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The purpose of this study is to compare the use of the Micro Vascular Plug (MVP) system and other embolic devices in treatment of PAVMs. Pulmonary Arteriovenous Malformations (PAVMs) are abnormal connections between the pulmonary vein and the pulmonary artery. This affects blood flow between the heart and lungs which puts patients at risk of stroke, brain abscess, hypoxia and even sudden death. The standard treatment of PAVMs is embolization. Embolization is the placing of an embolic (synthetic agent) into a blood vessel to block blood flow. The embolic is inserted via a catheter into the blood vessel. Detachable coils are the most commonly used embolic in the treatment of PAVMs. Despite long procedure times, numerous coils that are often required to occlude a single PAVM and recanalization rates ranging from 5% to 15%, the most widely used embolic device is still the detachable coil.
Transcatheter embolization has become the standard of care in the treatment of Pulmonary Arteriovenous Malformations (PAVMs). PAVM embolization is performed to prevent right to left shunting which puts patients at risk of stroke, brain abscess, hypoxia and even sudden death. Despite long procedure times, numerous coils that are often required to occlude a single PAVM and recanalization rates ranging from 5% to 15%, the most widely used embolic device is still the detachable coil delivered through a microcatheter. An alternative to coil embolization is the Amplatzer Vascular plug (AVP). AVPs allow for quick delivery of a single occluding device. AVPs, however, cannot be delivered through a microcatheter, limiting the AVPs' utility to larger PAVM with larger feeding arteries. The new MVPTM Micro Vascular Plug System (MVP, Medtronic) was designed to combine the best of both devices and allows for the occlusion of small vessels in a quick and predictable manner with a single embolic device through a micro catheter. At the investigators' institution the investigators have a very large PAVM practice, as the investigators are a large Hereditary Hemorrhagic Telangiectasia (HHT) center of excellence. Currently there is a paucity of data comparing these devices for the treatment of PAVMs. Specifically, there is little data to inform interventional radiologists' decision making process about which device to choose based on the patient's clinical characteristics, the size of the PAVM feeding artery, and cost.
The investigators will create a registry/database of all patients who undergo embolization for Pulmonary AVM at the investigators' HHT center of excellence collecting data and adding in data from the investigators' existing PAVM database dating back at least the last 7 years. Patients with MVP embolizations will be assessed and compared to patients who are embolized with other solid embolic devices (coils/plugs). The investigators will assess reperfusion rates, immediate technical success, procedural attributes including procedure time, fluoroscopy time, contrast administration, and finally embolic and overall procedural costs.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients treated for Pulmonary Arteriovenous Malformation | All participants in the study will be patients who have been treated for Pulmonary Arteriovenous Malformation using Microvascular Plugs, Amplatzer Vascular Plugs or Detachable coils. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Microvascular Plug (MVP) | Device | Patient's Pulmonary AVM(s) treated via transcatheter embolization with Microvascular Plugs. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Reperfusion Rates | Analyzed at 1 year and 3 years. Based on the investigators' preliminary data, reperfusion has been seen at 1-2 years in the patients the investigators have treated with coils and AVP making the 3-year goal for the investigators' prospective analysis feasible to cover reperfusion. | Up to 3 Years |
| Immediate post-procedural success | Immediate post-procedural technical success defined as complete occlusion of the feeding artery supplying the PAVM. | Immediately after procedure up to 5 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Procedure duration | Duration of procedure in minutes. | Up to 4 hours |
| Fluoroscopy time | Fluoroscopy time measured in minutes. | Up to 4 hours |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with Pulmonary Arteriovenous Malformation (PAVM) being treated through the Interventional Radiology clinic.
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| Name | Affiliation | Role |
|---|---|---|
| Clifford R Weiss, M.D. | Johns Hopkins University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Johns Hopkins University | Baltimore | Maryland | 21287 | United States |
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| ID | Term |
|---|---|
| C562404 | Pulmonary Arteriovenous Fistulas |
| D013683 | Telangiectasia, Hereditary Hemorrhagic |
| ID | Term |
|---|---|
| D020141 | Hemostatic Disorders |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D013684 | Telangiectasis |
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| Amplatzer Vascular Plug (AVP) | Device | Patient's Pulmonary AVM(s) treated via transcatheter embolization with Amplatzer Vascular Plugs. |
|
| Detachable coils | Device | Patient's Pulmonary AVM(s) treated via transcatheter embolization with detachable coils. |
|
| Contrast dose | Contrast dose in mL. | Up to 4 hours |
| Cost of embolic device per PAVM | The number of embolic used per procedure will be used to determine the cost per PAVM. | Up to 4 hours |
| Overall procedure cost for PAVM | Overall procedure cost for PAVM will be determined at 1 week after the procedure. | Up to 1 week |
| Radiation Dose Area Product (DAP) | Radiation DAP measured in milligray-centimeters squared (mGy-cm^2). | Up to 4 hours |
| Cumulative Air Kerma (AK) dose | Cumulative Air Kerma dose measured in milligray (mGy). | Up to 4 hours |
| D006474 |
| Hemorrhagic Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D054079 | Vascular Malformations |
| D018376 | Cardiovascular Abnormalities |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |