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Clinical outcomes of nonsurgical treatment for Preiser disease

To elucidate whether nonsurgical treatment for Preiser disease is effective. Eight patients with Preiser disease (median age 59 [47–69] years ) underwent nonsurgical treatment (median symptom-onset-to-treatment interval 8 [9–180] months). At presentation, 7 patients complained of constant pain and 1...

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Autores principales: Tomori, Yuji, Nanno, Mitsuhiko, Takai, Shinro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004783/
https://www.ncbi.nlm.nih.gov/pubmed/31977895
http://dx.doi.org/10.1097/MD.0000000000018883
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author Tomori, Yuji
Nanno, Mitsuhiko
Takai, Shinro
author_facet Tomori, Yuji
Nanno, Mitsuhiko
Takai, Shinro
author_sort Tomori, Yuji
collection PubMed
description To elucidate whether nonsurgical treatment for Preiser disease is effective. Eight patients with Preiser disease (median age 59 [47–69] years ) underwent nonsurgical treatment (median symptom-onset-to-treatment interval 8 [9–180] months). At presentation, 7 patients complained of constant pain and 1 of motion-related pain. Pain restricted wrist range of motion (median modified Mayo wrist score [MMWS] 17.5 [range 10–30]). Radiography revealed stages 1 to 3 disease (Herbert–Lanzetta classification). Median scapholunate angle was 62° (54°–75°), with 3 wrists suffering dorsal intercalated segment instability (DISI). Magnetic resonance imaging showed (Kalainov criteria) 4 stage 1 wrists (complete necrosis) and 4 stage 2 (incomplete necrosis). Two had concomitant Kienböck disease. All patients underwent nonsurgical treatment (ie, oral pain killer, immobilization, rest) and were monitored via radiographic and clinical evaluations. Scapholunate angles and the scaphoid area reduction ratio were calculated using radiography. Response criteria were the patients’ subjective and objective status. Endpoint was the time from start of non-surgical to surgical treatment. Immobilization lasting 0 to 24 months (median 1.8 months) did not relieve their symptoms. Follow-up radiography showed that the disease stage had progressed in 5 of 8 wrists, with 5 wrists having DISI. The median area reduction ratio of the scaphoid was 11% (4%–52%) on anteroposterior views and 4% (−23% to 17%) on lateral views. Compared with the contralateral wrist, the median wrist flexion-extension arc was 61% (50%–79%) and the median grip strength 39%. Median MMWS score was 17.5 (10–25) – poor in 6 of 8 patients. Surgery was thus necessary in all patients. Nonsurgical treatment for Preiser disease did not improve subjective or objective outcomes and did not prevent deterioration of radiographic findings. Type of study/level of evidence: Therapeutic, Level V.
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spelling pubmed-70047832020-02-19 Clinical outcomes of nonsurgical treatment for Preiser disease Tomori, Yuji Nanno, Mitsuhiko Takai, Shinro Medicine (Baltimore) 6900 To elucidate whether nonsurgical treatment for Preiser disease is effective. Eight patients with Preiser disease (median age 59 [47–69] years ) underwent nonsurgical treatment (median symptom-onset-to-treatment interval 8 [9–180] months). At presentation, 7 patients complained of constant pain and 1 of motion-related pain. Pain restricted wrist range of motion (median modified Mayo wrist score [MMWS] 17.5 [range 10–30]). Radiography revealed stages 1 to 3 disease (Herbert–Lanzetta classification). Median scapholunate angle was 62° (54°–75°), with 3 wrists suffering dorsal intercalated segment instability (DISI). Magnetic resonance imaging showed (Kalainov criteria) 4 stage 1 wrists (complete necrosis) and 4 stage 2 (incomplete necrosis). Two had concomitant Kienböck disease. All patients underwent nonsurgical treatment (ie, oral pain killer, immobilization, rest) and were monitored via radiographic and clinical evaluations. Scapholunate angles and the scaphoid area reduction ratio were calculated using radiography. Response criteria were the patients’ subjective and objective status. Endpoint was the time from start of non-surgical to surgical treatment. Immobilization lasting 0 to 24 months (median 1.8 months) did not relieve their symptoms. Follow-up radiography showed that the disease stage had progressed in 5 of 8 wrists, with 5 wrists having DISI. The median area reduction ratio of the scaphoid was 11% (4%–52%) on anteroposterior views and 4% (−23% to 17%) on lateral views. Compared with the contralateral wrist, the median wrist flexion-extension arc was 61% (50%–79%) and the median grip strength 39%. Median MMWS score was 17.5 (10–25) – poor in 6 of 8 patients. Surgery was thus necessary in all patients. Nonsurgical treatment for Preiser disease did not improve subjective or objective outcomes and did not prevent deterioration of radiographic findings. Type of study/level of evidence: Therapeutic, Level V. Wolters Kluwer Health 2020-01-24 /pmc/articles/PMC7004783/ /pubmed/31977895 http://dx.doi.org/10.1097/MD.0000000000018883 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 6900
Tomori, Yuji
Nanno, Mitsuhiko
Takai, Shinro
Clinical outcomes of nonsurgical treatment for Preiser disease
title Clinical outcomes of nonsurgical treatment for Preiser disease
title_full Clinical outcomes of nonsurgical treatment for Preiser disease
title_fullStr Clinical outcomes of nonsurgical treatment for Preiser disease
title_full_unstemmed Clinical outcomes of nonsurgical treatment for Preiser disease
title_short Clinical outcomes of nonsurgical treatment for Preiser disease
title_sort clinical outcomes of nonsurgical treatment for preiser disease
topic 6900
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004783/
https://www.ncbi.nlm.nih.gov/pubmed/31977895
http://dx.doi.org/10.1097/MD.0000000000018883
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