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Gabapentin, Concomitant Prescription of Opioids, and Benzodiazepines among Kidney Transplant Recipients

Gabapentinoids, commonly used for treating neuropathic pain, may be misused and coprescribed with opioid and benzodiazepine, increasing the risk of mortality and dependency among kidney transplant recipients. We identified adult kidney transplant recipients who enrolled in Medicare Part D in 2006-20...

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Published in:Clinical journal of the American Society of Nephrology 2023-01, Vol.18 (1), p.91-98
Main Authors: Chen, Yusi, Ahn, JiYoon B, Bae, Sunjae, Joseph, Corey, Schnitzler, Mark, Hess, Gregory P, Lentine, Krista L, Lonze, Bonnie E, Segev, Dorry L, McAdams-DeMarco, Mara
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container_issue 1
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container_title Clinical journal of the American Society of Nephrology
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creator Chen, Yusi
Ahn, JiYoon B
Bae, Sunjae
Joseph, Corey
Schnitzler, Mark
Hess, Gregory P
Lentine, Krista L
Lonze, Bonnie E
Segev, Dorry L
McAdams-DeMarco, Mara
description Gabapentinoids, commonly used for treating neuropathic pain, may be misused and coprescribed with opioid and benzodiazepine, increasing the risk of mortality and dependency among kidney transplant recipients. We identified adult kidney transplant recipients who enrolled in Medicare Part D in 2006-2017 using the United States Renal Data System/Medicare claims database. We characterized recipients' post-transplant concomitant prescription of gabapentinoids, opioids, and benzodiazepine stratified by transplant year and recipient factors (age, sex, race, and diabetes). We investigated whether concomitant prescriptions were associated with postkidney transplant mortality using Cox regression. Models incorporated inverse probability weighting to adjust for confounders. Among 63,359 eligible recipients, 13% of recipients filled at least one gabapentinoid prescription within 1 year after kidney transplant. The prevalence of gabapentinoid prescriptions increased by 70% over the study period (16% in 2017 versus 10% in 2006). Compared with nonusers, gabapentinoids users were more likely to have diabetes (55% versus 37%) and obesity (46% versus 34%). Of the 8509 recipients with gabapentinoid prescriptions, 45% were coprescribed opioids, 7% were coprescribed benzodiazepines, and 3% were coprescribed both opioids and benzodiazepines. Compared with no study prescriptions, gabapentinoid monotherapy (adjusted hazard ratio [aHR]=1.25; 95% confidence interval [CI], 1.16 to 1.32) and combination therapy (gabapentinoids and opioids [aHR=1.49; 95% CI, 1.39 to 1.60], gabapentinoids and benzodiazepines [aHR=1.46; 95% CI, 1.03 to 2.08], and coprescribing all three [aHR=1.88; 95% CI, 1.18 to 2.98]) were all associated with a higher risk of postkidney transplant mortality. Gabapentinoid coprescription with both benzodiazepines and opioids among kidney transplant recipients increased over time. Kidney transplant recipients prescribed gabapentinoids had a higher risk of post-transplant mortality, and the risk was higher with opioids or benzodiazepine coprescription.
doi_str_mv 10.2215/CJN.0000000000000019
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We identified adult kidney transplant recipients who enrolled in Medicare Part D in 2006-2017 using the United States Renal Data System/Medicare claims database. We characterized recipients' post-transplant concomitant prescription of gabapentinoids, opioids, and benzodiazepine stratified by transplant year and recipient factors (age, sex, race, and diabetes). We investigated whether concomitant prescriptions were associated with postkidney transplant mortality using Cox regression. Models incorporated inverse probability weighting to adjust for confounders. Among 63,359 eligible recipients, 13% of recipients filled at least one gabapentinoid prescription within 1 year after kidney transplant. The prevalence of gabapentinoid prescriptions increased by 70% over the study period (16% in 2017 versus 10% in 2006). Compared with nonusers, gabapentinoids users were more likely to have diabetes (55% versus 37%) and obesity (46% versus 34%). Of the 8509 recipients with gabapentinoid prescriptions, 45% were coprescribed opioids, 7% were coprescribed benzodiazepines, and 3% were coprescribed both opioids and benzodiazepines. Compared with no study prescriptions, gabapentinoid monotherapy (adjusted hazard ratio [aHR]=1.25; 95% confidence interval [CI], 1.16 to 1.32) and combination therapy (gabapentinoids and opioids [aHR=1.49; 95% CI, 1.39 to 1.60], gabapentinoids and benzodiazepines [aHR=1.46; 95% CI, 1.03 to 2.08], and coprescribing all three [aHR=1.88; 95% CI, 1.18 to 2.98]) were all associated with a higher risk of postkidney transplant mortality. Gabapentinoid coprescription with both benzodiazepines and opioids among kidney transplant recipients increased over time. 