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1.
J Pharm Pract ; 33(6): 882-894, 2020 Dec.
Article in English | MEDLINE | ID: mdl-31401932

ABSTRACT

Although the mortality from cardiovascular disease has declined, it remains the leading cause of morbidity and mortality in the United States. Dyslipidemia is a modifiable risk factor that plays a significant role in the development of atherosclerotic cardiovascular disease. Treating dyslipidemia by lowering cholesterol, predominately low-density lipoprotein cholesterol, has been shown to reduce cardiovascular events. The first article that provided dyslipidemia bibliographies was published in 2006. Since this time, new therapies have become available and older therapies that were once thought to provide benefit have since been shown to lack positive outcomes and have therefore fallen out of favor for routine use. As the body of evidence continues to expand, clinicians are faced with reevaluating their treatment strategies to ensure optimal outcomes and appropriate use of lipid-lowering therapies. Therefore, this compilation was created to serve as a resource for clinicians. This publication provides an update of key articles in dyslipidemia management including various guidelines and practice-changing randomized controlled trials.


Subject(s)
Dyslipidemias , Cardiovascular Diseases , Cholesterol , Cholesterol, LDL , Dyslipidemias/diagnosis , Dyslipidemias/drug therapy , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Practice Guidelines as Topic , Risk Factors , United States
2.
Curr Pharm Teach Learn ; 10(10): 1354-1362, 2018 10.
Article in English | MEDLINE | ID: mdl-30527365

ABSTRACT

BACKGROUND AND PURPOSE: To develop, integrate, and evaluate an innovative women's health and sexual health history interview activity in an elective course for pharmacy students. EDUCATIONAL ACTIVITY AND SETTING: Students reflected on personal experiences where a healthcare provider addressed sensitive health-related topics. Students used this reflection and other resources to prepare for and conduct an interview with an adult woman. Students wrote a reflection paper describing their interview experience. Female participants provided feedback on student performance via an anonymous, electronic survey. Analysis of student reflection papers explored the impact of students' personal health care experiences on their approach with the participant and achievement of activity learning objectives. FINDINGS: In 2015 and 2016, 38 of 51 (74.5%) participants interviewed completed the survey. In response to open-ended questions about student performance, 47% of participants stated the student helped them feel comfortable, 44% said the student was professional, and 13% stated the student seemed nervous or uncomfortable. All participants agreed or strongly agreed students used appropriate communication to obtain health information and asked sensitive questions professionally. Among 51 student reflections, all students were able to describe how their experience influenced them, and most described its application to future practice. Further reflection paper analysis revealed students tried to emulate behaviors, attitudes, and skills seen in personal encounters with clinicians. Examples of behaviors included empathy and patient-centered communication. DISCUSSION AND SUMMARY: Students achieved the activity learning objectives. Authors felt this unique activity may help students prepare for challenging patient interviews encountered in future practice.


Subject(s)
Interviews as Topic/methods , Patients , Students, Pharmacy/psychology , Women's Health/trends , Adult , Attitude of Health Personnel , Chicago , Curriculum/trends , Education, Pharmacy/methods , Education, Pharmacy/trends , Female , Humans , Interviews as Topic/standards , Students, Pharmacy/statistics & numerical data , Surveys and Questionnaires
3.
Am J Pharm Educ ; 82(10): 6748, 2018 12.
Article in English | MEDLINE | ID: mdl-30643312

ABSTRACT

Objective. To assess pharmacy students' ability to incorporate laptop computers into simulated patient encounters (SPEs) in the second professional year (P2) and assess their ability to retain these skills into the next professional year. Students' awareness and confidence in using computers was also assessed. Methods. P2 students were surveyed about their awareness of and confidence in incorporating a computer into an SPE. Their performance using a computer in an SPE was evaluated using a blinded rubric. Next, they received formal education on this skill. Students then completed the same questionnaire and were evaluated on their ability to use a computer in another SPE. In the third year, they were evaluated using the same rubric on four activities and completed the same questionnaire at the end of each semester. Results. There were 166 students in the two cohorts. Of those, 158 students were evaluated using the rubric and 166 students completed the four questionnaires. Student performance improved from the pre-instruction activity evaluation (43% earned acceptable) to post-instruction (66% earned acceptable). This performance improvement was retained for four activities in the third year (80%, 85%, 79%, and 92% earning acceptable ratings, respectively). Students' questionnaires reported an improved confidence incorporating a computer into the patient encounter after receiving formal instruction. This perception of improved confidence was maintained throughout the third year. Conclusion. Student performance improved throughout three semesters of computer use during SPEs. Students felt more confident and knowledgeable about integrating a computer into an SPE after instruction.


