Literature DB >> 32775535

Managing Device-Aided Treatments in Parkinson's Disease in Times of COVID-19.

Filomena Abate1, Roberto Erro1, Paolo Barone1, Marina Picillo1.   

Abstract

Entities:  

Keywords:  COVID‐1; DBS; LCIG; Parkinson's disease

Year:  2020        PMID: 32775535      PMCID: PMC7276832          DOI: 10.1002/mdc3.12985

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


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We read with interest the viewpoint review from Fasano and colleagues on the management of advanced therapies in patients with Parkinson's disease (PD) during the COVID‐19 pandemic. We agree with the authors that this crisis may be turned into an opportunity. Our national health care systems should actively support clinicians in the remote management of chronic neurological patients, including those with advanced PD. Similar to other countries, outpatient clinics have been suspended in Italy. Although recommendations are available to implement telemedicine for movement disorder clinics, Italy still lacks of a formal national system for the remote management of chronic patients, including dedicated emergency lines. , Thus, clinicians use alternative methods to ensure the most effective assistance to patients with PD on advanced therapies. Herein we share our experience on the remote management of 3 cases of patients with PD on device‐aided therapies by whatsapp video and phone calls and using a neurologist's private phone number. The first patient is a 56‐year‐old man with an 8‐year history of PD complicated by pathological gambling. Bilateral subthalamic nucleus deep brain stimulation was performed in February 2020 (Vercise; Boston Scientific, Marlborough, MA), and first programming was scheduled for March as per routine practice. As all routine visits were suspended because of the COVID‐19 emergency, first programming was scheduled on an urgent basis, and several initiatives were performed to maximize safety for both the patient and neurologist. First, both wore surgical masks and, instead of rigidity, bradykinesia was chosen to evaluate stimulation efficacy to maintain the recommended social distancing. The Bluetooth connection from the programmer to the patient's implanted pulse generator was helpful for this sake. A program for the upcoming weeks was proposed, and the patient was trained on the use of the remote control (Fig. 1).
FIG 1

Home program for stimulation tuning with remote control and stimulation management to avoid further hospital visits. Upper section. Pre‐established 4‐week program for stimulation tuning and dopaminergic medication management. Medications were slowly titrated since the patient was at risk for side effects from dopaminergic deprivation given the history of pathological gambling. Medications at the beginning included: Levodopa/Carbidopa/Entacapone 100 mg 2/die, Levodopa/Carbidopa/Entacapone 75 mg 3/die, Levodopa/Carbidopa/Entacapone 50 mg 1/die, Rotigotine patch 4 mg/die, Melevodopa/Carbidopa 100+25 3/die, Amantadine 100 mg 3/die. Lower section. Effective program was changed due to emergence of dyskinesia, increase of sexual drive and gait freezing. Over four weeks, the patient was able to finish programming [R STN C+ (2/3/4)‐ 1.3mA/60μs/130Hz; L STN C+ (5/6/7)‐ 1.3mA/60μs/130Hz) with a significant reduction of levodopa equivalent daily dose (LEDD from 1152 to 600 mg). Amantadine was unmodified. Motor symptoms were monitored with patients’ on‐off diaries. L STN, left subthalamic nucleus; LEDD, levodopa equivalent daily dose; Med, medications; R STN, right subthalamic nucleus; Stim: stimulation.

