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Pulmonary valve infective endocarditis caused by Mycobacterium abscessus

Abstract

Infective endocarditis caused by Mycobacterium abscessus is an uncommon event that, when it does occur, usually requires surgical valve replacement. The pulmonary valve is the least common heart valve involved in infective endocarditis. We present a rare case of isolated pulmonary valve endocarditis with Mycobacterium abscessus in a patient with recurrent sternal infections following repeated coronary artery bypass.

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Introduction

Right-sided infective endocarditis represents less than 10% of all infective endocarditis cases, with pulmonary valve involvement in less than 2% of cases [1]. Although rare, the incidence of right-sided infective endocarditis has steadily risen because of the increasing use of intravenous drugs [2]. In this report, we present a rare case of isolated pulmonary valve endocarditis attributable to Mycobacterium abscessus in a patient with recurrent sternal infections.

Case report

A 54-year-old male with a history of coronary artery disease, type II diabetes mellitus, hypertension, and past surgical history of coronary artery bypass grafting (CABG) presented to his primary care physician with chest pain. He was found to have significant coronary artery restenosis and underwent a redo sternotomy and CABG. During his redo CABG, an intraoperative injury to the pulmonary artery outflow tract necessitated pulmonary valve replacement with a 27 mm homograft valve and repair of the pulmonary artery with patch angioplasty.

Approximately one month following surgery, he presented with malodorous discharge from his sternal incision, requiring debridement with the placement of a Jackson-Pratt drain (Figs. 1 and 2). After sternal debridement, the patient was found to have persistent purulent drainage requiring additional six weeks of intravenous antibiotics along with the continuation of wound vacuum-assisted closure (VAC) changes. The patient underwent sternal wound washout with the removal of all sternal wires after completing the six-week regimen of antibiotics. Wound VAC therapy was continued, and his antibiotics were changed to Vancomycin and Piperacillin/Tazobactam.

Fig. 1
figure 1

Sternal wound infection prior to transfer to our center

Fig. 2
figure 2

Sternal wound status post debridement and washout

The patient had blood cultures growing Streptococcus dysgalactiae. However, surgical wound cultures showed no growth. Due to persistent sternal infection and sepsis, he was transferred to our center and underwent another sternal wound debridement with bilateral pectoralis major flap coverage and drain placement. The drain was removed before his discharge on post-debridement day seven. After consultation with the infectious disease team, we de-escalated his antibiotics to penicillin for four additional weeks. Cultures from both blood and sternum were negative to date.

Although the patient remained on intravenous antibiotics, he developed a fever of 102 F, and the workup showed concern for an infected subpectoral seroma. The blood culture obtained at this time grew Mycobacterium abscessus. The patient underwent evacuation of the infected seroma with sternal debridement, and cultures of the seroma grew Mycobacterium abscessus and Staphylococcus epidermidis. The patient was subsequently started on sensitive antibiotics for Mycobacterium abscessus.

However, he continued to have persistent intermittent fevers and underwent a radiological workup concerning an infected pulmonary artery pseudoaneurysm (Fig. 3). The patient was found to have an elevated procalcitonin level at 0.85 ng/mL. Given the complex clinical course, we discussed his case with our multidisciplinary team, and a week later, he underwent a redo sternotomy, resection of the pulmonary artery pseudoaneurysm with fresh pulmonary valve replacement, and chest wall reconstruction with a pectoralis muscle flap. Surgical cultures from the resected pulmonary artery pseudoaneurysm and the removed prosthetic pulmonary valve vegetations showed acid-fast bacilli. Wound cultures from the pulmonary valve also grew Mycobacterium abscessus. Based on sensitivities, he was started on amikacin, imipenem, and tigecycline. He was ultimately discharged to home on postoperative day 20 in stable condition. He has been followed up in the clinic and continued doing well two years after his most recent redo pulmonary valve surgery, with no evidence of acute or chronic infection.

Fig. 3
figure 3

CT scan illustrating infected pulmonary artery pseudoaneurysm

Discussion

Most infective endocarditis affects the left heart, and the most common organism is Staphylococcus aureus [3]. The right-sided endocarditis heart is much less common, and it usually involves the tricuspid valve when it does occur. Pulmonary valve endocarditis is even less common, accounting for less than 2% of all infective endocarditis cases [4]. Risk factors for the disease include intravenous drug use, central venous catheters, cyanotic congenital heart disease, and degenerative valve lesions. A 400-fold increase is observed in patients with prosthetic valves and a prior history of endocarditis [5]. In a retrospective study of 24 patients with pulmonary valve endocarditis, most had received prosthetic mechanical, autograft, or homograft valves [6].

