Abstract
Implantable cardioverter defibrillator lead endocarditis due to Brucella melitensis is a rare and life-threatening complication of brucellosis. Successful management requires a combination of medical treatment and device extraction. We present a case of relapsing brucellosis manifested as infective endocarditis colonizing the lead of the implantable cardioverter defibrillator with formation of vegetation on the lead. A 63-year-old male presented to the rehabilitation unit with hypotension. No other signs of infection were noted. The patient had a history of drinking unpasteurized milk since childhood and a previous episode of Brucella infective endocarditis. A transthoracic echocardiography showed an oscillating vegetation on the lead of the tip of the right atrial ICD, and the blood cultures were positive for Brucella melitensis. Surgical removal of the device was infeasible, and medical management was the only feasible option in this case.
1. Introduction
Brucellosis is one of the most encountered endemic zoonoses in many developing regions including the Middle East (ME), sub-Saharan Africa, South Asia, and South America [1]. This disease is caused by Brucella melitensis, a gram-negative, nonencapsulated, nonmotile, facultative intracellular coccobacillus [2, 3]. The mode of transmission of this infection is from infected animals to humans through either direct contact such as cut and aerosol inhalation or indirect contact such as ingestion of unpasteurized dairy products, urine, tissues, and products of conception (placenta) [4, 5]. Consumption of unpasteurized dairy products from contaminated milk is the main pathway of spread globally, especially in the Middle East [6].
Brucellosis presents with a broad spectrum of clinical manifestations including fever, arthralgia, myalgia, and back pain, and it is sometimes complicated with endocarditis, neurobrucellosis, and epididymo-orchitis [7]. Cardiovascular involvement is prevalent in 1% of brucellosis patients, with endocarditis being the most serious form and leading to brucellosis-related mortality [7, 8]. Although endocarditis caused by infection of a prosthetic device or implant is a rare complication of brucellosis, the most suitable therapeutic approach in this scenario is to remove the device. However, oftentimes the presence of multiple comorbidities and other factors, such as age, renders surgical management an infeasible approach, and the only option is to retain the device and place the patient on a prolonged antimicrobial treatment [9]. Due to the low number of reported cases of brucella infective endocarditis with device colonization, there is lack of consensus on the most appropriate approach for the management of these patients who are not candidates for surgery [10, 11].
A review of the literature revealed that about 25% of the reported cases of Cardiac Device-Related Brucella Endocarditis (CDRBrE) were in the Middle East [11–16]. In this report, we aim to describe the first case of recurrent brucellosis manifested as infective endocarditis colonizing the lead of the implanted cardioverter defibrillator (ICD) with formation of vegetation on the lead. To the best of our knowledge, this is also the first study to provide a comprehensive summary of CDRBrE cases reported in the literature.
2. Case Presentation
A 64-year-old Egyptian gentleman residing in Qatar, he has a long-standing history of hypertension, atrial fibrillation, and idiopathic dilated cardiomyopathy with a low ejection fraction (LV EF 26%), underwent implantation of a cardiac resynchronization therapy device (CRT-D) in 2013. Two years later, the CRT-D was downgraded to ICD.
On February 11th, 2020, the patient suffered from an ischemic stroke in the right middle cerebral artery for which he required decompressive craniectomy. Shortly after the procedure, his hospital stay was complicated with fever and malaise. Ingestion of partially boiled cow's milk was noted from the history. Blood cultures were positive for Streptococcus pneumoniae and Brucella melitensis. Based on these results, he was diagnosed with pneumonia and brucellosis, and antibiotics were commenced for treatment. As a result of the stroke, the patient suffered from hemiplegia which left him bed-bound and shifted to a rehabilitation centre for continuity of care. There, the patient showed only minor improvements in speech, but none in mobility. Nevertheless, the family refused to transfer him to a multispecialty hospital that provides medical, surgical, and long-term care.
