Poisoning Decontamination

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POISONING

DECONTAMINATION

DR. Med. dr. Untung Widodo, SpAn.KIC.


Department of Anesthesiology & Reanimation
Medicine Faculty of Gadjah Mada University
Yogyakarta,
2012
I. Introduction
 Poison = Toxin : substance that dangers via chemically
reaction in the body
(differs to drugs on dosing,
toxic effect = adverse effect of drug)
 Detoxification : to make no hazard/no harm for life …
chemically
 Decontamination (= elimination from the body)
physically (in their process may be involved chemically
reaction)
 Port of entry : Skin (& mucous parts), resp. system, TGI,
blood (circulation), like drug : i.c, s.c, i.m, iv., inhalasi,
topical.
 To make no harm and force elimination from the
site of contamination and from the body
Treatment, that we can do for
the toxin decontamination :
 Prevention of further absorption of a
poison :
Emesis (vomiting)
Gastric lavage
Chemical adsorption
Chemical inactivation
Purgation (Cathartics drug, bowel irrigation)
For topically : remove from exposure
Continuing introduction . . . .

 Enhanced Biotransformation and Excretion of


the poison
- induction of biotransforming hepatic enzymes
- inhibit of biotransforming hepatic enzyms
- enhance availability of conjugating detoxifying
substrate
- enhance biliary excretion
- inhibit reabsorbtion in renal tubulus, with diuretics
- Dialysis (hemodialysis, plasmaparesis)
Continuing introduction …

 Antagonism or chemical inactivation of


an absorbed poison
- functional and pharmacological antago-
nism of the effects of absorbed toxicants
- chelating agents (for metallic poison, etc)
- Antibodies (anti tetanus, anti snake poison,
anti digoxin etc.)
II. Poisoning via skin
 TOPICAL, (SKIN & MUCOUSAL SURFACE)
 WASHING WITH ANTISEPTIC
 INSEC BITE, SNAKE BITE
 CROS INCISION, FORCE ELIMINATE
FLUIDS FROM THE WOUND,
DEBRIDEMENT WITH ANTISEPTIC
 ANTIDOTUM or INACTIVATION (eg.SABU)
 CLINICAL SUPPORTIVE DRUGS &
TREATMENTS
III. Poison via respiration
system
 OXYGENATION, AND LIFE SUPPORTS
 ANTIDOTUM IV
 INCREASE METABOLISMS, ANTAGONISM,
INACTIVATION etc.
 INCREASE EXCRETIONS
 CLINICAL SUPPORTIVE DRUGS
IV. Poison via cardiovaskular
system
 FROM : S.c, i.m, iv.
 OXYGENATION, AND LIFE SUPPORTS
 ANTIDOTUM IV
 INCREASE METABOLISMS, ANTAGONISM,
INACTIVATION etc.
 INCREASE EXCRETIONS, HEMODIALYSIS
 CLINICAL SUPPORTIVE DRUGS
V. POISONING VIA TGI
 BEFORE GASTRIC EMPTYING,
STIMULATE VOMITING (no more recommend)
 GASTRIC WASHING WITH NGT (< 1 hour)
 > 1 HOURS : CATHARTICS
 MEDICAL CARBON (activated charcoal), Whole
bowel Irrigation (with Polyethylene glycol)
 ANTIDOTUM IV
 INCREASE METABOLISMS
 INCREASE EXCRETIONS, HEMODIALYSIS
 CLINICAL SUPPORTIVE DRUGS & TERATMENTS
ALCOHOL INTOXICATION
 ALCOHOL : ETANOL & METHANOL
 METHANOL WILL BE TRANSFORMED TO FORMIC ACID
BY ALCOHOL DEHYDROGENASE
(IT IS MORE TOXIS : ACIDOSIS, INHIBIT CYTOCHROME
OXYDASE, DIRECT NEUROTOXIS esp. RETINA & OPTIC
NERVES),
Tx. : FROM GASTRIC LAVAGE TO GIVING ETANOL TO
COMPETE IN THIS BIOTRANSFORMATION
 MILD TO MODERATE ETANOL INTOX. REQUIRES NO
SPECIAL TREATMENT OTHER THAN STOP INGESTION
 GENERAL CLINICAL LIFE SUPPORT
VI. LIFE THREATENING
ET CAUSA POISON
 TOXIS FOR : NEUROLOGICAL SYSTEM
 TOXIS FOR RESPIRATION SYSTEM
 TOXIN FOR CARDIOVASCULAR SYSTEM
 TOXIS FOR TGI
 TOXIS FOR KIDNEY
 TOXIS FOR BLOOD (hemolytic etc.)
 TOXIS FOR HOMEOSTASIS OF MILIEU
INTERNA
VII. CLINICAL SUPPORTIVE
TO PRESERVE LIFE
 FOR ALL PATIENTS OF ACUTE INTOXICATION
 SECURE A B C
 CLINICAL PROBLEM SOLVING
Respiration, Cardiovascular, gastrointestinal tract,
neurology, acid-base balances, electrolytes etc.
 DEFINITIVE DETOXIFICATION AND
 DEFINITIVE DECONTAMINATION
VIII. SUMMARY
IN ACUTE INTOXICATED PATIENTS
As soon as possible give :
. General live support
. Prevent the further absorption,
. Increase toxin elimination
. Increase Detoxification
. Reduce hazardous effect in the body
References
1. Goodman & Gilman’s The
Pharmacological Basis of Therapeutics 8th
Ed. Vol. 1, 1991, p:49-61
2. Texbook of Critical Care 5th Ed. 2005,
p:1587-1606
3. Oh’s Intensive Care Manual 6th Ed. 2009,
p:903-912

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