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  • 1
    In: Journal of Cardiovascular Electrophysiology, Wiley, Vol. 30, No. 11 ( 2019-11), p. 2618-2626
    Abstract: Loperamide, an antidiarrheal agent, is a µ‐opioid receptor agonist increasingly abused to prevent opioid withdrawal or to produce euphoric effects. At supra‐therapeutic doses, loperamide can cause cardiac toxicity due to blockade of Na and I Kr channels, resulting in wide QRS rhythms, severe bradycardia, prolonged QTc, polymorphic ventricular tachycardia, cardiac arrest, and death. There are limited data on the cardiotoxic effects of high dose loperamide. Methods and Results A case report of loperamide toxicity is presented and then added to a contemporary review of the literature. In total, the presentation and management of 36 cases of loperamide cardiotoxicity are summarized. The overall median daily dose (interquartile range) of loperamide was 200 (134‐400) mg. The median QRS duration was 160 (125‐170) ms. The median QTc duration was 620 (565‐701) ms. Ventricular tachycardia was experienced by 24/36 (67%) of patients, 20 of which were specified to be polymorphic. Treatment was supportive, providing advanced cardiopulmonary life support and aggressive electrolyte repletion. Isoproterenol infusion or overdrive pacing was employed in 19/36 (53%) of cases. The median time to electrocardiogram normalization or hospital discharge, whichever came first, was 5 (3.5‐10) days. Conclusion Loperamide overdose is a toxidrome that remains underrecognized, and in patients with unexplained cardiac arrhythmias, loperamide toxicity should be suspected. Prompt recognition is critical due to the delayed recovery and high risk for life‐threatening arrhythmias.
    Type of Medium: Online Resource
    ISSN: 1045-3873 , 1540-8167
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2037519-0
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2011
    In:  Circulation: Cardiovascular Quality and Outcomes Vol. 4, No. suppl_1 ( 2011-11)
    In: Circulation: Cardiovascular Quality and Outcomes, Ovid Technologies (Wolters Kluwer Health), Vol. 4, No. suppl_1 ( 2011-11)
    Abstract: Background: Coronary artery bypass surgery (CABG) is typically delayed until 5 days after last clopidogrel dose, waiting for restoration of platelet reactivity units (PRU). We have investigated cost-effectiveness of CABG timing strategy involving daily platelet PRU testing and operating when platelet inhibition (PI) is less than 30%. Material and Methods: All consenting patients underwent daily PRU testing with point of care VerifyNow P2Y12 assay after receiving 600 mg of clopidogrel at the time of catheterization. Twenty-four hour interval was given between integrillin administration and testing. 29 patients (41% females, 34% with diabetes) comprised study cohort. Daily hospital cost for room and board was $3,770; cost of PRU testing was $49.The study was approved by the institutional IRB. Results: 83% of patients were operated on day 6 after the last clopidogrel dose; an additional 5 patients waited for more than 6 days. At least 75% of the tested patients demonstrated less than 30% PI, traditionally considered “safe” for a surgical intervention. There were no significant differences in RBC (p=0.949) or platelet (p=0.864) transfusion, fresh frozen plasma (p=0.295) or cryoprecipitate (p=0.654) administration in patients whose surgery was delayed for more than 6 days. Employing a strategy of operating on the day when PI is less than 30%, time to the surgery can be decreased from 5.3+/- 0.6 days to 2.8+/-1.5 days, Mann-Whitney p 〈 0.0001. Assuming no other expenses than cost of room and board in patients managed traditionally and added cost of daily PRU testing in platelet reactivity directed approach, average cost would decrease from $19,890+/-2,447 to $10,535+/-5,558 (Mann-Whitney p 〈 0.0001). Conclusions: Unless dictated by other clinical considerations, delaying CABG beyond 5 days after last clopidogrel dose is not justified. Five day waiting period is excessive with the majority of clopidogrel-treated patients achieving “safe” platelet responsiveness in less than 5 days. A strategy, involving daily platelet reactivity testing and performing CABG when PI is less than 30%, promises to bring significant cost-savings without compromising quality of delivered care.
