
St. Jude Medical, Inc. Silzone Heart Valve Litigation
What is Silzone™ ?
St. Jude Medical trademark for a silver coating process that
was used to treat heart valve prosthesis sewing cuffs.
The concept was that the silver on the cuff would act as a
local antimicrobial agent, which would lead to a lower incidence
of
prosthetic valve endocarditis, a rare, but often fatal complication
of heart valve surgery.
The Products at Issue
» St.
Jude Master Series heart valves with Silzone™ Heart valves
» In
Canada and EU countries, the Regent™ and EPIC™ valves
also prior to January 2001 had Silzone™ .
» SJM
Tailor™ Annuloplasty Rings with Silzone™ coating
» SJM
Sequin™ Annuloplasty Rings with Silzone™coating
What is the concern here?
Starting in July, 1997, St Jude introduced Silzone™ coated
heart valve prosthetic products in Canada, Europe and the UK.
Starting in June 1998 it introduced a number of these products
in the U.S. and Australia.
On January 21, 2000, St. Jude initiated a voluntary worldwide
recall of all field inventory of heart valve replacement and
repair products incorporating its proprietary Silzone™ coating
on the sewing cuff fabric.
What is the concern?
Silzone™ taken off market following reports
of:
» Higher
rate of paravalvalar leakage in Silzone™ Master Series
valves compared to non Silzone product.
» Higher
rate of thromboembolic events (strokes, heart attacks,
TIA’s) in the Silzone valves compared to similar
non-Silzone product.
» Improper
healing tissue growth (e.g.- too much; not enough;
tissue friable; heart annulus appeared eaten away).
» 36,000 people
worldwide were implanted with defective Silzone™ coated
heart valves.
» 10,500 in
the United States.
» 2,500 in
Canada.
» 23,000 in
Europe and U.K.
What went wrong?
» Inadequate
research and testing of the silver coating prior to marketing.
» No
meaningful clinical study on safety and efficacy prior
to market release.
» Optimistic
views taken by SJM of equivocal evidence.
» Key
test and experiment results not provided to regulatory
bodies.
» Aggressive
marketing by SJM’s sales force.
» Co-opting
of key opinion and research leaders in
the field.
United Kingdom Medical Advisory
Over the last year MDA has received notification that 7 patients
suffered a stroke or peripheral embolism among a group of 51
patients implanted with Silzone® heart valves by a number
of surgeons at one UK centre. Six of these patients had received
a mitral Silzone® valve (including one who had received both
mitral and aortic valves). The adverse events occurred within
3 months of valve implantation, and in two cases extensive thrombus
was identified on the valve's silver coated sewing cuff. There
have been a further 5 suspected incidents of TIA among this patient
group.
Immediate Action:
» Follow up
all patients implanted with Silzone® mechanical heart
valves to identify any signs of stroke or transient ischemic
attack (TIA) and ensure adequate anticoagulation control.
» Consider
examining patients using Trans-Oesophageal Echocardiography
(TOE) to identify any signs of valve thrombus….
In addition a pathologist outside the UK [Canada] has reported
concerns based upon his evaluation of an unexpectedly high number
of Silzone® valve explants.
The Avert Study
» Artificial Valve Endocarditis Reduction Trial
» Sponsored
by SJM
» Multi-site – Headquartered
in Pittsburgh
» Designed
to see if Silzone reduced PVE
» Independent
Data and Safety Monitoring Board managing study advised
St. Jude on January
21 that further enrollment in the study was suspended
due to unacceptable level of explants due to paravalvular
leakage in the Silzone "arm" of AVERT.
Were there signals prior to recall? YES!
» Number
of Thromboembolic in Cardiff, Wales study commissioned by SJM
on Silzone valves reported to St. Jude in October, 1998.
» Toronto
Explant experience brought to SJM’s attention in
November, 1998.
» Canadian,
Belfast and Denmark hospitals stopped Silzone™ implants
due to complications.
» Animal
studies were indicative of problems.
» Silver
coated catheter studies showed there were problems
with the coating.
How to tell if you have a Silzone™ product?
» Date
of implant should be after July 1997 (June, 1998 in US) and
on or before Jan 21, 2000 (See Table)
» Check “pocket
card” patient is given
» On
mechanical valves look for an “S”in the
serial number
Examples: “19AS-601”; “19MS-601”;"19AECS-602";
"21MECS-602";
» Check
surgical or operative report records
Geography
|
SJM Masters
Mechanical Heart Valve w/Silzone
|
SJM Taylor
Annuloplasty Ring
|
SJM Epic Valve
Stented Tissue Valva
|
Sequin Ring
w/Silzone
|
SJM Regent
Valve
|
United States
FDA Approval
|
March 1998
|
August 1998
|
Not Available
|
October 1998
|
April 1999
Clinical site only
|
Europe
(CE Mark)
|
July 1997
|
May 1998
|
Sept. 1998
|
February 1999
|
February 1999
|
Canada
|
July 1997
|
Not Available
|
Not Available
|
Dec.1998
|
December 1998
|
China
|
June 1998
|
Not Available
|
Not Available
|
Not Available
|
Not Available
|
Australia
|
March 1998
|
July 1998
|
Not Available
|
March 1999
|
Not Available
|
Latin America
|
Not Available
|
Not Available
|
July 1998
|
Not Available
|
Not Available
|
Japan
|
Not Available
|
Not Available
|
Not Available
|
Not Available
|
Not Available
|
Current Litigation
Federal cases across the nation are assigned to MDL No. 1396
in Minnesota. These cases are being managed by Judge Tunheim.
State cases are centered in Ramsey County (St. Paul) Minnesota.
These cases are being managed by Judge Gearin. Cases are also
pending in Texas and Nevada.
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