Biomedical subjects

Richard J Powell

Publications and source records attributed to Richard J Powell.

40 records · Page 3Linked to original sources

PubMed2002

Prediction of early graft failure with intraoperative completion duplex ultrasound scan.

PURPOSE: The purpose of this study was to determine intraoperative hemodynamic parameters that predict early failure of infragenicular vein grafts with intraoperative completion duplex ultrasound scan. METHODS: We reviewed the results of intraoperative duplex scans that were selectively performed after completion of 45 tibial/pedal vein bypass grafts at high risk for failure. Bypass was performed for rest pain (39%) or tissue loss (61%), and 60% of the cases were disadvantaged because of compromised vein quality or poor arterial outflow. A 10-MHz low-profile transducer was used to scan the entire graft at bypass completion. All grafts were determined to be technically adequate (absence of retained valves, arteriovenous fistulas, or localized velocity increases and the presence of bypass-dependent distal pulses). Peak systolic velocity (PSV) and end diastolic velocity (EDV) were also measured at each anastomosis, in the outflow artery and in the proximal and distal portions of each graft. Resistive indices (RI) were calculated at each measurement point (PSV-EDV/PSV). Statistical analysis was performed with unpaired t test, chi(2) test, and multivariate analyses. RESULTS: Twenty infragenicular vein bypass grafts (44%) thrombosed within 12 months. Intraoperative hemodynamic parameters were significantly different between grafts that remained patent or thrombosed. EDV was lower (5 +/- 1 cm/s versus 13 +/- 3 cm/s; P =.02) and RI was higher (0.90 versus 0.81; P <.01) in the proximal portions of grafts that thrombosed within 12 months. Distal EDV was also lower (6 +/- 1 cm/s versus 15 +/- 2 cm/s; P <.01) and distal RI was higher (0.89 versus 0.78; P <.01) in grafts that thrombosed. With multivariate analysis, only low distal EDV was predictive of early graft failure (P <.05). Distal bypass EDV of less than 8 cm/s predicated early graft thrombosis with 76% sensitivity and 75% specificity (positive predictive value, 71%; negative predictive value, 78%). Absence of diastolic flow (EDV of 0 cm/s) predicted early graft failure with 100% specificity and 100% positive predictive value. CONCLUSION: In this initial experience, low EDV measured with intraoperative duplex scan was associated with early thrombosis of tibial level vein grafts. When such values are observed, measures should be taken to improve graft hemodynamic parameters. Prospective study of infragenicular vein bypass grafts may better define hemodynamic parameters predictive of early graft thrombosis.

Aged↗

PubMed2002

Internal iliac occlusion without coil embolization during endovascular abdominal aortic aneurysm repair.

PURPOSE: When abdominal aortic aneurysms and common iliac artery (CIA) aneurysms undergo concomitant endovascular repair, endograft limb extension into the external iliac artery is often necessary. Usually, the internal iliac artery (IIA) is coil embolized in such a case to prevent endoleak. It has been our practice to coil embolize the IIA only in cases where there is not adequate stent graft seal in the CIA immediately proximal to the IIA origin (effectively sealing the entire IIA origin). In this study, we evaluated the outcomes of this approach. METHODS: We retrospectively reviewed 204 consecutive endovascular abdominal aortic aneurysm repairs at Dartmouth-Hitchcock Medical Center from 1996 to 2001. Computed tomographic angiography with three-dimensional reconstruction was the primary preoperative imaging modality, and the decision to cover the IIA without concomitant coil embolization was based before surgery on the presence of adequate graft oversizing (> or =10% to 15%) in the most distal 5 mm of CIA and 15 mm of proximal external iliac artery, respectively. RESULTS: The IIA was occluded 33 times in 31 patients. In 22 cases (67%), the IIA was covered without coil embolization (COVER group). The remaining 11 patients (33%) with inadequate graft oversizing in the CIA underwent IIA coil embolization (COIL group). The follow-up periods for the COVER and COIL groups were 19 +/- 2 months and 10 +/- 3 months, respectively. All operations in both groups were technically successful without evidence of endoleak at completion angiography. No endoleaks, graft migrations, or aneurysm enlargements were associated with the covered or coiled IIAs during the follow-up period. No clinical sequelae were seen in the COVER group, with the exception of buttock claudication in six patients (27%) that resolved completely in five patients. In the COIL group, five patients (45%) had buttock claudication. In addition, one case of buttock necrosis and one case of ischemic neuropathy occurred in the COIL group. CONCLUSION: Covering the IIA without coiling effectively excluded the CIA aneurysm in every case and was associated with a low incidence rate of complications compared with coil embolization. With detailed preoperative imaging and patient selection, IIA coil embolization may not be necessary in as many as two thirds of patients who need IIA occlusion.

