Purpose: This guideline provides an evidence-based approach to managing methanol poisoning. It focuses on protecting the optic nerve and preventing permanent vision loss. The management covers the acute phase and extends up to six months after exposure under the supervision of the treating physician.

1. Principles of Care

Ophthalmology Interventions:

  • Acute phase optic nerve care is critical during the first two weeks following methanol poisoning. Intervention must start as early as possible, with continuous monitoring and treatment potentially extending for up to six months, depending on patient response and physician recommendations (Pakravan et al., 2016). Methanol poisoning survivors can experience progressive visual impairment even after discharge, with up to 40% developing long-term visual sequelae. Continuous monitoring through visual evoked potential (VEP) and retinal nerve fiber layer (RNFL) assessments every 3-6 months is critical to detect delayed optic nerve damage and provide timely intervention (Zakharov et al., 2015).

Medications:

  • Primary Medications:

  • Erythropoietin (EPO) is an effective adjunctive therapy for methanol-induced optic neuropathy (MON). When administered with corticosteroids, it improves visual outcomes in the acute phase. Studies have shown significant improvements in visual acuity and retinal nerve fiber layer thickness (Pakravan et al., 2016).

  • Methylprednisolone is recommended as it reduces inflammation in optic neuropathy and can be administered alongside EPO (Tabatabaei et al., 2023).

  • Supportive Medications:

    • Magnesium sulfate, Vitamin B12, and folic acid have been used to support nerve recovery, although their neuroprotective roles are less well-established than erythropoietin or methylprednisolone (Pakdel et al., 2018).

Drug Interactions and Contraindications:

  • Erythropoietin should be used with caution in patients with cardiovascular conditions, including uncontrolled hypertension, as it can increase the risk of thromboembolism (Pakravan et al., 2016).

  • Methylprednisolone interacts with anticonvulsants, anticoagulants, and NSAIDs and can cause complications in patients with pre-existing conditions such as osteoporosis and diabetes (Sanaei-Zadeh, 2012).

2. Detailed Treatment Guidelines

Administration of Erythropoietin (EPO):

  • Dosage: Administer 10,000 IU intravenously every 12 hours for three days. This dosage has significantly improved visual acuity in methanol-induced optic neuropathy (Pakravan et al., 2012).

  • Monitoring: Vital signs should be continuously monitored during administration, especially in patients over 40 who may require a cardiovascular assessment before treatment.

Administration of Methylprednisolone:

  • Dosage: 500 mg intravenously every 12 hours for three days, followed by oral prednisone (1 mg/kg) tapered over 1.5 months (Permaisuari et al., 2019).

  • Combination Therapy: Evidence suggests combining methylprednisolone with erythropoietin offers improved outcomes compared to corticosteroids alone (Pakravan et al., 2016).

Supportive Treatments:

  • Magnesium sulfate: 2 grams intravenously twice a day for five days.

  • Vitamin B12: 100 mg daily for one month.

  • Folic acid: 10 mg daily for one month, with continuation for up to six months based on patient response (Pakravan et al., 2016).

3. Follow-Up Care

Ophthalmology Follow-Up:

  • Imaging and Assessments: Retinal and optic nerve imaging (Optical Coherence Tomography, OCT) should be conducted within 48 hours of admission and every 48 hours during hospitalization. Regular evaluations with functional tests (visual field testing, visual evoked potentials) are recommended to monitor recovery (Pakravan et al., 2016). In some patients, visual function may continue to deteriorate even months after the initial poisoning event.

  • Long-term rehabilitation protocols, such as visual stimulation exercises or neuroprotective agents like erythropoietin (EPO), can improve outcomes, even when vision is initially lost (Pakdel et al., 2018). For this reason, follow-up imaging and functional tests, such as VEP and RNFL assessments, should be performed every 3-6 months to monitor for optic nerve degeneration (Nurieva et al., 2018).

Long-Term Monitoring:

  • Patients undergoing prolonged treatment should have monthly check-ups for visual acuity, CBC, liver enzymes, and renal function for up to six months (Pakdel et al., 2018).

4. Home Care Guidelines

  • Hydration: Drink plenty of water to support systemic detoxification.

  • Diet: A high-fiber diet rich in fruits and vegetables should be maintained.

  • Activity: Walking with assistance is encouraged to prevent muscle weakness, while bed rest should be minimized.

  • Lifestyle: Smoking, alcohol, and other harmful substances should be strictly avoided.

5. Contraindications and Drug Interactions

  • Erythropoietin: Should not be used in patients with a history of thromboembolism or uncontrolled hypertension. Monitoring for complications like elevated blood pressure and clot formation is essential (Pakravan et al., 2016).

