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OP0066 (2019)
EFFECTIVENESS OF SPECIALIZED HAND/FACE PHYSICAL-OCCUPATIONAL THERAPY IN PATIENTS WITH SYSTEMIC SCLEROSIS – PRELIMINARY RESULTS OF A ONE-YEAR CONTROLLED STUDY
Maja Špiritović1, Hana Smucrova2, Sabina Oreska3, Hana Štorkánová3, Barbora Heřmánková1, Petr Česák4, Adéla Rathouská2, Olga Růžičková3, Karel Pavelka3, Ladislav Šenolt3, Jiří Vencovský3, Radim Bečvář3, Michal Tomčík3
1Faculty of Physical Education and Sport, Charles University, Department of Physiotherapy, Prague, Czech Republic
2Institute of Rheumatology, Prague, Czech Republic
3Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic
4Faculty of Physical Education and Sport, Charles University, Human Movement Laboratory, Prague, Czech Republic

Background: Systemic sclerosis (SSc) is characterized by stiffness and contraction of tissues, which leads to a limitation in the execution of day-to-day activities. The aim of our study was to investigate the impact of specialized physical-occupational therapy (POT) focused on the hands/face and QoL of SSc patients.


Objectives: Fifty five patients fulfilled the EULAR/ACR criteria for SSc and had skin involvement leading to hand/face function impairment. 25 patients were recruited into the intervention group (IG) and 30 patients into the control group (CG). Both groups received an educational material for home exercise, but only the IG underwent a 6-month intervention with a subsequent 6-month follow-up period.


Methods: Patients were assessed by a physician and a physiotherapist blinded to intervention at months 0, 3, 6, and 12. Patients also filled out patient reported outcomes questionnaires and provided blood for routine laboratory analysis and bio-banking. Data analysis was done between groups and within the group.


Results: Compared to the observed statistically significant deterioration in the CG, we found a statistically significant improvement in the IG in objectively assessed function and strength of hand, distance between incisors and functional ability (SHAQ) (Table). Only numerical improvements in the IG during the intervention compared to numerical deterioration in CG that did not reach statistical significance were observed in subjectively assessed hand function and mouth handicap, functional ability (HAQ) and in some domains of QoL (SF-36) and fatigue (FIS – cognitive function). During the follow-up period, there was a significant deterioration or stagnation of the achieved positive results in the IG.

Parameter(unit) Intervention groupMean ± SEM Control groupMean ± SEM Intra-group analysis (Friedman+Dunn) Inter-group analysis (2WA)
Interevention gr. Control group
dFTP, dominant hand (cm) m0: 5.7 ± 0.5m3: 6.2 ± 0.5m6: 6.8 ± 0.6m12: 6.0 ± 0.6 m0: 6.8 ± 0.5m3: 6.2 ± 0.4m6: 5.9 ± 0.4m12: 5.6 ± 0.4 m0-3: p<0.01m3-6: p<0.05m0-6: p<0.0001m6-12: p<0.0001 m0-3: NS m3-6: NS m0-6: p<0.0001m6-12:NS p<0.0001
Hand grip strength, dominant hand (kg) m0: 17.2 ± 1.8m3: 19.2 ± 1.9m6: 19.7 ± 1.9m12: 17.5 ± 2.0 m0: 16.5 ± 1.2m3: 14.9 ± 1.3m6: 13.8 ± 1.2m12: 14.2 ± 1.3 m0-3: p<0.05m3-6: NS m0-6: p<0.001m6-12: p<0.05 m0-3: NS m3-6: NS m0-6: p<0.01m6-12: NS p<0.0001
HAMIS, dominant hand m0: 9.8 ± 1.3m3: 7.1 ± 1.3m6: 4.1 ± 0.9m12: 7.2 ± 1.2 m0: 3.9 ± 1.1m3: 6.3 ± 1.2m6: 8.9 ± 1.1m12: 9.8 ± 1.2 m0-3: p<0.01m3-6: p<0.001m0-6: p<0.0001m6-12: p<0.001 m0-3: NS m3-6: p<0.001m0-6: p<0.0001m6-12: NS p<0.0001
Inter-incisor distance (cm) m0: 2.9 ± 0.2m3: 3.2 ± 0.2m6: 3.5 ± 0.2m12: 3.2 ± 0.2 m0: 3.3 ± 0.1m3: 3.1 ± 0.1m6: 3.0 ± 0.1m12: 3.0 ± 0.1 m0-3: p<0.01m3-6: NS m0-6: p<0.0001m6-12: p<0.01 m0-3: p<0.01m3-6: NS m0-6: p<0.001m6-12: NS p<0.0001
SHAQ (mm) m0: 28.8 ± 3.9m3: 21.5 ± 3.4m6: 22.0 ± 3.5m12: 23.4 ± 3.7 m0: 21.5 ± 2.1m3: 24.6 ± 2.6 m6: 24.9 ± 2.9m12: 27.5 ± 3.3 m0-3: NS m3-6: NS m0-6: p<0.05m6-12: NS m0-3: NS m3-6: NS m0-6: NS m6-12: NS p=0.0015

Conclusion: Our program led to a significant improvement in the observed parameters that was clinically significant in a substantial proportion of patients, and prevention of the expected worsening of hand/face handicap and QoL.


Acknowledgement: Supported by AZV-16-33574A, SVV for FTVS UK 2019-260466, MHCR 023728.


Disclosure of Interests: Maja Špiritović: None declared, Hana Smucrova: None declared, Sabina Oreska: None declared, Hana Štorkánová: None declared, Barbora Heřmánková: None declared, Petr Česák: None declared, Adéla Rathouská: None declared, Olga Růžičková: None declared, Karel Pavelka: None declared, Ladislav Šenolt Grant/research support from: AbbVie, Consultant for: AbbVie, Bristol-Myers Squibb, Celgene Corporation, Merck Sharp and Dohme, Novartis, Pfizer, Roche, UCB, Amgen, Takeda, Speakers bureau: AbbVie, Amgen, Bristol-Myers Squibb, Celgene Corporation, Eli Lilly, Merck Sharp and Dohme, Novartis, Pfizer, Roche, UCB, Jiří Vencovský Consultant for: Samsung, Speakers bureau: AbbVie, Novartis, Pfizer, Sanofi, Eli Lilly, Biogen, UCB, MSD, Werfen, Roche, Radim Bečvář Consultant for: consultancy Actelion, Michal Tomčík: None declared

DOI: 10.1136/annrheumdis-2019-eular.4630


Citation: Ann Rheum Dis, volume 78, supplement 2, year 2019, page A105
Session: Myositis and SSc: Clinical highlights 2019 (Scientific Abstracts)