Bibliography

Research using CPRD data has informed drug safety guidance and clinical practice and resulted in over 2,800 peer-reviewed publications. The CPRD bibliography is updated on a monthly basis (last updated 5 October 2021) and papers are listed below and in the PDF below.

If you have published papers using CPRD data which are not included in this list, please contact us at enquiries@cprd.com so that we can update the bibliography.

Download:

 (PDF, 4MB, 241 pages) 

This work uses data provided by patients and collected by the NHS as part of their care and support. CPRD encourages researchers to use this citation in all publications using CPRD data. Find out more about acknowledging the use of patient data at the Understanding Patient Data website. 

 

 

Export 18 results:
Author Title Type [ Year(Asc)]
Filters: First Letter Of Title is Q  [Clear All Filters]
2021
R. Persson, Sponholtz, T., Vasilakis-Scaramozza, C., Hagberg, K. W., Williams, T., Kotecha, D., Myles, P., and Jick, S. S., “Quality and Completeness of Myocardial Infarction Recording in Clinical Practice Research Datalink Aurum”, Clin Epidemiol, vol. 13, pp. 745-753, 2021.
M. J. Schuemie, Weinstein, R., Ryan, P. B., and Berlin, J. A., “Quantifying bias in epidemiologic studies evaluating the association between acetaminophen use and cancer”, Regul Toxicol Pharmacol, vol. 120, p. 104866, 2021.
2020
S. S. Jick, Hagberg, K. W., Persson, R., Vasilakis-Scaramozza, C., Williams, T., Crellin, E., and Myles, P., “Quality and completeness of diagnoses recorded in the new CPRD Aurum Database: evaluation of pulmonary embolism”, Pharmacoepidemiol Drug Saf, 2020.
H. Carreira, Williams, R., Dempsey, H., Stanway, S., Smeeth, L., and Bhaskaran, K., “Quality of life and mental health in breast cancer survivors compared with non-cancer controls: a study of patient-reported outcomes in the United Kingdom”, J Cancer Surviv, 2020.
M. Quiroga, Shephard, E. A., Mounce, L. T. A., Carney, M., Hamilton, W. T., and Price, S. J., “Quantifying the impact of pre-existing conditions on the stage of oesophagogastric cancer at diagnosis: a primary care cohort study using electronic medical records”, Fam Pract, 2020.
2019
H. P. Booth, Gallagher, A. M., Mullett, D., Carty, L., Padmanabhan, S., Myles, P. R., Welburn, S. J., Hoghton, M., Rafi, I., and Valentine, J., “Quality improvement of prescribing safety: a pilot study in primary care using UK electronic health records”, Br J Gen Pract, 2019.
2018
R. I. Griffiths, McFadden, E. C., Stevens, R. J., Valderas, J. M., Lavery, B. A., Khan, N. F., Keating, N. L., and Bankhead, C. R., “Quality of diabetes care in breast, colorectal, and prostate cancer”, J Cancer Surviv, vol. 12, pp. 803-812, 2018.
2017
A. R. Tate, Dungey, S., Glew, S., Beloff, N., Williams, R., and Williams, T., “Quality of recording of diabetes in the UK: how does the GP's method of coding clinical data affect incidence estimates? Cross-sectional study using the CPRD database”, BMJ Open, vol. 7, p. e012905, 2017.
K. Wing, Bhaskaran, K., Pealing, L., Root, A., Smeeth, L., van Staa, T. P., Klungel, O. H., Reynolds, R. F., and Douglas, I., “Quantification of the risk of liver injury associated with flucloxacillin: a UK population-based cohort study”, J Antimicrob Chemother, vol. 72, pp. 2636-2646, 2017.
J. H. Humphreys, Warner, A., Costello, R., Lunt, M., Verstappen, S. M. M., and Dixon, W. G., “Quantifying the hepatotoxic risk of alcohol consumption in patients with rheumatoid arthritis taking methotrexate”, Ann Rheum Dis, vol. 76, pp. 1509-1514, 2017.
2016
H. J. Forbes, Bhaskaran, K., Thomas, S. L., Smeeth, L., Clayton, T., Mansfield, K., Minassian, C., and Langan, S. M., “Quantification of risk factors for postherpetic neuralgia in herpes zoster patients: A cohort study”, Neurology, vol. 87, pp. 94-102, 2016.
2015
E. A. Shephard, Neal, R. D., Rose, P. W., Walter, F. M., and Hamilton, W. T., “Quantifying the risk of Hodgkin lymphoma in symptomatic primary care patients aged >/=40 years: a case-control study using electronic records”, Br J Gen Pract, vol. 65, pp. e289-94, 2015.
E. A. Shephard, Neal, R. D., Rose, P., Walter, F. M., Litt, E. J., and Hamilton, W. T., “Quantifying the risk of multiple myeloma from symptoms reported in primary care patients: a large case-control study using electronic records”, Br J Gen Pract, vol. 65, pp. e106-13, 2015.
E. A. Shephard, Neal, R. D., Rose, P. W., Walter, F. M., and Hamilton, W. T., “Quantifying the risk of non-Hodgkin lymphoma in symptomatic primary care patients aged >/=40 years: a large case-control study using electronic records”, Br J Gen Pract, vol. 65, pp. e281-8, 2015.
2014
H. J. Forbes, Bhaskaran, K., Thomas, S. L., Smeeth, L., Clayton, T., and Langan, S. M., “Quantification of risk factors for herpes zoster: population based case-control study”, Bmj, vol. 348, p. g2911, 2014.
2012
A. M. Gallagher, de Vries, F., Plumb, J. M., Hass, B., Clemens, A., and van Staa, T. P., “Quality of INR control and outcomes following venous thromboembolism”, Clin Appl Thromb Hemost, vol. 18, pp. 370-8, 2012.
2010
N. F. Khan, Mant, D., and Rose, P. W., “Quality of care for chronic diseases in a British cohort of long-term cancer survivors”, Ann Fam Med, vol. 8, pp. 418-24, 2010.
1994
T. - P. Van Staa and Abenhaim, L., “The quality of information recorded on a UK database of primary care records: A study of hospitalizations due to hypoglycemia and other conditions”, Pharmacoepidemiology and Drug Safety, vol. 3, pp. 15-21, 1994.
[Page last reviewed 5 October 2021]