Subject(s)
Education, Pharmacy/methods , Educational Measurement/methods , Communication , Computers , Humans , Patient Simulation , Students, Pharmacy , Surveys and Questionnaires , Task Performance and Analysis
4.
Consult Pharm ; 32(3): 169-174, 2017 Mar 01.
Article in English | MEDLINE | ID: mdl-28270272

ABSTRACT

OBJECTIVE: The purpose of this study was to assess the effects of a clinical decision support (CDS) tool aimed at decreasing the prescribing of glyburide, a potentially inappropriate medication (PIM), in patients 65 years of age and older. DESIGN: Quasi-experimental, pre-post intervention study. SETTING: Ambulatory care clinics of an academic medical center. INTERVENTION: The tool appeared to providers when entering new prescriptions or refills for glyburide. Glimepiride, which is a more appropriate sulfonylurea, was suggested as an alternative at order entry. MAIN OUTCOME MEASURE(S): The primary outcome was the prescribing of glyburide orders, measured as a percentage of the total oral diabetic medications ordered in patients 65 years of age and older, during the study period. The secondary outcome measured was the response to the CDS tool (accept versus reject). RESULTS: The CDS tool alerted providers 101 times during the 90-day postimplementation period. When the tool appeared, patients were transitioned off of glyburide 17.8% of the time. Subanalysis found that when physicians viewed the alert, patients were transitioned off of glyburide 46.2% of the time. As a percentage of the total number of oral diabetic medications, glyburide prescribing was significantly decreased from pre- to postimplementation study period (3.3% vs. 1.2%; P < 0.001). CONCLUSIONS: A CDS tool can be used in the ambulatory care setting to influence prescribing and provide a safer alternative medication. Additional information is needed to test the use of a CDS tool in conjunction with education to ensure providers are comfortable with and understand implications of a CDS tool.


Subject(s)
Ambulatory Care , Decision Support Systems, Clinical/organization & administration , Medication Errors/prevention & control , Patient Safety , Prescription Drug Misuse/prevention & control , Aged , Diabetes Mellitus/drug therapy , Drug Interactions , Glyburide/administration & dosage , Humans , Hypoglycemic Agents/administration & dosage , Practice Guidelines as Topic , Practice Patterns, Physicians' , Sulfonylurea Compounds/administration & dosage
5.
J Pharm Pract ; 27(3): 234-42, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24742931

ABSTRACT

Acquired thrombophilia is associated with an increased risk of venous thromboembolism (VTE). Antiphospholipid syndrome (APS) is the most prevalent acquired thrombophilia and is associated with both venous and arterial thromboses. Human immunodeficiency virus (HIV) is another form of acquired thrombophilia. Risk factors associated with VTE in this population include those related to the disease itself, host factors, and the pharmacotherapy for HIV. A significant proportion of VTE events occur in patients with malignancies. There is an increase in mortality associated with patients having cancer who experience VTE when compared to patients having cancer without VTE. Combination oral contraceptive (COC) use infers risk of thromboembolic events. The risk is dependent upon the presence of an underlying inherited thrombophilia, the estrogen dose, and generation of progestin. Patients at highest risk of VTE include those receiving high-dose estrogen and fourth-generation, progesterone-containing contraceptives. With the exception of APS, thrombophilia status does not alter the acute treatment of an initial VTE in nonpregnant patients.


Subject(s)
Thrombophilia/complications , Thrombosis/etiology , Venous Thromboembolism/etiology , Antiphospholipid Syndrome/complications , HIV Infections/complications , Humans , Neoplasms/complications , Risk Factors , Thrombophilia/etiology , Thrombophilia/therapy , Thrombosis/prevention & control , Venous Thromboembolism/prevention & control
6.
J Pharm Pract ; 27(3): 243-52, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24742932

ABSTRACT

Pregnancy is associated with an increased risk of venous thromboembolism (VTE), with a reported incidence ranging from 0.49 to 2 events per 1000 deliveries. Risk factors include advanced maternal age, obesity, smoking, and cesarian section. Women with a history of previous VTE are at a 4-fold higher risk of recurrent thromboembolic events during subsequent pregnancies. Additionally, the presence of concomitant thrombophilia, particularly factor V Leiden (homozygosity), prothrombin gene mutation (homozygosity), or antiphospholipid syndrome (APS), increases the risk of pregnancy-related VTE. Low-molecular-weight heparin (LMWH) and unfractionated heparin (UFH) are the drugs of choice for anticoagulation during pregnancy. LMWH is preferred due to ease of use and lower rates of adverse events. Women with high thromboembolic risk particularly those with a family history of VTE should receive antepartum thromboprophylaxis. Women with low thromboembolic risk or previous VTE caused by a transient risk factor (ie, provoked), who have no family history of VTE, may undergo antepartum surveillance. Postpartum anticoagulation can be considered in women with both high and low thromboembolic risk.


Subject(s)
Anticoagulants/therapeutic use , Pregnancy Complications, Hematologic/prevention & control , Venous Thromboembolism/etiology , Anticoagulants/adverse effects , Cesarean Section/adverse effects , Female , Heparin/adverse effects , Heparin/therapeutic use , Heparin, Low-Molecular-Weight/adverse effects , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Maternal Age , Obesity/complications , Pregnancy , Pregnancy Complications, Hematologic/drug therapy , Risk Factors , Smoking/adverse effects , Venous Thromboembolism/drug therapy , Venous Thromboembolism/prevention & control
7.
J Pharm Pract ; 27(3): 227-33, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24739277

ABSTRACT

Thrombophilia alters normal hemostasis, shifting the balance in favor of thrombus formation. Inherited conditions include factor V Leiden (FVL), prothrombin G20210A mutation, deficiencies in natural anticoagulants (antithrombin [AT], protein C, and protein S), hyperhomocysteinemia, and elevations in clotting factors (factors VIII and XI). Although FVL and prothrombin mutation are common disorders, deficiencies in the natural anticoagulants are rare. The risk of initial thrombosis conferred by inherited thrombophilia varies with the highest risk in those homozygous for either FVL or prothrombin mutation, or with AT deficiency. In the nonpregnant patient, the presence of a thrombophilia does not affect treatment of an acute event. Although vitamin B supplementation has been shown to decrease the levels of homocysteine, the treatment has failed to show a benefit in thrombus prevention and is therefore not recommended.


Subject(s)
Homocysteine/metabolism , Thrombophilia/genetics , Thrombosis/etiology , Hemostasis/physiology , Humans , Mutation , Thrombophilia/complications , Thrombosis/prevention & control , Venous Thromboembolism/etiology , Venous Thromboembolism/prevention & control , Vitamin B Complex/administration & dosage
8.
J Pharm Pract ; 27(3): 253-9, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24739279

ABSTRACT

Although controversial, screening for thrombophilia has become common. Testing for antiphospholipid antibodies is indicated in order to guide treatment decisions if there is clinical suspicion for antiphospholipid syndrome. The utility of identifying other thrombophilias in symptomatic venous thromboembolism (VTE) is questionable, as the risk of recurrence does not appear to be increased by an appreciable degree with the most common disorders (heterozygosity for factor V Leiden or prothrombin mutation). Although recurrence appears to be increased in those with homozygous or multiple abnormalities and potentially deficiencies in natural anticoagulants, screening to detect these conditions is difficult to justify based on their rarity. The American College of Chest Physicians' current guidelines note the increased risk of recurrence with idiopathic, proximal events regardless of thrombophilia status. They suggest duration of anticoagulation therapy be based on location and provoking factors rather than whether or not the individual has a thrombophilia. Because routine prophylaxis in asymptomatic individuals with thrombophilia is not recommended, screening of asymptomatic family members is difficult to justify. Screening prior to prescribing combination oral contraceptives is not cost effective, may result in unwanted pregnancies, and may have little effect on the overall rate of VTE.


