Levodopa–Carbidopa–Entacapone Intestinal Gel in Advanced Parkinson Disease: A Multicenter Real-Life Experience

Author:

Szász József Attila12,Dulamea Adriana Octaviana34,Constantin Viorelia Adelina2,Mureşanu Dafin Fior56,Dumbravă Lăcrămioara Perju56,Tiu Cristina37,Jianu Dragoş Cătălin89,Simu Mihaela89,Ene Amalia7,Axelerad Any1011,Falup-Pecurariu Cristian1213,Lungu Mihaela14,Danci Adina Gabriela15,Sabau Monica16,Strilciuc ştefan5,Popescu Bogdan Ovidiu17

Affiliation:

1. Department of Neurology, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology, Târgu Mureş, Romania;

2. Neurology Department, Emergency Clinical County Hospital, Targu Mures, Romania;

3. “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania;

4. Department of Neurology, Fundeni Clinical Institute, Bucharest, Romania;

5. Department of Neuroscience, “Iuliu Haţieganu” University of Medicine and Pharmacy, Cluj-Napoca, Romania;

6. Neurology Department, Emergency Clinical County Hospital, Cluj-Napoca, Romania;

7. Neurology Department, Bucharest University Emergency Hospital, Bucharest, Romania;

8. Department of Neurology, “Victor Babeş” University of Medicine and Pharmacy, Timişoara, Romania;

9. Neurology Department, “Pius Brânzeu” Emergency Clinical County Hospital, Timişoara, Romania;

10. Department of Neurology, “Ovidius” University, Faculty of Medicine, Constanţa, Romania;

11. Neurology Department, Sfântul Andrei Emergency Clinical County Hospital, Constanţa, Romania;

12. Faculty of Medicine, Transilvania University, Braşov, Romania;

13. Neurology Department, Emergency Clinical County Hospital, Braşov, Romania;

14. Neurology Department, Emergency Clinical Hospital Galati, Faculty of Medicine and Pharmacy, Dunărea de Jos University, Galati, Romania;

15. Neurology Department, Cluj-Napoca Military Emergency Hospital, Cluj-Napoca, Romania;

16. Department of Psycho-Neuroscience and Medical Recovery, University of Medicine and Pharmacy Oradea, Emergency Clinical Hospital Bihor, Romania; and

17. Department of Clinical Neurosciences, Colentina Clinical Hospital, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania.

Abstract

Background: For Parkinson disease (PD) patients who have been diagnosed with advanced disease that can no longer be effectively controlled with optimized oral or transdermal medications, a range of device-aided therapies (DAT) are available, comprising either deep brain stimulation or infusion therapies providing continuous dopaminergic stimulation. Levodopa–entacapone–carbidopa intestinal gel (LECIG) infusion is the latest DAT for advanced PD (APD) that was approved in Romania in 2021. Study Question: What is the experience to date in real-world clinical practice in Romania regarding the efficacy and tolerability of LECIG in APD? Study Design: A retrospective evaluation of 74 APD patients treated with LECIG at 12 specialized APD centers in Romania. Measures and Outcomes: Demographic data and various clinical parameters were recorded, including Mini Mental State Evaluation score or Montreal Cognitive Assessment Test score. Levodopa-equivalent daily dose and the administered doses of levodopa and other PD medications were evaluated at baseline and after starting LECIG treatment. The efficacy of LECIG in reducing daily hours of off time, motor fluctuations, and dyskinesias were assessed. Any percutaneous endoscopic gastrojejunostomy system or device complications after starting LECIG treatment were noted. Results: At baseline, patients were taking oral levodopa for a mean of 5.3 times per day, with a high proportion also taking concomitant add-on therapies (dopamine agonists, 86%, monoamine oxidase type-B inhibitors, 53%; catechol-O-methyltransferase inhibitors, 64%). LECIG treatment significantly reduced daily off time versus baseline from 5.7 h/d to 1.7 hours per day (P < 0.01). Duration and severity of dyskinesias was also significantly reduced versus baseline, and improvements were observed in Hoehn and Yahr Scale scores. LECIG treatment also allowed a significant reduction in the use of concomitant oral medications. Conclusions: These findings suggest that LECIG treatment is an effective DAT option in APD that can simplify the treatment regimen.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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