Professor, Internal Medicine, Virginia Commonwealth University, Medical College of Virginia School of Medicine
Internal Medicine
Dr. Wally R. Smith, MD
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Wally Smith is an expert in the field of Internal Medicine. He attended University of Alabama Medical Center. University of Alabama Medical Center has a rank of 37 in research and a 17 in primary care Wally Smith is a published doctor and has 44 publications published. The lastest was: 'Randomized phase 2 study of GMI-1070 in SCD: reduction in time to resolution of vaso-occlusive events and decreased opioid use.' He accepts Medicare.
Publications
- Randomized phase 2 study of GMI-1070 in SCD: reduction in time to resolution of vaso-occlusive events and decreased opioid use.
- How Patients' Self-Disclosure about Sickle Cell Pain Episodes to Significant Others Relates to Living with Sickle Cell Disease.
- Fatigue in Adolescents and Young Adults With Sickle Cell Disease: Biological and Behavioral Correlates and Health-Related Quality of Life.
- Expanding concepts of opioid-taking behavior in sickle cell disease: A multi-phase, mixed methods study.
- Biopsychosocial-spiritual determinants of opioid-taking behavior in sickle cell disease: A multi-phase, mixed methods study.
- Expanding the Framework of Assessing Adherence and Medication-Taking Behavior.
- Disparities in breast and cervical cancer screening in women with mental illness: a systematic literature review.
- Hepatopulmonary syndrome associated with iron overload in sickle cell anaemia.
- Resilience training and physician well-being.
- Frequently asked questions by hospitalists managing pain in adults with sickle cell disease.
- Emerging biobehavioral factors of fatigue in sickle cell disease.
- Faculty values.
- Sickle-cell pain: advances in epidemiology and etiology.
- Evidence-based mini-review: Are systemic corticosteroids an effective treatment for acute pain in sickle cell disease?
- Health decision-making preferences among African American men recruited from urban barbershops.
- Comparisons of high versus low emergency department utilizers in sickle cell disease.
- Recruiting African-American barbershops for prostate cancer education.
- Depression and anxiety in adults with sickle cell disease: the PiSCES project.
- Daily assessment of pain in adults with sickle cell disease.
- A controlled trial of universal gloving versus contact precautions for preventing the transmission of multidrug-resistant organisms.
- Recommendations for teaching about racial and ethnic disparities in health and health care.
- Alcohol abuse in sickle cell disease: the Pisces Project.
- Patient satisfaction in specialized versus nonspecialized adult sickle cell care centers: the PiSCES study.
- Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES Project.
- Methadone-related Torsades de Pointes in a sickle cell patient treated for chronic pain.
- Use of an implantable drug delivery system for refractory chronic sickle cell pain.
- Understanding pain and improving management of sickle cell disease: the PiSCES study.
- Temperature changes, temperature extremes, and their relationship to emergency department visits and hospitalizations for sickle cell crisis.
- Special care for persons with Alzheimer's disease and related dementias in Virginia adult care residences.
- Timeliness of immunizations of children in a Medicaid primary care case management managed care program.
- Prognostic judgments and triage decisions for patients with acute congestive heart failure.
- Health related quality of life in sickle cell patients: the PiSCES project.
- Efficacy and safety of the Gardos channel blocker, senicapoc (ICA-17043), in patients with sickle cell anemia.
- Pain site frequency and location in sickle cell disease: the PiSCES project.
- The role of catastrophizing in sickle cell disease--the PiSCES project.
- Climatic and geographic temporal patterns of pain in the Multicenter Study of Hydroxyurea.
- Hydroxyurea and acute painful crises in sickle cell anemia: effects on hospital length of stay and opioid utilization during hospitalization, outpatient acute care con...
- Utilization of analgesics in the multicenter study of hydroxyurea in sickle cell anemia: effect of sex, age, and geographical location.
- Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III r...
- Somatic symptom burden in adults with sickle cell disease predicts pain, depression, anxiety, health care utilization, and quality of life: the PiSCES project.
- The association between hydroxyurea treatment and pain intensity, analgesic use, and utilization in ambulatory sickle cell anemia patients.
- Pain in sickle cell disease: the future of acute treatment.
- Opioid patient controlled analgesia use during the initial experience with the IMPROVE PCA trial: a phase III analgesic trial for hospitalized sickle cell patients wit...
Schools
University Of Birmingham
University Of Al Hospital
Doctors Specialties
- Internal Medicine
Accepted Insurances
Education
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University of Alabama Medical Center -
University of Alabama School of Medicine
Drug Facts
| NPI NUMBER | 1487743548 | |
| NPPES Provider LastName | SMITH | |
| NPPES Provider FirstName | WALLY | |
| NPPES Provider ZIPCode | 232980510 | |
| NPPES Provider State | VA | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 1290.0 | |
| Distinct Opioid Count | 9.0 | |
| Opioid Claim Count | 703.0 | |
| Percent Opioid Claims | 54.5 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1487743548 |
| Last Name Of The Provider | SMITH |
| First Name Of The Provider | WALLY |
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