On November 20th, 2020, while the patient was still in the rehabilitation centre, his health started to deteriorate. He was found to be hypotensive with a blood pressure of 80/40, but afebrile with an oral temperature of 37.0°C. His heart rate and respiratory rate were 93 beats/minute and 18 breaths/minute, respectively. Physical examination revealed no skin changes over the ICD pocket, no cardiac murmurs on auscultation, and no apparent localized signs of infection. Blood tests revealed a normal white blood cell count (5 × 103 cells/mm3) and high C-reactive protein level (77 mg/L). Blood cultures were positive for Brucella melitensis. These tests were followed with transthoracic echocardiography which showed a single oscillating mass measuring 0.8 × 0.4 cm attached to the tip of the right atrial lead of the ICD suggestive of vegetation (Figure 1).
Figure 1.

Vegetationson top of ICD lead. Transthoracic echocardiography, apical four-chamber view showing a large vegetation on the top of ICD atrial lead in a case of brucella endocarditis.
The patient was then transferred to the Heart Hospital as a case of relapsing brucellosis with brucella endocarditis and ICD-lead colonization. The Infectious Disease Team was consulted, and three-drug regimen was commenced including rifampicin (600 mg/day), gentamicin (5 mg/kg/day), and doxycycline (200 mg/day). Gentamicin was then increased to 7 mg/kg/day as the postdose peak levels were low, and trimethoprim/sulfamethoxazole (960 mg/12 h) was added to the treatment, with a recommendation to remove the ICD. A transesophageal echocardiography (TEE) was tried but was technically difficult to conduct due to the restricted neck movements and limited jaw mobility of the patient, which rendered the TEE probe impossible to insert. Therefore, a positron emission tomography (PET) scan was performed to confirm the nature of the vegetation, yet the results were being inconclusive.
The case was discussed in a multidisciplinary team (MDT) meeting, and all possibilities to deal with this infected ICD wires were explored. Due to the unavailability of laser-assisted lead extraction, surgery was proposed as an option; however, because of the patient's general condition, surgical removal was considered a high-risk procedure, and the final decision was to keep the ICD in place and to treat him conservatively with antibiotics. Another PET scan was requested that was also inconclusive, and a repeated echocardiogram revealed a slight increase in vegetative size (0.8 × 0.6 cm). Eventually, Gentamicin was stopped due to renal impairment.
On December 17th, 2020, the patient was medically fit for discharge and was sent home with oral antibiotics for 6 weeks.
On March 29th, 2021, the patient was doing well and still on oral antibiotics.
3. Discussion
Brucella infective endocarditis is a rare and life-threatening complication of brucellosis. A systematic review assessing the clinical manifestations of brucellosis revealed brucellosis-associated endocarditis was prevalent in an overall 1% of patients [7]. Another study found that 1 in 23 CDRIE cases was caused by Brucella melitensis [15]. Nevertheless, despite its low prevalence and insidious progression, infective endocarditis is a very severe complication of brucellosis, and it has been reported in a few of Cardiac Device-Related Infective Endocarditis (CDRIE) cases. In our review of 14 published CDRBrE cases, we found that 11 patients were males, two were females, and one was unidentified, none of them with involvement of the device lead. Moreover, their ages ranged between 38 and 82 years old (Table 1).
Table 1.
Case reports of brucellosis involving pacemakers and cardiac devices.