    Type of Medium: Online Resource
    ISSN: 1941-7713 , 1941-7705
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2011
    detail.hit.zdb_id: 2453882-6
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  • 3
    In: JAMA, American Medical Association (AMA), Vol. 325, No. 21 ( 2021-06-01), p. 2169-
    Type of Medium: Online Resource
    ISSN: 0098-7484
    RVK:
    Language: English
    Publisher: American Medical Association (AMA)
    Publication Date: 2021
    detail.hit.zdb_id: 2958-0
    detail.hit.zdb_id: 2018410-4
    SSG: 5,21
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  • 4
    In: Cureus, Springer Science and Business Media LLC
    Type of Medium: Online Resource
    ISSN: 2168-8184
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2020
    detail.hit.zdb_id: 2747273-5
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  • 5
    In: Circulation, Ovid Technologies (Wolters Kluwer Health), Vol. 143, No. 1 ( 2021-01-05), p. 7-17
    Abstract: The subcutaneous (S) implantable cardioverter-defibrillator (ICD) is safe and effective for sudden cardiac death prevention. However, patients in previous S-ICD studies had fewer comorbidities, had less left ventricular dysfunction, and received more inappropriate shocks (IAS) than in typical transvenous ICD trials. The UNTOUCHED trial (Understanding Outcomes With the S-ICD in Primary Prevention Patients With Low Ejection Fraction) was designed to evaluate the IAS rate in a more typical, contemporary ICD patient population implanted with the S-ICD using standardized programming and enhanced discrimination algorithms. Methods: Primary prevention patients with left ventricular ejection fraction ≤35% and no pacing indications were included. Generation 2 or 3 S-ICD devices were implanted and programmed with rate-based therapy delivery for rates ≥250 beats per minute and morphology discrimination for rates ≥200 and 〈 250 beats per minute. Patients were followed for 18 months. The primary end point was the IAS-free rate compared with a 91.6% performance goal, derived from the results for the ICD-only patients in the MADIT-RIT study (Multicenter Automatic Defibrillator Implantation Trial–Reduce Inappropriate Therapy). Kaplan-Meier analyses were performed to evaluate event-free rates for IAS, all-cause shock, and complications. Multivariable proportional hazard analysis was performed to determine predictors of end points. Results: S-ICD implant was attempted in 1116 patients, and 1111 patients were included in postimplant follow-up analysis. The cohort had a mean age of 55.8±12.4 years, 25.6% were women, 23.4% were Black, 53.5% had ischemic heart disease, 87.7% had symptomatic heart failure, and the mean left ventricular ejection fraction was 26.4±5.8%. Eighteen-month freedom from IAS was 95.9% (lower confidence limit, 94.8%). Predictors of reduced incidence of IAS were implanting the most recent generation of device, using the 3-incision technique, no history of atrial fibrillation, and ischemic cause. The 18-month all-cause shock-free rate was 90.6% (lower confidence limit, 89.0%), meeting the prespecified performance goal of 85.8%. Conversion success rate for appropriate, discrete episodes was 98.4%. Complication-free rate at 18 months was 92.7%. Conclusions: This study demonstrates high efficacy and safety with contemporary S-ICD devices and programming despite the relatively high incidence of comorbidities in comparison with earlier S-ICD trials. The inappropriate shock rate (3.1% at 1 year) is the lowest reported for the S-ICD and lower than many transvenous ICD studies using contemporary programming to reduce IAS. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02433379.
    Type of Medium: Online Resource
    ISSN: 0009-7322 , 1524-4539
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2021
    detail.hit.zdb_id: 1466401-X
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  • 6
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2008
    In:  Circulation Vol. 118, No. suppl_18 ( 2008-10-28)
    In: Circulation, Ovid Technologies (Wolters Kluwer Health), Vol. 118, No. suppl_18 ( 2008-10-28)
