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Volume 90, Issue 1, Pages 9-16.e2 (January 2009)


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Botulinum Toxin Dilution and Endplate Targeting in Spasticity: A Double-Blind Controlled Study

Presented as an abstract to the American Neurological Association, October 14, 2002, New York.

Jean-Michel Gracies, MDaCorresponding Author Informationemail address, Mara Lugassy, MDd, Donald J. Weisz, PhDb, Michele Vecchio, MDe, Steve Flanagan, MDc, David M. Simpson, MDa

Abstract 

Gracies J-M, Lugassy M, Weisz DJ, Vecchio M, Flanagan S, Simpson DM. Botulinum toxin dilution and endplate targeting in spasticity: a double-blind controlled study.

Objective

To determine the effects of botulinum neurotoxin type A (BTX-A) dilution and endplate-targeting in spastic elbow flexors.

Design

Double blind randomized controlled trial; 4-month follow-up after a 160-unit injection of BTX-A into spastic biceps brachii (4 sites). Randomization into: group 1: 100 mouse units (MU)/mL dilution, 0.4cc/site, 4-quadrant injection; group 2: 100MU/mL dilution, 0.4cc/site, 4 sites along endplate band; group 3: 20MU/mL dilution, 2cc/site, 4-quadrant injection (n=7 per group).

Setting

Institutional tertiary care ambulatory clinic.

Participants

Referred sample of 21 adults with spastic hemiparesis. No participant withdrew due to adverse effects.

Intervention

A 160-unit injection of BTX-A of different dilutions and locations into biceps brachii.

Main Outcome Measures

Primary: agonist and antagonist (cocontraction) mean rectified voltage (MRV) of elbow flexors/extensors during maximal isometric flexion/extension; secondary: maximal voluntary power of elbow flexion/extension; spasticity angle and grade in elbow flexors/extensors (Tardieu Scale); active range of elbow extension/flexion.

Results

BTX-A injection overall reduced agonist flexor MRV (–47.5%, P<0.0001), antagonist flexor MRV (–12%, P=.037), antagonist extensor MRV (–19%, P<.01), flexion maximal voluntary power (–33%, P<.001), elbow flexor spasticity angle (–30%, P<.001) and grade (–17%, P=.03), and increased extension maximal voluntary power (24%, P=.037) and active range of elbow extension (5.5%, 8°, P=.002). Agonist and antagonist flexor MRV reductions in group 3 (–81% and –31%) were greater than in groups 1 and 2, whereas increase in active range of elbow extension was greater in group 2 (10%) than in groups 1 and 3 (P<.05, analysis of covariance [ANCOVA]). Elbow flexor spasticity was significantly reduced in groups 2 and 3 only (P<.05, ANCOVA).

Conclusions

In spastic biceps, high-volume or endplate-targeted BTX-A injections achieve greater neuromuscular blockade, cocontraction and spasticity reduction, and active range of elbow extension improvement, than low volume, nontargeted injections.

a Department of Neurology, Mount Sinai Medical Center, New York, NY

b Department of Neurosurgery, Mount Sinai Medical Center, New York, NY

c Department of Rehabilitation Medicine, Mount Sinai Medical Center, New York, NY

d Department of Neurology, Columbia Presbyterian Hospital, New York, NY

e U.O. Physical Medicine and Rehabilitation, Vittorio Emanuele Hospital, Catania, Italy

Corresponding Author InformationCorrespondence to Jean-Michel Gracies, MD, Service de Médecine Physique et de Réadaptation, CHU Henri Mondor, 51, av du Maréchal De Lattre De Tassigny, 94010 Créteil, France

 Supported by a research grant from Allergan, Inc.

 A commercial party having a direct financial interest in the results of the research supporting this article has conferred or will confer a financial benefit on the author or one or more of the authors.

 Reprints are not available from the author.

PII: S0003-9993(08)01499-8

doi:10.1016/j.apmr.2008.04.030


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