MedPath

Role of Intralipid in Management of Organophosphorus Poisoning

Phase 2
Not yet recruiting
Conditions
Organophosphorus Poisoning
Interventions
Drug: Intralipid, 20% Intravenous Emulsion
Registration Number
NCT04393103
Lead Sponsor
Amani Hassan Abdel-Wahab
Brief Summary

Aim of the study:

To assess the role of intralipid emulsion in the acute man-agement of organophosphorus toxicity and its benefits in de-creasing mortality rates among victims.

Detailed Description

Organophosphates (OPs) are cholinesterase inhibitors that are widely used as pesticides and organophosphate (OP) poisoning is an important public health concern in Egypt especially in the rural farming population. Organophosphate toxicity lead to a characteristic toxidrome that includes muscarinic, nicotinic and central nervous system signs and symptoms and, without proper and early antidotal treatment, death. A new antidote is the need of the hour. Lipid emulsion being inexpensive, easily available and effective in management of other lipid soluble toxins may be a novel option. The exact mechanisms by which ILE exert their beneficial effects are not fully understood, and several have suggested synergistic effects of several mechanisms. The mechanisms of action can be divided into intravascular, membrane, and intracellular effects. The original theory explaining the mechanism of lipid rescue was that of "lipid sink", suggesting sequestration of lipophilic compounds to an expanded intravascular lipid phase, extracting the offending agent from the target tissue, and reversing the toxicity. Other hypotheses relate to the mechanism by which ILEs facilitate cardiac rescue from drug poisoning. These include:

1. increasing myocardial energy substrate delivery and a direct cardiotonic effect of ILE on the poisoned heart.

2. an effect of ILE on calcium ion channels through high levels of long-chain fatty acids, leading to increased cardiomyocyte calcium and positive inotropic effect.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age group of 18-60 years who are exposed to organophosphorus compounds.
  • Clinical manifestations of organophosphorus toxidromes (hyper-salivation, lacrimation, sweating, urinary incontinence, di-arrhea, vomiting and abdominal pain).
Exclusion Criteria
  1. Patient or relative in charge refusal.

  2. Chronic renal or liver disease manifested by history, clinical and investigatory diagnosis.

  3. Previous history of acute or chronic pancreatitis

  4. Combined poisoning with non OP compounds

  5. Asymptomatic patients.

  6. Contraindications to intralipid emulsion as:

    • disturbances of normal fat metabolism such as patho-logic hyperlipemia manifested by history, clinical and investigatory diagnosis.
    • lipoid nephrosis manifested by history, clinical and investigatory diagnosis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Follow upIntravenous Atropine SulfateFollow Up of 30 patients after administration of atropine.
intralipid 20% adjuvantIntralipid, 20% Intravenous Emulsion30 patients will receive atropine and intralipid AS AN ADJUVANT Three boluses of IFE 15 mg/kg were given over 3 minutes, 20 minutes apart.
intralipid 20% adjuvantIntravenous Atropine Sulfate30 patients will receive atropine and intralipid AS AN ADJUVANT Three boluses of IFE 15 mg/kg were given over 3 minutes, 20 minutes apart.
Primary Outcome Measures
NameTimeMethod
duration in days of hospitalization and ICU stayfour days

The primary outcome is to study the difference in total days of hospitalization and ICU stay between the study and control groups.

Secondary Outcome Measures
NameTimeMethod
mortality.four days

Death among cases under study.

© Copyright 2025. All Rights Reserved by MedPath