Evidence map›Paper›PMID 26448867›Full record

ArticleBMJ open diabetes research & care2015

Medication burden in the first 5 years following diagnosis of type 2 diabetes: findings from the ADDITION-UK trial cohort.

James A Black, Rebecca K Simmons, Clare E Boothby, Melanie J Davies, David Webb, Kamlesh Khunti, Gráinne H Long, Simon J Griffin

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Common, but not easy.Canadian family physician Medecin de famille canadien · 2019
    Article
  4. Review
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

8 authors.

James A BlackMRC Epidemiology Unit , University of Cambridge , Cambridge , UK.
Rebecca K SimmonsMRC Epidemiology Unit , University of Cambridge , Cambridge , UK.
Clare E BoothbyMRC Epidemiology Unit , University of Cambridge , Cambridge , UK.
Melanie J DaviesDepartment of Cardiovascular Sciences , Leicester Royal Infirmary , Leicester , UK.
David WebbDepartment of Cardiovascular Sciences , Leicester Royal Infirmary , Leicester , UK.
Kamlesh KhuntiDepartment of Cardiovascular Sciences , Leicester Royal Infirmary , Leicester , UK.
Gráinne H LongMRC Epidemiology Unit , University of Cambridge , Cambridge , UK.
Simon J GriffinMRC Epidemiology Unit , University of Cambridge , Cambridge , UK.

Funding

Department of Health 08/116/300Department of Health RP-PG-0606-1259Medical Research Council G0001164Medical Research Council MC_U106179474Medical Research Council MC_UU_12015/4
6 · The paper itself

Abstract

introductionIndividuals with screen-detected diabetes are likely to receive intensified pharmacotherapy to improve glycaemic control and general cardiometabolic health. Individuals are often asymptomatic, and little is known about the degree to which polypharmacy is present both before, and after diagnosis. We aimed to describe and characterize the pharmacotherapy burden of individuals with screen-detected diabetes at diagnosis, 1 and 5 years post-diagnosis.

methodsThe prescription histories of 1026 individuals with screen-detected diabetes enrolled in the ADDITION-UK trial of the promotion of intensive treatment were coded into general medication types at diagnosis, 1 and 5 years post-diagnosis. The association between change in the count of several medication types and age, baseline 10-year UK Prospective Diabetes Study (UKPDS) cardiovascular disease (CVD risk), sex, intensive treatment group and number of medications was explored.

resultsJust under half of individuals were on drugs unrelated to cardioprotection before diagnosis (42%), and this increased along with a rise in the number of prescribed diabetes-related and cardioprotective drugs. The medication profile over the first 5 years suggests multimorbidity and polypharmacy is present in individuals with screen-detected diabetes. Higher modeled CVD risk at baseline was associated with a greater increase in cardioprotective and diabetes-related medication, but not an increase in other medications.

conclusionAs recommended in national guidelines, our results suggest that treatment of diabetes was influenced by the underlying risk of CVD. While many individuals did not start glucose lowering and cardioprotective therapies in the first 5 years after diagnosis, more information is required to understand whether this represents unmet need, or patient-centered care. TRIAL REGISTRATION NUMBER: CNT00237549.

Indexed as

MedicationScreening

Identifiers

PMID26448867
PMCPMC4593027

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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.