Logo American Journal of Case Reports

Call: 1.631.629.4328
Mon-Fri 10 am - 2 pm EST

Contact Us

Logo American Journal of Case Reports Logo American Journal of Case Reports Logo American Journal of Case Reports

28 September 2020: Articles  Japan

Discontinuation of Cardiac Resynchronization Therapy for Heart Failure Due to Dilated Cardiomyopathy in a 61-Year-Old Female “ Super-Responder” with Return of a Reduced Left Ventricular Ejection Fraction to Normal

Unusual clinical course, Unusual or unexpected effect of treatment

Yasunari Hoshiba A* , Atsuhiko Sugimoto A , Shoko Doi A , Tomokazu Sawada A , Seiji Tamiya A , Daiki Ito A , Harukazu Iseki A

DOI: 10.12659/AJCR.926704

Am J Case Rep 2020; 21:e926704



BACKGROUND: Although cardiac resynchronization therapy (CRT) is widely used, it has been validated only during active pacing. “Super-responders” are patients with normalized or markedly improved left ventricular (LV) systolic function with CRT who may experience a decline in cardiac function with CRT discontinuation.

CASE REPORT: A 61-year-old woman with a nonischemic cardiomyopathy was admitted to our hospital in September 2008 for the treatment of heart failure (HF). Cardiac assessment revealed impaired LV function with an ejection fraction of 18%, LV dilatation, and left bundle branch block (LBBB). Despite optimized medical treatment, her HF progressed, with a rapid increase in LV chamber size, mitral regurgitation, and widening of the QRS complex. In July 2011, the patient initially refused CRT, but later consented to the procedure; CRT pacemaker implantation was subsequently performed. Thereafter, the LVEF improved from 27% to 46%, LV diastolic dimension decreased rapidly from 79 mm to 56 mm, and LVEF (65%) and LV size (47 mm) normalized within 1 year later. As of August 2012, battery exchange was needed within 1 year because of high LV pacing thresholds. In October 2012, although CRT discontinuation was not recommended, we discontinued CRT to conserve battery life with the patient’s consent, hoping to maintain her condition with pharmaceutical treatment. She remained stable through January 2020, with no indication of re-exacerbation.

CONCLUSIONS: We describe a female patient with a nonischemic cardiomyopathy and LBBB who demonstrated a super-response to CRT and maintained improvement in LV function and functional status for 8 years after discontinuing CRT.

Keywords: Ventricular Remodeling, cardiac resynchronization therapy, Cardiomyopathy, Dilated, Follow-Up Studies, Heart Failure, Middle Aged, Stroke Volume, Treatment Outcome, Ventricular Function, Left


Cardiac resynchronization therapy (CRT) is a treatment option for heart failure (HF) in patients with a reduced ejection fraction (EF) (≤35%) and intraventricular conduction delay (especially left bundle branch block [LBBB]), who are refractory to medication alone. Symptomatic HF is characterized by symptoms (e.g., breathlessness, ankle swelling, and fatigue) caused by a structural and/or functional cardiac abnormality. LBBB is a cardiac conduction abnormality seen on electrocardiography (ECG) that is mostly due to cardiac abnormality, and the QRS duration on ECG must be >120 ms. CRT has been reported to increase the left ventricular (LV) ejection fraction (LVEF), reduce LV size, and improve symptoms [1,2]; however, approximately 70% of patients benefit from CRT [3]. Patients are normally classified as either responders or nonresponders based on changes in the LVEF, LV size, and clinical symptoms, although unified definitions of CRT response and nonresponse have not yet been established [3,4]. Additionally, the concept of a CRT super-response has recently been introduced; this has been defined as an improvement in LVEF to >50% and/or a decrease in LV size of >25–30% by 6 months to 1 year after implantation [4,5]. Super-responders may also react differently to CRT discontinuation by exhibiting a rapid decrease in the LVEF and an increase in both mitral regurgitation (MR) and QRS complex width [6,7].

Some studies have reported that discontinuation of CRT results in a decline in cardiac function due to recurrence of remodeling, even in super-responders [5,6]; therefore, CRT should be continued as long as possible. Here, we report a case of dilated cardiomyopathy (DCM) treated with CRT and medication in which the patient, classified as a CRT super-responder, was able to successfully discontinue CRT.

Case Report

A 61-year-old woman with no medical history was admitted to our hospital in September 2008 for 2 months of progressive dyspnea. She was documented to have decompensated HF with New York Heart Association (NYHA) II functional limitations. She had no history of tobacco smoking, alcohol consumption, or substance abuse. Results of the physical examination were: height, 150 cm; weight, 42 kg; body mass index (BMI), 18.7 kg/m2; blood pressure, 120/66 mmHg; heart rate, 73 beats/min; and oxygen saturation, 94% (room air). Her dyspnea on exertion was class II based on the NYHA classification. On auscultation, a third heart sound (S3) and an apical systolic murmur were detected.