| Study/year | Country | Gender | Age (years) | Type of device | Brucella relapse | Brucella blood culture | Miscellaneous cultures | Device and leads removed | Antibiotics | Treatment duration |
|---|---|---|---|---|---|---|---|---|---|---|
| de la Fuente et al. [28] | Spain | Male | 63 | Chamber end cavitary pacemaker | Yes | No | Pacemaker, leads, pus, necrotic tissue | Yes | Doxycycline Rifampin Streptomycin |
45 days 45 days 21 days |
| Francia et al. [29] | Spain | Male | 71 | Pacemaker | Yes | No | Pacemaker and leads. Negative TEE | Yes | Doxycycline Rifampin |
6 weeks 8 weeks |
| Ulkar et al. [12] | Turkey | Male | 68 | Pacemaker | No | Yes | Abscess culture | Yes | Doxycycline Rifampin |
6 weeks 6 weeks |
| Miragliotta et al. [10] | Italy | Female | 70 | Single-chamber pacemaker | Yes | Yes | Cutaneous swab from fresh wound of recent removal and replacement of pacemaker | No | Rifampicin Ciprofloxacin Minocycline |
6 weeks 6 weeks 6 weeks |
| Dourakis et al. [17] | Greece | Male | 70 | ICD | Yes | Yes | TEE showed mass on tricuspid, pacemaker, and leads had vegetation | Yes | Doxycycline Ciprofloxacin Rifampin |
12 months 12 months 12 months |
| Al-Majid [13] | Saudi Arabia | Male | 38 | Pacemaker | Yes | Yes | Leads | Yes | Doxycycline Rifampin |
6 weeks 6 weeks |
| Gungor et al. [14] | Turkey | Male | 61 | Pacemaker | No | Yes | Ultrasonography revealed an abscess and a fistula. Cultures from sputum samples, drained materials from the abscess, and the pacemaker pocket |
Yes | Doxycycline Rifampin |
6 weeks 6 weeks |
| Osmonov et al. [15] | Turkey | N/A | N/A | Pacemaker | N/A | Yes | Lead culture TEE showed vegetation |
Yes | N/A | 6 weeks |
| Elmardi et al. [16] | Saudi Arabia | Female | 54 | ICD | No | No | TEE showed large masses attached to all leads. Culture from pocket fluid and tissues |
Yes | N/A | N/A |
| Saudi Arabia | Male | 52 | Single-chamber ICD | Yes | No | Culture from pocket tissue | Yes | Cotrimoxazole Doxycycline Gentamicin |
N/A | |
| Al-Adsani and Al-Mousa [11] | Kuwaiti | Male | 70 | Pacemaker | No | Yes | Transthoracic echo showed calcification and thickening of the aortic valve with two mobile masses attached to the aortic valve. TEE was unremarkable. |
No | Doxycycline Rifampin Cotrimoxazole Gentamicin |
3 months 3 months 3 months 2 weeks |
| Dhand and Ross [18] | United States | Male | 66 | ICD | No | No | Cultures from superficial specimen, tissue from the pocket, ICD, and leads | Yes | Gentamicin Ciprofloxacin Doxycycline |
6 weeks 6 weeks |
| Enjalbert et al. [30] | France | Male | 65 | ICD | N/A | No | Culture from device | Yes | N/A | N/A |
| Kanji and Saxinger [19] | Canada | Male | 82 | Pacemaker | No | No | Cultures from leads and ventricular tissue | Yes | Gentamicin Doxycycline Rifampin |
12 weeks 12 weeks |
Diagnosing brucellosis begins with an assessment of epidemiological factors. Our patient mentioned a history of drinking unpasteurized milk since childhood. A history of contact with animals (sheep and goats), consumption of dairy products, or consumption of uncooked meat was noted in several studies as a common trait of the majority of brucellosis patients [11, 12, 16–19]. An assay of blood, bone marrow, or other body fluids or tissue cultures are considered the gold standards for the diagnosis of brucellosis.
However, it is imperative to underscore that Brucella is a fastidious bacteria requires special culture media with a variable and more prolonged incubation period, which could justify why only seven patients had positive blood cultures (Table 1). There are multiple serological tests used to diagnose brucellosis, with the most common being the serum agglutination test. In general, agglutination titres ≥ 1 : 160 are considered diagnostic, although a titre of ≥1 : 320 is considered diagnostic in endemic areas. Enzyme-linked immunosorbent assay (ELISA) is another popular serological method used to diagnose brucellosis. ELISA detects total Brucella immune-specific IgM, IgA, and IgG immunoglobulins [20–22].
Optimal management of CDRIE should include removal of the whole device and prolonged antibiotic therapy to eradicate the pathogen from the body, especially in the presence of unusual organisms such as Brucella melitensis. This treatment is also recommended when CDRIE is suspected in the case of occult infections without any known source of disease [9]. Considering the inherent risk of an open surgical operation, our patient was deemed a high-risk candidate for surgical device removal and medical management was adopted in place [23]. The same approach was reported in two other studies on brucella CDRIE with good outcomes. In both studies, the patients had an implanted pacemaker which was not removed, while they received medical treatment for brucellosis. Follow-up examination revealed that they were both in good condition without any remaining signs of infection, and no recurrence of the illness was reported (Table 1) [10, 11]. On the other hand, other studies show that medical therapy alone is associated with high risk of disease recurrence and mortality [24]. It remains to be seen in the near future whether our patient and the patients in the previous studies will remain disease-free [10, 11]. In most cases of brucella CDRIE, device removal and lead extraction followed by extended antibiotic therapy are required for the effective treatment of this disease (Table 1).
