1. Effectiveness and Tolerability of Nifedipine GITS in Patients with Chronic Kidney Disease and Uncontrolled Hypertension: A Prospective, Multicenter, Observational Study (ADRENAL)
- Author
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Wei Li, Qinkai Chen, Henglan Wu, Cuihong Liu, Tao Zhang, Shizhong Shen, Feng Yu, Jian Huang, Xiaoru Zhang, Hong Cheng, Rong Li, Wang Jijun, Rong Lv, Fuyuan Hong, Jie Liu, Huamin Wang, Xiao Hua, Jianghua Chen, Wenbin Song, and Lixin Wei
- Subjects
medicine.medical_specialty ,Nifedipine ,Diastole ,Blood Pressure ,Nifedipine GITS ,Internal medicine ,Chronic kidney disease ,Observational study ,medicine ,Clinical endpoint ,Humans ,Pharmacology (medical) ,cardiovascular diseases ,Prospective Studies ,Renal Insufficiency, Chronic ,Adverse effect ,Antihypertensive Agents ,Original Research ,business.industry ,General Medicine ,medicine.disease ,Confidence interval ,Blood pressure ,Tolerability ,Hypertension ,business ,medicine.drug ,Kidney disease ,circulatory and respiratory physiology - Abstract
Introduction Achieving target blood pressure (BP) goals in patients with chronic kidney disease (CKD) and uncontrolled hypertension is a challenge. Various studies have shown the efficacy of nifedipine gastrointestinal therapeutic system (GITS) 60 mg in patients with hypertension. However, there is a paucity of clinical studies in patients with CKD. Hence, we conducted this study to evaluate the effectiveness and tolerability of nifedipine GITS 60 mg in Chinese patients with CKD and uncontrolled hypertension in real-world clinical settings. Methods In a prospective, multicenter, observational study, Chinese patients with CKD and uncontrolled hypertension were given nifedipine GITS 60 mg with a primary endpoint of change in office systolic BP (SBP) at 12 weeks. The secondary endpoints included changes at 12 weeks in office diastolic BP (DBP), office SBP and DBP in SBP subgroups (140–160 mmHg and ≥ 160 mmHg) and CKD stages subgroups, SBP and DBP control rate, and the adverse events (AEs). Statistical analysis was performed using SAS® version 9.4. Results In total, 871 and 622 patients were included in the safety analysis set and efficacy analysis set respectively. The mean office SBP and DBP at baseline were 162.9 and 97.3 mmHg, respectively. At week 12, the mean change in SBP was − 24.0 mmHg (95% confidence interval [CI] − 25.32, − 22.65 mmHg); after missing data were accounted for, it was − 23.9 mmHg (95% CI − 25.25, − 22.60 mmHg). Marked decreases in DBP, and office SBP and DBP in baseline SBP subgroups as well as CKD stages were observed at week 12. The BP control rate at week 12 was 50.0%. Twenty-three (2.6%) patients reported at least one drug-related AEs. No event of hypotension or death occurred during the study. Conclusion Nifedipine GITS 60 mg showed effectiveness and tolerability in reducing office SBP and DBP in Chinese patients with CKD and uncontrolled hypertension. Trial Registration ClinicalTrials.gov identifier NCT03194633. Supplementary Information The online version contains supplementary material available at 10.1007/s12325-021-01850-3.
- Published
- 2021