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Introduction
Post-Polio Syndrome (PPS) is a disorder of the nervous system
that can break out in individuals who have suffered from polio.
1–4
Symptoms include reacquired muscle weakness, fatigue, and muscle
and joint pain, which may result in impaired functionality.
5
Pain is one of the most frequent occurrences in PPS, being reported
by up to 86% of patients.
6
Its origin is predominantly related to
impaired body mechanics, caused by either musculoskeletal overuse
or disuse.
6
To help diagnosis, PPS was divided into three categories:
type I pain is post-polio pain, which occurs only in the muscles affected
by it; type II pain includes injuries to tissues, muscles, tendons, bursae
and ligaments; type III pain, or biomechanical pain, occurs due to
joint degeneration.
7
Energy preservation is of paramount importance in the treatment of
PPS and Guidelines for Rehabilitation of People with PPS syndrome
and co-morbidities advocate managing pain through physical
rehabilitation, lifestyle changes and drug treatment.
8
Physical rehabilitation helps in the improvement of body
mechanics, in gait adjustments, and in muscle and joint overload
relief.
7,8
Lifestyle changes include daily routine changes, home and
workplace adaptations, weight control and compliance with pain-
relief domestic guidelines, such as limbering, heat applications, self-
massage and rest.
7–8
Drug treatment is essential for pain control in
PPS and, to date, benzodiazepine-class muscle relaxants are the most
effcient drugs.
7,11
Several drugs have been evaluated in the treatment of PPS pain,
including prednisone, amantadine, and intravenous immunoglobulin,
but none of them have shown entirely satisfactory results.
12–14
Piracetam is a nootropic agent, distinguished by increasing neuron
effciency, restoring the functioning of cortical cells and activating
cognitive functions
15
and L-Carnitine is a quaternary ammonium
compound, which facilitates the intramitochondrial transportation of
fat in type 1 muscle fber, generating energy for the functioning of
muscles.
16,17
Considering that pain in PPS is associated with musculoskeletal
activity (overuse or disuse), it is assumed that supplementation with a
fxed-dose combination of L-Carnitine + Piracetam improves energy
performance of muscles and, hence, reduces pain.
Objectives
To analyze the therapeutic effect of a fxed-dose combination of
L-Carnitine + Piracetam in the pain of patients with PPS.
Method
This was a randomized, double-blind, placebo-controlled clinical
trial that compared the use of a fxed-dose combination of L-Carnitine
+ Piracetam to placebo, as an adjuvant therapy in the treatment of
pain in patients with PPS. It was approved by the Comitê de Ética e
Pesquisa – CET (Ethics and Research Committee) of the Universidade
Federal de São Paulo-UNIFESP/EPM (Federal University of São
Int Phys Med Rehab J. 2020;5(6):233‒236. 233
©2020 Campos et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and build upon your work non-commercially.
Assessment of a fxed-dose combination of
l-carnitine + piracetam in the treatment of pain in
post-poliomyelitis syndrome
Volume 5 Issue 6 - 2020
Katia Maria de Campos,
1
Abrahão Augusto
Juviniano Quadros,
1
Marcio Falci,
2
Acary
Souza Bulle Oliveira
1
1
Department of Neurology and Neurosurgery, Research Section
of Neuromuscular Diseases, Federal University of São Paulo,
Paulista Medical School (UNIFESP/EPM), Brasil
2
Advisor to the Scientifc Chair of Biolab Sanus Farmaceutica
Ltda, Brasil
Correspondence: Katia Maria de Campos, Department
of Neurology and Neurosurgery, Research Section of
Neuromuscular Diseases, Federal University of São Paulo,
Paulista Medical School (UNIFESP/EPM), Rua Josefna Arnoni,
115 apto. 161 bl.3 São Paulo/SP, Brazil, CEP -02374-050,
Tel 5511 999319115, Email
Received: October 14, 2020 | Published: November 09, 2020
Abstract
Introduction: Pain is one of the most frequent symptoms of Post Poliomyelitis Syndrome
(PPS) and its treatment also includes medication. The no otropic agent Piracetam enhances
neuronal effectiveness and the compound L-Carnitine generates muscle energy. Considering
that pain in PPS is related to muscle overuse or disuse, it is assumed that supplementation
with a fxed-dose combination of L-Carnitine + Piracetam improves muscle performance,
reducing pain.
Objective: To analyze the effect of a fxed-dose combination of L-Carnitine + Piracetam
on pain in PPS patients.
Method: A randomized, double-blind clinical trial, has compared the use of a fxed-dose
combination of L-Carnitine + Piracetam to placebo, in the treatment of pain in 94 patients
at the PPSambulatory care center of UNIFESP.
Results: Both groups reported a reduction inpain, however, only the active group improved
functional performance after using the medication.
Conclusion: the use of a fxed-dose combination of L-Carnitine + Piracetam is effcient in
the treatment of pain in PPS patients.
Keywords: drug treatment, L-carnitine, pain, piracetam, post poliomyelitis syndrome,
rehabilitation
International Physical Medicine & Rehabilitation Journal
Research Article
Open Access