Showing posts with label poisoning. Show all posts
Showing posts with label poisoning. Show all posts

Thursday, 2 June 2016

Iron Overdose

Iron overdose is common, but it is infrequent that it causes severe problems. I have seen it frequently in children, who take their parents well woman tablets, or similar.

Background
When thinking about iron, the first thing that must be done is to convert the amount of iron taken, to the amount of elemental iron ingested. This varies considerably between different types of iron tablets, depending on the type of ferrous or ferric salt:

  ferrous sulfate (dried) — divide dose by 3.3
  ferrous sulfate (heptahydrate) — divide dose by 5
  ferrous gluconate — divide dose by 9
  ferrous fumarate — divide dose by 3
  ferric chloride — divide dose by 3.5
  ferrous chloride — divide dose by 4

You can then risk stratify, by the amount of elemental iron they have ingested:
  <20mg/kg –– asymptomatic
  20-60mg/kg –– GI symptoms only
  60-120mg/kg –– potential for systemic toxicity
  >120mg/kg –– potentially lethal

Peak serum iron levels occur 4-6 hours following iron ingestion, then levels fall due to intracellular shift. Levels do not clearly correlate with clinical toxicity, but > 90 micromol/L (500 mcg/dL) is generally considered predictive of systemic toxicity (equivalent to >60mg/kg)

Pathophysiology
Local Effects - corrosive injury to the GI mucosa (vomiting, diarrhoea, haematemeis, melaena) . Can lead to gastric strictures.

Systemic Effects - cellular toxin, targeting the cardiovascular syndrome. Severe lactic acidosis from hypoperfusion due to volume loss, vasodilation and negative inotropic effects.


Clinical Symptoms


Investigations
Blood gas - can look like DKA. Anion gap metabolic acidosis.
BMs - can be hyperglycaemic
AXR
LFTs, Coags — hepatic failure
U&E — renal failure
Iron levels

Management
**Not adsorbed by activated charcoal**
Whole bowel irrigation for ingestion >60mg/kg
Surgical or endoscopy removal if >120mg/kg or WBI not feasible

Desferroxamine Chelation:
    level >90 micromol/L at 4-6 hours post-ingestion
    evidence of systemic toxicity
    shock
    metabolic acidosis
    altered mental status

Chelates free irons that can be renally excreted. Ferrioxamine is then excreted unchanged in the urine which classically, not reliably, turns a vin rose colour.

15 mg/kg/h, reduced if hypotension occurs, may be titrated up to 40mg/kg/h in severe toxicity
cardiac monitoring is mandatory. Can cause hypersensitivity, ARDS, toxic retinopathy or yersinia sepsis. Can be stopped when the patient is stable and serum iron is <60micromol/L - usually 56 hours.



References
http://learning.bmj.com/learning/modules/elucidat/57067260702df.html?moduleId=10055999&status=LIVE&action=start&_flowId=ELU&sessionTimeoutInMin=90&locale=en_GB&shouldStartAtQuestionSection=false

https://www.aliem.com/2014/management-iron-toxicity/
http://lifeinthefastlane.com/ccc/iron-overdose/
http://lifeinthefastlane.com/toxicology-conundrum-034/
https://wikem.org/wiki/Iron_toxicity
http://lifeinthefastlane.com/tox-library/antidote/desferrioxamine/
http://www.foamem.com/2014/08/06/management-of-iron-toxicity/
http://adc.bmj.com/content/87/5/400.full 
http://lifeinthefastlane.com/cicm-saq-2009-2-q18/ 




Wednesday, 27 January 2016

Methaemoglobin

Pathogenesis
- Oxidisation of the haem of haemoglobin by free radicals or things like hydrogen peroxide and nitric oxide. 
- Shifts O2 dissociation curve to the left. 

Causes

- Hereditary / Congenital: Hb and NADH-MetHb reductase deficiency
- Acquired: 
  *   Medications eg. Amyl nitrite, Benzocaine, Dapsone, Lidocaine, Nitroglycerin, Nitroprusside, Phenacetin, Phenazopyridine, Prilocaine, Quinones, Sulfonamides (eg. sulfamethoxazole). Chloroquine. 
  *   Chemical agents eg. Aniline dye derivatives (shoe dyes, inks) Butyl nitrite, Chlorobenzene, Nitrate-containing foods, Isobutyl nitrite, Naphthalene, Nitrophenol, Nitrous gases, Silver nitrate, and Trinitrotoluene. Sodium nitrite - used in food preservation. 

Signs & Symptoms

- chocolate brown discoloration of the blood. 
- SaO2 readings go crazy 

0-10% - Features unlikely


10-30%- Mild effects 

Blue-grey ‘apparent’ central cyanosis, fatigue, dizziness, headaches

30-50% - Moderate effects – weakness, tachypnoea, tachycardia


50-70% - Severe effects 

stupor, coma, convulsions, respiratory depression, cardiac arrhythmias, acidosis

> 70% - Potentially fatal


Treatment

<20% - nothing
20 - 30% - oxygen therapy 
>30% - methylene blue
            1-2 mg/kg IV over 5 minutes - 1% (10mg/ml solution) 
            repeat up to 7 mg/kg 
SpO2 normally dives as you give the methylene blue. 
Recheck levels after an hour 

Interesting Note

Hydrogen sulfide poisoning is similar to cyanide poisoning and can be treated by inducing metHb. 




References

http://stemlynsblog.org/feeling-blue-at-st-emlyns/
http://www.rcemlearning.co.uk/modules/papa-smurf-has-a-seizure/
http://emergencymedicineireland.com/2011/07/why-methaemoglobinaemia-is-a-good-thing/
http://emergencymedicineireland.com/2011/07/why-methaemoglobinaemia-is-a-bad-thing/