Differences in medication adherence by sex and organ type among adolescent and young adult solid organ transplant recipients
Background Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients. Methods This multice...
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Published in | Pediatric transplantation Vol. 27; no. 2; pp. e14446 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.03.2023
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ISSN | 1397-3142 1399-3046 1399-3046 |
DOI | 10.1111/petr.14446 |
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Abstract | Background
Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients.
Methods
This multicenter study of prevalent kidney, liver and heart transplant recipients 14–25 years assessed adherence 3 times (0, 3, 6 months post‐enrollment) with the BAASIS self‐report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non‐adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ.
Results
Across all visits, males (n = 150, median age 20.4 years, IQR 17.2–23.3) had lower odds of self‐reported adherence than females (n = 120, median age 19.8 years, IQR 17.1–22.7) (OR 0.41, 95% CI 0.21–0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30–4.82). No significant differences in adherence (by self‐report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients.
Conclusion
Females show better self‐reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self‐reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type. |
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AbstractList | Background
Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients.
Methods
This multicenter study of prevalent kidney, liver and heart transplant recipients 14–25 years assessed adherence 3 times (0, 3, 6 months post‐enrollment) with the BAASIS self‐report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non‐adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ.
Results
Across all visits, males (n = 150, median age 20.4 years, IQR 17.2–23.3) had lower odds of self‐reported adherence than females (n = 120, median age 19.8 years, IQR 17.1–22.7) (OR 0.41, 95% CI 0.21–0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30–4.82). No significant differences in adherence (by self‐report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients.
Conclusion
Females show better self‐reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self‐reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type. Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients. This multicenter study of prevalent kidney, liver and heart transplant recipients 14-25 years assessed adherence 3 times (0, 3, 6 months post-enrollment) with the BAASIS self-report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non-adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ. Across all visits, males (n = 150, median age 20.4 years, IQR 17.2-23.3) had lower odds of self-reported adherence than females (n = 120, median age 19.8 years, IQR 17.1-22.7) (OR 0.41, 95% CI 0.21-0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30-4.82). No significant differences in adherence (by self-report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients. Females show better self-reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self-reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type. BackgroundIdentification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients.MethodsThis multicenter study of prevalent kidney, liver and heart transplant recipients 14–25 years assessed adherence 3 times (0, 3, 6 months post‐enrollment) with the BAASIS self‐report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non‐adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ.ResultsAcross all visits, males (n = 150, median age 20.4 years, IQR 17.2–23.3) had lower odds of self‐reported adherence than females (n = 120, median age 19.8 years, IQR 17.1–22.7) (OR 0.41, 95% CI 0.21–0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30–4.82). No significant differences in adherence (by self‐report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients.ConclusionFemales show better self‐reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self‐reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type. Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients.BACKGROUNDIdentification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared immunosuppressive medication adherence between males and females, and between kidney, liver and heart transplant recipients.This multicenter study of prevalent kidney, liver and heart transplant recipients 14-25 years assessed adherence 3 times (0, 3, 6 months post-enrollment) with the BAASIS self-report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non-adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ.METHODSThis multicenter study of prevalent kidney, liver and heart transplant recipients 14-25 years assessed adherence 3 times (0, 3, 6 months post-enrollment) with the BAASIS self-report tool. At each visit, participants were classified as adherent if they missed no doses in the prior 4 weeks and non-adherent otherwise. Adherence was also assessed using the coefficient of variation (CV) of tacrolimus trough levels; CV < 30% was classified as adherent. We used multivariable mixed effects logistic regression models adjusted for potential confounders to compare adherence by sex and by organ.Across all visits, males (n = 150, median age 20.4 years, IQR 17.2-23.3) had lower odds of self-reported adherence than females (n = 120, median age 19.8 years, IQR 17.1-22.7) (OR 0.41, 95% CI 0.21-0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30-4.82). No significant differences in adherence (by self-report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients.RESULTSAcross all visits, males (n = 150, median age 20.4 years, IQR 17.2-23.3) had lower odds of self-reported adherence than females (n = 120, median age 19.8 years, IQR 17.1-22.7) (OR 0.41, 95% CI 0.21-0.80) but higher odds of adherence by tacrolimus CV (OR 2.50, 95% CI 1.30-4.82). No significant differences in adherence (by self-report or tacrolimus CV) were noted between the 184 kidney, 58 liver, and 28 heart recipients.Females show better self-reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self-reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type.CONCLUSIONFemales show better self-reported adherence than males but greater variability in tacrolimus levels. Social desirability bias, more common in females than males, may contribute to better self-reported adherence among females. Higher tacrolimus variability among females may reflect biologic differences in tacrolimus metabolism between males and females rather than sex differences in adherence. There were no significant differences in adherence by organ type. |
Author | Urschel, Simon Johnston, Olwyn Vaisbourd, Yulia Matsuda‐Abedini, Mina Phan, Veronique BScPhm, Jennifer Harrison Zhang, Xun Dahhou, Mourad Mital, Seema Bissonnette, Janice Cardinal, Heloise Tibbles, Lee Anne De Geest, Sabina Hamiwka, Lorraine Schiff, Jeffrey Allen, Upton Sapir‐Pichhadze, Ruth Birk, Patricia Foster, Bethany J. Blydt‐Hansen, Tom D. Avitzur, Yaron |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36478059$$D View this record in MEDLINE/PubMed |
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Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared... Identification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared... BackgroundIdentification of differences in medication adherence by sex or organ type may help in planning interventions to optimize outcomes. We compared... |
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SubjectTerms | Adolescent Adult Female Females Graft Rejection - drug therapy Graft Rejection - prevention & control Heart transplantation Heart transplants Humans Immunosuppressive Agents - therapeutic use Kidney Transplantation Liver transplantation Male Males Medication Adherence Patient compliance Regression analysis sex Sex differences Social desirability solid organ transplantation Tacrolimus Tacrolimus - therapeutic use Teenagers Transplant Recipients Young Adult |
Title | Differences in medication adherence by sex and organ type among adolescent and young adult solid organ transplant recipients |
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