Nuclear studies such as positron emission tomography (PET) scan and single photon emission computed tomography (SPECT) are used in the diagnosis of the difficult cases of device-related endocarditis [25]; however, in our patient, the result of PET scan was inconclusive because of the intense physiologic left ventricular myocardial uptake, and the area of the right ventricle lead could not be evaluated.
The proposed therapy for brucellosis endocarditis by the European Society of Cardiology (ESC) includes doxycycline (200 mg/24 h), cotrimoxazole (trimethoprim and sulfamethoxazole) (960 mg/12 h), and rifampin (300–600/24 h) for 3–6 months, with some recommending gentamicin to be added for the first 3 weeks, while the addition of streptomycin (15 mg/kg/24 h in 2 doses) for the first few weeks is optional [9]. An alternative regimen includes doxycycline and rifampin for a total of 6 weeks, but this regimen shows a higher failure rate, and it is not recommended for osteoarticular disease [25]. The relapse rate in patients treated with the latter is 14.4% and 22.6% [26, 27]. In our case, we followed the recommendations of ESC and used a combination of rifampicin (600 mg/day), doxycycline (200 mg/day), septrin (trimethoprim and sulfamethoxazole) (960 mg/12 h), and gentamicin (7 mg/kg/day); the latter administered at a low dose for fear of renal impairment. Only one study adopted this medical management and reported good outcomes with no relapse up to date [11]. A study that reported multiple relapses used rifampicin (600 mg/day) and minocycline (100 mg bd), for 12 weeks; rifampicin (600 mg/day) and ciprofloxacin (500 mg bd), for 6 weeks; rifampicin (600 mg/day), trimethoprim-sulfamethoxazole (2 g intravenous bd), and minocycline (100 mg bd); rifampicin, ciprofloxacin, and minocycline, for 6 weeks, on 4 separate occasions for treatment [10].
Interestingly, brucella CDRIE can occur practically at any time after device implantation, where relapse of brucella CDRIE was noted in six cases as well as in our patient (Table 1) [10, 13, 16, 17, 28, 29]. Routine follow-ups should be a requirement in cases of systemic brucella infection to avoid overlooking the rare complication of relapsing infective endocarditis. This must be implemented in the care plan of our patient and any future patients when surgical intervention is impractical.
4. Conclusion
The present case report highlights the possibility of brucella being an agent that can complicate the placement of an ICD. A high degree of awareness of the possibility of colonization of implanted devices with brucella in patients residing in endemic regions is fundamental for early laboratory recognition of this virulent pathogen to ameliorate the course of the disease. Routine follow-ups must be conducted on patients with ICD recovering from brucellosis who are not good candidates for surgical management.
Acknowledgments
We are thankful to the management of Hamad Medical Corporation for the support.
Abbreviations
- ME:
Middle East
- CDRIE:
Cardiac Device-Related Infective Endocarditis
- ICD:
Implantation of cardioverter defibrillator
- CRT-D:
Cardiac resynchronization therapy device
- TEE:
Transesophageal echocardiography
- PET:
Positron emission tomography
- ESC:
European Society of Cardiology.
Data Availability
The data used to support the findings of this case study are stored in the patient file in the Cerner but restricted by the HMC ethics board in order to protect patient privacy. Data are approachable by the corresponding author and other researchers who meet the criteria for access to confidential data.
Ethical Approval
This case report was approved by the Institutional Review Board (IRB) at (HMC) (MRC 4-21-281).
Consent
Written consent was obtained from the patient.
Conflicts of Interest
The authors declare that they have no conflict of interests.
