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What Drugs Cause Central Serous Retinopathy? An Expert Guide

4 min read

According to the American Society of Retina Specialists, systemic exposure to corticosteroids is the most common and widely reported trigger for Central Serous Chorioretinopathy (CSR). Understanding what drugs cause central serous retinopathy is crucial for early detection and management of this vision-threatening condition.

Quick Summary

This article explores various medications known to be associated with central serous retinopathy, focusing on corticosteroids, sympathomimetics, certain cancer therapies, and other drugs linked to retinal fluid buildup and vision issues.

Key Points

  • Corticosteroids Are the Primary Culprit: Systemic, inhaled, topical, and nasal corticosteroids are the most common medications strongly linked to causing central serous retinopathy (CSR).

  • Diverse Medication Classes Can Be Implicated: Beyond steroids, several other drug types, including cancer therapies (MEK/BRAF inhibitors), stimulants, and psychiatric drugs (quetiapine), have been associated with CSR.

  • Multiple Routes of Exposure Are Risky: Even localized steroid applications like nasal sprays or topical creams can increase the risk, not just oral or injectable forms.

  • Diagnosis Requires Specialized Imaging: An ophthalmologist uses Optical Coherence Tomography (OCT) and Fluorescein Angiography (FA) to confirm the diagnosis and pinpoint the source of leakage.

  • Medication Discontinuation Is Key to Recovery: Often, the CSR resolves on its own after the causative medication is stopped, though this should always be done under the supervision of a doctor.

  • Early Intervention Minimizes Permanent Damage: Prompt identification of the drug and appropriate management greatly increases the likelihood of full visual recovery and prevents long-term vision loss.

In This Article

Central Serous Retinopathy (CSR), also known as Central Serous Chorioretinopathy (CSCR), is a condition where fluid accumulates under the retina, causing central vision to become blurry or distorted. While factors like stress and Type A personality traits have been linked to CSR, a significant number of cases are attributed to exogenous (outside the body) and endogenous (inside the body) corticosteroids. Beyond steroids, a growing list of medications, from cancer treatments to common over-the-counter drugs, have been implicated in triggering or exacerbating this retinal disorder. The key to management often involves identifying and, under medical supervision, discontinuing the offending medication.

The Strongest Link: Corticosteroids

Corticosteroids, a class of anti-inflammatory drugs, have the most robust association with CSR. Their use is strongly correlated with an increased risk of developing the condition, regardless of the route of administration.

Systemic Corticosteroids

These are typically taken orally or via injection for conditions such as autoimmune disorders, asthma, and inflammatory diseases. Studies have found a dramatically increased odds ratio for CSR in patients using systemic steroids. High doses and prolonged use are particularly risky, but even low-dose oral steroids can trigger CSR.

Inhaled and Topical Corticosteroids

It is a common misconception that localized steroid use is safe for the eyes. Case reports demonstrate that inhaled corticosteroids for asthma and nasal sprays for allergies can cause CSR. Similarly, high-potency topical steroid creams used on the skin have been linked to the condition. This underscores the importance of a comprehensive medical history when evaluating a patient with CSR, as all forms of steroid exposure should be considered.

Other Medications Linked to Central Serous Retinopathy

While corticosteroids are the primary culprits, research has identified a diverse range of other drugs that can contribute to or trigger CSR.

Cancer Medications

  • MEK Inhibitors: Used to treat certain types of melanoma and other cancers, MEK inhibitors like cobimetinib and trametinib can cause serous retinal detachments.
  • BRAF Inhibitors: Often used in combination with MEK inhibitors, these drugs can also trigger CSR.
  • Checkpoint Inhibitors: Some immunotherapies can induce a variety of ocular side effects, including serous retinal detachments.
  • Tamoxifen: This breast cancer drug has toxic effects on the retinal pigment epithelium and can lead to fluid accumulation.

Psychiatric and Neurological Drugs

  • Quetiapine: This atypical antipsychotic has been associated with CSR, potentially by affecting choroidal blood flow through dopamine and serotonin pathways.
  • Pregabalin: Case reports suggest this medication, used for neuropathic pain and anxiety, may trigger CSR.

Cardiovascular and Stimulant Drugs

  • Sympathomimetics: Drugs that increase sympathetic nervous system activity, such as Adderall (dextroamphetamine-amphetamine), pseudoephedrine (a decongestant), and illicit substances like MDMA (ecstasy), have been linked to CSR.
  • Phosphodiesterase-5 (PDE-5) Inhibitors: Medications for erectile dysfunction, like sildenafil (Viagra), have been associated with CSR.
  • Aspirin: High doses of aspirin, particularly in the context of hypercoagulability, have been explored as a potential contributor.

