A multivariable model was then used to determine independent risk factors for the performance
of revision surgery.
The results suggest that the risk
of revision surgery and most other complications of shoulder arthroplasty increases along with BMI in obese patients.
«These data will provide valuable information in preoperative counseling for patients and physicians regarding patient and procedural characteristics associated with higher rates
of revision surgery,» the authors conclude.
Not exact matches
The International Statistical Classification
of Diseases and Related Health Problems, 10th
Revision, codes were used to determine patients» co-existing conditions and complications after
surgery.
The research team, led by the University
of Bristol, conducted a study that reviewed patient data from 44 studies to compare the effectiveness
of the two types
of surgery currently used to treat infections — one - stage and two - stage
revisions.
Published
revision rates for septorhinoplasty procedures in the current facial plastic
surgery literature are limited to a small number
of studies focused on a single institution or a single surgeon.
Patient characteristics associated with increased
revision were younger age, being female, having a history
of anxiety or autoimmune disease, and
surgery for cosmetic or congenital nasal deformities, the study suggests.
A study from Hospital for Special
Surgery (HSS) finds that in morbidly obese patients, bariatric surgery performed prior to a total hip or knee replacement can reduce in - hospital and 90 - day postoperative complications and improve patient health, but it does not reduce the risk of needing a revision s
Surgery (HSS) finds that in morbidly obese patients, bariatric
surgery performed prior to a total hip or knee replacement can reduce in - hospital and 90 - day postoperative complications and improve patient health, but it does not reduce the risk of needing a revision s
surgery performed prior to a total hip or knee replacement can reduce in - hospital and 90 - day postoperative complications and improve patient health, but it does not reduce the risk
of needing a
revision surgerysurgery.
Levels
of pain, assessment
of general health, complications, the need for
revision surgery, and mortality were measured postoperatively for up to four years.
Only five per cent
of patients require
revision surgery over a 10 - year period.
Because
of the higher
revision rate
of partial knee replacement
surgery, which is traditionally regarded as the most important factor to determine the choice
of implant, its use in the treatment
of end - stage osteoarthritis is controversial, with only about 7,000 being performed annually in the UK.
For patients undergoing shoulder joint replacement
surgery (arthroplasty), higher body mass index is linked to increased complications — including the need for «revision» surgery, reports a study in the June 7 issue of The Journal of Bone & Joint S
surgery (arthroplasty), higher body mass index is linked to increased complications — including the need for «
revision»
surgery, reports a study in the June 7 issue of The Journal of Bone & Joint S
surgery, reports a study in the June 7 issue
of The Journal
of Bone & Joint
SurgerySurgery.
Patients who received a
revision joint replacement
surgery, a TJR following a fracture, patients with a history
of blood clots, or patients taking hormone replacement therapy were excluded from the study.
«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.
Main Outcomes and Measures
Revision surgery after an index septorhinoplasty was the main outcome measure, and the rate of revision was calculated within subgroups of patients based on different demographic and clinical characte
Revision surgery after an index septorhinoplasty was the main outcome measure, and the rate
of revision was calculated within subgroups of patients based on different demographic and clinical characte
revision was calculated within subgroups
of patients based on different demographic and clinical characteristics.
Of patients undergoing revision surgery, the median time to revision was 1.2 years after the index procedure, while 50.0 % of patients underwent revision between 8 months and 2.3 year
Of patients undergoing
revision surgery, the median time to
revision was 1.2 years after the index procedure, while 50.0 %
of patients underwent revision between 8 months and 2.3 year
of patients underwent
revision between 8 months and 2.3 years.
We are very enthusiastic regarding the ongoing development
of our orthopedic services including lameness diagnosis, trauma care, non-emergent orthopedic
surgery (cranial cruciate ligament rupture, medial patellar luxation), limb deformity, minimally invasive
surgery, arthroscopy, total joint replacement, orthopedic
revision surgery, sports medicine, physical rehabilitation, and regenerative medicine.
Consumers have reported side effects
of the BioMet hip replacements such as severe pain, swelling and difficulty walking, and many have required hip
revision surgery.
The National Joint Registry
of England & Wales found that
revision rates were higher for
surgeries using these products at the five - year point.
While artificial hips are supposed to last at least 15 years, DePuy was forced to recall its ASR devices nearly four years ago in the wake
of rising device failure rates, with many patients having to undergo
revision surgery within five years
of getting their device.
With a Monday, January 6, 2014 deadline looming for people looking to avail
of a multibillion - dollar DePuy ASR settlement deadline, many
of those who were forced to undergo
revision surgery to replace their faulty hip implants are rushing to meet the deadline to register their claim.
It noted, «Thus, the «
revision»
surgery for that fracture was simply further treatment
of the initial injury.»
The insurance company took the position that, because Conners had failed to follow medical advice during his recovery from the first
surgery, his negligence (and not the accident) was the cause
of the nonunion, the
revision surgery, and the resulting drug reaction.
Depuy Hip Implants — Involving the Pinnacle Implant — where the patient has had to undergo a removal and replacement
of the implant (a
revision surgery).
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.
In particular, he carries out a large number
of revision spinal procedures in patients who have had previous spinal
surgery elsewhere.
Some defective hip implant patients have needed
revision surgery to remove the implant, which creates a separate set
of risks.
The FDA stated that the use
of a Transvaginal mesh implant like the Bard Avaulta, Johnson & Johnson, American Medical Systems, Boston Scientific, and other vaginal mesh is no more effective compared to other
surgeries yet is much more likely to cause injury and require
revision surgery.
(Because
of the nature
of these particular hip systems,
revision surgery can prove particularly challenging to perform and traumatic for the patient.)
Two months before the recall, Stryker is reported to have put out a warning to medical professionals and affected parties over concern that the rubbing together
of its parts could Adverse Local Tissue Reaction, including necrosis, metallosis, osteolysis, tumor - like formations, and pain serious enough to warrant
revision surgery.
In 2010, reports disclosed that approximately 9 %
of people with the Zimmer NexGen CR - Flex Porous Femoral component knee replacement required a
revision surgery within two years.
Hip Implant Failure Any type
of hip implant failure likely means that the patient will have to undergo at least one another
revision surgery to have the device removed and replaced.
In her hip injury lawsuit, Lincoln claims that her ABG II system implant caused her to develop a number
of health issues, including metallosis, and she has been forced to undergo
revision surgery.
Recent studies have shown that 24 %
of patients who had
revision surgery experienced worsening symptoms.
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.
Many doctors have stopped using the devices as companies halt sales amid allegations
of mesh side effects, including severe pain, limited mobility and
revision surgery.
The Gynecare Prolift is the subject
of the first transvaginal mesh lawsuit to go to trial in New Jersey, where Linda Gross alleges the device failed and required 18
revision surgeries.
The Saskatchewan Ministry
of Health turned down their request to cover the
revision surgery because it will not fund out -
of - country medical procedures.
The cases being filed by Georgia DePuy Hip Implant lawyers seek compensation for the patients to cover the cost
of having a second
revision surgery.
One internal analysis in 2011 is said to have found that close to 36 %
of the devices would likely failed within five years - way below generally accepted standards that say that no more than 5 %
of patients should undergo
revision hip replacement
surgery during this timeframe.
The FDA issued a mesh warning after receiving an influx
of complaints from patients who allege that their transvaginal mesh device were causing severe complications, pain and sometimes
revision surgery.
As with any kind
of surgery, there are risks involved and, in certain circumstances, more than one
revision procedure may be required.
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.
This is considered to be the main risk with rhinoplasty and it accounts for 5 - 15 %
of the cases that cause
revision surgery as based on studies.