Ila M. Harris
University of Minnesota
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Featured researches published by Ila M. Harris.
Pharmacotherapy | 2000
Lucinda G. Miller; Anne L. Hume; Ila M. Harris; Eric Jackson; Tina J. Kanmaz; Jacintha S. Cauffield; Thomas W. F. Chin; Maureen Knell
: Individuals increasingly are taking a more active role in their health care, and herbal products have emerged as a common choice among self-care therapies. Pharmacists are active participants in the care of patients who are taking herbal products. Currently, most pharmacists are not educated adequately about herbal products and other types of alternative medicine. Furthermore, good information about many of these products is not available. These combined factors present a challenge for pharmacists as they seek to provide optimal care and counseling to patients who use herbs or supplements. We recommend the following actions to place pharmacists in better positions as effective agents protecting public safety: Regulations should be implemented at a federal level to require basic levels of standardization and quality control in the manufacture of herbal products. Indexing terms in medical bibliographic systems should be expanded to target herbal products. Funding should be increased for scientific research evaluating herbal products. Pharmacy schools should include a competency statement in their curricula regarding herbal medicines. Continuing education in herbal products should be available and encouraged for all pharmacists. Pharmacists should approach the use of all therapeutic interventions with scientific rigor, whether they are traditional or complementary in nature. Patients will benefit as more information is known and widely disseminated. By actively embracing the responsibility for counseling individuals on the appropriate use of herbal products, pharmacists will become a recognized source of expert information in this rapidly growing area, yielding important improvements in the quality of care.
Pharmacotherapy | 2000
Ila M. Harris
Dietary supplements are commonly used, and many are effective or hold promise for treating various conditions. However, they do not require Food and Drug Administration (FDA) approval. Impurities and adulterants have been found in the products, mostly due to the lack of requirements for good manufacturing practices. In addition, as no standardization is required, the active ingredient may be absent or highly variable among manufacturers. The FDA published its 10‐year plan for dietary supplements that addresses safety, labeling, boundaries, enforcement, research, and outreach. This endeavor, if put into place, will be instrumental in providing consumers with more confidence in the safety, composition, and labeling of dietary supplements.
Journal of The American Pharmacists Association | 2009
Ila M. Harris; Sarah M. Westberg; Michael J. Frakes; James S. Van Vooren
OBJECTIVE To evaluate the effects of pharmacist-conducted medication therapy review (MTR) and intervention on the quality of care of patients in a family medicine clinic. DESIGN Prospective, observational, cohort study. SETTING Family medicine clinic in Minnesota during 2000-2001. PATIENTS Patients were enrolled in a statewide nonprofit managed care organization; selected patients were seen by a clinical pharmacist. INTERVENTION Following MTR, medication-related problems (MRPs) were identified and resolved. MAIN OUTCOME MEASURES MRPs identified and resolved, improvement in clinical status, achievement of therapeutic goals, important medication use, and reduction in number of medications. RESULTS 92 patients were included in the study, with a total of 203 patient encounters. MRPs were identified in 90% of patients, with a total of 250 identified. Overall status of medical conditions improved in 45% of patients, 46% stayed the same, and 9% declined (P < 0.001). Significant improvement in status was found for hypertension (P = 0.007), dyslipidemia (P = 0.002), and asthma (P = 0.011). Significant improvement was seen for aspirin use for myocardial infarction prevention (50% vs. 93%, P = 0.031) and inhaled steroids for asthma (36% vs. 64%, P = 0.031). The number of medications was reduced from an average of 3.92 to 3.04 (P < 0.001) per patient. CONCLUSION MTR and intervention by a pharmacist positively affected quality of care in this family medicine clinic.
Headache | 2017
Taeho Greg Rhee; Ila M. Harris
We examined whether the prevalence of complementary and alternative medicine (CAM) use varies by gender, and assessed the interaction of gender and CAM use on moderate mental distress (MMD) in U.S. adults with migraines/severe headaches.
American Journal of Public Health | 2017
Ann M. Philbrick; Cherilyn M. Wicks; Ila M. Harris; Grant M. Shaft; James S. Van Vooren
An editorial is presented which addresses various aspects of the provision of health care services to refugees in America in the wake of the 2016 U.S. presidential election, and it mentions the impacts of language barriers, cultural and religious beliefs, and access to medical insurance problems on a refugees ability to obtain medical care. Refugee resettlement in the U.S. is addressed, along with Medicaid health insurance benefits and the medical needs of Somali refugees.
