UroToday.com - Botulinum toxin (BTX) is used therapeutically seeing that various disorders associated with disproportionate powerful contractions including central dystonias. Recently BTX has been successfully used for the treatment of disorders of the gastrointestinal and urinary tracts. Nevertheless, controversy exists with respect to refuge of this treatment.
Respective studies reported autonomic effects of BTX, particularly of BTX B used to reception of cervical dystonia, including dry speak, blurred vision, lightheadedness and constipation.(1,2,3)
In the present boning up intraprostatic injection of BTX A has been successfully used to abridge voiding dysfunction in 77 patients with Non-virulent Prostatic Hyperplasia (BPH).
In another clinical experience, seven patients, all of whom reported no symptomatic improvement with BTX A treatment, have been treated using intraprostatic injection of BTX B (NeuroBloc, Elan, Ireland) with the for all that technique, in order to avoid the risk of resistance to BTX A and to obtain long-lasting results. The NeuroBloc equivalent was determined by multiplying by 50 the dose as Botox units, so 10000 U of BTX B were used.
Two months after injections, AUA score decreased from 23.6 ±1.7 to 12.3 ±2 points (P =0.00001), serum PSA from 4.1 ±0.6 to 2.0 ±0.8 ng per ml (P =0.0004), prostatic quantity from 47.8 ±9.8 to 26.1 ±6.0 ml (P =0.0009), and residuary volume from 76 ±26 to 47 ±7.6 ml (P =0.02). At the done on the dot, middling tip urinary flow grade increased from 9.4 ±3.0 to 14.4 ±0.7 ml per second (P =0.002). Two of the seven patients (40%) professional erectile dysfunction and unembellished mouth.
Furthermore, to enquire cardiovascular autonomic effects of BTX A, we possess studied six patients, from 22 to 62 years old, without detectable cardiovascular or autonomic diseases, treated with 150 units (0.75 ml) of BTX A (Dysport, Ipsen SpA, Milan, Italy) in place of lingering anal fissure. We have utilized the Ewing usage at baseline (before treatment) and repeated the tests within 96 hours and within 30 days after treatment with BTX. The Ewing treaty, including calculation of heart rate changes during deep breathing, Valsalva maneuver and duration up; blood-pressure measurement during handgrip and during standing up, make been developed to assess the autonomic control of cardiovascular technique and to distinguish autonomic neuropathy. To class the rigidity of damage of ANS, a score (0 = normal response; 1 = borderline; 2 = abnormal) is given to each trial. The final get laid can change from 0/10-1/10 (normal pattern), to 2/10-4/10 (borderline pattern), to 5/10-10/10 (abnormal pattern). No person of the patients had worsening of test scores after toxin injections. In specifically, before treatment a borderline pattern (2/10 score) was set in 4 patients. At 96-hour ranking, a borderline pattern (2/10 score) was rest in 1 patient. At 30 days evaluation, all patients who had previously reported strange vocal score no longer had such scores, and a normal pattern (0/10) was found in all treated patients.
In these clinical trials BTX did not bring up any pensive cardiovascular adverse events. Besides, BTX B caused significant reduction of saliva movie and erectile dysfunction in 40% of patients. According to our results, in a recent duplicated blind randomized trial BTX A and B were compared in the treatment of 20 patients with cervical dystonia; patients treated with BTX B showed dry mouth and greater hardness of habitual constipation in non-existence of onerous autonomic dysfunctions in each group of patients. (3)
Although BTX B affects neuromuscular cholinergic synapses, its clinical effects on autonomic cholinergic synapses are considerably stronger, as reflected by the adverse events reported. It is unclear whether this reflects either a rather higher fondness of BTX B, as compared to BTX A, for the sake of autonomic synapses, or the observation that doses of BTX B for production of neuromuscular effects in humans are several-fold higher than those of toxin A, such that at remedial neuromuscular doses, autonomic synapses are stimulated by BTX B. However, in our patients it seems conceivable that erectile dysfunction and dry mouth may represent, respectively, a local diffusion to autonomic targets and a systemic effect. Thus, accustomed its side effect profile, BTX B should be used carefully in patients with pre-existing autonomic dysfunction, other anticholinergic treatment, or conditions in which anticholinergics are contraindicated.
References:
1. Tintner R, Gross R, Winzer UF, Smalky KA, Jankovic J. Autonomic function after botulinum toxin type A or B: A double unthinking, randomized trial. Neurology 2005; 65: 765-767
2. Jankovich J. Treatment of cervical dystonia with botulinum toxin. Mov Disord 2004;19: S109-115
3. DresslerD, Benecke R. Autonomic side effects of botulinum toxin type B treatment of cervical dystonia and hyperidrosis. Eur Neurol 2003; 49: 34-38
Written by Giuseppe Brisinda, MD, Federica Cadeddu, MD, and Giorgio Maria MD as part of Beyond the Theoretical on UroToday.com
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Giuseppe Brisinda
Department of Surgery
Catholic School of Medicine
University Hospital “Agostino Gemelli”
Largo Agostino Gemelli 8
00168 Rome (Italy)
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