In veterinary patients it has not been proven to be necessary and some believe it may contribute to scar tissue formation, surgical failure, and the
need for revision surgery in the future.
Morbid obesity (a body mass index greater than or equal to 40 kg / m2) is associated with poor postoperative outcomes after total knee arthroplasty (TKA) and total hip arthroplasty (THA), including increased
risk for revision surgery, postoperative infection, and medical complications.
«The
reasons for revision surgery are varied and can include infection, instability and loosening of the prostheses, and the need for revision can occur within the first few months after implantation,» Pourzal says.
If you have suffered tissue damage, bone erosion, severe pain, or the need
for a revision surgery following an artificial hip implant, contact Altman & Altman, LLP today for a free and confidential consultation about your case.
Several manufacturers have issued transvaginal mesh recalls after studies linked the devices to severe complications and potential
need for revision surgery.
Levels of pain, assessment of general health, complications, the need
for revision surgery, and mortality were measured postoperatively for up to four years.
In human patients, excessive decompression can be detrimental due to cerebellar slouching and result in the need
for revision surgery.
If you or a loved one have suffered serious complications, such as hernia recurrence or need
for revision surgery, following placement of either Physiomesh of C - Qur hernia mesh, contact us today for a free legal consultation.
Bone fractures, joint dislocations, improperly positioned components, infection, defective stem designs, and poor cementing techniques may contribute to the loosening of stem components and the need
for a revision surgery.
Many transvaginal mesh manufacturers such as Johnson & Johnson and C. R. Bard have stopped selling their mesh devices after thousands of women have complained of severe pain, limited mobility and the need
for revision surgery.
Women implanted with a transvaginal mesh patch have complained of limited mobility, debilitating pain and a need
for revision surgery.
The FDA has reported various complications associated with hernia mesh products, including intestinal adhesions (occurs when parts of the intestine adhere to the mesh), reactions to the mesh, infection, severe and chronic pain, injuries to organs and nerves, and the need
for revision surgery.
The knee replacement systems are designed to last up to 15 years, however are often susceptible to complications including loosening and other failures, which sometimes result in the need
for revision surgery.