Journal of Diabetes | 2018
Taeho Greg Rhee; Sarah M. Westberg; Ila M. Harris
Although complementary and alternative medicine (CAM) is increasingly used, little is known about the reasons for CAM use (treatment, wellness, or both), or the self‐reported perceived benefits among US adults with diabetes. In this study we estimated prevalence rates of overall and specific types of CAM, as well as the perceived benefits of CAM, by reason for use among US diabetic adults.
The American Journal of Pharmaceutical Education | 2016
Jody L. Lounsbery; Chrystian R. Pereira; Ila M. Harris; Jean Y. Moon; Sarah M. Westberg; Claire Kolar
Objective. To determine if the amount of exposure to patient encounters and clinical skills correlates to student clinical competency on ambulatory care advanced pharmacy practice experiences (APPEs). Design. Students in ambulatory care APPEs tracked the number of patients encountered by medical condition and the number of patient care skills performed. At the end of the APPE, preceptors evaluated students’ competency for each medical condition and skill, referencing the Dreyfus model for skill acquisition. Assessment. Data was collected from September 2012 through August 2014. Forty-six responses from a student tracking tool were matched to preceptor ratings. Students rated as competent saw more patients and performed more skills overall. Preceptors noted minimal impact on workload. Conclusions. Increased exposure to patient encounters and skills performed had a positive association with higher Dreyfus stage, which may represent a starting point in the conversation for more thoughtful design of ambulatory care APPEs.
Diabetes Care | 2018
Taeho Greg Rhee; Sarah M. Westberg; Ila M. Harris
Older adults with diabetes are at high risk for having multiple chronic conditions and diabetes complications and often take multiple medications concomitantly. Studies have shown that many Americans are using complementary and alternative medicine (CAM) to either improve or manage their health (1,2). Individuals have diverse purposes for using CAM, from treating specific conditions, such as back and neck pain (e.g., acupuncture and chiropractic), to improving general health and wellness (e.g., meditation and tai chi). Since relatively little is known about the prevalence and patterns of CAM use in older adults with diabetes, we investigated this topic to guide integrated, patient-centered health care use for this population. We used data from the 2012 National Health Interview Survey (NHIS), which is an annual cross-sectional in-person interview survey demonstrating health care trends among noninstitutionalized civilians in the U.S. (3). The NHIS collects comprehensive CAM-related information every 5 years. The sample included adults aged 65 or older who reported having …
Journal of The American Pharmacists Association | 2015
Ann M. Philbrick; Ila M. Harris; Jon C. Schommer; Christopher J. Fallert
OBJECTIVE To describe the number of medication discrepancies associated with subsequent medication reconciliations by a clinical pharmacist in an ambulatory family medicine clinic and the proportion of subsequent medication reconciliation visits that were associated with hospital discharge, long-term anticoagulation management, or both. METHODS Data on medication reconciliations were collected over a 2-year time period in an ambulatory family medicine clinic for patients taking 10 or more medications. RESULTS Medication reconciliation was performed 752 times for 500 patients. A total of 5,046 discrepancies were identified, with more than one-half deemed clinically important. A mean (± SD) of 6.7 ± 4.6 discrepancies per visit (3.5 ± 3.2 clinically important) were identified. The findings showed that the distribution of total discrepancies identified by pharmacist-performed medication reconciliation was significantly different over the course of subsequent medication reconciliations. However, the distribution of clinically important discrepancies was not significantly different; important discrepancies were as likely to be found in later reconciliations as in earlier ones. As subsequent medication reconciliation visits were performed, an increasing proportion consisted of post-hospital discharge visits, long-term anticoagulation managed by a clinical pharmacist, or both. CONCLUSION Patients with a recent hospital discharge, on long-term anticoagulation management, or both, were more likely to have multiple sessions with a clinical pharmacist for medication reconciliation. These findings can help identify patients for whom medication reconciliation is warranted.
American Journal of Health-system Pharmacy | 2014
Ila M. Harris; Ann M. Philbrick; Christopher J. Fallert; Ahmed M. Soliman
Adverse drug events (ADEs) occur in approximately 27% of outpatients, with approximately 1.5 million preventable ADEs occurring each year in the United States, mostly in the outpatient setting.[1][1],[2][2] The Food and Drug Administration (FDA) responds to new clinically significant ADEs and risks