_10_1016_S0140_6736_25_01391_1 crossref_primary_10_1093_jamia_ocaa283 crossref_primary_10_1093_ajh_hpad047 crossref_primary_10_1161_JAHA_124_033995 |
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| Title | Translating clinical trial results into personalized recommendations by considering multiple outcomes and subjective views |
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