Home program for stimulation tuning with remote control and stimulation management to avoid further hospital visits. Upper section. Pre‐established 4‐week program for stimulation tuning and dopaminergic medication management. Medications were slowly titrated since the patient was at risk for side effects from dopaminergic deprivation given the history of pathological gambling. Medications at the beginning included: Levodopa/Carbidopa/Entacapone 100 mg 2/die, Levodopa/Carbidopa/Entacapone 75 mg 3/die, Levodopa/Carbidopa/Entacapone 50 mg 1/die, Rotigotine patch 4 mg/die, Melevodopa/Carbidopa 100+25 3/die, Amantadine 100 mg 3/die. Lower section. Effective program was changed due to emergence of dyskinesia, increase of sexual drive and gait freezing. Over four weeks, the patient was able to finish programming [R STN C+ (2/3/4)‐ 1.3mA/60μs/130Hz; L STN C+ (5/6/7)‐ 1.3mA/60μs/130Hz) with a significant reduction of levodopa equivalent daily dose (LEDD from 1152 to 600 mg). Amantadine was unmodified. Motor symptoms were monitored with patients’ on‐off diaries. L STN, left subthalamic nucleus; LEDD, levodopa equivalent daily dose; Med, medications; R STN, right subthalamic nucleus; Stim: stimulation. The second patient was a 73‐year‐old man with a 10‐year‐history of PD and on intrajejunal infusion of levodopa/carbidopa intestinal gel (LCIG) since last year. On March 2020, his infusion pump stopped working properly likely the result of an obstruction of the percutaneous endoscopic transgastric jejunostomy (PEG‐J) tube. Although the PEG‐J tube was washed repeatedly, the issue persisted. Thus, the patient was switched from LCIG to regular levodopa, maintaining a stable levodopa‐equivalent dose (from LCIG 3.4 mL/h per 14 hr/day to levodopa/carbidopa 250 + 25 mg 4 tablets per day), and continued to wash the PEG‐J tube daily. After about 1 week he was able to switch back to LICG with no further complaints. The third patient is 70‐year‐old woman with a 7‐year‐history of PD with dementia and on LCIG for 2 years (2.6 mL/hr for 12–14 hr/day). As the result of the recent worsening of a preexisting abdominal tumor, she presented an aggravation of her general condition and severe dysphagia. Thus, it was suggested to the patient's caregiver to use the PEG‐J (15 Fr) for enteral nutrition through the gastric port. Her neurological condition has been stable since then. We provided a few examples supporting the role of video and phone contacts for the management of emergencies in advanced therapies in PD. Such observations should prompt national and local health care systems to support clinicians in the remote management of chronic patients. The usefulness of the patients' remote control for deep brain stimulation management was also emphasized.

Author Roles

(1) Research Project: A. Conception, B. Organization, C. Execution; (2) Manuscript Preparation: A. Writing of the First Draft, B. Review and Critique. F.A.: 2A R.E.: 2B P.B.: 2B M.P.: 1A, 1B, 1C, 2A, 2B

Disclosures

Ethical Compliance Statement: The study has been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. The patient signed written informed consent. We confirm that we have read the Journal's position on issues involved in ethical publication and affirm that this work is consistent with those guidelines. Funding Sources and Conflict of Interest: On behalf of all authors, the corresponding author states that there are neither funding sources nor conflict of interest. Financial Disclosures for the previous 12 months: Marina Picillo is supported by the Michael J Fox Foundation for Parkinson's Research; Paolo Barone received consultancies as a member of the advisory board for Zambon, Lundbeck, UCB, Chiesi, Abbvie, and Acorda. Roberto Erro has received honorarium from Bial, the International Parkinson's Disease and Movement Disorder Society, and the American Academy of Neurology. He receives royalties for the publication of Case Series in Movement Disorders–Common and Uncommon Presentations, Cambridge University Press. The other authors report no financial disclosures for the previous 12 months.
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1.  Tele-health for patients with deep brain stimulation: The experience of the Ontario Telemedicine Network.

Authors:  Onanong Jitkritsadakul; Rajasumi Rajalingam; Carol Toenjes; Renato P Munhoz; Alfonso Fasano
Journal:  Mov Disord       Date:  2017-11-09       Impact factor: 10.338

Review 2.  Programming Deep Brain Stimulation for Parkinson's Disease: The Toronto Western Hospital Algorithms.

Authors:  Marina Picillo; Andres M Lozano; Nancy Kou; Renato Puppi Munhoz; Alfonso Fasano
Journal:  Brain Stimul       Date:  2016-02-12       Impact factor: 8.955

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Authors:  Julien F Bally; Mohamad Rohani; Marta Ruiz-Lopez; Vijayashankar Paramanandam; Renato P Munhoz; Mojgan Hodaie; Suneil K Kalia; Andres M Lozano; Pierre R Burkhard; Antoine Poncet; Alfonso Fasano
Journal:  J Neurol       Date:  2019-06-13       Impact factor: 4.849

Review 4.  Management of Advanced Therapies in Parkinson's Disease Patients in Times of Humanitarian Crisis: The COVID-19 Experience.

Authors:  Alfonso Fasano; Angelo Antonini; Regina Katzenschlager; Paul Krack; Per Odin; Andrew H Evans; Thomas Foltynie; Jens Volkmann; Marcelo Merello
Journal:  Mov Disord Clin Pract       Date:  2020-05-04
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