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110 citation(s) found for "Wade, R C".

A Multicenter, Retrospective Study of Patients with Pulmonary Arterial Hypertension Transitioned from Parenteral Prostacyclin Therapy to Inhaled Iloprost
Channick, Richard N. , Frantz, Robert P. , Palevsky, Harold I. , Tumuluri, Ramagopal, Sulica, Roxana, Lauto, Paula, Benton, Wade W. , Boisblanc, Bennett de, Channick, Richard N. , Kawut, Steven M. , Frantz, Robert P

Pulmonary Circulation | July 8, 2013 | Volume: 3 | Issue: 2 | Pages: 381-388

10.4103/2045-8932.114768 | PMID 24015339 Get It

Pulmonary arterial hypertension (PAH) is characterized by progressive increases in pulmonary vascular resistance, leading to right heart failure and death. Guidelines recommend customization of treatment, necessitating the development of effective strategies for transitioning patients among treatments. In this study, we characterized our experience with patient transitions from parenteral prostacyclin to inhaled iloprost. We retrospectively assessed records from 11 centers of 37 consecutive patients with PAH aged ≥ 18 years who were treated with intravenous (IV) or subcutaneous (SC) prostacyclin analogues and transitioned to inhaled iloprost. The transition period began on the first day of inhaled iloprost with the intent of discontinuing parenteral prostacyclin and ended on the first day on inhaled iloprost free of parenteral prostacyclin. Persistence was defined as the absence of (1) parenteral prostacyclin while remaining on inhaled iloprost during post‐transition Days 1–90 and (2) no reinitiation of parenteral prostacyclin during post‐transition Days 90–365. All patients were clinically stable before transitioning to inhaled iloprost. The mean age was 46.5 years, 70.3% were female, 51.4% had idiopathic PAH, and 43.0% were in New York Heart Association Functional Class III. Among patients with an overlapping transition, the mean transition period was 10.5 days. A transition dosing algorithm was used in 10 patients (27.0%). At one year, 78.4% of the patients remained persistent on inhaled iloprost and 81.1% were free of clinical worsening. In selected patients on background oral PAH therapy, transitioning from parenteral prostacyclin to inhaled iloprost appears safe and feasible and is associated with long‐term success. Further study is needed to define the optimal patient selection criteria and transition algorithm.
Online Problem-Solving Therapy for Executive Dysfunction After Child Traumatic Brain Injury
Kurowski, Brad G. , Wade, Shari L. , Kirkwood, Michael W. , Brown, Tanya M. , Stancin, Terry , Taylor, Hudson Gerry

Pediatrics | June 11, 2013 | Volume: 132 | Issue: 1 | Pages: e158-e166

10.1542/peds.2012-4040 | PMID 23753094 Get It

OBJECTIVE: Executive dysfunction after traumatic brain injury (TBI) in children is common and leads to significant problems in functioning across multiple settings. The objective of this study was to evaluate the efficacy of a web-based counselor-assisted problem solving (CAPS) intervention compared with an Internet resource comparison (IRC) for treatment of executive dysfunction within 12 months after complicated mild to severe TBI in adolescents. We hypothesized that CAPS would significantly improve parent ratings of executive dysfunction compared with an IRC. METHODS: Participants included 132 adolescents aged 12 to 17 years who sustained a complicated mild to severe TBI within 1 to 6 months before study enrollment. Study design was a multisite, assessor-blinded, randomized controlled trial. Study sites included 3 tertiary pediatric hospitals and 2 tertiary general medical centers. The main outcome measure was primary caregiver Behavioral Rating Inventory of Executive Function Global Executive Composite at baseline and 6-month follow-up. Generalized linear models that controlled for baseline scores were used to compare the CAPS and IRC scores. RESULTS: In older teens, the CAPS group showed significant improvement in executive function behaviors at 6-month follow-up compared with the IRC group (F = 6.74, P = .01, Cohen’s d = 0.63). CONCLUSIONS: Findings indicate that web-based CAPS improves primary caregiver-rated executive functioning within the first 12 months after TBI in older adolescents. Future research needs to define the optimal timing after injury for delivery of CAPS and characteristics of individuals and families who are most likely to benefit from CAPS.
Patient Body Mass Index Does Not Predict Six-Month Clinical Outcome of Depression Managed Under Collaborative Care
Angstman, Kurt B. , Wade, Todd W., DeJesus, Ramona S. , Rundell, James R., Altrichter, Paul M.

