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Dive into the research topics where Dana Oliver is active.

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Featured researches published by Dana Oliver.


Gut | 2008

Development and validation of a simple NAFLD clinical scoring system for identifying patients without advanced disease

Stephen A. Harrison; Dana Oliver; Hays Arnold; Sudhanshu Gogia; Brent A. Neuschwander-Tetri

Background: Clinical predictors of advanced non-alcoholic liver disease (NAFLD) are needed to guide diagnostic evaluation and treatment. Methods: To better understand the demographics of NAFLD and risk factors for advanced disease, this study analysed 827 patients with NAFLD at two geographically separate tertiary medical centres. Results: The cohort was 51% female and had a median body mass index (BMI) of 33 kg/m2; 3% had a normal BMI. Common co-morbidities included hypertension (60%) and diabetes (35%); insulin resistance was present in 91% and advanced fibrosis in 24% of patients. When comparing patients with no fibrosis or mild fibrosis to those with advanced fibrosis, BMI ⩾28 kg/m2, age >50 years, and aspartate transaminase/alanine aminotransferase (AST/ALT) ratio ⩾0.8, a quantitative assessment check index (QUICKI) score <0.294 (equivalent to homeostatasis model assessment (HOMA) >6.2) and the presence of diabetes mellitus (DM) were individually associated by univariate analysis with odds ratios (ORs) of ⩾2.4 for advanced fibrosis. Based on the results of forced entry logistic regression analysis, three variables were combined in a weighted sum (BMI ⩾28 = 1 point, AAR of ⩾0.8 = 2 points, DM = 1 point) to form an easily calculated composite score for predicting advanced fibrosis called the BARD score. A score of 2–4 was associated with an OR for advanced fibrosis of 17 (confidence interval 9.2 to 31.9) and a negative predictive value of 96%. Conclusions: Insulin resistance and its co-morbidities are often present in patients with NAFLD. An easily calculated score based on readily available clinical data can reliably exclude the presence of advanced fibrosis in these patients, particularly among non-diabetics.


American Journal of Nephrology | 2004

Vitamin D Insufficiency and Deficiency in Chronic Kidney Disease

Esther Gonzalez; Ashutosh Sachdeva; Dana Oliver; Kevin J. Martin

Background: Kidney disease has been identified as a risk factor for vitamin D deficiency in hospitalized patients, and low levels of 25-hydroxyvitamin D have been suggested to be a risk factor for hyperparathyroidism in patients with chronic kidney disease (CKD). However, little is known about the magnitude of vitamin D deficiency in patients with CKD living in the United States. Methods: In this regard, we examined the levels of 25(OH)D in 43 patients with CKD and serum creatinine between 1 and 5 mg/dl (calculated glomerular filtration rate 111–11 ml/min per 1.73 m2) as well as in 103 patients undergoing hemodialysis. Results: In the predialysis patients, we found that 37 of the 43 patients (86%) had suboptimal levels of vitamin D (<30 ng/ml). Regression analysis indicated that there was a negative correlation between 25(OH)D and intact parathyroid hormone (PTH). Alkaline phosphatase showed a similar but less sensitive relationship. Serum albumin levels correlated with 25(OH)D levels. In contrast to findings reported in normal individuals, the levels of calcitriol correlated with those of 25(OH)D in the patients with CKD. In the group undergoing maintenance hemodialyis, we found that 97% of the patients had vitamin D levels in the suboptimal range, and there was no correlation of 25(OH)D levels with either PTH or serum albumin values. These data indicate that vitamin D insufficiency and deficiency are highly prevalent in patients with CKD and may play a role in the development of hyperparathyroidism. The functional significance of low levels of 25(OH)D in patients with stage 5 CKD remains to be determined.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2005

SURGICAL MARGIN DETERMINATION IN HEAD AND NECK ONCOLOGY: CURRENT CLINICAL PRACTICE. THE RESULTS OF AN INTERNATIONAL AMERICAN HEAD AND NECK SOCIETY MEMBER SURVEY

Jeremy D. Meier; Dana Oliver; Mark A. Varvares

Our aim was to investigate the ways in which surgeons who perform head and neck ablative procedures on a regular basis define margins, how they use frozen sections to evaluate margins, and the effect of chemoradiation on determining tumor margins.


