What happens between injury and our perception of pain? This book is about the first unifying law of Pain that explains the origin of all types of pain: from Arthritis to Fibromyalgia and from Migraine to Sciatica.

 

Designed for quick access to pain drugs information, Sota Omoigui's Pain Drugs Handbook is a complete clinical guide in a handy portable format

 

As a synopsis of anesthetic pharmacology it is a useful review for the beginning trainee and the advanced practitioner. An all-time best seller, The Anesthesia Drugs Handbook has been translated into Italian, Japanese, Malaysian, Polish and Portuguese.

 

This booklet is written to guide those who suffer or know someone suffering from pain. It provides the most current information about the common painful syndromes, the right medications, useful herbs and various treatments that can be utilized in the home, clinic or hospital to successfully ease pain.

 

One of the best books on Self Improvement and Management ever published. Animals have been taking care of business much longer than humans and they do it with an instinct few humans possess.

 

The Universal
Drug Infusion Ruler

Drug Infusions Made Easy

 

 

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MEDICAL PUBLICATIONS

 

 

Med Hypotheses. 2007 Jan 18; [Epub ahead of print]
The biochemical origin of pain - Proposing a new law of pain: The origin of all pain is inflammation and the inflammatory response. Part 1 of 3 - A unifying law of pain.
Omoigui S.

L.A. Pain Clinic, Hawthorne, California

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Med Hypotheses. 2005;65(3):559-69
Cholesterol Synthesis is the Trigger
Omoigui S. MD.

L.A. Pain Clinic, Los Angeles, California, USA.

Read the full Article


Pain Med. 2004 Jun;5(2):229-30
Subcutaneous Injection of Anakinra
Omoigui S. MD.

L.A. Pain Clinic, Los Angeles, California, USA.

Read the full Article
 



Regional Anesthesia and Pain Medicine 23 (4): 427, 1998
A Safer Technique for Epidural Lysis of Adhesions
Omoigui S. MD.

L.A. Pain Clinic, Los Angeles, California, USA.

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Anesth Analg. 1991 Mar;72(3):392-3
Blind nasal intubation with Audio-Capnometry
Omoigui S, Glass P, Martel DL, Watkins K, Williams KL, Whitefield SM, Wooten LL.

L.A. Pain Clinic, Los Angeles, California, USA.

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 Medical News for Today

BREAKING NEWS!!!!!!:
New Breakthrough Biotechnology Treatment for Pain


Medical Publications
                U.S. Patents

 

Pain Med. 2005 Mar-Apr;6(2):149-51
Treatment of ptosis as a complication of botulinum toxin injection.


Omoigui S, Irene S.


 

Key words: Botulinum toxin; Ptosis; Migraine; Apraclonidine.

Introduction:  Botulinum toxin Type A injection has been used for the
treatment of migraine headache, tension headache and chronic daily headache.1 Botulinum toxins are potent nerve toxins, which bind to transport proteins in nerve cells and block the release of nerve transmitters from nerve endings. One of these transmitters is acetylcholine, which is released by nerve cells and transported into muscle cells to signal the muscle to contract. Botulinum toxin by this mechanism reduces muscle hyperactivity and decreases muscle tension. Muscle tension may trigger or aggravate migraine headaches.1 By interfering with transport proteins in nerve cells, studies have shown that Botulinum toxin may also inhibit the release of excitatory nerve transmitter glutamate2 and inflammatory mediators such as Arachidonic acid (AA), 3 Vasoactive intestinal peptide (VIP) and Neuropeptide Y (NPY) 4,5.  Botulinum toxins also inhibit the release of tumor necrosis factor alpha (TNF-alpha) from immune cells and thus can alleviate pain and spasm produced by the inflammatory response.6 By reducing the neurogenic flare, Botulinum toxin may reduce the central sensitization from hyper-excitable peripheral nerves that lower the threshold for headache in migraine. When used to treat migraine, Botulinum toxin is injected to denervate the Frontalis, Orbicularis Oculi, Corrugator Supercillis, Temporalis and the Procerus muscles.   One of the complications of Botulinum toxin injection is ptosis. Ptosis is commonly managed conservatively. Ptosis also can occur in Horner’s syndrome and has been effectively treated with apraclonidine HCL.7 There is no case report in the literature of the treatment of ptosis caused by injection of Botulinum toxin. While Botulinum toxin-induced ptosis is a well-documented complication8.9, we have always used great caution and proper technique to avoid this complication in our practice. Nevertheless, the risk of ptosis is real and, unfortunately, only anecdotal remedies or passive treatments have been offered to patients in the past. This case report documents our only experience with Botulinum toxin-induced ptosis, and its dramatic reversal using apraclonidine.

CASE REPORT

A forty seven year old woman with chronic migraine had injections of Botulinum toxin Type A as part of a treatment regimen.  0.1 ml of Lidocaine 1% with 2.5 units of the Botulinum toxin was injected into each muscle belly of the bilateral Orbicularis Oculi, bilateral Corrugator Supercillis, and the midline Procerus muscles. 0.1 ml of Lidocaine 1% with 2.5 units of the Botulinum toxin was injected into five sites in the Frontalis muscle, and five sites in each Temporalis Muscle. A total of 50 units of the Botulinum toxin and 2 mls of Lidocaine 1% were injected.

