Botulism historical perspective: Difference between revisions

Jump to navigation Jump to search
Line 4: Line 4:
{{MJM}}
{{MJM}}
==Historical Perspective==
==Historical Perspective==
The German physician and poet Justinus Kerner called botulinum toxin "sausage [[poison]]", or "Canadian bacon pathogen" as this [[bacterium]] often causes poisoning by growing in badly handled or prepared meat products. He first conceived a possible therapeutic use of botulinum toxin. In 1870, Muller (another German physician) coined the name [[botulism]], from [[Latin]] ''botulus'' = "sausage". In 1895, Emile Van Ermengem first isolated the bacterium ''Clostridium botulinum''. In 1944, Edward Schantz cultured ''Clostridium botulinum'' and isolated the toxin, and, in 1949, Burgen's group discovered that botulinum toxin blocks [[neuromuscular]] transmission.  
The German physician and poet Justinus Kerner called botulinum toxin "sausage [[poison]]", or "Canadian bacon pathogen" as this [[bacterium]] often causes poisoning by growing in badly handled or prepared meat products. He first conceived a possible therapeutic use of botulinum toxin. In 1870, Muller (another German physician) coined the name [[botulism]], from [[Latin]] ''botulus'' = "sausage". In 1895, Emile Van Ermengem first isolated the bacterium ''Clostridium botulinum''. In 1944, Edward Schantz cultured Clostridium botulinum and isolated the toxin, and, in 1949, Burgen's group discovered that botulinum toxin blocks [[neuromuscular]] transmission.  
{{#widget:SchemaSnippet}}
{{#widget:SchemaSnippet}}
By 1973, Alan B Scott, MD, of [[Smith-Kettlewell Institute]] used botulinum toxin type A (BTX-A) in monkey experiments, and, in 1980, he officially used BTX-A for the first time in humans to treat [[strabismus]]. In December 1989, BTX-A (BOTOX) was approved by the US [[Food and Drug Administration]] (FDA) for the treatment of [[strabismus]], [[blepharospasm]], and [[hemifacial]] [[spasm]] in patients over 12 years old. The [[cosmetic]] effect of BTX-A was initially described by [[ophthalmologist]] Jean Carruthers and [[dermatologist]] Alastair Carruthers, a husband-and-wife team working in Vancouver, Canada, although the effect had been observed by a number of independent groups. On April 15, 2002, the FDA announced the approval of botulinum toxin type A (BOTOX Cosmetic) to temporarily improve the appearance of moderate-to-severe frown lines between the [[eyebrows]] (glabellar lines). BTX-A has also been approved for the treatment of excessive underarm [[sweating]]. The acceptance of BTX-A use for the treatment of [[spasticity]] and [[muscle]] pain disorders is growing, with approvals pending in many European countries and studies on [[headaches]] (including [[migraine]]), [[prostatic]] symptoms, [[asthma]], [[obesity]] and many other possible indications are ongoing.
By 1973, Alan B Scott, MD, of [[Smith-Kettlewell Institute]] used botulinum toxin type A (BTX-A) in monkey experiments, and, in 1980, he officially used BTX-A for the first time in humans to treat [[strabismus]]. In December 1989, BTX-A (BOTOX) was approved by the US [[Food and Drug Administration]] (FDA) for the treatment of [[strabismus]], [[blepharospasm]], and [[hemifacial]] [[spasm]] in patients over 12 years old. The [[cosmetic]] effect of BTX-A was initially described by [[ophthalmologist]] Jean Carruthers and [[dermatologist]] Alastair Carruthers, a husband-and-wife team working in Vancouver, Canada, although the effect had been observed by a number of independent groups. On April 15, 2002, the FDA announced the approval of botulinum toxin type A (BOTOX Cosmetic) to temporarily improve the appearance of moderate-to-severe frown lines between the [[eyebrows]] (glabellar lines). BTX-A has also been approved for the treatment of excessive underarm [[sweating]]. The acceptance of BTX-A use for the treatment of [[spasticity]] and [[muscle]] pain disorders is growing, with approvals pending in many European countries and studies on [[headaches]] (including [[migraine]]), [[prostatic]] symptoms, [[asthma]], [[obesity]] and many other possible indications are ongoing.

Revision as of 21:51, 18 December 2012

Botulism Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Botulism from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

CT

MRI

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Botulism historical perspective On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Botulism historical perspective

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Botulism historical perspective

CDC on Botulism historical perspective

Botulism historical perspective in the news

Blogs on Botulism historical perspective

Directions to Hospitals Treating Botulism

Risk calculators and risk factors for Botulism historical perspective

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Michael Maddaleni, B.S.

Historical Perspective

The German physician and poet Justinus Kerner called botulinum toxin "sausage poison", or "Canadian bacon pathogen" as this bacterium often causes poisoning by growing in badly handled or prepared meat products. He first conceived a possible therapeutic use of botulinum toxin. In 1870, Muller (another German physician) coined the name botulism, from Latin botulus = "sausage". In 1895, Emile Van Ermengem first isolated the bacterium Clostridium botulinum. In 1944, Edward Schantz cultured Clostridium botulinum and isolated the toxin, and, in 1949, Burgen's group discovered that botulinum toxin blocks neuromuscular transmission.

By 1973, Alan B Scott, MD, of Smith-Kettlewell Institute used botulinum toxin type A (BTX-A) in monkey experiments, and, in 1980, he officially used BTX-A for the first time in humans to treat strabismus. In December 1989, BTX-A (BOTOX) was approved by the US Food and Drug Administration (FDA) for the treatment of strabismus, blepharospasm, and hemifacial spasm in patients over 12 years old. The cosmetic effect of BTX-A was initially described by ophthalmologist Jean Carruthers and dermatologist Alastair Carruthers, a husband-and-wife team working in Vancouver, Canada, although the effect had been observed by a number of independent groups. On April 15, 2002, the FDA announced the approval of botulinum toxin type A (BOTOX Cosmetic) to temporarily improve the appearance of moderate-to-severe frown lines between the eyebrows (glabellar lines). BTX-A has also been approved for the treatment of excessive underarm sweating. The acceptance of BTX-A use for the treatment of spasticity and muscle pain disorders is growing, with approvals pending in many European countries and studies on headaches (including migraine), prostatic symptoms, asthma, obesity and many other possible indications are ongoing.

Botox is manufactured by Allergan Inc (U.S.) for both therapeutic as well as cosmetic use. The formulation is best stored at cold temperature of 2-8 degrees Celsius. Dysport is a therapeutic formulation of the type A toxin developed and manufactured in the UK and which is licensed for the treatment of focal dystonias, symptoms of cerebral palsy, and certain cosmetic uses in many territories world wide.

Botulinum Toxin Type B (BTX-B) received FDA approval for treatment of cervical dystonia on December 21, 2000. Trade names for BTX-B are Myobloc in the United States, and Neurobloc® in the European Union.

References



Template:WikiDoc Sources

Cookies help us deliver our services. By using our services, you agree to our use of cookies.

Navigation menu