Transcutaneous port for continuous duodenal levodopa/carbidopa administration in Parkinson's disease
Identifieur interne : 001302 ( Main/Exploration ); précédent : 001301; suivant : 001303Transcutaneous port for continuous duodenal levodopa/carbidopa administration in Parkinson's disease
Auteurs : Anne Marthe Meppelink [Pays-Bas] ; Rickard Nyman [Suède] ; Teus Van Laar [Pays-Bas] ; Martje Drent [Pays-Bas] ; Ted Prins [Pays-Bas] ; Klaus Leonhard Leenders [Pays-Bas]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-02-01.
English descriptors
- KwdEn :
- Administration, Cutaneous, Adult, Aged, Antiparkinson Agents (administration & dosage), Antiparkinson Agents (therapeutic use), Carbidopa (administration & dosage), Carbidopa (therapeutic use), Drug Combinations, Duodenum, Female, Humans, Levodopa (administration & dosage), Levodopa (therapeutic use), Male, Middle Aged, Parkinson Disease (drug therapy), Parkinson's disease, Patient Satisfaction, Quality of Life, Severity of Illness Index, Treatment Outcome, T‐port, duodopa.
- MESH :
- chemical , administration & dosage : Antiparkinson Agents, Carbidopa, Levodopa.
- chemical , therapeutic use : Antiparkinson Agents, Carbidopa, Levodopa.
- drug therapy : Parkinson Disease.
- Administration, Cutaneous, Adult, Aged, Drug Combinations, Duodenum, Female, Humans, Male, Middle Aged, Patient Satisfaction, Quality of Life, Severity of Illness Index, Treatment Outcome.
Abstract
Motor fluctuations in Parkinson's disease (PD) can be reduced by intraduodenal infusion of levodopa‐carbidopa (Duodopa®) via percutaneous endoscopic gastrojejunostomy (PEG). We applied the transcutaneous soft‐tissue anchored titanium port (T‐port) in 15 PD patients with motor fluctuations; 7 Duodopa‐naive (non‐PEG), and 8 previously receiving Duodopa (former‐PEG). Motor scores (UPDRS‐III) and quality of life (QOL, PDQ‐8) were assessed at baseline and 6 month follow‐up. Six patients had local irritation shortly after implantation, persisting in one patient at 6 month follow‐up, which led to explantation. After having finished the protocol, four T‐ports were explanted in total. UPDRS‐III and PDQ‐8 scores improved moderately in the non‐PEG patients, but remained similar in the former‐PEG users. Two former‐PEG users developed polyneuropathy. No obstructions, retractions, or leakages occurred. Technical and hygienic properties of the T‐port were preferred by most patients. The T‐port seems to be suitable for most PD patients qualifying for Duodopa therapy, although local infection may lead to explantation during longer‐term follow‐up. © 2010 Movement Disorder Society.
Url:
DOI: 10.1002/mds.23408
Affiliations:
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Le document en format XML
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<term>Antiparkinson Agents (therapeutic use)</term>
<term>Carbidopa (administration & dosage)</term>
<term>Carbidopa (therapeutic use)</term>
<term>Drug Combinations</term>
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<term>Levodopa (administration & dosage)</term>
<term>Levodopa (therapeutic use)</term>
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<front><div type="abstract" xml:lang="en">Motor fluctuations in Parkinson's disease (PD) can be reduced by intraduodenal infusion of levodopa‐carbidopa (Duodopa®) via percutaneous endoscopic gastrojejunostomy (PEG). We applied the transcutaneous soft‐tissue anchored titanium port (T‐port) in 15 PD patients with motor fluctuations; 7 Duodopa‐naive (non‐PEG), and 8 previously receiving Duodopa (former‐PEG). Motor scores (UPDRS‐III) and quality of life (QOL, PDQ‐8) were assessed at baseline and 6 month follow‐up. Six patients had local irritation shortly after implantation, persisting in one patient at 6 month follow‐up, which led to explantation. After having finished the protocol, four T‐ports were explanted in total. UPDRS‐III and PDQ‐8 scores improved moderately in the non‐PEG patients, but remained similar in the former‐PEG users. Two former‐PEG users developed polyneuropathy. No obstructions, retractions, or leakages occurred. Technical and hygienic properties of the T‐port were preferred by most patients. The T‐port seems to be suitable for most PD patients qualifying for Duodopa therapy, although local infection may lead to explantation during longer‐term follow‐up. © 2010 Movement Disorder Society.</div>
</front>
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