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1.
Int J Artif Organs ; 43(7): 494-499, 2020 Jul.
Article in English | MEDLINE | ID: mdl-31964206

ABSTRACT

Driveline infection is the most common infectious complication in patients with left ventricular assist devices. Minimum inhibitory concentration changes are not well described in relapsed driveline infections. This retrospective descriptive epidemiology study of patients with left ventricular assist device implantation between January 1, 2013, and August 1, 2017, who developed driveline infection with positive cultures aimed to describe minimum inhibitory concentration changes. Of the 330 patients underwent left ventricular assist device implantation, 30 (9%) met criteria for driveline infection. Median duration of follow-up was 26 months (interquartile range 16, 39) and time to first driveline infection was 171 days (interquartile range 83, 403). There were 74 driveline infections: 40 new and 34 relapsed. Staphylococcus aureus was most common in new and relapsed driveline infection. Thirteen patients comprised the 34 relapsed infections, 9 of which experienced a minimum inhibitory concentration change. Median time to first minimum inhibitory concentration change was 56 days (interquartile range 36-88), and type of minimum inhibitory concentration change was an increase in five cases, decrease in two cases, and both increase and decrease in two cases. Minimum inhibitory concentration changes did not result in resistance in S. aureus but did in Pseudomonas aeruginosa and Mycobacterium fortuitum relapsed driveline infection. Time to first relapse from initial infection was longer in those who received suppressive therapy, 60 days versus 83 days, p = 0.047. Relapsed driveline infections were most common with S. aureus. Minimum inhibitory concentration changes were quite variable and may not be the major contributor to relapsed infection in gram-positive driveline infection.


Subject(s)
Heart Failure/therapy , Heart-Assist Devices/adverse effects , Mycobacterium Infections, Nontuberculous/epidemiology , Prosthesis-Related Infections/microbiology , Pseudomonas Infections/epidemiology , Staphylococcal Infections/epidemiology , Adult , Anti-Infective Agents/therapeutic use , Female , Heart Failure/microbiology , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Mycobacterium Infections, Nontuberculous/diagnosis , Mycobacterium Infections, Nontuberculous/drug therapy , Mycobacterium fortuitum , Prosthesis-Related Infections/drug therapy , Prosthesis-Related Infections/epidemiology , Pseudomonas Infections/diagnosis , Pseudomonas Infections/drug therapy , Pseudomonas aeruginosa , Recurrence , Retrospective Studies , Staphylococcal Infections/diagnosis , Staphylococcal Infections/drug therapy , Staphylococcus aureus , Time Factors
2.
ASAIO J ; 65(5): 530-532, 2019 07.
Article in English | MEDLINE | ID: mdl-30299299

ABSTRACT

We compared maximal plasma concentrations (Cmax) of sildenafil and metabolite n-desmethyl sildenafil in 12 inpatients with left ventricular assist devices (LVADs) on sildenafil (60 mg/day) to the reference range. Sildenafil Cmax (156.8 ± 124.5 ng/ml) was elevated in 66% of patients, with a two to fivefold increase over the upper limit of the reference range in 25% of patients. Metabolite Cmax (133.3 ± 102.0 ng/ml) was elevated in 75% of patients, with a three to sevenfold increase over the upper limit of the reference range in 40% of patients. Patients with heart failure and LVADs are at increased risk of concentrated-related sildenafil adverse events.


Subject(s)
Heart-Assist Devices , Phosphodiesterase 5 Inhibitors/blood , Phosphodiesterase 5 Inhibitors/pharmacokinetics , Sildenafil Citrate/blood , Sildenafil Citrate/pharmacokinetics , Humans , Male , Middle Aged
3.
Pharmacotherapy ; 37(8): 944-955, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28543813

