MIND study

The MIND study involving the ARTEMIS Penumbra System.

Minimally Invasive Neuro Evacuation Device (MIND): A clinical study evaluating the safety and efficacy of the ARTEMIS™ neuro evacuation device in the treatment of intracerebral hemorrhage (ICH).

### 📌 Objective: To evaluate whether minimally invasive aspiration using ARTEMIS can safely reduce hematoma volume and potentially improve clinical outcomes in patients with spontaneous ICH.

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### 📋 Study Design: - Prospective, multicenter, single-arm observational study. - Sponsored by Penumbra Inc. - Involved patients with deep ICH (e.g., basal ganglia, thalamus) eligible for minimally invasive evacuation. - Primary endpoints:

1. Safety (mortality, procedure-related complications).
2. Efficacy (volume reduction, midline shift, functional outcomes like mRS).

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### ✅ Key Strengths:

- Real-world data from multiple centers. - Use of modern, targeted aspiration technique (ARTEMIS catheter). - Focused on deep hematomas, often harder to access surgically. - Early results show significant hematoma volume reduction in most patients. - Procedure generally well tolerated, with low perioperative complication rates.

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### ⚠️ Limitations and Critique:

1. Lack of control group:

1. Being a single-arm study, it lacks a comparison against conservative treatment or other surgical approaches (e.g., craniotomy, MISTIE-style catheter+lysis).

2. Functional outcomes unclear:

1. Volume reduction was achieved, but meaningful clinical recovery (e.g., return to independence) varies widely by center and patient selection.
2. Small sample size so far makes it hard to generalize.

3. Timing of intervention:

1. There's variability in when patients were treated (early vs. delayed aspiration), which affects the results.
2. No clear guidelines yet on optimal time window for ARTEMIS use.

4. No long-term follow-up published yet:

1. Cognitive and neurological outcomes beyond 90 days are not well documented.

5. Commercial interest:

1. As it’s industry-sponsored, results must be interpreted carefully with independent validation.

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### 🧾 Conclusion:

The MIND study confirms that the ARTEMIS™ system is: - Technically feasible, - Safe for aspiration of deep ICH, - Effective in reducing hematoma volume.

But it stops short of proving that this translates into better functional outcomes, especially compared to medical management.

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### 📊 What's Needed Next:

- A randomized controlled trial (RCT) comparing ARTEMIS vs. standard care or vs. other minimally invasive techniques. - Stratified analysis of ICH volume, location, and timing. - Cost-effectiveness evaluations. - Long-term outcome tracking.