Chest radiography revealed cardiomegaly and bilateral pleural effusions. ECG showed a sinus rhythm with LBBB and a QRS complex duration of 140 ms (Figure 1A–1E). Echocardiography revealed severe LV enlargement with impaired systolic function and an LVEF of 18% (normal range, 55–65%). LV diastolic to systolic dimension (LVDd/LVDs) was 56/48 mm (normal range, 40–55/30–45 mm), and moderate MR was observed. Based on these findings, the patient was admitted with a diagnosis of HF.

Secondary cardiomyopathy associated with autoimmune disease, metabolic disease, and inflammatory disease may show echocardiographic findings similar to DCM. Blood tests results were normal and ruled out these diseases. Coronary angiography was also performed to exclude ischemic cardiomyopathy, and it did not demonstrate significant coronary artery disease. Cardiac magnetic resonance imaging demonstrated LV dilation with an LVEF of 16% and no evidence of abnormal gadolinium enhancement. Thus, no findings were suggestive of secondary cardiomyopathy after these examinations. Along with these results, and based on the 2006 American Heart Association Classification of “Contemporary definitions and classification of the cardiomyopathies,” we reached a final diagnosis of DCM.

Diuretic treatment was initiated (furosemide: 40 mg/day, initially administered via intravenous injection and then orally) in combination with an angiotensin II receptor blocker (candesartan: 4 mg/day) and a β-blocker (carvedilol) for secondary prevention of HF. As the prognostic improvement associated with β-blockers is dose-dependent, the guidelines recommended increasing the dosage in accordance with the tolerance level of the patient [8,9]. In our case, the carvedilol dosage was increased to 10 mg/day. The use of mineralocorticoid/aldosterone receptor antagonists and a further increase in the carvedilol dosage were not possible because of hypotension. The patient’s HF improved, and she was subsequently discharged.

In October 2009, the patient was readmitted because of HF re-exacerbation, despite ongoing pharmaceutical treatment. Echocardiography revealed an LVEF of 30% and an LVDd/LVDs of 67/54 mm, and ECG indicated a QRS width of 144 ms. We determined that CRT was required; however, the patient refused because of fear of surgery. Hence, pharmaceutical treatment alone was continued. In June 2011, the patient’s HF worsened, and she was readmitted with significant widening of the QRS complex (160 ms), decreased LVEF (27%), and rapidly increased LVDd/LVDs (79/69 mm). In July 2011, she consented to CRT, and a pacemaker (AllureTM, St Jude Medical, MN, USA) was implanted. The placement of the LV leads resulted in a high LV pacing threshold; however, no other positions were feasible because there was no other coronary vein branch wherein the LV lead could be inserted with a good threshold. Immediately after implantation, the LVEF increased and QRS width decreased.

Echocardiography performed in August 2011 revealed significant improvements in both the LVEF (46%) and LV enlargement (LVDd/Ds of 56/43 mm), the QRS width was 124 ms, and we were able to increase the carvedilol dosage to 20 mg/day. Follow-up echocardiography performed in June 2012 confirmed the improvement in the LVEF (65%) and LVDd/LVDs (47/30 mm), revealed QRS width of 136 ms, and showed mild MR.

At this point, due to the high threshold of the LV pacing lead, the remaining battery power was estimated to last less than 1 year; thus, we decided to discontinue biventricular pacing. Although the LBBB persisted, follow-up ECG and echocardiography indicated that the QRS width had not increased (136 ms) and there was no deterioration in MR or LVEF. Therefore, with the patient’s consent, CRT was discontinued in October 2012 to preserve the battery. We changed the mode from DDD to AAI as there was a mild bradycardia, possibly due to the increased β-blocker dose. It was clearly communicated to the patient that CRT would be promptly restarted if there was any sign of HF re-exacerbation; she was carefully monitored for the following 4 years, during which there was no deterioration of cardiac function. Echocardiography and ECG revealed an LVEF of 69%, LVDd/LVDs of 44/27 mm, and a QRS width of 130 ms during follow-up in August 2014, and an LVEF of 60%, LVDd/LVDs of 42/30 mm, and a QRS width of 126 ms in June 2016. The latest follow-up in November 2018 revealed an LVEF of 64%, LVDd/LVDs of 44/30 mm, and a QRS width of 132 ms.

In anticipation of probable cardiac remodeling that could re-exacerbate the HF, and thus require prompt resumption of CRT, a generator exchange surgery was performed in June 2016. At the most recent follow-up in 2020, CRT had not been resumed and the patient’s status remained stable without signs of re-exacerbation (Figure 2A, 2B).