Other Drug Classes

  • Antibiotics: Some antibiotics, including rifampin, have been linked to CSR.
  • Sulfa-derived drugs: These medications can cause choroidal effusion and retinal folds, mimicking or potentially causing CSR.
  • Interferon: Used for conditions like multiple sclerosis and hepatitis, interferon can induce ocular toxicity, including CSR.
  • Finasteride: Some reports have linked this drug for prostate enlargement and hair loss to CSR.

Comparison of Key Drug Categories and CSR Risk

Drug Category Examples Routes of Administration Mechanism of Action Risk Level
Corticosteroids Prednisone, Dexamethasone, Flonase, Hydrocortisone cream Oral, IV, Inhaled, Topical, Nasal Upregulation of mineralocorticoid receptors; altered choroidal blood flow High and Confirmed
Sympathomimetics Adderall, Pseudoephedrine, MDMA Oral, Nasal, Illicit Increased sympathetic activity and vascular changes Probable/Case Reports
MEK/BRAF Inhibitors Cobimetinib, Trametinib Oral Disrupts intracellular signaling pathways, causing retinal detachment High for Chronic Users
PDE-5 Inhibitors Sildenafil (Viagra) Oral Altered blood flow and vascular permeability in the choroid Probable/Case Reports
Atypical Antipsychotics Quetiapine Oral Modulates dopamine/serotonin, affecting choroidal circulation Probable/Case Reports

Pathophysiology and Diagnosis

Though not fully understood, the underlying mechanism of drug-induced CSR involves an abnormal increase in the permeability of the choroidal capillaries, the blood vessel layer beneath the retina. This leads to fluid leakage, which collects under the retina and separates it from the underlying tissue. Retinal pigment epithelium (RPE) cells are also affected, contributing to the fluid buildup.

Diagnosis is confirmed through a comprehensive eye exam by an ophthalmologist, which includes retinal imaging techniques. Optical Coherence Tomography (OCT) is crucial for visualizing the subretinal fluid. Fluorescein Angiography (FA), a test using a fluorescent dye, can detect the specific leakage sites. The doctor will also take a detailed history of all medications to identify potential culprits.

Conclusion

The association between certain medications and the development of central serous retinopathy is well-documented, with corticosteroids being the most prominent cause. However, it is important for both physicians and patients to be aware that other drug classes, including cancer therapies, stimulants, and psychiatric medications, can also trigger this condition. The potential for vision-related side effects from seemingly unrelated drug therapies highlights the need for a thorough medical and medication history in patients presenting with CSR symptoms. Early detection and, where appropriate, discontinuing the offending medication under a doctor's care are often key steps toward successful visual recovery.

For more detailed information, consult the resource on Drug Induced Maculopathy from the American Society of Retina Specialists.

What to Do If You Suspect Drug-Induced CSR

If you experience blurred or distorted vision, especially if you are taking any of the medications listed above, it is essential to contact an ophthalmologist promptly. A retinal specialist can properly diagnose the condition and determine if a medication is the likely cause. Do not stop any prescribed medication without first consulting your prescribing physician, as abrupt discontinuation can be medically unsafe.

Frequently Asked Questions

CSR is a condition in which fluid leaks from the choroid (the vascular layer beneath the retina) and collects under the retina, causing a serous detachment and distorting central vision.

Yes, case reports confirm that even locally administered corticosteroids, such as nasal allergy sprays and topical skin creams, can trigger CSR.

Some cancer medications, notably MEK inhibitors (e.g., cobimetinib, trametinib) and BRAF inhibitors, are known to cause serous retinal detachments similar to CSR.

Sympathomimetic agents, which include stimulants like Adderall and decongestants, are thought to cause CSR by increasing sympathetic nervous system activity and altering choroidal blood flow.

No, you should never stop a prescribed medication on your own. It is essential to consult with both your ophthalmologist and the doctor who prescribed the medication to safely manage your treatment.

While many cases of CSR resolve spontaneously after stopping the medication, some persistent cases may require additional treatment, and permanent vision changes can occur, though this is rare.

Research suggests there may be a genetic tendency for CSR, as a higher incidence is sometimes found among relatives. This indicates that certain individuals may be more susceptible to drug triggers.

Yes, endogenous (naturally produced) corticosteroids released during periods of high emotional stress are also considered a risk factor for CSR, especially in individuals with 'Type A' personality traits.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.