Quality assurance for Quantitative Sensory Testing laboratories: development and validation of an automated evaluation tool for the analysis of declared healthy samples
Quantitative Sensory Testing (QST) is a psychophysical method assessing the somatosensory nervous system. A premise for comparable results between laboratories is standardized testing. Its quality can be proven by analyzing healthy subjects, because their results should lie within confidence interva...
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| Published in | Pain (Amsterdam) Vol. 156; no. 12; pp. 2423 - 2430 |
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| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
International Association for the Study of Pain
01.12.2015
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0304-3959 1872-6623 1872-6623 |
| DOI | 10.1097/j.pain.0000000000000300 |
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| Abstract | Quantitative Sensory Testing (QST) is a psychophysical method assessing the somatosensory nervous system. A premise for comparable results between laboratories is standardized testing. Its quality can be proven by analyzing healthy subjects, because their results should lie within confidence intervals estimated from large database samples. However, it is unclear how many abnormal values can be tolerated. Based on a binomial distribution, a tool for assessing samples of healthy subjects was developed to detect inclusion errors (inclusion of nonhealthy subjects) or measuring errors (inaccuracies in single QST parameters). Sensitivity and specificity of detecting inclusion errors were assessed in 431 healthy subjects and 833 patients with neuropathic pain syndromes from the German Research Network on Neuropathic Pain (DFNS) database. Measuring errors were simulated by raising all absolute values in a single parameter by 0.5 SD. We calculated optimal cutoff values for group sizes of 16 healthy subjects, as implemented in the DFNS certification procedures. The algorithm was applied in the certification process of 18 European QST laboratories. With a specificity of 95% and a sensitivity of 60%, inclusion errors can be assumed for ≥4 abnormal values per subject, whereas ≥6 abnormal values per QST parameter and laboratory indicate measuring errors. Subsequently, in the certification process of 5 of 18 centers, inclusion or measuring errors were detected. In most cases, inclusion errors were verified and reasons for measuring errors were illuminated by the centers. This underlines the usefulness and validity of our tool in quality assurance of QST laboratories using the DFNS protocol. |
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| AbstractList | Quantitative Sensory Testing (QST) is a psychophysical method assessing the somatosensory nervous system. A premise for comparable results between laboratories is standardized testing. Its quality can be proven by analyzing healthy subjects, because their results should lie within confidence intervals estimated from large database samples. However, it is unclear how many abnormal values can be tolerated. Based on a binomial distribution, a tool for assessing samples of healthy subjects was developed to detect inclusion errors (inclusion of nonhealthy subjects) or measuring errors (inaccuracies in single QST parameters). Sensitivity and specificity of detecting inclusion errors were assessed in 431 healthy subjects and 833 patients with neuropathic pain syndromes from the German Research Network on Neuropathic Pain (DFNS) database. Measuring errors were simulated by raising all absolute values in a single parameter by 0.5 SD. We calculated optimal cutoff values for group sizes of 16 healthy subjects, as implemented in the DFNS certification procedures. The algorithm was applied in the certification process of 18 European QST laboratories. With a specificity of 95% and a sensitivity of 60%, inclusion errors can be assumed for ≥4 abnormal values per subject, whereas ≥6 abnormal values per QST parameter and laboratory indicate measuring errors. Subsequently, in the certification process of 5 of 18 centers, inclusion or measuring errors were detected. In most cases, inclusion errors were verified and reasons for measuring errors were illuminated by the centers. This underlines the usefulness and validity of our tool in quality assurance of QST laboratories using the DFNS protocol. Quantitative Sensory Testing (QST) is