Artigo Acesso aberto Revisado por pares

Hiccups and Dysphonic Metallic Voice

2006; Lippincott Williams & Wilkins; Volume: 114; Issue: 15 Linguagem: Inglês

10.1161/circulationaha.106.626788

ISSN

1524-4539

Autores

Maurizio Gasparini, François Regoli, Carlo Ceriotti, Elisa Gardini,

Tópico(s)

Pathogenesis and Treatment of Hiccups

Resumo

HomeCirculationVol. 114, No. 15Hiccups and Dysphonic Metallic Voice Free AccessReview ArticlePDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessReview ArticlePDF/EPUBHiccups and Dysphonic Metallic VoiceA Unique Presentation of Twiddler Syndrome Maurizio Gasparini, MD, François Regoli, MD, Carlo Ceriotti, MD and Elisa Gardini, MD Maurizio GaspariniMaurizio Gasparini From the Electrophysiology and Pacing Unit, IRCCS Istituto Clinico Humanitas, Rozzano-Milano, Italy. , François RegoliFrançois Regoli From the Electrophysiology and Pacing Unit, IRCCS Istituto Clinico Humanitas, Rozzano-Milano, Italy. , Carlo CeriottiCarlo Ceriotti From the Electrophysiology and Pacing Unit, IRCCS Istituto Clinico Humanitas, Rozzano-Milano, Italy. and Elisa GardiniElisa Gardini From the Electrophysiology and Pacing Unit, IRCCS Istituto Clinico Humanitas, Rozzano-Milano, Italy. Originally published10 Oct 2006https://doi.org/10.1161/CIRCULATIONAHA.106.626788Circulation. 2006;114:e534–e535Twiddler syndrome refers to a rare complication observed in patients with implanted pacemakers or defibrillators that causes device malfunction. The condition arises as a result of the patient's conscious or unconscious manipulation of the device, causing its rotation in the pocket, resulting in torsion and dislodgment of the implanted lead(s).A 65-year-old obese woman with idiopathic dilated cardiomyopathy and diabetes mellitus had undergone implantation of a biventricular implantable cardioverter-defibrillator (CRT-D, Medtronic Insync Maximo 7304) with the positioning of 3 leads: a passive bipolar lead in the auricula of the right atrium (Medtronic Capsure Z Novus 5554), a bipolar, single-coil, screw-in lead (Medtronic Sprint 6931) in the apex of the right ventricle (RV), and a unipolar left-ventricular (LV) pacing lead (Medtronic Attain 4193) in an anterolateral tributary of the coronary sinus.Approximately 1 month after implantation, the patient presented to the emergency room with effort dyspnea followed by gradually worsening hiccups associated with dysphonia (a metallic or "pseudo-robot" voice was observed). The device was investigated: During threshold testing of the RV, no effective capture could be observed, even at maximum output. In contrast, when testing the unipolar LV lead (which in this model closes off on the RV coil), the symptoms of hiccups and "pseudo-robot" voice were immediately reproduced. The device was reprogrammed in VVI mode 30 bpm so that underlying spontaneous sinus rhythm emerged, and symptoms ceased immediately.Chest radiography (Figure 1) showed a macrodislodgment of the screw-in RV coil lead into the brachiocephalic vein (at the level of the esophagus) and an impressive cluster of catheter tangles in the subcutaneous pocket. The right atrium lead, although slightly retracted and with a large loop, appeared to have the tip in the correct position, with good sensing and pacing values. The LV unipolar lead (with the dipole closing on the RV coil in the brachiocephalic vein) initially presented a slight retraction but with good sensing and pacing threshold. Download figureDownload PowerPointFigure 1. Chest radiograph shows the configuration of electrodes when the patient presented in the emergency room with hiccups and a dysphonic metallic voice. ATR indicates atrial bipolar lead; RV, screw-in right ventricular coil lead; and LV, left ventricular electrode in the coronary sinus.Four days later, the patient underwent a revision procedure aiming at repositioning both the LV and RV coil leads. The chest radiograph