![]() Currently, there is no unique procedure code for AF ablation. Our target population consisted of Medicare patients who had undergone RFA for AF from Octoto September 30, 2006. The validity of identifying comorbid conditions from such administrative data has been previously established. For each hospitalization, the MedPAR files contain information on basic patient demographics (age, gender, race) quarter and year the admission and discharge occurred principal discharge diagnosis, coded according to the International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) up to eight secondary ICD-9-CM diagnosis codes up to six ICD-9-CM procedural codes length of stay and discharge status. short-stay hospitals for services provided to Medicare beneficiaries. MedPAR files contain administrative data for all claims submitted to the Centers for Medicare and Medicaid Services (CMS) by U.S. Medicare beneficiaries, the objectives of this study were to assess trends in the number of hospitals performing RFA for AF and the volume of cases performed to identify the rates of significant procedural complications and changes in these rates over time and to assess variation in complication rates according to patient demographics and clinical characteristics.ĭata for the current analysis were obtained from Medicare Provider Analysis and Review (MedPAR) files for fiscal years 2001–2006. hospitals other than in selected, primarily academic centers. Little is known about the utilization, success rates, and frequency of complications in older patient populations and in U.S. Furthermore, most studies on the outcomes of AF ablation have included relatively young patients 8 despite the fact that most patients with AF are older than 65 years. Typically, these centers are teaching hospitals that perform a large volume of procedures 7 and therefore might be expected to have better outcomes than smaller, less experienced centers. The majority of data regarding the safety of RFA for AF come from selected centers with considerable interest and experience in catheter ablation. 2 Reported success rates and complication rates vary widely, with most studies suggesting major complication rates between 1% and 8%. 1 Radiofrequency catheter ablation (RFA) involving, but not limited to, electrical isolation of the pulmonary veins has evolved into an important treatment option for AF, and its utilization also is increasing. Personally visits the Medanta for returning the Device.Atrial fibrillation (AF) is the most common sustained arrhythmia in humans, and its incidence is increasing. Refund of DepositĪmount shall be made through the same mode of payment as that of purchase in cases where the User The refund of DepositĪmount shall be subject to return of the Device in working and undamaged condition. In cases where the User has opted for availing the Services through rented Device, a refundable depositĪmount of ₹ 5,000 (“ Deposit Amount”) shall be applicable and paid by the User. The extended program availed by the User shall be activated automatically on expiry of existing program of services. For the said purposes, the User can call our helpline number +414 or visit ![]() Provided that the Device has not been unboxed.īefore the expiry of service duration, the User can extend the services by availing various program Service on the day of purchase in which case, full amount of service fees shall be refunded to the User The services once availed cannot be cancelled except in cases where the User requests to cancel the Neither does Medanta endorse or promote the Device in any manner nor will Medanta be liableįor any claims, representations or warranties, whether express or implied as to the safety, reliability,ĭurability and performance of the device. Of services by Medanta is being provided on “as is” and “as available” basis through Alivecor India Private The User hereby agrees and acknowledges that the Device (hardware and software) used in the provision The User agrees and acknowledges that the User has read, understood and accepts the terms and conditions contained in the brochure provided with the Device (“ Device”) with respect to its usage, operations, return / replacement and warranty policy.
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