    Abstract: Non-steroidal anti-inflammatory drugs (NSAIDs) increase risk of CV events. We sought to evaluate hospital outcomes associated with NSAID therapy in patients undergoing percutaneous coronary interventions (PCI). Data on NSAID use in single institution treated, consecutive PCI patients (treatment period 2004 –2006, rofecoxib-treated subjects excluded) was merged with NY State Angioplasty Registry database, and studied with ANOVA, chi-square, Kaplan-Meier, and logistic regression analyses. Of 2933 ASA-treated PCI patients (29% females) only 78 (2.7%) were treated with non-selective (ns) NSAIDs and 15 (0.5%) with Celecoxib. Most commonly used ns-NSAIDs were Ibuprofen (n=47) and Ketorolac (n=16). Most common indications for NSAIDs were musculoskeletal pain (35%) or “non-cardiac” chest pain (9%). NSAID-treated patients were younger (56+/−12 in ns-NSAID, 60+/−12 in Celecoxib, and 62+/−12 years old in “no NSAID” groups; p 〈 0.001). More NSAID-treated patients had a history of myocardial infarction (p 〈 0.001) or reduced ejection fraction (p=0.008). NSAIDs treatment did not affect post-PCI in-hospital mortality (p=0.769). However, post-procedural myocardial infarction (MI) was more common in ns-NSAID-treated patients (5% in ns-NSAID, 0% in Celecoxib, and 1% in “no NSAID” groups, p=0.002), odds ratio 5.4 (95%CI of 1.9 –15.9, p=0.002). Post-procedural length of stay in survivors was also significantly longer in the ns-NSAID group (3.9+/− 3.4 days), as compared to Celecoxib (1.1+/− 0.3 days) or “no NSAID” groups (2.2 +/−3.3 days; p 〈 0.001). Ns-NSAID treatment remained predictive of prolonged hospital stay (p=0.011) after adjustment for age (p=0.033), ejection fraction (p 〈 0.001), and history of previous (p 〈 0.001) or post-procedural MI (p=0.001). We observed an increased incidence of peri-procedural MI and longer post-PCI length-of-stay in patients treated with non-selective NSAIDs, but not with Celecoxib. Poor outcomes in ns-NSAIDs treated PCI patients may be due to attenuation of aspirin’s anti-platelet effects by ns-NSAIDs. Pending results of the randomized trials, providers should limit use on non-selective NSAIDs in patients with coronary artery disease undergoing PCI.
    Type of Medium: Online Resource
    ISSN: 0009-7322 , 1524-4539
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2008
    detail.hit.zdb_id: 1466401-X
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  • 7
    In: JAMA Neurology, American Medical Association (AMA), Vol. 80, No. 1 ( 2023-01-01), p. 99-
    Abstract: The Stroke of Known Cause and Underlying Atrial Fibrillation (STROKE AF) trial found that approximately 1 in 8 patients with recent ischemic stroke attributed to large- or small-vessel disease had poststroke atrial fibrillation (AF) detected by an insertable cardiac monitor (ICM) at 12 months. Identifying predictors of AF could be useful when considering an ICM in routine poststroke clinical care. Objective To determine the association between commonly assessed risk factors and poststroke detection of new AF in the STROKE AF cohort monitored by ICM. Design, Setting, and Participants This was a prespecified analysis of a randomized (1:1) clinical trial that enrolled patients between April 1, 2016, and July 12, 2019, with primary follow-up through 2020 and mean (SD) duration of 11.0 (3.0) months. Eligible patients were selected from 33 clinical research sites in the US. Patients had an index stroke attributed to large- or small-vessel disease and were 60 years or older or aged 50 to 59 years with at least 1 additional stroke risk factor. A total of 496 patients were enrolled, and 492 were randomly assigned to study groups (3 did not meet inclusion criteria, and 1 withdrew consent). Patients in the ICM group had the index stroke within 10 days before insertion. Data were analyzed from October 8, 2021, to January 28, 2022. Interventions ICM monitoring vs site-specific usual care (short-duration external cardiac monitoring). Main Outcomes and Measures The ICM device automatically detects AF episodes 2 or more minutes in length; episodes were adjudicated by an expert committee. Cox regression multivariable modeling included all parameters identified in the univariate analysis having P values & amp;lt;.10. AF detection rates were calculated using Kaplan-Meier survival estimates. Results The analysis included the 242 participants randomly assigned to the ICM group in the STROKE AF study. Among 242 patients monitored with ICM, 27 developed AF (mean [SD] age, 66.6 [9.3] years; 144 men [60.0%]; 96 [40.0%] women). Two patients had missing baseline data and exited the study early. Univariate predictors of AF detection included age (per 1-year increments: hazard ratio [HR], 1.05; 95% CI, 1.01-1.09; P  = .02), CHA 2 DS 2 -VASc score (per point: HR, 1.54; 95% CI, 1.15-2.06; P  = .004), chronic obstructive pulmonary disease (HR, 2.49; 95% CI, 0.86-7.20; P  = .09), congestive heart failure (CHF; with preserved or reduced ejection fraction: HR, 6.64; 95% CI, 2.29-19.24; P   & amp;lt; .001), left atrial enlargement (LAE; HR, 3.63; 95% CI, 1.55-8.47; P  = .003), QRS duration (HR, 1.02; 95% CI, 1.00-1.04; P  = .04), and