a psychophysical method assessing the somatosensory nervous system. A premise for comparable results between laboratories is standardized testing. Its quality can be proven by analyzing healthy subjects, because their results should lie within confidence intervals estimated from large database samples. However, it is unclear how many abnormal values can be tolerated. Based on a binomial distribution, a tool for assessing samples of healthy subjects was developed to detect inclusion errors (inclusion of nonhealthy subjects) or measuring errors (inaccuracies in single QST parameters). Sensitivity and specificity of detecting inclusion errors were assessed in 431 healthy subjects and 833 patients with neuropathic pain syndromes from the German Research Network on Neuropathic Pain (DFNS) database. Measuring errors were simulated by raising all absolute values in a single parameter by 0.5 SD. We calculated optimal cutoff values for group sizes of 16 healthy subjects, as implemented in the DFNS certification procedures. The algorithm was applied in the certification process of 18 European QST laboratories. With a specificity of 95% and a sensitivity of 60%, inclusion errors can be assumed for ≥4 abnormal values per subject, whereas ≥6 abnormal values per QST parameter and laboratory indicate measuring errors. Subsequently, in the certification process of 5 of 18 centers, inclusion or measuring errors were detected. In most cases, inclusion errors were verified and reasons for measuring errors were illuminated by the centers. This underlines the usefulness and validity of our tool in quality assurance of QST laboratories using the DFNS protocol.Quantitative Sensory Testing (QST) is a psychophysical method assessing the somatosensory nervous system. A premise for comparable results between laboratories is standardized testing. Its quality can be proven by analyzing healthy subjects, because their results should lie within confidence intervals estimated from large database samples. However, it is unclear how many abnormal values can be tolerated. Based on a binomial distribution, a tool for assessing samples of healthy subjects was developed to detect inclusion errors (inclusion of nonhealthy subjects) or measuring errors (inaccuracies in single QST parameters). Sensitivity and specificity of detecting inclusion errors were assessed in 431 healthy subjects and 833 patients with neuropathic pain syndromes from the German Research Network on Neuropathic Pain (DFNS) database. Measuring errors were simulated by raising all absolute values in a single parameter by 0.5 SD. We calculated optimal cutoff values for group sizes of 16 healthy subjects, as implemented in the DFNS certification procedures. The algorithm was applied in the certification process of 18 European QST laboratories. With a specificity of 95% and a sensitivity of 60%, inclusion errors can be assumed for ≥4 abnormal values per subject, whereas ≥6 abnormal values per QST parameter and laboratory indicate measuring errors. Subsequently, in the certification process of 5 of 18 centers, inclusion or measuring errors were detected. In most cases, inclusion errors were verified and reasons for measuring errors were illuminated by the centers. This underlines the usefulness and validity of our tool in quality assurance of QST laboratories using the DFNS protocol. |
| Author | Enax-Krumova, Elena K. Maier, Christoph Tölle, Thomas Hüllemann, Philipp Vollert, Jan Treede, Rolf-Detlef Mainka, Tina Pfau, Doreen Barbara Baron, Ralf |
| AuthorAffiliation | Department of Pain Medicine, BG University Hospital Bergmannsheil GmbH, Ruhr University, Bochum, Germany Centre of Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany Department of Neurology, BG University Hospital Bergmannsheil GmbH, Ruhr-University Bochum, Germany Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany |
| AuthorAffiliation_xml | – name: Department of Pain Medicine, BG University Hospital Bergmannsheil GmbH, Ruhr University, Bochum, Germany Centre of Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany Department of Neurology, BG University Hospital Bergmannsheil GmbH, Ruhr-University Bochum, Germany Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany |
