Quality of life predicts outcome of deep brain stimulation in early Parkinson disease

authors

  • Schuepbach W.M. Michael
  • Tonder Lisa
  • Schnitzler Alfons
  • Krack Paul
  • Rau Joern
  • Hartmann Andreas
  • Hälbig Thomas
  • Pineau Fanny
  • Falk Andrea
  • Paschen Laura
  • Paschen Stephen
  • Volkmann Jens
  • Dafsari Haidar
  • Barbe Michael
  • Fink Gereon
  • Kühn Andrea
  • Kupsch Andreas
  • Schneider Gerd-H.
  • Seigneuret Eric
  • Fraix Valérie
  • Kistner Andrea
  • Chaynes P. Patrick
  • Ory-Magne Fabienne
  • Brefel-Courbon Christine
  • Vesper Jan
  • Wojtecki Lars
  • Derrey Stéphane
  • Maltête David
  • Damier Philippe
  • Derkinderen Pascal
  • Sixel-Döring Friederike
  • Trenkwalder Claudia
  • Gharabaghi Alireza
  • Wächter Tobias
  • Weiss Daniel
  • Pinsker Marcus O.
  • Regis Jean-Marie
  • Witjas Tatiana
  • Thobois Stéphane
  • Mertens Patrick
  • Knudsen Karina
  • Schade-Brittinger Carmen
  • Houeto Jean-Luc
  • Agid Yves
  • Vidailhet Marie
  • Timmermann Lars
  • Deuschl Günther

document type

ART

abstract

Objective To investigate predictors for improvement of disease-specific quality of life (QOL) after deep brain stimulation (DBS) of the subthalamic nucleus (STN) for Parkinson disease (PD) with early motor complications. Methods We performed a secondary analysis of data from the previously published EARLYSTIM study, a prospective randomized trial comparing STN-DBS (n = 124) to best medical treatment (n = 127) after 2 years follow-up with disease-specific QOL (39-item Parkinson’s Disease Questionnaire summary index [PDQ-39-SI]) as the primary endpoint. Linear regression analyses of the baseline characteristics age, disease duration, duration of motor complications, and disease severity measured at baseline with the Unified Parkinson’s Disease Rating Scale (UPDRS) (UPDRS-III“off”and “on” medications, UPDRS-IV) were conducted to determine predictors of change in PDQ-39-SI. Results PDQ-39-SI at baseline was correlated to the change in PDQ-39-SI after 24 months in both treatment groups (p < 0.05). The higher the baseline score (worse QOL) the larger the improvement in QOL after 24 months. No correlation was found for any of the other baseline characteristics analyzed in either treatment group. Conclusion Impaired QOL as subjectively evaluated by the patient is the most important predictor of benefit in patients with PD and early motor complications, fulfilling objective gold standard inclusion criteria for STN-DBS. Our results prompt systematically including evaluation of disease-specific QOL when selecting patients with PD for STN-DBS.

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