Evidence map›Paper›PMID 26331311›Full record

Observational studyClinical and experimental hypertension (New York, N.Y. : 1993)2016

Combination therapy with nifedipine GITS 60 mg: subanalysis of a prospective, 12-week observational study (AdADOSE).

Ahmed K Motaweih, Elena Usova, Wajid Hussain, Ziad Dello, Thomas Petri

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical and experimental hypertension (New York, N.Y. : 1993), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Ahmed K Motaweiha Cardiovascular Medicine Department, Faculty of Medicine, Azhar University , Giza , Egypt .
Elena Usovab Outpatient Department , Clinical Hospital 122 , Saint Petersburg , Russia .
Wajid Hussainc Department of Cardiology , Baqai Institute of Cardiovascular Diseases , Karachi , Pakistan .
Ziad Dellod Department of Cardiology , Dallah Hospital , Riyadh , Saudi Arabia , and.
Thomas Petrie Global Medical Affairs Primary Care, Bayer Pharma AG , Berlin , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdADOSE was a 12-week, international, observational study conducted in the Middle East and Russia where patients received nifedipine gastrointestinal therapeutic system (GITS) at a daily dose of 30, 60, or 90 mg as part of an antihypertensive combination therapy. This subgroup analysis of the AdADOSE study assesses the efficacy and tolerability of nifedipine GITS combination therapy when used specifically at the 60-mg strength.

methodsPatients with hypertension who received a daily nifedipine GITS dose of 60 mg, either at constant dose (n = 686) or up-titrated from 30 mg (n = 392), were analyzed. Target blood pressure (BP) was <140/90 mmHg (or <130/80 mmHg for those at high/very high cardiovascular risk).

resultsFollowing nifedipine GITS combination therapy, target BP was achieved by 33.7% patients in the 60 mg group (previously untreated, 42.5%; previously treated, 32.0%) and 32.4% patients in the 30-60 mg group (previously untreated, 45.2%; previously treated, 30.7%). Mean systolic BP/diastolic BP changes were -40.3/-20.7 mmHg and -35.6/-18.5 mmHg, respectively, and were similar regardless of previous antihypertensive treatment or the number of concomitant diseases. Incidences of drug-related adverse events (AEs) were low (3.2%, 60 mg; 2.0%, 30-60 mg group), few patients discontinued because of AEs (0.6% and 1.0%, respectively), and there were no serious AEs.

conclusionCombination therapy with nifedipine GITS 60 mg in a real-life observational setting was effective and well tolerated in hypertensive patients, with low rates of treatment-related AEs.

Indexed as

Blood PressureHypertensionNifedipineAdultAntihypertensive AgentsBlood Pressure DeterminationDelayed-Action PreparationsDose-Response Relationship, DrugDrug MonitoringDrug Therapy, CombinationFemaleHumansMaleMiddle AgedMiddle EastProspective StudiesAntihypertensive AgentsDelayed-Action PreparationsNifedipineAdADOSEcardiovascularhypertensionnifedipine GITSobservational study

Identifiers

PMID26331311
PMCPMC4720040

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.