Journal of Primary Care & Community Health | July 18, 2012 | Volume: 4 | Issue: 2 | Pages: 119-123

10.1177/2150131912454012 | PMID 23799719 Get It

Obesity and depression are often comorbid conditions. There appears to be a bidirectional relationship between these. Obesity at baseline has been shown to increase the risk of onset of depression and depression at baseline increased the odds for developing obesity. Less is understood about the impact of obesity on depression treatment outcomes. The authors’ hypothesis was that obesity (body mass index [BMI] ≥30 kg/m 2 ) and morbid obesity (BMI ≥ 40 kg/m 2 ) would each have negative effects on depression remission rates after 6 months of enrollment into collaborative care management for depression. In a retrospective analysis of 1111 depressed patients with a PHQ-9 (Patient Health Questionnaire) score of 10 or greater, multivariate analysis for the odds ratio of achieving remission at 6 months demonstrated that the patient’s BMI at baseline was not an independent risk factor for depression outcome at 6 months. Collaborative care management for depression has been shown to be effective for improving depression outcomes, yet minimal prior research has focused on other clinical comorbidities that might affect outcomes. Although obesity was common in the study population, it was reassuring, based on this study that 6-month depression treatment outcomes do not appear to be significantly affected by the patient’s baseline BMI.
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia
Skibola, Christine F., Bernardo, Maria Chiara Di, Conde, Lucía , Broderick, Peter , McDonnell, Shannon K. , Goldin, Lynn R. , Croft, Naomi, Holroyd, Amy, Harris, Shelley , Riby, Jacques, Serie, Daniel, Call, Timothy G. , Bracci, Paige M. , Halperin, Eran , Lanasa, Mark C., Cunningham, Julie M. , Leis, José F., Morrison, Vicki A., Spector, Logan G. , Vachon, Celine M. , Strom, Sara S., Camp, Nicola J. , Weinberg, J. Brice , Matutes, Estella , Caporaso, Neil E., Wade, Rachel , Dyer, Martin J.S. , Dearden, Claire , Cerhan, James R. , Catovsky, Daniel , Houlston, Richard S. , Slager, Susan L. , Kay, Neil E. , Vachon, Celine M. , Shanafelt, Tait D. , Cerhan, James R , Houlston, Richard S , McDonnell, Shannon K

Blood | June 15, 2012 | Volume: 120 | Issue: 4 | Pages: 843-846

10.1182/blood-2012-03-413591 | PMID 22700719 Get It

Abstract We performed a meta-analysis of 3 genome-wide association studies to identify additional common variants influencing chronic lymphocytic leukemia (CLL) risk. The discovery phase was composed of genome-wide association study data from 1121 cases and 3745 controls. Replication analysis was performed in 861 cases and 2033 controls. We identified a novel CLL risk locus at 6p21.33 (rs210142; intronic to the BAK1 gene, BCL2 antagonist killer 1; P = 9.47 × 10−16). A strong relationship between risk genotype and reduced BAK1 expression was shown in lymphoblastoid cell lines. This finding provides additional support for polygenic inheritance to CLL and provides further insight into the biologic basis of disease development.
Transabdominal and Transcervical Chorionic Villus Sampling Models to Teach Maternal-Fetal Medicine Fellows
McWeeney, Dennis, Schwendemann, Wade, Nitsche, Joshua F. , Rose, Carl H., Davies, Norman, Watson, William J. , Brost, Brian

American Journal of Perinatology | April 11, 2012 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1055/s-0032-1310518 | PMID 22495896 Get It

Clinical Stroke Trials
Brott, Thomas, Kothari, Rashmi, Smith, Wade S. , Goldstein, Larry B.

Stroke | June 17, 2011 | Volume: 30 | Issue: 6 | Pages: 1165-1166

10.1161/01.str.30.6.1165 | PMID 10356093 Get It

Large-Scale Analysis of DNA Methylation In Chronic Lymphocytic Leukemia
Rahmatpanah, Farahnaz, Carstens, Stephanie, Hooshmand, Sam , Welsh, Elise C, Sjahputera, Ozy, Taylor, Kristen H. , Bennett, Lynda , Shi, Huidong , Arthur, Gerald L., Wooldridge, James E. , Caldwell, Charles W., Davis, J. Wade , Shanafelt, Tait D. , Kay, Neil E.

Epigenomics | October 6, 2009 | Volume: 1 | Issue: 1 | Pages: 39-61

10.2217/epi.09.10 | PMID 20495622 Get It

A Patient-Centered Approach to Weight Management Coaching
Rohrer, James E. , Bartel, Greg, Wade, Todd W., Yapuncich, Victor P., Bartel, Gregory A.

Obesity Management | February 13, 2008 | Volume: 4 | Issue: 1 | Pages: 27-30

10.1089/obe.2008.0119 Get It

Polypropylene Mesh Tape for Stress Urinary Incontinence: Complications of Urethral Erosion and Outlet Obstruction
SWEAT, SUSAN D., Itano, Nancy B., Bushman, Wade , Gruenenfelder, Jennifer, McGuire, Edward J., Lightner, Deborah J., Clemens, J. Quentin

Journal of Urology | January 17, 2006 | Volume: 168 | Issue: 1 | Pages: 144-146

10.1016/s0022-5347(05)64848-3 Get It