IVC Filter Complications

In addition to the problem of filter migration, embolization of the struts and penetration of the IVC, there is an additional complication: the blockage or occlusion of the filter due to blood clots being captured by the filter or forming as a result of filter placement. According to a February 2013 study in Vascular Medicine, placement of an IVC filter may promote the formation of blood clots. “Occlusion of IVC filters remains their most frequent complication,” the authors wrote.

IVC Filter Complications – The MAUDE Database

One of the best sources of information about IVC filter complications is within a database maintained by the U.S. Food and Drug Administration known as the Manufacturer and User Facility Device Experience (MAUDE) database. Researchers use this database to study problems associated with the filters.

Federal law requires manufacturers and importers of medical devices, as well as medical facilities (such as hospitals, ambulatory surgical centers, nursing homes and outpatient clinics), to let U.S. Food and Drug Administration (FDA) know when they have learned of significant problems associated with a medical device.

They must file reports and those reports, along with the information contained in them, are then stored in the MAUDE database. Sometimes voluntary reports are also filed by health care professionals and consumers.

Perhaps the most important element to realize about the reports in the MAUDE database is that each report involves either death, serious injury or malfunctions that “would be likely to cause or contribute to a death or serious injury” if these defects were to occur again.

“He allegedly experienced worsening pain and discomfort as fragments of the filter ‘became embedded in the tissue throughout his body.’ Decedent allegedly took his own life…after being ‘unable to find relief from constant pain.’” -From a MAUDE database report submitted to the FDA on October 22, 1015.

MAUDE Database in Medical Research

In 2014, doctors in Northwestern University’s Department of Radiology published the results of their investigation into IVC filter incident reports contained in the MAUDE database. They searched the database for adverse events that had been reported between January 2009 and December 2012 and found 1,606 such events involving 1,057 IVC filters. 1,394 events involved retrievable filters, those that are meant to be removed as soon as there is no longer a need, and 212 were tied to permanent filters. Not surprisingly, the filing of an IVC filter lawsuit is most often tied to the retrievable type filters.

Out of 1,606 adverse events reported, the researchers found the following complications:

As mentioned above, the limbs of the IVC filter may pierce through the inferior vena cava and come into contact with nearby organs. The Northwestern doctors found 28 cases in which the device had penetrated into the duodenum or small bowel, 14 cases of penetration into the aorta, and 12 cases of penetration into structures adjacent to the IVC, including vertebral bodies and disks—nine producing bleeding.

A recent IVC filter lawsuit has alleged (backed by autopsy findings) that the filter pierced the inferior vena cava, causing internal bleeding which led to a woman’s death.

In another IVC filter lawsuit, a Mississippi man alleges that the filter perforated the inferior vena cava and was leaning against the abdominal aorta—the blood vessel that supplies oxygenated blood to the organs around the abdomen and pelvis, as well as to the legs. The position of the device made it too dangerous to remove.

MAUDE database report submitted to the FDA on November 3, 2015:

“Event description: It was reported that approximately five years post vena cava filter deployment; an inferior vena cava gram performed allegedly demonstrated a detached limb in the right kidney, with two filter limbs penetrating the IVC wall. There was no report of an attempt to retrieve the filter or detached limb was made. Approximately six years post vena cava filter deployment an open surgical procedure was performed to remove the filter; reportedly four filter limbs had perforated the IVC wall. The filter was removed successfully….possible complications include, but are not limited to, the following: perforation or other acute or chronic damage of the IVC wall…. All of the above complications have been associated with serious adverse events such as medical intervention and/or death.”

IVC Filter Complications and Filter Brands

Information in the database suggests that certain IVC filter complications are more closely associated with one brand than another, perhaps due to filter design. The Northwestern University study authors found that fracture of the filter device was most commonly reported in Bard filters. They also noted that filter fracture and migration were cited as reasons the Bard Recovery and G2 filters were removed from the market. Penetration of the IVC by the filter limbs was most common with the Cook Celect filter, which has been reported in the medical literature to have a rate of IVC penetration of 86.1%. Placement malfunctions were associated more with the OPTEASE and Cook Günther Tulip filters.

If you or a loved one has been injured by an IVC filter, or is under threat of injury, the IVC filter team at Wisner Baumwould like to hear from you. Please contact our firm for a free consultation.