Aged↗

PubMed2002

The TNF receptor-associated periodic syndrome (TRAPS): emerging concepts of an autoinflammatory disorder.

The present report describes and expands the clinical and genetic spectrum of the autoinflammatory disorder, tumor necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS). A total of 20 mutations have been identified since our initial discovery of 6 missense mutations in TNF receptor super family 1A (TNFRSF1A) in 1999. Eighteen of the mutations result in amino acid substitutions within the first 2 cysteine-rich domains (CRDs) of the extracellular portion of the receptor. A single splicing mutation also affects the first CRD by causing the insertion of 4 amino acids. Haplotype analysis of the most commonly occurring and ethnically heterogeneous mutation, R92Q, demonstrates an ancient founder; however, analysis of the T50M mutation, another commonly occurring mutation in Irish and Scottish families, does not, suggesting that T50M is a recurring mutation. Mutations that result in cysteine substitutions demonstrate a higher penetrance of the clinical phenotype (93% versus 82% for noncysteine residue substitutions), and also increase the probability of developing life-threatening amyloidosis (24% versus 2% for noncysteine residue substitutions). Retrospective and prospective evaluation of more than 50 patients, representing 10 of the 20 known mutations, allows us to expand and better define the clinical spectrum of TRAPS. Recurrent episodes of fever, myalgia, rash, abdominal pain, and conjunctivitis that often last longer than 5 days are the most characteristic clinical features of TRAPS. Defective shedding of TNFRSF1A can only partially explain the pathophysiologic mechanism of TRAPS, since some mutations have normal shedding. Consequently, other mechanisms may be mediating the observed phenotype. We are currently investigating other possible mechanisms using stable and transiently transfected cell systems in vitro, as well as developing a knockin mouse model. Preliminary data suggest that etanercept may be effective in decreasing the severity, duration, and frequency of symptoms in TRAPS patients. Additionally, it provides a viable therapeutic alternative to glucocorticoid therapy, which has numerous serious, long-term adverse effects. Two clinical trials are being conducted to evaluate the efficacy of etanercept in decreasing the frequency and severity of symptoms in TRAPS. Lastly, we have summarized data that R92Q and P46L, and probably as yet undiscovered substitutions, represent very low penetrance mutations that may play a much larger role in more broadly defined inflammatory diseases such as rheumatoid arthritis. Our laboratories are currently undertaking both clinical and basic research studies to define the role of these mutations in more common inflammatory diseases.

Adolescent↗

PubMedDate not supplied

The eye in systemic inflammatory diseases.

Systemic inflammatory diseases commonly affect the sclera, cornea, retina, and orbit, and can pose a serious threat to sight. They encompass both primary and secondary vasculitic disorders and specific granulomatous inflammatory conditions. As well as direct eye involvement from the systemic inflammatory process, there can be signs of ocular ischaemia due to carotid or ophthalmic arteritis, hypertensive retinopathy, and ocular complications such as chloroquine maculopathy related to anti-inflammatory drug treatment. Additionally, systemic infection relating to the eye, either as the result of primary infective disease processes or infection secondary to immunosuppression, might be mistaken as endogenous intraocular inflammation. Infection can closely mimic the ocular signs of endogenous inflammation, and in selected patients (such as those who have been immunosuppressed to treat vasculitis and who additionally have had invasive surgery, indwelling intravenous catheters, or systemic sepsis), it might be necessary to specifically exclude infection by the sampling and culturing of intraocular fluids and tissue.

Diagnosis, Differential↗