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Bos, Johan M

0000-0002-3635-2003

Mayo Clinic

Department of Pediatric and Adolescent Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN, USA.

Citations 76

Hypertrophic Cardiomyopathy, Athlete’s Heart, or Both
Kebed, Kalie, Bos, J. Martijn , Anavekar, Nandan S., Ackerman, Michael J. , Ommen, Steve R. , Kebed, Kalie Y, Mulvagh, Sharon L. , Bos, Johan M

Circulation: Cardiovascular Imaging | July 11, 2015 | Volume: 8 | Issue: 7 | Pages: No page available

10.1161/circimaging.115.003312 Get It

Genotype-phenotype Correlations of Hypertrophic Cardiomyopathy When Diagnosed in Children, Adolescents, and Young Adults
Loar, Robert W. , Bos, J. Martijn , Will, Melissa L., Ommen, Steve R. , Ackerman, Michael J. , Bos, Johan M

Congenital Heart Disease | June 11, 2015 | Volume: 10 | Issue: 6 | Pages: 529-536

10.1111/chd.12280 Get It

Breath Holding Spells in Children with Long QT Syndrome
Robinson, Jeffrey A. , Bos, J. Martijn , Etheridge, Susan P. , Ackerman, Michael J. , Bos, Johan M

Congenital Heart Disease | April 27, 2015 | Volume: 10 | Issue: 4 | Pages: 354-361

10.1111/chd.12262 Get It

Effects on Repolarization Using Dynamic QT Interval Monitoring in Long‐QT Patients Following Left Cardiac Sympathetic Denervation
Bos, J. Martijn , Bos, Katy M., Liang, Jackson J. , Patel, Nikhil A. , Hodge, David O. , Noheria, Amit , Asirvatham, Samuel J. , Ackerman, Michael J. , DeSimone, Christopher V. , Asirvatham, Samuel J , Bos, Johan M , Liang, Jackson

Journal of Cardiovascular Electrophysiology | January 5, 2015 | Volume: 26 | Issue: 4 | Pages: 434-439

10.1111/jce.12609 Get It

Dynamic QT Interval Monitoring Post‐LCSDBackgroundVideoscopic left cardiac sympathetic denervation (LCSD) is an adjunct therapy for reduction of arrhythmia‐induced events in patients with long‐QT syndrome (LQTS). LCSD reduces LQTS‐triggered breakthrough cardiac events. The temporal effects of QTc changes post‐LCSD have not been studied.MethodsWe utilized continuous QTc monitoring on 72 patients with LQTS. We evaluated acute and long‐term QTc changes in comparison to 12‐lead ECG‐derived QTc values prior to surgery, 24 hours postsurgery, and at follow up ≥3 months.ResultsSeventy‐two patients underwent LCSD at our institution (46% male, mean age at LCSD was 14 ± 10 years). The mean baseline, pre‐LCSD QTc was 505 ± 56 ms, which had decreased significantly at ≥3 months post‐LCSD to 491 ± 40 ms (P = 0.001). QTc monitoring revealed that the majority of the cohort (53/72; 74%) had a transient increase >30 ms in QTc from baseline, with an average maximum increase of 72 ± 30 ms. Resolution within 10 ms of baseline or less occurred in 57% (30/53) at 24 hours post‐LCSD.ConclusionsAlthough LQTS patients may have a paradoxically increased QTc post‐LCSD, the effects are transient in most patients. Importantly, no patients experienced any arrhythmias in the postoperative setting related to this transient rise in QTc.
Sudden Cardiac Arrest During Sex in Patients with Either Catecholaminergic Polymorphic Ventricular Tachycardia or Long‐QT Syndrome: A Rare But Shocking Experience
Loar, Robert W. , Bos, J. Martijn , Cannon, Bryan C. , Ackerman, Michael J. , Bos, Johan M

Journal of Cardiovascular Electrophysiology | December 16, 2014 | Volume: 26 | Issue: 3 | Pages: 300-304

10.1111/jce.12600 Get It

Sudden Cardiac Arrest During Sex in Cardiac ChannelopathiesBackgroundPatients with catecholaminergic polymorphic ventricular tachycardia (CPVT) and long‐QT syndrome (LQTS) are susceptible to cardiac events during sympathetic nervous system activation. Herein, we sought to determine the risk of cardiac events associated with sex in CPVT and LQTS patients.Methods and ResultsWe reviewed the electronic medical record of patients seen in the Genetic Heart Rhythm Clinic. There were 445 patients ≥18 years diagnosed with LQTS (N = 402, age at diagnosis 30 ± 16 years) or CPVT (N = 43, age at diagnosis 25 ± 15 years). No sex‐induced cardiac events occurred in the LQTS population, and 2 occurred in the CPVT population. Sex‐induced events were more likely in CPVT (2/43, 4.7%) than LQTS (0/402, 0%, P = 0.008). One case involved a 22‐year‐old CPVT1 female with prior cardiac arrest, who experienced several appropriate implantable cardioverter defibrillator shocks during intercourse while taking β‐blockers. The second case was a 52‐year‐old CPVT1 male with history of recurrent exercise‐triggered syncope, who had syncope during sex in the setting of β‐blocker noncompliance. Extrapolating from published estimates of intercourse frequency by age, the overall event rate was only 0.0004%, and 0.005% among the CPVT cohort.ConclusionsPotentially life‐threatening cardiac events during sex in patients with CPVT are rare and even rarer in LQTS. Overall, the cardiac event per intercourse rate is extremely low. Patients and their partners should be reassured that sex is a low‐risk activity from a cardiac standpoint.
Genotype-Phenotype Correlations in Apical Variant Hypertrophic Cardiomyopathy
Towe, Eric, Bos, J. Martijn , Ommen, Steve R. , Ackerman, Michael J. , Towe, Eric C, Gersh, Bernard J. , Bos, Johan M

