The Amazing Benefits of esketamine (Spravato) for Treatment-Resistant Depression

Dr. Danish and his team of practitioners at Philadelphia Integrative Psychiatry are experienced in the use of both ketamine and esketamine (Spravato) for the treatment of treatment-resistant depression (TRD). Our extensive experience allows us to tailor treatments to the unique needs of each patient, ensuring the best possible outcomes. We are happy to offer both options, given the insurance backing of Spravato and the higher relative efficacy of ketamine. This dual approach enables us to provide flexible and effective solutions for those struggling with TRD.

High Efficacy for Depression 

The research article titled Efficacy and safety of ketamine and esketamine for unipolar and bipolar depression: an overview of systematic reviews with meta-analysis highlights the positive results of esketamine for Major Depressive Disorder (MDD). Esketamine significantly reduced depressive symptoms and suicidal ideation, with effects lasting up to 3-6 days and showing consistent efficacy beyond this period. The response and remission rates were higher in the esketamine groups compared to controls, especially within the first 24-48 hours. Esketamine was noted for its sustained efficacy in unipolar depression, making it a promising treatment option for patients with treatment-resistant depression (TRD).

Regarding dosing and side effects, esketamine is typically administered intranasally, which offers convenience and efficacy. The initial phase involves twice-weekly administration, followed by weekly or biweekly maintenance doses. Common side effects included dizziness, nausea, and increased blood pressure, with esketamine showing a higher incidence of nausea and vomiting compared to control groups. Dissociative symptoms were also noted, persisting even in the long term. Despite these side effects, esketamine was generally well-tolerated, with dropout rates similar to those of control interventions.

Indications and Limitations of Use

Spravato (esketamine) nasal spray is indicated for adults with treatment-resistant depression and depressive symptoms in adults with major depressive disorder (MDD) with acute suicidal ideation or behavior. However, it is important to note that Spravato is not approved for preventing suicide or reducing suicidal ideation or behavior. Additionally, it is not approved as an anesthetic agent.

Efficacy of esketamine (Spravato)

The efficacy of esketamine (Spravato) in treating treatment-resistant depression is highly promising. According to the research article titled "Efficacy and safety of ketamine and esketamine for unipolar and bipolar depression: an overview of systematic reviews with meta-analysis," esketamine significantly reduces depressive symptoms and suicidal ideation. The effects are notable, lasting up to 3-6 days, with consistent efficacy beyond this period.

Rapid Onset and Sustained Effects

One of the most remarkable aspects of esketamine is its rapid onset of action. Patients often experience significant improvements within the first 24-48 hours of administration. This rapid response is crucial for individuals suffering from severe depressive episodes, providing quick relief from debilitating symptoms. Moreover, the sustained efficacy of esketamine in unipolar depression makes it a promising treatment option for patients with TRD, offering hope where other treatments have failed.

High Response and Remission Rates

The response and remission rates for esketamine are notably higher compared to control groups. This means that a greater proportion of patients experience a significant reduction in depressive symptoms and achieve remission when treated with esketamine. These positive outcomes underscore the potential of esketamine to transform the treatment landscape for TRD, offering a new avenue of hope for patients who have not responded to traditional therapies.

Important Safety Information

Sedation and Dissociation

Spravato can cause sedation and dissociative effects, such as perceptual changes, derealization, and depersonalization. Patients must be monitored for at least two hours post-administration to ensure they are clinically stable before leaving the healthcare setting.

Respiratory Depression

There is a theoretical risk of respiratory depression with Spravato use. Patients should be monitored for changes in respiratory status during and after treatment sessions.

Abuse and Misuse

As a Schedule III controlled substance, Spravato has the potential for abuse and misuse. Healthcare providers must assess each patient's risk and monitor for signs of abuse or dependence.

Blood Pressure Increases

Spravato can cause significant increases in blood pressure, peaking around 40 minutes post-administration. Patients with cardiovascular conditions should be carefully evaluated before starting treatment.

Adverse Reactions

Common adverse reactions to Spravato include dissociation, dizziness, nausea, sedation, vertigo, hypoesthesia, anxiety, lethargy, increased blood pressure, vomiting, and a feeling of being drunk. For patients with MDD and acute suicidal ideation, additional reactions may include euphoric mood and vertigo.

Special Populations

Geriatric Use

No significant differences in safety were observed between older and younger patients. However, patients with moderate hepatic impairment may require longer monitoring for adverse reactions.

Pregnancy and Lactation

Spravato is not recommended during pregnancy due to potential fetal harm. Breastfeeding is also not recommended during treatment due to the risk of neurotoxicity.

Getting in Touch with Dr. Danish and his Team

At Philadelphia Integrative Psychiatry, we continue to stay on top of the latest research related to esketamine (Spravato) for treatment-resistant depression so we can provide the best quality care in a safe manner. Our holistic and integrative approach ensures that we consider all aspects of our patients' well-being in developing personalized treatment plans. If you or a loved one are seeking support for TRD or similar conditions, please text or call 610-999-6414 to learn how we can help.



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