Evidence map›Paper›PMID 33496201›Full record

Trial reportJournal of the American Heart Association2021

Achieving Optimal Medical Therapy: Insights From the ORBITA Trial.

Michael Foley, Christopher A Rajkumar, Matthew Shun-Shin, Sashiananthan Ganesananthan, Henry Seligman, James Howard, Alexandra N Nowbar, Thomas R Keeble, John R Davies, Kare H Tang and 9 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02062593 (Defining a Gold Standard for Ischaemia), which is not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02062593 nacompletednot on this map

Defining a Gold Standard for Ischaemia: Effects of Interventional Revascularisation Versus Optimum Medical Therapy on Exercise Capacity in Patients With Stable Coronary Artery Disease

TypeinterventionalSponsorImperial College LondonRan2013 to 2017Enrolled230ConditionsStable AnginaArmsCoronary angioplasty
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Achieving Optimal Medical Therapy: Insights From the ORBITA Trial.Journal of the American Heart Association · 2021
    Trial
  7. Article
  8. Remote digital smart device follow-up in prospective clinical trials: early insights from ORBITA-2, ORBITA-COSMIC, and ORBITA-STAR.European heart journal supplements : journal of the European Society of Cardiology · 2022
    Article
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 1 country.

Michael FoleyNational Heart and Lung InstituteImperial College London London UK.
Christopher A RajkumarNational Heart and Lung InstituteImperial College London London UK.
Matthew Shun-ShinNational Heart and Lung InstituteImperial College London London UK.
Sashiananthan GanesananthanImperial College Healthcare NHS Trust London UK.
Henry SeligmanNational Heart and Lung InstituteImperial College London London UK.
James HowardNational Heart and Lung InstituteImperial College London London UK.
Alexandra N NowbarNational Heart and Lung InstituteImperial College London London UK.
Thomas R KeebleEssex Cardiothoracic Centre Basildon UK.
John R DaviesEssex Cardiothoracic Centre Basildon UK.
Kare H TangEssex Cardiothoracic Centre Basildon UK.
Robert GerberEast Sussex Healthcare NHS Trust Hastings UK.
Peter O'KaneRoyal Bournemouth and Christchurch NHS Trust Bournemouth UK.
Andrew S P SharpUniversity Hospital of Wales Cardiff UK.
Ricardo PetracoNational Heart and Lung InstituteImperial College London London UK.
Iqbal S MalikNational Heart and Lung InstituteImperial College London London UK.
Sukhjinder NijjerNational Heart and Lung InstituteImperial College London London UK.
Sayan SenNational Heart and Lung InstituteImperial College London London UK.
Darrel P FrancisNational Heart and Lung InstituteImperial College London London UK.
Rasha Al-LameeNational Heart and Lung InstituteImperial College London London UK.
Imperial College Healthcare NHS Trust · GBEssex Cardiothoracic Centre · GBEast Sussex Healthcare NHS Trust · GBRoyal Bournemouth and Christchurch Hospitals NHS Foundation Trust · GBUniversity Hospital of Wales · GB

Funding

Department of Health NIHR300166Medical Research Council MR/S021108/1
6 · The paper itself

Abstract

Background In stable coronary artery disease, medications are used for 2 purposes: cardiovascular risk reduction and symptom improvement. In clinical trials and clinical practice, medication use is often not optimal. The ORBITA (Objective Randomised Blinded Investigation With Optimal Medical Therapy of Angioplasty in Stable Angina) trial was the first placebo-controlled trial of percutaneous coronary intervention. A key component of the ORBITA trial design was the inclusion of a medical optimization phase, aimed at ensuring that all patients were treated with guideline-directed truly optimal medical therapy. In this study, we report the medical therapy that was achieved. Methods and Results After enrollment into the ORBITA trial, all 200 patients entered a 6-week period of intensive medical therapy optimization, with initiation and uptitration of risk reduction and antianginal therapy. At the prerandomization stage, the median number of antianginals established was 3 (interquartile range, 2-4). A total of 195 patients (97.5%) reached the prespecified target of ≥2 antianginals; 136 (68.0%) did not stop any antianginals because of adverse effects, and the median number of antianginals stopped for adverse effects per patient was 0 (interquartile range, 0-1). Amlodipine and bisoprolol were well tolerated (stopped for adverse effects in 4/175 [2.3%] and 9/167 [5.4%], respectively). Ranolazine and ivabradine were also well tolerated (stopped for adverse effects in 1/20 [5.0%] and 1/18 [5.6%], respectively). Isosorbide mononitrate and nicorandil were stopped for adverse effects in 36 of 172 (20.9%) and 32 of 141 (22.7%) of patients, respectively. Statins were well tolerated and taken by 191 of 200 (95.5%) patients. Conclusions In the 12-week ORBITA trial period, medical therapy was successfully optimized and well tolerated, with few drug adverse effects leading to therapy cessation. Truly optimal medical therapy can be achieved in clinical trials, and translating this into longer-term clinical practice should be a focus of future study. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT02062593.

Indexed as

AmlodipineBisoprololCardiovascular AgentsCoronary AngiographyCoronary Artery DiseaseDose-Response Relationship, DrugDrug Therapy, CombinationFemaleFollow-Up StudiesFractional Flow Reserve, MyocardialHumansHydroxymethylglutaryl-CoA Reductase InhibitorsIsosorbide DinitrateMaleMiddle AgedNicorandilAmlodipineBisoprololCardiovascular AgentsHydroxymethylglutaryl-CoA Reductase Inhibitorsisosorbide-5-mononitrateIsosorbide DinitrateNicorandilRanolazineVasodilator Agentsadverse effectsanginacompliance/adherencemedical therapyrandomized controlled trial

Identifiers

PMID33496201
PMCPMC7955412
OpenAlexW3122241184

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.