CRT has been reported to improve symptoms and mortality in patients with HF who present with prolongation of the QRS complex and low LVEF despite standard medical therapy [1,2]. Approximately 60–70% of patients respond to CRT [10,11]. CRT responders show that the beneficial clinical outcomes are due in part to significant reductions in the LV end-systolic volume, so-called reverse remodeling (RR), and the occurrence of RR is closely related to prognosis [4]. It is considered that RR occurred in this case, resulting in the improvement in LVEF and LV size. Additionally, a high degree of RR may have made this case a super-responder. Further, this case is characterized by an extremely fast rate of improvement, as can be seen from the fact that the EF improved from 27% to 46% and the LVDd/LVDs decreased from 79/69 mm to 56/43 mm within 1 month of CRT. This may be because RR progressed rapidly.

Hsu et al. reported that a QRS duration of ≥150 ms, LBBB, BMI <30 kg/m2, and smaller baseline left atrial volume index, as well as being female and having no prior myocardial infarction, were all predictors of a CRT super-response [12]. This case was classified as a super-responder. Remarkably, this patient met all of these criteria, which may have been the reason for the high and rapid RR.

Standard, evidence-based medical treatments for HF with a low EF have included β-blockers, angiotensin-converting enzyme inhibitors, and mineralocorticoid/aldosterone receptor antagonists [9]. Among these drugs, β-blockers promote RR to the greatest extent [13]. In many patients, it is possible to increase the β-blocker dosage up to that recommended by the guidelines after CRT; however, such an increase is not possible before CRT [14,15]. Thus, the stable outcome of our patient after CRT discontinuation may have been related to the increased dosage of β-blockers after CRT. These factors may explain the high degree of RR progression.

In this case, we also noticed that the improvement of the EF was accompanied by shortening of the QRS width, and even after CRT was discontinued, the QRS width did not increase again. It is hypothesized that an increase in the QRS width indicates electrical remodeling, whereas a decrease in the EF indicates mechanical remodeling. Shortening of the QRS width in our case may have implied electrical RR, and the lack of re-increase in the QRS width may be due to the absence of electrical RR recurrence following discontinuation of CRT.

Another study demonstrated that prolonged mechanical dys-synchrony as a result of the LBBB may have triggered mechanical and electrical remodeling [16]. CRT is reported to improve both electrical and mechanical remodeling by modifying mechanical dyssynchrony. In our case, indeed, it seemed that high degrees of electrical and mechanical RR had occurred.

Liang et al. demonstrated that even super-responders sometimes exhibited a recurrence of electrical and mechanical remodeling after CRT discontinuation [5]; therefore, CRT should be continued when possible to promote these protective factors. In our patient, CRT was discontinued because of the high rate of battery consumption; however, this was a special case, and current evidence and guidelines do not recommend the discontinuation of CRT.

A previous study reported that CRT was interrupted in approximately 4–10% of the patients for various reasons (this excludes interruption due to arrhythmias and includes only those caused by device or lead issues) [17,18]. In such cases, CRT should be continued in accordance with guidelines and supporting evidence, using methods such as reoperation. There may be cases where it is difficult to continue CRT for various reasons. We believe our case is unique, as it demonstrates that remodeling may not occur despite discontinuation of CRT. However, because of limited data, we cannot elucidate the mechanisms involved. Many studies and guidelines have recommended that CRT should be continued as long as possible [5,6,19] and discontinuation is not recommended. In this case, although CRT was discontinued, good results were achieved, and HF did not recur.


We present a rare case of DCM treated with CRT and medication in a female patient who demonstrated a super-response to CRT and was able to successfully discontinue CRT without re-exacerbation of HF. Guidelines and evidence do not recommend discontinuation of CRT; however, there have been reports of patients who have had difficulty continuing CRT for various reasons. As in this case, super-responders or those with rapidly progressing RR may be suitable for CRT discontinuation. Nevertheless, clear indicators for discontinuing CRT are currently unknown because of a lack of evidence.

We hope that this case will provide evidence for similar studies in the field and assist in the identification of alternative treatment strategies for cardiomyopathy, as we have considered these results to be not only exceptional, but also interesting and impressive.