ABSTRACT

Right ventricular failure (RVF) after cardiac transplant (CTX) or implantation of a continuous-flow left ventricular assist device (CF-LVAD) is associated with significant postoperative morbidity and mortality. A variety of modalities have been used to treat postoperative RVF, including management of volume status, intravenous inotropes and vasodilators, and right-sided mechanical support. Inhaled vasodilator agents are a unique treatment option aimed at minimizing systemic absorption by delivering therapy directly to the pulmonary vasculature. Current LVAD and CTX guidelines endorse inhaled vasodilators for managing postoperative RVF; however, no guidance is offered regarding agent selection, dosing, or administration. A review of the current literature confirms that inhaled pulmonary vasodilator agents have been shown to decrease pulmonary artery pressure when used in the perioperative period of CF-LVAD implant or CTX. However, the literature regarding the potential impact on clinical outcomes (e.g., survival or risk of developing RVF) is lacking with these medications. Based on our assessment of the literature, we suggest that when RVF occurs in the setting of a normal pulmonary vascular resistance (PVR), traditional inotropic therapy (e.g., dobutamine) should be used. Conversely, if the PVR is elevated (> 250 dynes/sec/cm5 or 3 Wood units), or the patient has other evidence of a high right ventricular afterload (i.e., a transpulmonary gradient > 12 mm Hg), then an inhaled pulmonary vasodilator would be the preferred initial pharmacologic agent. Drug selection depends largely on the institution's capacity to safely prepare and administer the medication, along with formulary considerations, such as the high costs associated with inhaled iloprost and inhaled nitric oxide.


Subject(s)
Heart Transplantation , Heart-Assist Devices , Vasodilator Agents/administration & dosage , Ventricular Dysfunction, Right/drug therapy , Administration, Inhalation , Humans , Iloprost/administration & dosage , Milrinone/administration & dosage , Nitric Oxide/administration & dosage , Postoperative Period
4.
Am J Health Syst Pharm ; 74(1): e72-e75, 2017 Jan 01.
Article in English | MEDLINE | ID: mdl-28007724

ABSTRACT

PURPOSE: The influence of targeted strategies implemented to increase member engagement on a social media page of a professional pharmacy organization was studied. METHODS: The Ohio Society of Health-System Pharmacists (OSHP) implemented posting strategies to increase member engagement with its social media page in late 2013. Data were collected retrospectively for a nine-month period in 2013 (preimplementation) and a matching nine-month period in 2014 (postimplementation). The primary endpoint was reach (as provided by the social media website). Data regarding reach were reported to OSHP page administrators on a weekly basis. Posts during the study period were characterized by the day of week, time of day, type of post, and corresponding reach. Continuous variables were represented using means and standard deviations or medians and interquartile ranges (IQRs); categorical data were represented by percentages. RESULTS: The total reach of posts during the nine-month study period increased postimplementation, from 10,826 to 32,338. Further, the median reach per post on the OSHP Facebook page was higher postimplementation (214; IQR, 107-380) versus preimplementation (152; IQR, 89-224; p = 0.035). Evening posts had significantly greater reach compared with nonevening posts. The median reach for evening posts was 232 (IQR, 143-378) versus 131 (IQR, 77-200) for nonevening posts (p < 0.001). There was no significant difference in the median reach of weekday posts (179.5; IQR, 85.5-339.5) versus weekend posts (192; IQR, 113-252). Posts with photos or pictures had the highest reach of all post types. CONCLUSION: Implementation of targeted strategies resulted in an increase in the number of users reached by a state health-system pharmacy organization's social media page.


Subject(s)
Pharmaceutical Services/organization & administration , Pharmacists , Pharmacy/organization & administration , Social Media , Work Engagement , Humans , Ohio , Pharmacy/methods , Retrospective Studies , Societies, Pharmaceutical/organization & administration
5.
J Pharm Pract ; 30(5): 571-575, 2017 Oct.
Article in English | MEDLINE | ID: mdl-27353145

ABSTRACT

Hydroxychloroquine (HQ) is commonly prescribed for autoimmune diseases such as systemic lupus erythematosus. We report a case of a 75-year-old female presenting with de novo decompensated heart failure and restrictive cardiomyopathy (left ventricular ejection fraction: 40%-45%) after treatment with HQ for more than 11 years. Hydroxychloroquine was discontinued, and follow-up echocardiogram 57 days after discontinuation showed normalization of her left ventricular ejection fraction. A score of 7 on the Naranjo Adverse Drug Reaction Probability Scale indicates that HQ is a probable cause of this patient's cardiomyopathy. An adverse drug effect due to HQ should be considered in treated patients who present with restrictive cardiomyopathy. Discontinuation may allow for partial or complete reversal of the cardiomyopathy.


Subject(s)
Antimalarials/adverse effects , Cardiomyopathy, Restrictive/chemically induced , Cardiomyopathy, Restrictive/diagnostic imaging , Hydroxychloroquine/adverse effects , Lupus Erythematosus, Systemic/drug therapy , Aged , Antimalarials/administration & dosage , Drug Administration Schedule , Female , Humans , Hydroxychloroquine/administration & dosage , Time Factors
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