Clinical Gastroenterology and Hepatology | 2005

Effect of Significant Histologic Steatosis or Steatohepatitis on Response to Antiviral Therapy in Patients With Chronic Hepatitis C

Stephen A. Harrison; Elizabeth M. Brunt; Rizwan A. Qazi; Dana Oliver; Brent A. Tetri; Adrian M. Di Bisceglie; Bruce R. Bacon

BACKGROUND & AIMS Treatment of chronic hepatitis C (CHC) results in an average sustained viral response (SVR) rate of 54%-63%. Most previous studies have not separately reported SVR rates for patients who have CHC and concomitant significant hepatic steatosis (>33%) or histologic evidence of steatohepatitis (SH). The aim of this study was to evaluate SVR in patients with CHC plus steatosis or SH on biopsy examination, compared with a group of controls with CHC and no significant steatosis or SH. METHODS Our surgical pathology database and clinical files were queried for CHC between 1997 to 2002. Biopsy specimens with both CHC and significant steatosis (>33%) or SH were categorized as group 1. Of the patients treated with antiviral therapy, information on either SVR (hepatitis C virus [HCV] RNA negative at 6 months posttreatment) or lack of SVR (nonresponse as early as 12 weeks into therapy and relapsers) with either interferon (IFN)/ribavirin or pegylated IFN/ribavirin was found in 84 patients. A control group (group 2) of 231 CHC patients was identified by using a 2-year database (January 2000-June 2001) of patients without evidence of greater than 33% steatosis or SH. RESULTS The overall SVR was 28% in group 1, compared with 44% for group 2 ( P = .001). For HCV genotype 1, the SVR was 23% vs 34% for group 2 ( P = .19). For HCV genotypes 2 and 3, the SVR was 42% vs 78% for groups 1 and 2 ( P = .008), respectively. CONCLUSIONS Overall SVR for patients with HCV and significant steatosis or SH is considerably lower than for HCV and steatosis less than 33% and no SH.


Brain Research | 2005

Effect of testosterone on functional recovery in a castrate male rat stroke model

Yi Pan; Haibo Zhang; Aninda B. Acharya; Ping Patrick; Dana Oliver; John E. Morley

Both increased and decreased testosterone levels have been reported to correlate with poor outcome after acute ischemic stroke. The present study focused on the role of testosterone during recovery from neurological deficits in a rat focal ischemia model. Castrate male rats were subjected to behavioral tests after 90 min of middle cerebral artery occlusion (MCAO). On day 7 post-MCAO, neurological deficit-matched rats were assigned to a treatment group implanted with subcutaneous testosterone pellets or a control group implanted with sham cholesterol pellets. After 4 weeks post-MCAO, the average infarct volume was not significantly different between the two groups. Rats in the testosterone group demonstrated significantly earlier improvement in neurological deficits and shortened latency of adhesive tape removal compared with the control group as analyzed by Wilcoxon signed ranks test. Walking on parallel bars improved in both groups with a trend towards early recovery observed in the testosterone group. Biased left body swings persisted during the test period in both groups post-MCAO. Serum testosterone was within physiological levels in the treatment group but was not detectable in the control group by radioimmunoassay. GAP-43 and synaptophysin expression did not differ between groups. Less GFAP expression and reactive astrocyte hypertrophy were found around the infarct area in testosterone-treated rats compared with control rats. In conclusion, testosterone replacement post-MCAO accelerated functional recovery in castrate rats, suggesting a potential therapeutic role for testosterone replacement in stroke recovery.


Clinical Nuclear Medicine | 2009

F-18 FDG PET/CT characterization of talc pleurodesis-induced pleural changes over time: a retrospective study.

Nghi Nguyen; Isaac Tran; Christopher N. Hueser; Dana Oliver; Hussein Farghaly; Medhat Osman

Purpose: The current study characterized pleural changes induced by talc pleurodesis (TP), based on serial positron emission tomography/computer-tomography (PET/CT) with F-18 fluorodeoxyglucose (FDG). Materials and Methods: A total of 8 cancer patients who had both TP and PET/CT and no evidence of active pleural involvement after TP were retrospectively evaluated. Maximum standard uptake values, maximum Hounsfield units (HU), and thickness were followed over time. Results: The 8 patients had 25 PET/CT scans performed in an average of 22 months after TP. An increased FDG uptake was associated with an increase in pleural thickness within 5 months after TP, and both parameters showed statistical significance as compared with findings before TP. After 5 months of TP, the standard uptake value appeared to persist or increase further, and the pleural thickening stabilized. The formation of calcification was a slow process and might lag behind the changes in FDG metabolism and pleural thickness. The HU did not change significantly once pleural calcification had been formed. Conclusions: Knowledge of aforementioned pleural changes may help differentiate TP induced pleural inflammation from pleural malignancy and to avoid false-positive interpretation of FDG PET/CT exams.


