Ambulatory continuous peripheral nerve blocks to treat postamputation phantom limb pain: a multicenter, randomized, quadruple-masked, placebo-controlled clinical trial.

dc.contributor.author

Ilfeld, Brian M

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Khatibi, Bahareh

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Maheshwari, Kamal

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Madison, Sarah J

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Esa, Wael Ali Sakr

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Mariano, Edward R

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Kent, Michael L

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Hanling, Steven

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Sessler, Daniel I

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Eisenach, James C

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Cohen, Steven P

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Mascha, Edward J

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Ma, Chao

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Padwal, Jennifer A

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Turan, Alparslan

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PAINfRE Investigators

dc.date.accessioned

2021-05-01T13:44:56Z

dc.date.available

2021-05-01T13:44:56Z

dc.date.issued

2021-03

dc.date.updated

2021-05-01T13:44:55Z

dc.description.abstract

Phantom limb pain is thought to be sustained by reentrant neural pathways, which provoke dysfunctional reorganization in the somatosensory cortex. We hypothesized that disrupting reentrant pathways with a 6-day-long continuous peripheral nerve block reduces phantom pain 4 weeks after treatment. We enrolled patients who had an upper- or lower-limb amputation and established phantom pain. Each was randomized to receive a 6-day perineural infusion of either ropivacaine or normal saline. The primary outcome was the average phantom pain severity as measured with a Numeric Rating Scale (0-10) at 4 weeks, after which an optional crossover treatment was offered within the following 0 to 12 weeks. Pretreatment pain scores were similar in both groups, with a median (interquartile range) of 5.0 (4.0, 7.0) for each. After 4 weeks, average phantom limb pain intensity was a mean (SD) of 3.0 (2.9) in patients given local anesthetic vs 4.5 (2.6) in those given placebo (difference [95% confidence interval] 1.3 [0.4, 2.2], P = 0.003). Patients given local anesthetic had improved global impression of change and less pain-induced physical and emotional dysfunction, but did not differ on depression scores. For subjects who received only the first infusion (no self-selected crossover), the median decrease in phantom limb pain at 6 months for treated subjects was 3.0 (0, 5.0) vs 1.5 (0, 5.0) for the placebo group; there seemed to be little residual benefit at 12 months. We conclude that a 6-day continuous peripheral nerve block reduces phantom limb pain as well as physical and emotional dysfunction for at least 1 month.

dc.identifier

00006396-202103000-00030

dc.identifier.issn

0304-3959

dc.identifier.issn

1872-6623

dc.identifier.uri

https://hdl.handle.net/10161/22718

dc.language

eng

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Ovid Technologies (Wolters Kluwer Health)

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Pain

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10.1097/j.pain.0000000000002087

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PAINfRE Investigators

dc.title

Ambulatory continuous peripheral nerve blocks to treat postamputation phantom limb pain: a multicenter, randomized, quadruple-masked, placebo-controlled clinical trial.

dc.type

Journal article

duke.contributor.orcid

Kent, Michael L|0000-0002-9051-2645

pubs.begin-page

938

pubs.end-page

955

pubs.issue

3

pubs.organisational-group

School of Medicine

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Anesthesiology, Ambulatory

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Duke

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Anesthesiology

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Clinical Science Departments

pubs.publication-status

Published

pubs.volume

162

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