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Use of dothiepin for management of Wenkebachtype second degree heart block Jeenal Patel, Jayne Hui Box Hill Hospital, Eastern Health Background Dothiepin is a tricyclic antidepressant (TCA) which inhibits the reuptake of noradrenaline and serotonin and blocks cholinergic and alpha-adrenergic receptors1. Infrequent adverse effects (0.1-1%) of TCAs include snius tachycardia, arrhythmias and QT prolongation1,2. Objective To report a successful case of dothiepin use in treating PR prolongation due to Wenkebachtype second degree heart block. Day 6 -Medical review -Ventricular pauses likely due to increased vagal tone in setting of sepsis. -Wenckebach pattern seen on ECG -Isoprenaline ceased -Atropine PRN commenced Day 0 -Admission with urosepsis -JJ Stent inserted -Ceftriaxone 1g initiated Day 3 - Ventricular pauses seen on ECG - Transfer to cardiology ward - IV isoprenaline commenced - Ceftriaxone ceased Figure 1: Timeline of Clinical Presentation and Management Figure 3: Relevant Biochemistry during Patient Admission Clinical Features An 80 year old caucasian female was admitted with E.coli urosepsis, successfully treated with JJ stent insertion and ceftriaxone 1g IV daily. Ventricular pauses were seen on electrocardiogram (ECG) day 3 post procedure and the patient was transferred to the cardiology unit. Discussion Wenkebach-type second degree heart block describes non-conducted P waves that occur due to prolongation of the PR interval, because of fatigue of AV node cells.3 As there is minimal progression to third degree heart block, only symptomatic patients are treated. Atropine is the treatment standard.3 Case Progress and Outcomes Initially, cardiology planned for permanent pacemaker (PPM) insertion when sepsis was resolved. On day 6, ECG highlighted Wenckebach pattern of PR prolongation prior to ventricular pauses, suggesting type-1 second degree heart block.3 Isoprenaline was ceased and atropine as required commenced. There is paucity of evidence to support the use of dothiepin in this setting, as a known side effect of TCAs is PR prolongation.4 However, past literature does suggest tricyclic antidepressants such as imipramine may demonstrate anti-arrythmic effect.4 This is the first case report of such dothiepin use to our knowledge. The mechanism of action for this effect has not been established. Permanent pacemakers are not required for Wenkebachtype second degree heart block. Dothiepin 25mg daily was initiated on Day 9 and increased over three days to 50mg, resulting in less ventricular pauses on telemetry. The patient was discharged on dothiepin 50mg daily. Day 9 - Dothiepin 25mg daily initiated by cardiology team Day 11 -Dothiepin dose increased to 50mg daily - Patient discharged Day 1 Day 3 Day 6 Day 10 Hb - 116 118 128 Na+ - 140 140 139 K+ - 4.0 4.3 4.6 Mg2+ - 1.0 - 0.89 Cr - 56 62 60 eGFR - 85 82 83 BP (mmHg) 130/66 141/76 - 130/65 Heart Rate (BPM) 108 58 - 80 Conclusion This case demonstrates the successful initial use of dothiepin in the management of ventricular pauses in a patient with Wenckebach-type second degree heart block. Further research is vital in ascertaining this mechanism of action and duration of treatment. Figure 2: Past Medical History and Medications Taken Prior to Admission Past Medical History Medications on admission Hypertension amlodipine 10mg/ valsartan 160mg 1 po daily Glaucoma brinzolamide 1% eye drops; travoprost 0.004% eye drops Hypercholesterolaemia Untreated Osteoarthritis Untreated For further information, please contact Jeenal Patel at [email protected] References 1. Australian Medicines Handbook. Adelaide; Australian Medicines Handbook Pty Ltd; 2016 2. Dothiepin. In: Adverse Effects [database on the Internet]. Ann Arbor (MI): Truven Health Analytics; 2016 [cited 20 Sept 2016]. Available from:www.micromedexsolutions.com 3. AV Block: 2nd degree, Mobitz I. Life in the Fast Lane;2016 [cited 20 Sept 2016]. Available from: http://lifeinthefastlane.com/ecg-library/basics/wenckebach/ 4. Glassman A. Cardiovascular Effects of Therapeutic Doses of Tricyclic Antidepressants. Arch Gen Psychiatry; 1981, 38:815-820.