1.. Bristow MR, Saxon LA, Boehmer J: N Engl J Med, 2004; 350; 2140-50

2.. Cleland JG, Daubert JC, Erdmann E: N Engl J Med, 2005; 352; 1539-49

3.. Abraham WT, Fisher WG, Smith AL: N Engl J Med, 2002; 346; 1845-53

4.. Ypenburg C, van Bommel RJ, Borleffs CJ: J Am Coll Cardiol, 2009; 53; 483-90

5.. Liang Y, Wang Q, Zhang M: J Cardiovasc Electrophysiol, 2018; 29; 1548-55

6.. Knappe D, Pouleur AC, Shah AM: J Card Fail, 2013; 19; 149-55

7.. Ypenburg C, Lancellotti P, Tops LF: J Am Coll Cardiol, 2007; 50; 2071-7

8.. Bristow MR, Gilbert EM, Abraham WT: Circulation, 1996; 94; 2807-16

9.. Ponikowski P, Voors AA, Anker SD: Eur Heart J, 2016; 37; 2129-200

10.. Solomon SD, Foster E, Bourgoun M: Circulation, 2010; 122; 985-92

11.. John Sutton M, Ghio S, Plappert T: Circulation, 2009; 120; 1858-65

12.. Hsu JC, Solomon SD, Bourgoun M: J Am Coll Cardiol, 2012; 59; 2366-73

13.. Kramer DG, Trikalinos TA, Kent DM: J Am Coll Cardiol, 2010; 56; 392-406

14.. Kachboura S, Ben Halima A, Ibn Elhadj : Ann Cardiol Angeiol (Paris), 2014; 63; 17-22

15.. Martens P, Verbrugge FH, Nijst P: J Card Fail, 2017; 23; 597-605

16.. Duchenne J, Turco A, Ünlü S: Circ Arrhythm Electrophysiol, 2019; 12; e007224

17.. Knight BP, Desai A, Coman J: J Am Coll Cardiol, 2004; 44; 72-77

18.. Schuchert A, Muto C, Maounis T: Europace, 2013; 15; 71-76

19.. Ypenburg C, Van Bommel RJ, Marsan NA: Am J Cardiol, 2008; 102; 718-21


13 May 2022 : Case report  Japan

A case of exacerbation of haloperidol-induced rhabdomyolysis following the onset of COVID-19

Am J Case Rep In Press; DOI: 10.12659/AJCR.936589  

13 May 2022 : Case report  USA

Acute Disseminated Encephalomyelitis After SARS-CoV-2 Vaccination

Am J Case Rep In Press; DOI: 10.12659/AJCR.936574  

20 April 2022 : Case report  Indonesia

Progressive Worsening of Neurological Manifestations in HIV-Associated Opportunistic Central Nervous System...

Am J Case Rep In Press; DOI: 10.12659/AJCR.936257  

20 April 2022 : Case report  USA

A 62-Year-Old Man Presenting with Bilateral Tremor of the Upper Limb After a Diagnosis of COVID-19 with Con...

Am J Case Rep In Press; DOI: 10.12659/AJCR.934955  

In Press

16 May 2022 : Case report  Saudi Arabia

Primary Central Nervous System Burkitt Lymphoma, Presenting with Long-Term Fluctuating Level of Consciousne...

Am J Case Rep In Press; DOI: 10.12659/AJCR.936401  

16 May 2022 : Case report  USA

Long-Term Efficacy of Dupilumab in Alopecia Areata

Am J Case Rep In Press; DOI: 10.12659/AJCR.936488  

16 May 2022 : Case report  USA

Stellate Hypopigmentation in a Pediatric Patient After Treatment with Intralesionally-Injected Corticosteroid

Am J Case Rep In Press; DOI: 10.12659/AJCR.935898  

13 May 2022 : Case report  Japan

A case of exacerbation of haloperidol-induced rhabdomyolysis following the onset of COVID-19

Am J Case Rep In Press; DOI: 10.12659/AJCR.936589  

Most Viewed Current Articles

23 Feb 2022 : Case report  USA

Penile Necrosis Associated with Local Intravenous Injection of Cocaine

DOI :10.12659/AJCR.935250

Am J Case Rep 2022; 23:e935250

17 Feb 2022 : Case report  Oman

Myocarditis, Pulmonary Hemorrhage, and Extensive Myositis with Rhabdomyolysis 12 Days After First Dose of P...

DOI :10.12659/AJCR.934399

Am J Case Rep 2022; 23:e934399

06 Dec 2021 : Case report  Brazil

Lipedema Can Be Treated Non-Surgically: A Report of 5 Cases

DOI :10.12659/AJCR.934406

Am J Case Rep 2021; 22:e934406

19 Feb 2022 : Case report  USA

A Rare Case of Coronavirus Disease 2019 Vaccine-Associated Cerebral Venous Sinus Thrombosis Treated with Me...

DOI :10.12659/AJCR.935355

Am J Case Rep 2022; 23:e935355

Your Privacy

We use cookies to ensure the functionality of our website, to personalize content and advertising, to provide social media features, and to analyze our traffic. If you allow us to do so, we also inform our social media, advertising and analysis partners about your use of our website, You can decise for yourself which categories you you want to deny or allow. Please note that based on your settings not all functionalities of the site are available. View our privacy policy.

American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923