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Catalog Number UNK - VEPTR |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Unspecified Infection (1930)
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Event Type
Injury
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Event Description
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This report is being filed after the subsequent review of the following journal article: " scoliosis research society 47th annual meeting and course final program".Abstract# 41: ajeya joshi and et al: management of thoracic insufficiency syndrome (tis) in congenital scoliosis patients using vertical expandable prosthetic titanium rib (veptr) a review of 32 cases of progressive congenital scoliosis (pcs) with thoracic insufficiency syndrome (tis) treated with vertical expandable prosthetic titanium rib.Patients averaged 4.1 +/- 3.1 years at first vertical expandable prosthetic titanium rib implant, with average follow-up of 3.8 +/- 1.2 years.Charts were reviewed for operative course, assisted ventilation rate (avr) changes, and complications.Sitting radiographs were measured for cobb angle, sagittal profile, thoracic height and width, and space available for lungs (sal).Opening wedge thoracostomy (owt) usually accompanied initial device implantation and was repeated later in a subset of patients.Device dislodgements occured in 16 patients and infections occured in 6 patients.This is report 4 of 4 for (b)(4).This report is for unknown veptr, implanted in 6 patients.
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Manufacturer Narrative
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Device was used for treatment, not diagnosis.Date the abstract was published is unknown.This report is for unknown veptr, unknown part/unkown lot.This report for 6 unknown veptr.Implant date: unknown.Joshi et al, management of thoracic insufficiency syndrome (tis) in congenital scoliosis patients using vertical expandable prosthetic titanium rib (veptr), pg# 78 abstract# 41, scoliosis research society, 47th annual meeting & course, sep 5-8, 2012.Without a lot number the device history records review could not be completed.The investigation could not be completed; no conclusion could be drawn, as no product was received.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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