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Continuous Subcutaneous Apomorphine Infusion before Subthalamic Deep Brain Stimulation: A Prospective, Comparative Study in 20 Patients.
Fernández-Pajarín, Gustavo; Sesar, Ángel; Ares, Begoña; Jiménez-Martín, Isabel; Gelabert, Miguel; Arán-Echabe, Eduardo; Relova, José Luis; Castro, Alfonso.
Afiliação
  • Fernández-Pajarín G; Department of Neurology Hospital Clínico Universitario de Santiago Santiago Spain.
  • Sesar Á; Grupo Clínico de Trastornos del Movimiento Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS) Santiago Spain.
  • Ares B; Department of Neurology Hospital Clínico Universitario de Santiago Santiago Spain.
  • Jiménez-Martín I; Grupo Clínico de Trastornos del Movimiento Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS) Santiago Spain.
  • Gelabert M; Department of Neurology Hospital Clínico Universitario de Santiago Santiago Spain.
  • Arán-Echabe E; Grupo Clínico de Trastornos del Movimiento Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS) Santiago Spain.
  • Relova JL; Department of Neurology Hospital Clínico Universitario de Santiago Santiago Spain.
  • Castro A; Grupo Clínico de Trastornos del Movimiento Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS) Santiago Spain.
Mov Disord Clin Pract ; 8(8): 1216-1224, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34761055
ABSTRACT

BACKGROUND:

Studies comparing the clinical efficacy of apomorphine infusion (APO) with subsequent subthalamic deep brain stimulation (STN-DBS) in advanced Parkinson's disease (aPD) are currently lacking. Retrospective data have shown that patients treated with APO are usually older, have a more prolonged disease, and a more severe phenotype.

OBJECTIVE:

To compare the benefit of APO with that of STN-DBS on motor, non-motor, cognitive, and quality of life in the same patient when given sequentially.

METHODS:

We prospectively analyzed 20 aPD patients over 3 different treatment phases baseline (optimized medical treatment), during APO treatment, and during subsequent STN-DBS treatment. The APO and STN-DBS phases were stable for 6 months, and evaluation of the different treatments was separated by 6 months.

RESULTS:

Compared to baseline, APO, and STN-DBS reduced mean daily off time by 70.5% and 89.3% (P = 0.012), respectively, and scores for Unified Parkinson's Disease Rating Scale (UPDRS) IV by 27.5% and 80.5% (P ≤ 0.001), Non-motor symptoms scale (NMSS) by 24.6% and 49.3% (P ≤ 0.001), Montgomery Asberg depression scale (MADRS) by 7.4% and 39.0% (P = 0.27), Starkstein apathy scale (SAS) by 51.1% and 39.9% (P = 0.734), Parkinson's disease sleep scale 2 (PDSS-2) by 25.7% and 56.7% (P ≤ 0.001), and Parkinson's disease questionnaire 39 item (PDQ-39) by 39.6% and 64.9% (P ≤ 0.001). Global cognition did not change with either therapy, but phonetic fluency worsened after STN-DBS compared to APO (P = 0.022).

CONCLUSIONS:

Both APO and STN-DBS improved motor and non-motor symptoms and quality of life compared to optimized medical treatment in aPD. Overall, STN-DBS was the most effective treatment, but APO showed a pronounced benefit on motor symptoms. Effective treatment for aPD should not be delayed, even when waiting for surgery.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article