| Author_xml | – sequence: 1 givenname: Jan surname: Vollert fullname: Vollert, Jan organization: Department of Pain Medicine, BG University Hospital Bergmannsheil GmbH, Ruhr University, Bochum, Germany Centre of Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany Division of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany Department of Neurology, BG University Hospital Bergmannsheil GmbH, Ruhr-University Bochum, Germany Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany – sequence: 2 givenname: Tina surname: Mainka fullname: Mainka, Tina – sequence: 3 givenname: Ralf surname: Baron fullname: Baron, Ralf – sequence: 4 givenname: Elena surname: Enax-Krumova middlename: K. fullname: Enax-Krumova, Elena K. – sequence: 5 givenname: Philipp surname: Hüllemann fullname: Hüllemann, Philipp – sequence: 6 givenname: Christoph surname: Maier fullname: Maier, Christoph – sequence: 7 givenname: Doreen surname: Pfau middlename: Barbara fullname: Pfau, Doreen Barbara – sequence: 8 givenname: Thomas surname: Tölle fullname: Tölle, Thomas – sequence: 9 givenname: Rolf-Detlef surname: Treede fullname: Treede, Rolf-Detlef |
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| Cites_doi | 10.1007/s00482-008-0771-4 10.1016/j.pain.2010.07.026 10.1016/j.pain.2012.08.007 10.1016/j.pain.2010.05.002 10.1093/clinchem/39.4.561 10.1016/j.pain.2006.01.041 10.1016/j.pain.2014.02.004 10.1097/AJP.0b013e31821d8fce 10.2307/2531595 10.1016/j.pain.2010.01.011 10.1016/j.pain.2013.05.047 |
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| References_xml | – volume: 12 start-page: 393 year: 2012 ident: R6-7-20210126 article-title: Neuropathic pain: is quantitative sensory testing helpful Curr Diab R publication-title: ep – volume: 23 start-page: 65 year: 2009 ident: R5-7-20210126 article-title: Procedure for certification of QST laboratories in German. publication-title: Schmerz doi: 10.1007/s00482-008-0771-4 – volume: 151 start-page: 598 year: 2010 ident: R7-7-20210126 article-title: Reference data for quantitative sensory testing (QST): refined stratification for age and a novel method for statistical comparison of group data. publication-title: PAIN doi: 10.1016/j.pain.2010.07.026 – volume: 153 start-page: 2403 year: 2012 ident: R11-7-20210126 article-title: Quantitative sensory testing somatosensory profiles in patients with cervical radiculopathy are distinct from those in patients with nonspecific neck-arm pain. publication-title: PAIN doi: 10.1016/j.pain.2012.08.007 – volume: 150 start-page: 439 year: 2010 ident: R8-7-20210126 article-title: Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): somatosensory abnormalities in 1236 patients with different neuropathic pain syndromes. publication-title: PAIN doi: 10.1016/j.pain.2010.05.002 – volume: 39 start-page: 561 year: 1993 ident: R13-7-20210126 article-title: Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine. publication-title: Clin Chem doi: 10.1093/clinchem/39.4.561 – volume: 123 start-page: 231 year: 2006 ident: R10-7-20210126 article-title: Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): standardized protocol and reference values. publication-title: PAIN doi: 10.1016/j.pain.2006.01.041 – volume: 155 start-page: 1002 year: 2014 ident: R9-7-20210126 article-title: Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): reference data for the trunk and application in patients with chronic postherpetic neuralgia. publication-title: PAIN doi: 10.1016/j.pain.2014.02.004 – volume: 27 start-page: 782 year: 2011 ident: R12-7-20210126 article-title: Pain-associated mild sensory deficits without hyperalgesia in chronic non-neuropathic pain. publication-title: Clin J Pain doi: 10.1097/AJP.0b013e31821d8fce – volume: 44 start-page: 837 year: 1988 ident: R4-7-20210126 article-title: Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. publication-title: Biometrics doi: 10.2307/2531595 – volume: 149 start-page: 76 year: 2010 ident: R2-7-20210126 article-title: Reference values for quantitative sensory testing in children and adolescents: developmental and gender differences of somatosensory perception. publication-title: PAIN doi: 10.1016/j.pain.2010.01.011 – volume: 154 start-page: 1807 year: 2013 ident: R1-7-20210126 article-title: Value of quantitative sensory testing in neurological and pain disorders: NEUPSIG consensus. publication-title: PAIN doi: 10.1016/j.pain.2013.05.047 |
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| Title | Quality assurance for Quantitative Sensory Testing laboratories: development and validation of an automated evaluation tool for the analysis of declared healthy samples |
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