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10.1093/ajhp/zxab215

http://scihub22266oqcxt.onion/10.1093/ajhp/zxab215
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suck abstract from ncbi


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pmid34013341      Am+J+Health+Syst+Pharm 2021 ; 78 (24): 2245-2255
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  • Serum potassium changes due to concomitant ACEI/ARB and spironolactone therapy: A systematic review and meta-analysis #MMPMID34013341
  • Villa-Zapata L; Carhart BS; Horn JR; Hansten PD; Subbian V; Gephart S; Tan M; Romero A; Malone DC
  • Am J Health Syst Pharm 2021[Dec]; 78 (24): 2245-2255 PMID34013341show ga
  • PURPOSE: To provide evidence of serum potassium changes in individuals taking angiotensin-converting enzyme inhibitors (ACEIs) and/or angiotensin receptor blockers (ARBs) concomitantly with spironolactone compared to ACEI/ARB therapy alone. METHODS: PubMed, Embase, Scopus, and Web of Science were searched for studies including exposure to both spironolactone and ACEI/ARB therapy compared to ACEI/ARB therapy alone. The primary outcome was serum potassium change over time. Main effects were calculated to estimate average treatment effect using random effects models. Heterogeneity was assessed using Cochran's Q and I2. Risk of bias was assessed using the revised Cochrane risk of bias tool. RESULTS: From the total of 1,225 articles identified, 20 randomized controlled studies were included in the meta-analysis. The spironolactone plus ACEI/ARB group included 570 patients, while the ACEI/ARB group included 547 patients. Treatment with spironolactone and ACEI/ARB combination therapy compared to ACEI/ARB therapy alone increased the mean serum potassium concentration by 0.19 mEq/L (95% CI, 0.12-0.26 mEq/L), with intermediate heterogeneity across studies (Q statistic = 46.5, P = 0.004; I2 = 59). Sensitivity analyses showed that the direction and magnitude of this outcome did not change with the exclusion of individual studies, indicating a high level of reliability. Reporting risk of bias was low for 16 studies (80%), unclear for 3 studies (15%) and high for 1 study (5%). CONCLUSION: Treatment with spironolactone in combination with ACEI/ARB therapy increases the mean serum potassium concentration by less than 0.20 mEq/L compared to ACEI/ARB therapy alone. However, serum potassium and renal function must be monitored in patients starting combination therapy to avoid changes in serum potassium that could lead to hyperkalemia.
  • |*Angiotensin Receptor Antagonists[MESH]
  • |*Spironolactone/adverse effects[MESH]
  • |Angiotensin-Converting Enzyme Inhibitors/adverse effects[MESH]
  • |Humans[MESH]
  • |Potassium[MESH]


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