Subject(s)
Mass Screening/methods , Thrombophilia/diagnosis , Antibodies, Antiphospholipid/analysis , Anticoagulants/administration & dosage , Antiphospholipid Syndrome/complications , Antiphospholipid Syndrome/diagnosis , Humans , Practice Guidelines as Topic , Recurrence , Thrombophilia/complications , Thrombophilia/drug therapy , Venous Thromboembolism/etiology , Venous Thromboembolism/prevention & control
9.
J Am Pharm Assoc (2003) ; 52(3): 358-62, 2012.
Article in English | MEDLINE | ID: mdl-22618976

ABSTRACT

OBJECTIVES: To determine whether a difference exists in hospital readmission rates at 60 days postdischarge between patients who saw (intervention group) or did not see (control group) a pharmacist within 60 days of discharge and to describe the number and type of pharmacist interventions. DESIGN: Retrospective electronic record review. SETTING: Austin, TX, from January 2006 to January 2010. PATIENTS: 131 adult patients aged 18 to 65 years who were on at least three prescription medications. INTERVENTION: Pharmacist visit within 60 days post-hospital discharge. MAIN OUTCOME MEASURE: Hospital readmission rates at 60 days postdischarge. RESULTS: The intervention and control groups did not differ regarding age or gender, but the control group had a higher percentage of whites, fewer medications, and fewer diseases. Chi-square analyses revealed that of 65 patients in the control group, 28 (43.1%) were readmitted to the hospital within 60 days of discharge compared with 12 of 66 (18.2%) intervention group patients (P = 0.0020). Pharmacists provided approximately two interventions per patient. The most frequently provided pharmacist interventions were medication counseling (88.1%) and drug dosage adjustment (52.2%). CONCLUSION: Patients on multiple prescription medications and with chronic diseases may benefit from a pharmacist visit within 60 days of hospital discharge. However, future studies are needed to further determine the effectiveness of pharmacists' interventions post-hospital discharge.


Subject(s)
Patient Discharge/statistics & numerical data , Patient Readmission/statistics & numerical data , Pharmacists , Adolescent , Adult , Aged , Counseling , Drug Prescriptions , Electronic Health Records , Female , Humans , Male , Medication Therapy Management , Middle Aged , Pharmaceutical Preparations/administration & dosage , Retrospective Studies , Young Adult
10.
Postgrad Med ; 124(1): 74-82, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22314117

ABSTRACT

Patients are diagnosed as having resistant hypertension when they have blood pressure readings that remain above goal despite the concomitant use of 3 optimally dosed antihypertensive agents from different classes, with 1 of the agents being a diuretic. Prior to diagnosing a patient as having resistant hypertension, it is important to document adherence and exclude white-coat hypertension, inaccurate measurement of blood pressure, and secondary causes of hypertension (eg, aldosterone excess). After determining resistance, optimization of the medication regimen is essential. Combination strategies, which might include dual renin-angiotensin-aldosterone blockade with spironolactone as 1 agent, have been proven successful. This article focuses on the safety and efficacy of spironolactone when added to an optimized 3-drug regimen. Additionally, the use of spironolactone in chronic kidney disease and obstructive sleep apnea complicated by resistant hypertension is discussed. These 2 clinical entities are frequently accompanied by resistant hypertension and are indications for the use of spironolactone as well.


Subject(s)
Antihypertensive Agents/therapeutic use , Hypertension/drug therapy , Mineralocorticoid Receptor Antagonists/therapeutic use , Spironolactone/therapeutic use , Diuretics/therapeutic use , Drug Resistance , Drug Therapy, Combination , Humans , Hypertension/diagnosis , Hypertension/etiology , Hypertension/metabolism , Renal Insufficiency, Chronic/complications , Renal Insufficiency, Chronic/drug therapy , Renin-Angiotensin System/physiology , Sleep Apnea, Obstructive/complications , Sleep Apnea, Obstructive/drug therapy
11.
Article in English | MEDLINE | ID: mdl-22879787

ABSTRACT

The prevalence of diabetes mellitus (DM) in the elderly population currently represents almost one-half of the overall diabetic population. Treatment of DM often requires a multidrug regimen that includes insulin therapy; however, due to concomitant comorbidities such as dementia, vision loss, neuropathies, poor mobility, and poor manual dexterity, elderly patients may be at increase risk for hypoglycemia and other dosing errors that are associated with insulin administration. Insulin pen devices have been shown to provide more reliable, accurate, and simplified dosing, and therefore may be a safer, easier, and more acceptable method of insulin delivery in the elderly population. This review will describe the various insulin pen devices available today, as well as discuss the potential advantages of these devices in the elderly population.

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