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We identified adult kidney transplant recipients who enrolled in Medicare Part D in 2006-2017 using the United States Renal Data System/Medicare claims database. We characterized recipients' post-transplant concomitant prescription of gabapentinoids, opioids, and benzodiazepine stratified by transplant year and recipient factors (age, sex, race, and diabetes). We investigated whether concomitant prescriptions were associated with postkidney transplant mortality using Cox regression. Models incorporated inverse probability weighting to adjust for confounders. Among 63,359 eligible recipients, 13% of recipients filled at least one gabapentinoid prescription within 1 year after kidney transplant. The prevalence of gabapentinoid prescriptions increased by 70% over the study period (16% in 2017 versus 10% in 2006). Compared with nonusers, gabapentinoids users were more likely to have diabetes (55% versus 37%) and obesity (46% versus 34%). Of the 8509 recipients with gabapentinoid prescriptions, 45% were coprescribed opioids, 7% were coprescribed benzodiazepines, and 3% were coprescribed both opioids and benzodiazepines. Compared with no study prescriptions, gabapentinoid monotherapy (adjusted hazard ratio [aHR]=1.25; 95% confidence interval [CI], 1.16 to 1.32) and combination therapy (gabapentinoids and opioids [aHR=1.49; 95% CI, 1.39 to 1.60], gabapentinoids and benzodiazepines [aHR=1.46; 95% CI, 1.03 to 2.08], and coprescribing all three [aHR=1.88; 95% CI, 1.18 to 2.98]) were all associated with a higher risk of postkidney transplant mortality. Gabapentinoid coprescription with both benzodiazepines and opioids among kidney transplant recipients increased over time. Kidney transplant recipients prescribed gabapentinoids had a higher risk of post-transplant mortality, and the risk was higher with opioids or benzodiazepine coprescription.</description><subject>Adult</subject><subject>Aged</subject><subject>Analgesics, Opioid - therapeutic use</subject><subject>Benzodiazepines - therapeutic use</subject><subject>Drug Prescriptions</subject><subject>Gabapentin - therapeutic use</subject><subject>Humans</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Medicare Part D</subject><subject>Original</subject><subject>Retrospective Studies</subject><subject>Transplantation</subject><subject>United States - epidemiology</subject><issn>1555-9041</issn><issn>1555-905X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLBDEMx4sovr-BSI8edrXPGeckuvheVETBW-l00rWy047trOB-eivqoiaHBJL8kvBHaIeSfcaoPBhd3eyTP0arJbROpZTDisin5UUu6BraSOmFECE4k6tojRclrWhB19HkXNe6A987P8Cj4E1oXa99j-8iJBNd17vgcbD4tnPBNWmAtW_wCfh5aJyeQ-c8JKzb4Cf42jUe3vFD1D5100_IPRjXuUxPW2jF6mmC7e-4iR7PTh9GF8Px7fnl6Hg8NFwe9sNSN7aRDGRhbckqKbTgtZFSA-NFxagVNWdai4ZQZmh-o7ZlDUUFzAhjOeeb6OiL283qFhqTd0c9VV10rY7vKmin_la8e1aT8KYoyV6QKhP2vgkxvM4g9ap1ycA0PwRhlhQrS8o5o2WRW8VXq4khpQh2sYcS9SmSyiKp_yLlsd3fNy6GflThHz8mj6w</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Chen, Yusi</creator><creator>Ahn, JiYoon B</creator><creator>Bae, Sunjae</creator><creator>Joseph, Corey</creator><creator>Schnitzler, Mark</creator><creator>Hess, Gregory P</creator><creator>Lentine, Krista L</creator><creator>Lonze, Bonnie E</creator><creator>Segev, Dorry L</creator><creator>McAdams-DeMarco, Mara</creator><general>American Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230101</creationdate><title>Gabapentin, Concomitant Prescription of Opioids, and Benzodiazepines among Kidney Transplant Recipients</title><author>Chen, Yusi ; 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We identified adult kidney transplant recipients who enrolled in Medicare Part D in 2006-2017 using the United States Renal Data System/Medicare claims database. We characterized recipients' post-transplant concomitant prescription of gabapentinoids, opioids, and benzodiazepine stratified by transplant year and recipient factors (age, sex, race, and diabetes). We investigated whether concomitant prescriptions were associated with postkidney transplant mortality using Cox regression. Models incorporated inverse probability weighting to adjust for confounders. Among 63,359 eligible recipients, 13% of recipients filled at least one gabapentinoid prescription within 1 year after kidney transplant. The prevalence of gabapentinoid prescriptions increased by 70% over the study period (16% in 2017 versus 10% in 2006). Compared with nonusers, gabapentinoids users were more likely to have diabetes (55% versus 37%) and obesity (46% versus 34%). Of the 8509 recipients with gabapentinoid prescriptions, 45% were coprescribed opioids, 7% were coprescribed benzodiazepines, and 3% were coprescribed both opioids and benzodiazepines. Compared with no study prescriptions, gabapentinoid monotherapy (adjusted hazard ratio [aHR]=1.25; 95% confidence interval [CI], 1.16 to 1.32) and combination therapy (gabapentinoids and opioids [aHR=1.49; 95% CI, 1.39 to 1.60], gabapentinoids and benzodiazepines [aHR=1.46; 95% CI, 1.03 to 2.08], and coprescribing all three [aHR=1.88; 95% CI, 1.18 to 2.98]) were all associated with a higher risk of postkidney transplant mortality. Gabapentinoid coprescription with both benzodiazepines and opioids among kidney transplant recipients increased over time. Kidney transplant recipients prescribed gabapentinoids had a higher risk of post-transplant mortality, and the risk was higher with opioids or benzodiazepine coprescription.</abstract><cop>United States</cop><pub>American Society of Nephrology</pub><pmid>36719161</pmid><doi>10.2215/CJN.0000000000000019</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source Open Access: PubMed Central; Highwire Press American Society of Nephrology
subjects Adult
Aged
Analgesics, Opioid - therapeutic use
Benzodiazepines - therapeutic use
Drug Prescriptions
Gabapentin - therapeutic use
Humans
Kidney Transplantation - adverse effects
Medicare Part D
Original
Retrospective Studies
Transplantation
United States - epidemiology
title Gabapentin, Concomitant Prescription of Opioids, and Benzodiazepines among Kidney Transplant Recipients
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