at that point (Figure 2) revealed further retraction of both the RV and LV leads (no LV pacing was possible at that point). After incision into the skin and gentle extraction of the device, an impressive cluster of twisted catheter tangles connected to the device (Figure 3) was found. The device had rotated innumerous times on its central axis. As a consequence of the numerous loops and twists, both the RV lead coil and the LV lead had been deformed and needed replacement. Download figureDownload PowerPointFigure 2. Chest radiography performed a few days later showed further retraction of both the RV and LV leads. ATR indicates atrial bipolar lead; RV, screw-in right ventricular coil lead; and LV, left ventricular electrode in the coronary sinus.Download figureDownload PowerPointFigure 3. Intraoperative image showing the cluster of catheter tangles found in the device pocket.Twiddler syndrome is a rare and potentially dangerous cause of lead dislodgment in patients with pacemakers and implantable cardioverter-defibrillators.1–4 The peculiar clinical presentations of Twiddler syndrome in conventional pacemakers include abdominal pulsation2 and stimulation of the pectoral major muscle.3 Patients who are most at risk for this condition include middle-aged obese women4 and patients with mental disorders such as dementia.5 To our knowledge, this is the first report of Twiddler syndrome in a CRT-D device with retraction of a screw-in defibrillation lead. The unique symptoms of hiccups and dysphonic metallic voice have never been reported before and were the result of the particular technical characteristics of the Medtronic CRT-D device system, in which the unipolar tip of the LV lead uses the RV defibrillator coil as the anode. The macrodislodgment of the RV coil (retracted into the brachiocephalic vein, at the level of esophagus) with consequent anatomic proximity to both recurrent and phrenic nerves caused an electrical irritation of these nerves, hence explaining the very odd symptoms. Treatment measures to avoid or limit Twiddler syndrome in patients at increased risk include limiting the pocket size and the suturing of the device to the fascia.6DisclosuresNone.FootnotesCorrespondence to Dr Maurizio Gasparini, IRCCS Istituto Clinico Humanitas, Rozzano-Milano, Italy, Via Manzoni 56 Rozzano-Milano, Italy. 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Konishi H, Tokano T, Nakazato Y, Komatsu S, Suwa S, Komatsu K, Hayashi H, Sekita G, Sumiyoshi M, Bito F, Kizu K and Daida H (2012) Twiddler's syndrome detected by patient's complaint of implantable cardioverter-defibrillator rotation in the subcutaneous pocket, Journal of Arrhythmia, 10.1016/j.joa.2011.12.003, 28:4, (239-241), Online publication date: 1-Aug-2012. van Oostrom A and Boersma L (2011) Hazardous twiddling of a subpectoral internal cardioverter defibrillator, Netherlands Heart Journal, 10.1007/s12471-011-0131-3, 19:6, (304-304), Online publication date: 1-Jun-2011. Benouda L, Zerhouni K, Saïdi A, Kidouche R, Tonyiga K, Vignat N, Khellaf A, Monsuez J and Artigou J (2011) Le twiddler syndrome, Archives des Maladies du Coeur et des Vaisseaux - Pratique, 10.1016/S1261-694X(11)70200-0, 2011:196, (27-29), Online publication date: 1-Mar-2011. 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Patel M, Pandya K, Shah A, Lojewski E, Castellani M and Thakur R (2008) Reel syndrome—not a twiddler variant, Journal of Interventional Cardiac Electrophysiology, 10.1007/s10840-008-9288-0, 23:3, (243-246), Online publication date: 1-Dec-2008. October 10, 2006Vol 114, Issue 15 Advertisement Article InformationMetrics https://doi.org/10.1161/CIRCULATIONAHA.106.626788PMID: 17030694 Originally publishedOctober 10, 2006 PDF download Advertisement SubjectsCatheter Ablation and Implantable Cardioverter-DefibrillatorCongenital Heart DiseasePacemaker

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