American Journal of Roentgenology | 2010

18F-FDG PET/CT of Patients With Cancer: Comparison of Whole-Body and Limited Whole-Body Technique

Medhat Osman; Bassem T. Chaar; Razi Muzaffar; Dana Oliver; Hans Joachim Reimers; Bruce Walz; Nghi Nguyen

OBJECTIVE Use of the routine field of view for whole-body (18)F-FDG PET/CT can lead to underestimation of the true extent of the disease because metastasis outside the typical base of skull to upper thigh field of view can be missed. The purpose of this study was to evaluate the incremental added value of true whole-body as opposed to this limited whole-body PET/CT of cancer patients. MATERIALS AND METHODS True whole-body FDG PET/CT, from the top of the skull to the bottom of the feet, was performed on 500 consecutively registered patients. A log was kept of cases of suspected malignancy outside the typical limited whole-body field of view. Suspected lesions in the brain, skull, and extremities were verified by correlation with surgical pathologic or clinical follow-up findings. RESULTS Fifty-nine of 500 patients had PET/CT findings suggestive of malignancy outside the limited whole-body field of view. Thirty-one of those patients had known or suspected malignancy outside the limited whole-body field of view at the time of the true whole-body study. Among the other 28 patients, follow-up data were not available for two, six had false-positive findings, and new cancerous involvement was confirmed in 20. Detection of malignancy outside the limited whole-body field of view resulted in a change in management in 65% and in staging in 55% of the 20 cases. CONCLUSION Our study showed that 20 of 500 (4.0%) of patients had previously unsuspected malignancy outside the typical limited whole-body field of view. Detection of such malignancy resulted in a change in management in 13 of 500 cases (2.6%). We propose that adopting a true whole-body field of view in the imaging of cancer patients may lead to more accurate staging and restaging than achieved with the routinely used limited whole-body field of view.


Transfusion | 2009

TRANSFUSION PRACTICE: Liver donor's age and recipient's serum creatinine predict blood component use during liver transplantation

Kian A. Modanlou; Dana Oliver; Brenda J. Grossman

BACKGROUND: Excessive use of blood components during liver transplantation should be avoided because it has been associated with poor outcomes and it may stress blood bank resources.


Transfusion | 2009

Liver donor's age and recipient's serum creatinine predict blood component use during liver transplantation.

Kian A. Modanlou; Dana Oliver; Brenda J. Grossman

BACKGROUND: Excessive use of blood components during liver transplantation should be avoided because it has been associated with poor outcomes and it may stress blood bank resources.


Journal of Clinical Apheresis | 2008

A retrospective review of the outcome of plasma exchange and aggressive medical therapy in antibody mediated rejection of renal allografts: A single center experience

Wisam Al-Badr; Dorina Kallogjeri; Kamel Madaraty; Dana Oliver; Bahar Bastani; Brenda J. Grossman

Antibody‐mediated rejection (AMR) has been recognized as a major cause of renal allograft loss. Protocols using plasma exchange (PE) to reverse rejection have mixed results. Methods: A retrospective chart review was performed to determine the clinical response to PE inpatients with AMR of renal allograft. A good response to treatment was defined as a decline in serum creatinine (SCr) to within 25% above the prerejection value or discontinuation of dialysis with a SCr <2 mg/dl within 3 months of discharge from the hospital and disappearance of donor‐specific alloantibodies (DSA). Results: Twenty‐two patients, treated with PE for biopsy proven AMR with or without acute‐cellular rejection (ACR), were included in the study. Sixty‐four percent of patients had concurrent AMR and ACR. Fifty‐two percent of all patients had a good response to antirejection therapy, whereas 63% of patients with only AMR and 46% of patients with both AMR and ACR had a good response. Good response to PE did not correlate with the number of plasma volumes exchanged (P = 0.09), but correlated with a shorter period from transplantation to the rejection episode (P = 0.002). Conclusion: Only a shorter interval between transplantation and the acute rejection episode correlated with a good response to PE. J. Clin. Apheresis, 2008.

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Nghi Nguyen

Saint Louis University

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Bruce Walz

Saint Louis University

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Isaac Tran

Saint Louis University

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Brenda J. Grossman

Washington University in St. Louis

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Elizabeth M. Brunt

Washington University in St. Louis

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