kidney dysfunction (HR, 3.58; 95% CI, 1.35-9.46; P  = .01). In multivariable modeling (n = 197), only CHF (HR, 5.06; 95% CI, 1.45-17.64; P  = .05) and LAE (HR, 3.32; 1.34-8.19; P  = .009) remained significant predictors of AF. At 12 months, patients with CHF and/or LAE (40 of 142 patients) had an AF detection rate of 23.4% vs 5.0% for patients with neither (HR, 5.1; 95% CI, 2.0-12.8; P   & amp;lt; .001). Conclusions and Relevance Among patients with ischemic stroke attributed to large- or small-vessel disease, CHF and LAE were associated with a significantly increased risk of poststroke AF detection. These patients may benefit most from the use of ICMs as part of a secondary stroke prevention strategy. However, the study was not powered for clinical predictors of AF, and therefore, other clinical characteristics may not have reached statistical significance. Trial Registration ClinicalTrials.gov Identifier: NCT02700945
    Type of Medium: Online Resource
    ISSN: 2168-6149
    Language: English
    Publisher: American Medical Association (AMA)
    Publication Date: 2023
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  • 8
    Online Resource
    Online Resource
    Elsevier BV ; 2020
    In:  Journal of the American College of Cardiology Vol. 75, No. 11 ( 2020-03), p. 2010-
    In: Journal of the American College of Cardiology, Elsevier BV, Vol. 75, No. 11 ( 2020-03), p. 2010-
    Type of Medium: Online Resource
    ISSN: 0735-1097
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2020
    detail.hit.zdb_id: 1468327-1
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  • 9
    In: Journal of the American College of Cardiology, Elsevier BV, Vol. 67, No. 13 ( 2016-04), p. 823-
    Type of Medium: Online Resource
    ISSN: 0735-1097
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 1468327-1
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  • 10
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2012
    In:  Circulation: Cardiovascular Quality and Outcomes Vol. 5, No. suppl_1 ( 2012-04)
    In: Circulation: Cardiovascular Quality and Outcomes, Ovid Technologies (Wolters Kluwer Health), Vol. 5, No. suppl_1 ( 2012-04)
    Abstract: Background: It has been suggested that proton pump inhibitor (PPI) administration may decrease clinical efficacy of clopidogrel. We have studied changes in platelet reactivity during brief discontinuation of chronic PPI administration in patients on clopidogrel maintenance therapy. Methods: Study was approved by institutional IRB and informed consent was obtained in all patients. Study population consisted of 9 outpatients (6 females, 68+/-6 years old) on chronic clopidogrel and PPI therapy. VerifyNow P2Y12 point of care assay was used to measure P2Y12 platelet reactivity unit (PRU) and percent platelet inhibition. Platelet reactivity was measured on PPI therapy, 10 days after stopping PPI, and 10 days after re-starting PPI. Control baseline platelet reactivity testing was conducted on each occasion and remained unchanged (on enrollment 321+/-44 PRU vs. off clopidogrel 327+/-33 PRU vs. on clopidogrel 342+/-36, p=0.159). Repeated measurements ANOVA analysis was used to study overall changes in platelet reactivity. Fisher’s protected least significance difference intervals test was used to compare individual groups. All tests were 2-tailed, p 〈 0.05 was considered significant. Results: We observed a significant reduction in platelet reactivity after PPI discontinuation (baseline PRU 205+/-111 vs. PRU 159+/-116 on day 10 post last PPI dose, p=0.028). Resuming PPI resulted in increased platelet reactivity (228+/-94 PRU after 10 days of PPI, p=0.002). Accordingly, PPI discontinuation was associated with significantly enhanced platelet inhibition (baseline percent inhibition 38+/-31 vs. 52+/-33% on day 10 after stopping PPI, p=0.029). Re-starting PPI resulted in significantly less effective platelet inhibition (percent inhibition 34+/-23% 10 days after PPI resumption, p=0.009). There were no significant differences in platelet reactivity (p=0.243) and percent inhibition (p=0.596) when baseline values were compared with ones obtained after 10 days of PPI treatment. Conclusions: We have documented dynamic changes in clopidogrel induced platelet inhibition associated with discontinuation and resumption of PPI therapy. Clopidogrel appears to provide significantly less effective platelet inhibition when PPI is administered simultaneously.
    Type of Medium: Online Resource
    ISSN: 1941-7713 , 1941-7705
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2012
    detail.hit.zdb_id: 2453882-6
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