Haemodialysis for lithium poisoning: Translating EXTRIP recommendations into practical guidelines
Nicholas A Buckley1, Sonia Cheng2,3, Katherine Isoardi4
1Pharmacology, University of Sydney, Sydney, Australia.
Insights
Applying Extracorporeal Treatments in Poisoning (EXTRIP) criteria to lithium toxicity is too broad. Modifications can better target haemodialysis for patients at risk of neurological sequelae.
Area of Science:
- Nephrology
- Toxicology
- Pharmacology
Background:
- Lithium is a common treatment for bipolar disorder.
- Lithium toxicity can lead to severe neurological complications.
- The Extracorporeal Treatments in Poisoning (EXTRIP) Workgroup developed criteria for managing poisoning.
Purpose of the Study:
- To evaluate the impact of applying EXTRIP Workgroup criteria to lithium toxicity cases.
- To assess the effectiveness of haemodialysis in lithium poisoning.
- To develop a predictive method for lithium concentration at 36 hours.
Main Methods:
- Retrospective analysis of medical records for lithium poisoning patients (≥1.3 mmol/L).
- Evaluation of patient data against EXTRIP criteria.
- Development and validation of a nomogram using Estimated Glomerular Filtration Rate (eGFR) to predict lithium concentration.
Main Results:
- 2.5% of patients received haemodialysis; 6.7% experienced neurological sequelae.
- Applying EXTRIP criteria would have indicated dialysis for 58% of patients.
- A developed nomogram accurately predicted lithium concentration at 36 hours for chronic toxicity.
Conclusions:
- EXTRIP criteria for lithium toxicity are overly broad.
- Modifications to EXTRIP criteria can help target haemodialysis to high-risk patients.
- A predictive nomogram aids in managing chronic lithium poisoning.
Objectives:
This study aimed to determine the impact on practice of applying the Extracorporeal Treatments in Poisoning (EXTRIP) Workgroup criteria to lithium toxicity.
Method:
We retrospectively examined the medical records of patients from three hospitals who presented with chronic or acute on chronic lithium poisoning with a lithium concentration ≥1.3 mmol/L (2008-2018). We determined which criteria were met by patients and their subsequent course. We developed and validated a method to predict if lithium concentration would be >1mmol/L at 36 hours.
Results:
There were 111 acute on chronic and 250 chronic lithium toxic patients. Nine patients (2.5%) were treated with haemodialysis. Six chronic patients had neurological sequelae. The "estimated lithium concentration at 36 hours > 1 mmol/L" criterion required pharmacokinetic calculations. A simple nomogram was developed using Estimated Glomerular Filtration Rate (eGFR) and lithium concentration. For chronic toxicity, the nomogram would have correctly predicted lithium concentration >1.4 mmol/L at 36 hours in all except two patients. If EXTRIP criteria were followed, dialysis would have been instituted for 211 patients (58%). However, only 51 patients with chronic toxicity fulfilled both a concentration and a clinical criterion. Late neurological sequelae were observed in five out of six patients who fulfilled a concentration and a clinical criterion on admission, with the sixth meeting these criteria shortly after admission.
Conclusions:
The EXTRIP criteria are too broad, but minor modifications allow haemodialysis to be targeted to those most at risk of sequelae. Most acute on chronic poisonings do not need haemodialysis, but it might shorten hospital stay in those with very high concentrations. The nomogram accurately predicts the fall in lithium concentration for chronic poisoning.
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