Congenital Heart Disease | December 15, 2014 | Volume: 10 | Issue: 3 | Pages: E139-E145

10.1111/chd.12242 Get It

Impact of clinical decision support preventing the use of QT-prolonging medications for patients at risk for torsade de pointes
Sorita, Atsushi , Bos, J. Martijn , Morlan, Bruce W., Tarrell, Robert F., Ackerman, Michael J. , Caraballo, Pedro J. , Bos, Johan M

Journal of the American Medical Informatics Association | October 17, 2014 | Volume: 22 | Issue: e1 | Pages: e21-e27

10.1136/amiajnl-2014-002896 Get It

AbstractWe developed and implemented a ‘CPOE-QT Alert’ system, that is, clinical decision support integrated in the computerized physician order entry system (CPOE), in 2011. The system identifies any attempts to order medications with risk of torsade de pointes (TdP) for patients with a history of significant QT prolongation (QTc ≥500 ms) and alerts the provider entering the order. We assessed its impact by comparing orders and subsequent medication administration before and after activation of the system. We found a significant decrease in the proportion of completed order per ordering attempt after system activation (94% (1293/1379) vs 77% (1888/2453), difference 16.8%; p<0.001). This resulted in a 13.9% reduction in the administration of those medications to patients. A significant decrease was observed across all provider types, educational levels, and specialties. The CPOE-QT Alert system successfully reduced exposure to QT-prolonging medications in high risk patients.
Epilepsy Misdiagnosed as Long QT Syndrome: It Can Go Both Ways
Medford, Beth A., Bos, J. Martijn , Ackerman, Michael J. , Bos, Johan M

Congenital Heart Disease | June 10, 2013 | Volume: 9 | Issue: 4 | Pages: E135-E139

10.1111/chd.12104 Get It

Left Cardiac Sympathetic Denervation in Long QT Syndrome
Bos, J. Martijn , Bos, Katy M., Johnson, Jonathan N. , Moir, Christopher R. , Ackerman, Michael J. , Bos, Johan M

Circulation: Arrhythmia and Electrophysiology | June 1, 2013 | Volume: 6 | Issue: 4 | Pages: 705-711

10.1161/circep.113.000102 Get It

Background— Long QT syndrome (LQTS) is a potentially lethal but highly treatable cardiac channelopathy. Treatment options include pharmacotherapy, device therapy, and left cardiac sympathetic denervation (LCSD). Here, we sought to determine the characteristics of LQTS patients who have had ≥1 LQTS-related breakthrough cardiac event (BCE) after LCSD. Methods and Results— We performed retrospective chart review for 52 consecutive patients (24 males; mean age at diagnosis, 10.0±10 years; mean QTc, 528±74 ms) with LQTS who underwent LCSD between 2005 and 2010 (mean age at LCSD, 14.1±10 years) and have been followed up for 3.6±1.3 years. A BCE was defined as either (1) an appropriate ventricular fibrillation-terminating implantable cardioverter defibrillator shock or (2) arrhythmogenic syncope, seizures, or aborted cardiac arrest after LCSD. Thirty-three patients (61%) had LCSD as primary prevention because of either high-risk assessment or β-blocker intolerance. So far, 12 of 52 (23%) patients (7 males) have experienced ≥1 BCE post LCSD. The clinical phenotype of patients with BCEs was significantly more severe than patients without a BCE. No BCEs were seen in patients undergoing LCSD for β-blocker intolerance (0/12 versus 17/40; P <0.001). Conclusions— Although a marked reduction in number of cardiac events is usually seen after LCSD, ≈50% of high-risk LQTS patients have experienced ≥1 post-LCSD breakthrough. Therefore, LCSD must not be viewed as curative or as an alternative in implantable cardioverter defibrillator for high-risk patients. Prophylactic LCSD may provide another option to counter a suboptimal quality of life resulting from medication-related side effects.
Sudden Cardiac Arrest in a Young Patient with Hypertrophic Cardiomyopathy and Zero Canonical Risk Factors: The Inherent Limitations of Risk Stratification in Hypertrophic Cardiomyopathy
Kohorst, John J. , Bos, J. Martijn , Hagler, Donald J. , Ackerman, Michael J. , Bos, Johan M

Congenital Heart Disease | May 7, 2013 | Volume: 9 | Issue: 2 | Pages: E51-E57

10.1111/chd.12073 Get It