References
- 1.Franc K. A., Krecek R. C., Häsler B. N., Arenas-Gamboa A. M. Brucellosis remains a neglected disease in the developing world: a call for interdisciplinary action. BMC Public Health. 2018;18(1):p. 125. doi: 10.1186/s12889-017-5016-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Wyatt H. Lessons from the history of brucellosis. Revue Scientifique et Technique de l'OIE. 2013;32(1):17–25. doi: 10.20506/rst.32.1.2181. [DOI] [PubMed] [Google Scholar]
- 3.George F. Update on laboratory diagnosis of human brucellosis. International Journal of Antimicrobial Agents. 2010;36(Supplemnt 1):S12–S17. doi: 10.1016/j.ijantimicag.2010.06.014. [DOI] [PubMed] [Google Scholar]
- 4.Mantur B., Amarnath S., Shinde R. J. Review of clinical and laboratory features of human brucellosis. Indian Journal of Medical Microbiology. 2007;25(3):188–202. doi: 10.1016/S0255-0857(21)02105-8. [DOI] [PubMed] [Google Scholar]
- 5.Heymann D. L. Control of communicable diseases manual: an official report of the American Public Health Association. 18th. Washington DC: World Health Organization/American Public Health Association; 2004. [Google Scholar]
- 6.María Pía F., Maximilian M., Gilman R., Smits H. J. L. I. D. Human brucellosis. The Lancet. 2007;7(12):775–786. doi: 10.1016/S1473-3099(07)70286-4. [DOI] [PubMed] [Google Scholar]
- 7.Dean A. S., Crump L., Greter H., Hattendorf J., Schelling E., Zinsstag J. J. P. N. T. D. Clinical manifestations of human brucellosis: a systematic review and meta-analysis. PLoS Neglected Tropical Diseases. 2012;6(12, article e1929) doi: 10.1371/journal.pntd.0001929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Pappas G., Akritidis N., Bosilkovski M., Tsianos E. Brucellosis. The New England Journal of Medicine. 2005;352(22):2325–2336. doi: 10.1056/NEJMra050570. [DOI] [PubMed] [Google Scholar]
- 9.Habib G., Lancellotti P., Antunes M. J., et al. 2015 ESC guidelines for the management of infective endocarditis. European Heart Journal. 2015;36(44):3075–3128. doi: 10.1093/eurheartj/ehv319. [DOI] [PubMed] [Google Scholar]
- 10.Miragliotta G., Mosca A., Tantimonaco G., De Nittis R., Antonetti R., Di Taranto A. J. I. H. J. Relapsing brucellosis related to pacemaker infection. Italian Heart Journal. 2005;6(7):612–613. [PubMed] [Google Scholar]
- 11.al-Adsani W., Ahmad A., al-Mousa M. A case of Brucella melitensis endocarditis in a patient with cardiovascular implantable electronic device. Infection and drug resistance. 2018;11:387–390. doi: 10.2147/IDR.S152771. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ulkar U. G., Demiray T., Aydoğan H., Dansuk Z., Kocakavak C., Mert A. Pacemaker infection due to Brucella melitensis: a case report. Archives of internal medicine. 2001;161(15):1910–1911. doi: 10.1001/archinte.161.15.1910. [DOI] [PubMed] [Google Scholar]
- 13.Al-Majid F. M. Pacemaker lead endocarditis due to Brucellosis. Saudi Medical Journal. 2010;31(4):448–450. [PubMed] [Google Scholar]
- 14.Gungor O., Yalcin M., Ozel E., Biberoglu K., Topal K. Pacemaker infection due to Brucella melitensis. Hippokratia. 2012;16(4):390–391. [PMC free article] [PubMed] [Google Scholar]
- 15.Osmonov D., Ozcan K. S., Erdinler I., et al. Cardiac device-related endocarditis: 31-years’ experience. Journal of Cardiology. 2013;61(2):175–180. doi: 10.1016/j.jjcc.2012.08.019. [DOI] [PubMed] [Google Scholar]
- 16.Elmardi M., al Hebaishi Y., al Kassab S., et al. Implantable cardioverter device infection due to Brucella melitensis in two patients. Hellenic Journal of Cardiology. 2016;57(4):271–272. doi: 10.1016/j.hjc.2015.06.004. [DOI] [PubMed] [Google Scholar]
