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Assessing the effectiveness of a combined drug regimen on ambulatory blood pressure monitoring in stage 2 hypertension

Giyosova NigoraDepartment of Nephrology and Hemodialysis, Bukhara State Medical Institute named after Abu Ali ibn Sino, Bukhara, UzbekistanEsanov DostonbekNavoi Branch of the Republican Scientific and Practical Center of Emergency Medical Care, Navoi, UzbekistanShodiyeva GulzodaPhD, Department of Internal Diseases, Samarkand State Medical University, Samarkand, UzbekistanMaksadjon KhakimovPhD, Department of Traumatology, Orthopedics and Neurosurgery, Andijan State Medical Institute, Andijan, UzbekistanKamola SattarovaPhD, Department of Obstetrics and gynecology, reproductology, Tashkent state medical university, Tashkent, UzbekistanБобоева, Угилой ФатуллаевнаPhD, Assistant of the 2nd Department of Pediatrics, Bukhara State Medical Institute named after Abu Ali ibn Sino, Bukhara, UzbekistanRahimov NurbekDepartment of Internal medicine, Bukhara State Medical Institute named after Abu Ali ibn Sino, Bukhara, UzbekistanBogdanovich GennadiyDepartment of Russian Language Theory and Translation Studies, Andijan State Institute of Foreign Languages, Andijan, UzbekistanSobirjon Muhammadiyevassistant, Department of Trauma and orthopedics, Fergana medical institute of public health, Fergana, Uzbekistan
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Abstract

Stage 2 hypertension poses a major cardiovascular threat in Uzbekistan, where monotherapy often fails to achieve 24-hour control. This study assessed the efficacy of a fixed-dose telmisartan 80 mg/amlodipine 10 mg combination using ambulatory blood pressure monitoring (ABPM) in treatment-naïve patients. In this prospective, single-center trial at Tashkent's Republican Specialized Scientific-Practical Medical Center of Cardiology (January 2024–June 2025), 100 adults (mean age 54 years, 58% male) with office BP ≥140/90 mmHg received once-daily therapy for 12 weeks, alongside lifestyle counseling. ABPM (Oscar 2) captured 24-hour, daytime, and nighttime pressures at baseline and endpoint. Primary outcome: change in 24-hour mean BP. Analyses used paired t-tests and chi-square (p<0.05), powered for 12 mmHg systolic reduction. Therapy yielded significant reductions as 24-hour BP fell by 19.6/12.3 mmHg (p<0.001), daytime 20.7/13.1 mmHg, nighttime 17.4/10.5 mmHg (all p<0.001). Normal dipping rose from 32% to 72% (p<0.001); 92% were systolic responders, 78% achieved <130/80 mmHg 24-hour targets. Office BP dropped 22.8/13.8 mmHg (p<0.001). Adverse events were mild (24%, mainly edema); labs remained stable. Adherence exceeded 87%. Telmisartan-amlodipine combination excels in stage 2 hypertension, delivering robust ABPM control and dipping restoration with excellent tolerability. These findings support its first-line use in Central Asian settings to bridge persistent management gaps.

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