  • Methylprednisolone: Requires caution in patients with existing coagulopathies and those on anticoagulants or NSAIDs (Sharma et al., 2012). Steroids, like methylprednisolone, may interact with common medications such as blood thinners (e.g., warfarin) and anticonvulsants (e.g., phenytoin). These interactions can increase the risk of side effects, making it essential to adjust doses and closely monitor the patient (Sanaei-Zadeh et al., 2011)

6. Recommendations for High-Dose Treatment

  • In severe cases, pulse therapy with erythropoietin (up to 20,000 units/day for three days) and methylprednisolone (up to 1,000 mg/day) is recommended, particularly when vision recovery is urgent (Pakdel et al., 2018).

  • Long-term Monitoring: Regular follow-up is necessary to assess for adverse effects like increased hemoglobin or hypertension (Pakravan et al., 2016).

  • High-dose methylprednisolone and erythropoietin aim to reduce inflammation and protect the optic nerve from further damage. These treatments can improve visual outcomes, but it is important to monitor patients closely for side effects like elevated blood pressure and electrolyte imbalances, which are common with high-dose steroids and EPO (Pakdel et al., 2018).

Conclusion

This guideline integrates the latest evidence on using erythropoietin and methylprednisolone for methanol-induced optic neuropathy. Early intervention with combined therapy significantly improves visual outcomes, but regular monitoring is essential to avoid complications.

References:

  1. Nurieva, O., Diblík, P., Kuthan, P., Sklenka, P., Meliska, M., Bydžovský, J., Heissigerova, J., Urban, P., Kotíková, K., Navrátil, T., Komarc, M., Seidl, Z., Vaněčková, M., Pelclova, D., & Zakharov, S. (2018). Progressive Chronic Retinal Axonal Loss Following Acute Methanol-induced Optic Neuropathy: Four-Year Prospective Cohort Study. American journal of ophthalmology, 191, 100-115. https://doi.org/10.1016/j.ajo.2018.04.015.

  2. Pakravan, M., Esfandiari, H., Sanjari, N., & Ghahari, E. (2016). Erythropoietin as an adjunctive treatment for methanol-induced toxic optic neuropathy. The American Journal of Drug and Alcohol Abuse, 42, 633 - 639. https://doi.org/10.1080/00952990.2016.1198800.

  3. Pakdel, F., Sanjari, M., Naderi, A., Pirmarzdashti, N., Haghighi, A., & Kashkouli, M. (2018). Erythropoietin in Treatment of Methanol Optic Neuropathy. Journal of Neuro-Ophthalmology, 38, 167–171. https://doi.org/10.1097/WNO.0000000000000614.

  4. Permaisuari, N., Rahmawati, N., Nusanti, S., & Thamrin, H. (2019). Efficacy of high-dose intravenous steroid treatment in methanol-induced optic neuropathy: A systematic review. International Journal of Applied Pharmaceutics, 11, 97-100. https://doi.org/10.22159/IJAP.2019.V11S6.33557.

  5. Sanaei-Zadeh, H. (2012). METHANOL-INDUCED BLINDNESS TREATED BY ERYTHROPOIETIN; A RAY OF HOPE IN THE DARKEST OF CLOUDS. , 81, 188-189. https://doi.org/10.31482/MMSL.2012.026.

  6. Sanaei-Zadeh, H., Zamani, N., & Shadnia, S. (2011). Outcomes of visual disturbances after methanol poisoning. Clinical Toxicology, 49, 102 - 107. https://doi.org/10.3109/15563650.2011.556642.

  7. Sharma, R., Marasini, S., Sharma, A., Shrestha, J., & Nepal, B. (2012). Methanol Poisoning: Ocular and Neurological Manifestations. Optometry and Vision Science, 89, 178-182. https://doi.org/10.1097/OPX.0b013e31823ee128.

  8. Tabatabaei, S., Amini, M., Haydar, A., Soleimani, M., Cheraqpour, K., Shahriari, M., Hassanian‐Moghaddam, H., Zamani, N., & Akbari, M. (2023). Outbreak of methanol-induced optic neuropathy in early COVID-19 era; effectiveness of erythropoietin and methylprednisolone therapy. World Journal of Clinical Cases, 11, 3502–3510. https://doi.org/10.12998/wjcc.v11.i15.3502.

  9. Zakharov, S., Pelclova, D., Diblík, P., Urban, P., Kuthan, P., Nurieva, O., Kotíková, K., Navrátil, T., Komarc, M., Běláček, J., Seidl, Z., Vaněčková, M., Hubacek, J., Bezdicek, O., Klempír, J., Yurchenko, M., Růžička, E., Miovský, M., Janíková, B., & Hovda, K. (2015). Long-term visual damage after acute methanol poisonings: Longitudinal cross-sectional study in 50 patients. Clinical Toxicology, 53, 884 - 892. https://doi.org/10.3109/15563650.2015.1086488.

 

Related Guidelines