- 17.Dourakis S., Sambatakou H., Tsiachris D., Kittou N., Alexopoulou A., Archimandritis A. J. A 70-year-old stock-breeder with tricuspid valve and defibrillator lead brucella endocarditis. International Journal of Cardiology. 2008;126(3):e47–e49. doi: 10.1016/j.ijcard.2007.01.018. [DOI] [PubMed] [Google Scholar]
- 18.Dhand A., Ross J. J. Implantable cardioverter-defibrillator infection due to Brucella melitensis: case report and review of brucellosis of cardiac devices. Clinical Infectious Diseases. 2007;44(4):e37–e39. doi: 10.1086/511079. [DOI] [PubMed] [Google Scholar]
- 19.Kanji J. N., Saxinger L. J. C. Brucella infection at cardiac pacemaker site in a patient who had consumed raw caribou meat in Northern Canada. CMAJ. 2018;190(37):E1108–E1110. doi: 10.1503/cmaj.170234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Franco M. P., Mulder M., Gilman R. H., Smits H. G. Human brucellosis. The Lancet. 2007;7(12):775–786. doi: 10.1016/S1473-3099(07)70286-4. [DOI] [PubMed] [Google Scholar]
- 21.Kasper D., Fauci A. Harrison’s Infectious Diseases. McGraw-Hill Education. 2017. pp. 560–564. 3rd edition.
- 22.del Río A., Anguera I., Miró J. M., et al. Surgical treatment of pacemaker and defibrillator lead endocarditis: the impact of electrode lead extraction on outcome. Chest. 2003;124(4):1451–1459. doi: 10.1378/chest.124.4.1451. [DOI] [PubMed] [Google Scholar]
- 23.Peery T. M., Belter L. F. Brucellosis and heart disease: II. Fatal brucellosis: a review of the literature and report of new cases. The American Journal of Pathology. 1960;36(6):673–697. [PMC free article] [PubMed] [Google Scholar]
- 24.Solís García del Pozo J., Solera J. Systematic review and meta-analysis of randomized clinical trials in the treatment of human brucellosis. PLoS One. 2012;7(2, article e32090) doi: 10.1371/journal.pone.0032090. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Erba P. A., Lancellotti P., Vilacosta I., et al. Recommendations on nuclear and multimodality imaging in IE and CIED infections. European Journal of Nuclear Medicine and Molecular Imaging. 2018;45(10):1795–1815. doi: 10.1007/s00259-018-4025-0. [DOI] [PubMed] [Google Scholar]
- 26.Karabay O., Sencan I., Kayas D., Şahin I. Ofloxacin plus rifampicin versus doxycycline plus rifampicin in the treatment of brucellosis: a randomized clinical trial [ISRCTN11871179] BMC Infectious Diseases. 2004;4(1):p. 18. doi: 10.1186/1471-2334-4-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Hasanain A., Mahdy R., Mohamed A., Ali M. A randomized, comparative study of dual therapy (doxycycline-rifampin) versus triple therapy (doxycycline-rifampin-levofloxacin) for treating acute/subacute brucellosis. The Brazilian Journal of Infectious Diseases. 2016;20(3):250–254. doi: 10.1016/j.bjid.2016.02.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.de la Fuente A., Sanchez J. R., Uriz J., Reparaz J., Lopez-Coronado J. L., Moriones I. J. T. H. I. J. Infection of a pacemaker by Brucella melitensis. Texas Heart Institute Journal. 1997;24(2):129–130. [PMC free article] [PubMed] [Google Scholar]
- 29.Francia E., Domingo P., Sambeat M. A., et al. Pacemaker infection by Brucella melitensis: a rare cause of relapsing brucellosis. Archives of Internal Medicine. 2000;160(21):3327–3328. doi: 10.1001/archinte.160.21.3327. [DOI] [PubMed] [Google Scholar]
- 30.Enjalbert L., Moatti N., Chabanon G., Castany P., Gaurand P. The cardiac pacemaker and melitococcus. La Nouvelle Presse Médicale. 1977;6(4):p. 277. [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data used to support the findings of this case study are stored in the patient file in the Cerner but restricted by the HMC ethics board in order to protect patient privacy. Data are approachable by the corresponding author and other researchers who meet the criteria for access to confidential data.