One week later, the patient was seen in the clinic with a complaint of weakness in opening the right eye. She stated that the weakness started three days after the Chemodenervation procedure with Botulinum toxin. On examination the patient had ptosis in the right eye with an inability to fully open the eye on command. The Margin Reflex Distance (MRD) on the right eye was 2 mm, and 5 mm on the left eye. The normal MRD for this patient was 6 mm in both right and left eyes. The patient was advised that the ptosis would be temporary. No medications were prescribed. Five days later, the patient returned to the clinic stating the weakness in the right eye had not resolved and she also had weakness in opening her left eye.  On examination, the patient had ptosis of both eyes. The Margin Reflex Distance in both right and left eyes was 2 mm. The ptosis was associated with pain, excessive lacrymation, and conjunctiva injection in both eyes. The patient was prescribed the following medications. Apraclonidine 0.5 % ophthalmic solution 1-2 drops to be instilled in both eyes q 8hr to treat the ptosis, and dexamethasone 0.1% / tobramycin 0.3% ophthalmic suspension instilled in both eyes q 4hr to treat the conjunctival inflammation.

The patient returned to the clinic, five days after treatment was started.  She stated that her eye opening improved one day after commencing treatment, and by the third day excessive lacrymation and conjuctival injection were completely resolved. On examination there was only mild ptosis in the right eye (MRD 4 mm) and the left eye ptosis had resolved (MRD 6 mm). The conjunctiva was clear in both eyes. On re-evaluation nine days later the right eye ptosis was completely resolved and MRD in bilateral eyes was 6 mm. 

Discussion – Prevention of ptosis requires care during injection and in the post-procedure period. When injecting Botulinum toxin, care should be taken not to inject the lower Frontalis or Orbicularis oculi muscles at sites that are lateral to the mid-pupillary line. And also the needle should be pointing superiorly away from the orbit. These are to prevent the toxin from tracking downward and denervating the muscles that raise the eyelid, resulting in ptosis. The Levator Palpebrae Superioris and Superior Tarsal muscles elevate the eyelid. The Levator Palpebrae Superioris is a voluntary muscle innervated by the Oculomotor nerve, while the Superior Tarsal (Müller) muscle is a smooth muscle innervated by sympathetic nerves that have preganglionic cell bodies in the upper thoracic levels of the spinal cord and postsynaptic cell bodies in the superior cervical ganglion. The Superior Tarsal muscle has its origins from the undersurface of the Levator Superioris. Approximately 12 mm length, it inserts superiorly on the tarsal border and elevates the upper lid approximately 2 mm. At rest, the lid is just below the top part of the iris (the colored part of the eye). This is measured with the patient looking straightforward with the head vertical. The lid position is measured relative to the visual axis using the margin reflex distance (MRD). This is the distance from the eyelid margin to the corneal light reflex with the patient looking straight ahead at a penlight. Normal MRD is usually greater than 2.5 mm.  Ptosis due to Botulinum toxin injection was successfully reversed with apraclonidine ophthalmic solution. Apraclonidine an alpha-adrenergic receptor agonist possibly reversed the ptosis by directly stimulating the sympathetic innervations of the Superior Tarsal muscle. There is currently no treatment for Botulinum toxin-induced ptosis. Patients who suffer such a complication have to wait for several weeks until the effects of the toxin wear off. This case report suggests that apraclonidine can provide a reversal option for physicians and their patients.

 

References

1.Loder E, Biondi D. Use of Botulinum toxins for chronic headaches: a focused review.

 Clin J Pain 2002 Nov-Dec; 18(6 Suppl): S 169-76.

2. Sanchez-Prieto J et al. Botulinum toxin A blocks glutamate exocytosis from guinea pig                    

cerebral cortical synaptosomes.

Eur J Biochem 1987 Jun15; 165(3): 675-81

3.Ray P, Berman JD, Middleton W, Brendle J. Botulinum toxin inhibits arachidonic acid release associated with acetylcholine release from PC12 cells.

J Biol Chem 1993 May 25; 268(15): 11057-64.

4. Hardebo JE, Suzuki N, Ekbald E, Owman C. Vasoactive intestinal polypeptide and acetylcholine coexist with neuropeptides Y, dopamine-beta-hydroxylase, tyrosine hydroxylase, substance P or calcitonin gene-related peptide in neuronal subpopulations in cranial parasympathetic ganglia of rat.

Cell Tissue Res 1992 Feb; 267(2): 291-300.

5. Omoigui S. The Biochemical Origin of Pain: How a new law and new drugs have led to a medical breakthrough in the treatment of persistent pain. Hawthorne, CA. State-of-the-Art Technologies Publishers, 2002. p. 78-79

6. Imamura K, Spriggs D, Ohno T, Kufe D. Effects of Botulinum toxin type D on secretion of tumor necrosis factor from human monocytes.

Mol Cell Biol 1989 May; 9(5): 2239-43.

7. Jose Morales et al. Ocular Effects of Apraclonidine in Horner Syndrome.

Arch Ophthal. 2000;118:951-954.

8. Benabent EC, Garcia Hermosa P, Arrazola MT, Alio y Sanz JL. Botulinum toxin injection without electromyographic assistance.  J Pediatr Ophthalmol Strabismus. 2002 Jul-Aug;39(4):231-4..

9. Redaelli A, Forte R. How to avoid brow ptosis after forehead treatment with botulinum toxin. J Cosmet Laser Ther. 2003 Dec;5(3-4):220-2.

 

 

Copyright 2002. Sota Omoigui, M.D. All rights reserved. Book1 Book2