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Observational Study
. 2019 Jun 12;9(6):e028062.
doi: 10.1136/bmjopen-2018-028062.

Trends in kidney function testing in UK primary care since the introduction of the quality and outcomes framework: a retrospective cohort study using CPRD

Affiliations
Observational Study

Trends in kidney function testing in UK primary care since the introduction of the quality and outcomes framework: a retrospective cohort study using CPRD

Benjamin Feakins et al. BMJ Open. .

Erratum in

Abstract

Objectives: To characterise serum creatinine and urinary protein testing in UK general practices from 2005 to 2013 and to examine how the frequency of testing varies across demographic factors, with the presence of chronic conditions and with the prescribing of drugs for which kidney function monitoring is recommended.

Design: Retrospective open cohort study.

Setting: Routinely collected data from 630 UK general practices contributing to the Clinical Practice Research Datalink.

Participants: 4 573 275 patients aged over 18 years registered at up-to-standard practices between 1 April 2005 and 31 March 2013. At study entry, no patients were kidney transplant donors or recipients, pregnant or on dialysis.

Primary outcome measures: The rate of serum creatinine and urinary protein testing per year and the percentage of patients with isolated and repeated testing per year.

Results: The rate of serum creatinine testing increased linearly across all age groups. The rate of proteinuria testing increased sharply in the 2009-2010 financial year but only for patients aged 60 years or over. For patients with established chronic kidney disease (CKD), creatinine testing increased rapidly in 2006-2007 and 2007-2008, and proteinuria testing in 2009-2010, reflecting the introduction of Quality and Outcomes Framework indicators. In adjusted analyses, CKD Read codes were associated with up to a twofold increase in the rate of serum creatinine testing, while other chronic conditions and potentially nephrotoxic drugs were associated with up to a sixfold increase. Regional variation in serum creatinine testing reflected country boundaries.

Conclusions: Over a nine-year period, there have been increases in the numbers of patients having kidney function tests annually and in the frequency of testing. Changes in the recommended management of CKD in primary care were the primary determinant, and increases persist even after controlling for demographic and patient-level factors. Future studies should address whether increased testing has led to better outcomes.

Keywords: chronic kidney disease; kidney function; monitoring; primary care; proteinuria; serum creatinine.

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Conflict of interest statement

Competing interests: NRH is currently employed by Bristol-Meyers Squibb Limited, a company that manufactures ACE inhibitors, which are drugs indicated in the treatment of chronic kidney disease, when present in conjunction with other comorbidities such as type 2 diabetes. CT reports speaker fees from Vifor and Novartis and non-financial support from Roche outside of the submitted work. All other authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Rates of kidney function testing (per year), stratified by CKD stage. CKD, chronic kidney disease.
Figure 2
Figure 2
Rates of kidney function testing (per year), stratified by eGFR and albuminuria categories. eGFR, estimated glomerular filtration rate.
Figure 3
Figure 3
Rates of kidney function testing per financial year, stratified by CKD stage. CKD, chronic kidney disease; QOF, Quality and Outcomes Framework.
Figure 4
Figure 4
Percentage of patients that have had 1, 2, 3, 4 or more than four kidney function tests per financial year. NSAIDs, non-steroidal anti-inflammatory drugs; OACs, oral anticoagulants.
Figure 5
Figure 5
Rates of kidney function testing per financial year, stratified by age category. QOF, Quality and Outcomes Framework.
Figure 6
Figure 6
Rates of kidney function testing per financial year, stratified by comorbidity. AFib, atrial fibrillation; HF, eart failure; HTN, hypertension; IHD, ischaemic heart disease; PVD, peripheral vascular disease; QOF, Quality and Outcomes Framework; TIA, transient ischaemic attack; THY, thyroid.
Figure 7
Figure 7
Rates of kidney function testing per financial year, stratified by concomitant pharmacotherapy. ACE-is, ACE inhibitors; ARBs, angiotensin II receptor blockers; Darones, amiodarone or dronedarone; Immuno, other (non-methotrexate) immunosuppressants; NSAIDs, non-steroidal anti-inflammatory drugs; OACs, oral anticoagulants; QOF, Quality and Outcomes Framework.

References

    1. National Institute for Health and Care Excellence, “Chronic kidney disease in adults: assessment and management. Clinical guideline [CG182]. 2014. https://www.nice.org.uk/guidance/cg182. - PubMed
    1. National Kidney Foundation. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis 2002;39(2 Suppl 1):S1–S266. - PubMed
    1. Department of Health, The National Services Framework for Renal Services. Part One: Dialysis and Transplantation, 2004.
    1. British Medical Association. “Revisions to the GMS contract 2006/07. 2006. http://www.nhsemployers.org/-/media/Employers/Documents/Primary-care-con....
    1. National Institute for Health and Care Excellence. NICE Clinical Guideline 73: Chronic Kidney Disease: Early Identification and Management of Chronic Kidney Disease in Adults in Primary and Secondary Care. 2008. https://www.nice.org.uk/guidance/CG73.

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