<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jakubowski BE</submitter><funding>National Institute for Health Research Professorship</funding><funding>National Institute for Health Research (NIHR)</funding><funding>National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research (CLAHRC)</funding><funding>Primary Care Research Trust</funding><funding>National Institute for Health Research Oxford Biomedical Research Centre</funding><pagination>2142-2148</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9790635</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>129(13)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To determine the accuracy of self-testing for proteinuria during pregnancy.&lt;h4>Design&lt;/h4>Diagnostic accuracy study.&lt;h4>Setting&lt;/h4>Antenatal clinics, maternity assessment units and inpatient wards at three hospital sites.&lt;h4>Population or sample&lt;/h4>345 pregnant women.&lt;h4>Methods&lt;/h4>Pregnant women self-tested in-clinic for urinary protein using visually read dipsticks with samples then sent for laboratory estimation of the spot protein-creatinine ratio (PCR) (primary reference test). Secondary index tests included testing by antenatal healthcare professionals and an automated colorimetric reader.&lt;h4>Main outcome measures&lt;/h4>Sensitivity, specificity, negative predictive value, positive predictive value and likelihood ratios were calculated for self-testing (primary index test) along with healthcare professional and colorimetric testing compared to the primary reference test (PCR).&lt;h4>Results&lt;/h4>335/345 (97%) had sufficient data to be included in the analysis. Self-testing had a sensitivity of 0.71 (95% confidence interval [CI] 0.62-0.79) and a specificity of 0.89 (95% CI 0.84-0.92) compared to PCR. Sensitivity and specificity of testing by healthcare professionals and the colorimetric reader were similar: sensitivity 0.73 (95% CI 0.64-0.80) and 0.78 (95% CI 0.69-0.85), respectively; specificity 0.88 (95% CI 0.82-0.92) and 0.83 (95% CI 0.78-0.88), respectively.&lt;h4>Conclusion&lt;/h4>Pregnant women can visually read a dipstick for urinary protein with similar accuracy to antenatal healthcare professionals. Automated colorimetric testing was not significantly different, in contrast to some previous studies. Self-testing has the potential to form part of a self-monitoring regime in pregnancy.</pubmed_abstract><journal>BJOG : an international journal of obstetrics and gynaecology</journal><pubmed_title>Cross-sectional diagnostic accuracy study of self-testing for proteinuria during hypertensive pregnancies: The UDIP study.</pubmed_title><pmcid>PMC9790635</pmcid><funding_grant_id>NIHR-RP-R2-12-015</funding_grant_id><funding_grant_id>RP‐PG‐0614‐20005</funding_grant_id><funding_grant_id>RP-PG-0614-20005</funding_grant_id><pubmed_authors>Lavallee L</pubmed_authors><pubmed_authors>Hodgkinson J</pubmed_authors><pubmed_authors>Stevens R</pubmed_authors><pubmed_authors>Chappell LC</pubmed_authors><pubmed_authors>Wilson H</pubmed_authors><pubmed_authors>Brittain L</pubmed_authors><pubmed_authors>Mackillop L</pubmed_authors><pubmed_authors>Jakubowski BE</pubmed_authors><pubmed_authors>McManus RJ</pubmed_authors><pubmed_authors>Crawford C</pubmed_authors><pubmed_authors>Tucker KL</pubmed_authors><pubmed_authors>Hinton L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cross-sectional diagnostic accuracy study of self-testing for proteinuria during hypertensive pregnancies: The UDIP study.</name><description>&lt;h4>Objective&lt;/h4>To determine the accuracy of self-testing for proteinuria during pregnancy.&lt;h4>Design&lt;/h4>Diagnostic accuracy study.&lt;h4>Setting&lt;/h4>Antenatal clinics, maternity assessment units and inpatient wards at three hospital sites.&lt;h4>Population or sample&lt;/h4>345 pregnant women.&lt;h4>Methods&lt;/h4>Pregnant women self-tested in-clinic for urinary protein using visually read dipsticks with samples then sent for laboratory estimation of the spot protein-creatinine ratio (PCR) (primary reference test). Secondary index tests included testing by antenatal healthcare professionals and an automated colorimetric reader.&lt;h4>Main outcome measures&lt;/h4>Sensitivity, specificity, negative predictive value, positive predictive value and likelihood ratios were calculated for self-testing (primary index test) along with healthcare professional and colorimetric testing compared to the primary reference test (PCR).&lt;h4>Results&lt;/h4>335/345 (97%) had sufficient data to be included in the analysis. Self-testing had a sensitivity of 0.71 (95% confidence interval [CI] 0.62-0.79) and a specificity of 0.89 (95% CI 0.84-0.92) compared to PCR. Sensitivity and specificity of testing by healthcare professionals and the colorimetric reader were similar: sensitivity 0.73 (95% CI 0.64-0.80) and 0.78 (95% CI 0.69-0.85), respectively; specificity 0.88 (95% CI 0.82-0.92) and 0.83 (95% CI 0.78-0.88), respectively.&lt;h4>Conclusion&lt;/h4>Pregnant women can visually read a dipstick for urinary protein with similar accuracy to antenatal healthcare professionals. Automated colorimetric testing was not significantly different, in contrast to some previous studies. Self-testing has the potential to form part of a self-monitoring regime in pregnancy.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T12:09:52.869Z</modification><creation>2025-04-04T12:09:52.869Z</creation></dates><accession>S-EPMC9790635</accession><cross_references><pubmed>35412672</pubmed><doi>10.1111/1471-0528.17180</doi></cross_references></HashMap>