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Amlodipine and calcineurin inhibitor-induced nephrotoxicity following allogeneic hematopoietic stem cell transplant.
Jensen, Ryan R; Healy, Regan M; Ford, Clyde D; Child, Berrie; Majers, Jacob; Draper, Brent; Hasan, Yousef; Hoda, Daanish.
Affiliation
  • Jensen RR; Intermountain Healthcare Acute Leukemia, Blood and Marrow Transplant Program, LDS Hospital, Salt Lake City, Utah.
  • Healy RM; Department of Pharmacy, LDS Hospital, Salt Lake City, Utah.
  • Ford CD; Intermountain Healthcare Acute Leukemia, Blood and Marrow Transplant Program, LDS Hospital, Salt Lake City, Utah.
  • Child B; Department of Pharmacy, LDS Hospital, Salt Lake City, Utah.
  • Majers J; Intermountain Healthcare Acute Leukemia, Blood and Marrow Transplant Program, LDS Hospital, Salt Lake City, Utah.
  • Draper B; Intermountain Healthcare Acute Leukemia, Blood and Marrow Transplant Program, LDS Hospital, Salt Lake City, Utah.
  • Hasan Y; Department of Pharmacy, LDS Hospital, Salt Lake City, Utah.
  • Hoda D; Intermountain Healthcare Acute Leukemia, Blood and Marrow Transplant Program, LDS Hospital, Salt Lake City, Utah.
Clin Transplant ; 33(7): e13633, 2019 07.
Article in En | MEDLINE | ID: mdl-31177566
Studies in the renal transplant population have suggested calcium-channel blockers (CCBs) may protect against calcineurin inhibitor (CNI)-induced nephrotoxicity. However, this has not been evaluated in the hematopoietic stem cell transplant (HSCT) population. This retrospective study reviews data from 350 consecutive patients who underwent allogeneic HSCT to determine whether amlodipine improved renal outcomes. Subject data included up to one year from CNI initiation. Patients in the amlodipine group (n = 130) received an average of 143 days treatment with amlodipine and experienced a smaller decrease in creatinine clearance (CrCl) through day 180. At day 30, change in CrCl was -17.4 mL/min in the amlodipine cohort and -33.8 mL/min in the control (P < 0.001). At day 180, change in CrCl was -40.9 and -50.6 mL/min, respectively (P = 0.005). Incidence of hospitalization with acute kidney injury (AKI) was significantly lower in patients receiving amlodipine, 7.7% (10/132) vs 16.4% (36/220) (hazard ratio [HR] 0.44; 95% confidence interval [CI] 0.22-0.89). Median blood pressure in the amlodipine group remained <132/78 through day 360. Our data support the use of amlodipine for hypertension in the allogeneic HSCT population and provide evidence suggesting that CCBs protect against CNI-induced nephrotoxicity.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amlodipine / Hematopoietic Stem Cell Transplantation / Acute Kidney Injury / Calcineurin Inhibitors / Antihypertensive Agents Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Clin Transplant Journal subject: TRANSPLANTE Year: 2019 Document type: Article Country of publication: Denmark

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amlodipine / Hematopoietic Stem Cell Transplantation / Acute Kidney Injury / Calcineurin Inhibitors / Antihypertensive Agents Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Clin Transplant Journal subject: TRANSPLANTE Year: 2019 Document type: Article Country of publication: Denmark