The Reliability of Remembered Pretreatment Visual Analog Scale Scores among Hand-Surgery Patients
- PMID: 32280175
- PMCID: PMC7141901
- DOI: 10.1055/s-0039-1683462
The Reliability of Remembered Pretreatment Visual Analog Scale Scores among Hand-Surgery Patients
Abstract
Background In clinical audits in which preoperative visual analog scale (VAS) scores were not recorded, it would be useful if such scores could be re-created at the time of review. Patients and Methods We recorded VAS score for pain during the past week before surgery for 245 consecutive hand-surgery patients scheduled for planned surgery during a 6-month period. A total of 30 patients who refused to participate or were unable to respond were excluded. The remaining 215 patients were contacted after 21 months and asked to furnish a new VAS score of the pain they remembered to have had during the last week before surgery. Responses were analyzed with a Bland-Altman plot. Results One hundred and thirty-one (61%) of the patients responded. The mean remembered preoperative score was higher than the mean real preoperative score in all diagnosis groups. The mean difference was 10 mm (standard deviation: 22 mm; standard error of the mean: 2 mm). The lower and upper limits of 95% agreement for individual scores were -33 and 53 mm, whereas the lower and upper limits of the 95% confidence interval of the mean were 6 and 14 mm. Conclusion It may be possible to predict the mean real preoperative VAS score in groups of patients with accuracy using the remembered preoperative score. In individual patients, remembered preoperative VAS scores are far too inaccurate to be of value. However, real preoperative scores should be used whenever possible.
Keywords: accuracy; pain; recall; remembered; visual analog score.
© Thieme Medical Publishers.
Conflict of interest statement
Ethical ApprovalNoteAuthors’ ContributionsAvailability of Data and MaterialConflict of Interest This study was approved in writing by the regional committee for medical health research ethics for central Norway (ref. 2015/456). Patients were fully informed in writing about the purpose of our request for the remembered VAS and that the results would be published in a scientific paper. Those who responded to our letter and returned a remembered VAS were considered to have given their implied consent. V.F. conceived the study, analyzed the data, and wrote the paper. S.H. collected the data, analyzed the data, and wrote the paper. I.F. collected the data, analyzed the data, and wrote the paper. All data generated or analyzed during this study are included in the Supplementary Material (available in the online version). None declared.
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