Mycobacterium abscessus is a non-tuberculous, rapidly growing mycobacterium species that is exceptionally drug-resistant. It commonly infects indwelling medical devices such as catheters and prosthetic valves but is an uncommon agent of endocarditis. Through a literature search using PubMed/Medline, we identified 20 cases reporting infective endocarditis caused by Mycobacterium abscessus, including a review article summarizing ten cases published on or before 2008 and another ten sporadical cases published after 2008 (Table 1) [7,8,9,10,11,12,13,14,15,16,17]. Among these, eight (40%) involved prosthetic valve infections. The associated in-hospital mortality with endocarditis caused by Mycobacterium abscessus was very high (n = 12, 60%), despite surgery and prolonged antimicrobial therapy. Of note, only one case (5%) involved the pulmonary valve.

Table 1 Infective endocarditis caused by Mycobacterium abscessus published in the literature

Our patient had a sternal wound infection which may have seeded the infective endocarditis. Cultures from deep sternal wound infections often grow Staphylococcus aureus, coagulase-negative Staphylococcus species, and multiple mixed organisms [18]. Sternal mycobacterial infections are very uncommon, which further contributes to the uniqueness of this case.

Conclusion

In summary, our patient represents the conjunction of several unusual clinical events, including isolated pulmonary valve infective endocarditis and Mycobacterium abscessus infection. This case highlights that mycobacterial infections may be difficult to identify, resistant to antibiotics and debridement therapy, and consequential in the outcome.

Availability of data and materials

The raw data are available on reasonable request due to privacy or ethical restrictions.

References

  1. Akinosoglou K, Apostolakis E, Koutsogiannis N, Leivaditis V, Gogos CA. Right-sided infective endocarditis: surgical management. Eur J Cardiothorac Surg. 2012;42(3):470–9.

    Article  PubMed  Google Scholar 

  2. Deo SV, Raza S, Kalra A, et al. Admissions for infective endocarditis in intravenous drug users. J Am Coll Cardiol. 2018;71(14):1596–7.

    Article  PubMed  Google Scholar 

  3. Baddour LM, Wilson WR, Bayer AS, et al. Infective endocarditis in adults: diagnosis, antimicrobial therapy, and management of complications: a Scientific Statement for Healthcare Professionals from the American Heart Association. Circulation. 2015;132(15):1435–86.

    Article  CAS  PubMed  Google Scholar 

  4. Datar Y, Yin K, Wang Y, et al. Surgical outcomes of pulmonary valve infective endocarditis: a US population-based analysis. Int J Cardiol. 2022;361:50–4.

    Article  PubMed  Google Scholar 

  5. Steckelberg JM, Wilson WR. Risk factors for infective endocarditis. Infect Dis Clin North Am. 1993;7(1):9–19.

    Article  CAS  PubMed  Google Scholar 

  6. Isaza N, Shrestha NK, Gordon S, et al. Contemporary outcomes of Pulmonary Valve Endocarditis: a 16-Year single centre experience. Heart Lung Circ. 2020;29(12):1799–807.

    Article  PubMed  Google Scholar 

  7. Tsai WC, Hsieh HC, Su HM, et al. Mycobacterium abscessus endocarditis: a case report and literature review. Kaohsiung J Med Sci. 2008;24(9):481–6.

    Article  PubMed  Google Scholar 

  8. Williamson JC, Miano TA, Morgan MR, Palavecino EL. Fatal Mycobacterium abscessus endocarditis misidentified as Corynebacterium spp. Scand J Infect Dis. 2010;42(3):222–4.

    Article  PubMed  Google Scholar 

  9. Al-Benwan K, Ahmad S, Mokaddas E, Johny M, Kapoor MM. Diagnosis of endocarditis caused by Mycobacterium abscessus. Ann Saudi Med. 2010;30(5):408–11.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Garcia DC, Nascimento R, Soto V, Mendoza CE. A rare native mitral valve endocarditis successfully treated after surgical correction. BMJ Case Rep. 2014;2014:bcr2013202610.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Mahajan S, Mishra V, Sorabjee J. Mycobacterium abscessus: causing fatal endocarditis after cardiac catheterization. J Postgrad Med. 2015;61(2):131–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Huth RG, Douglass E, Mondy K, Vasireddy S, Wallace RJ. Treatment of Mycobacterium abscessus subsp. massiliense tricuspid valve endocarditis. Emerg Infect Dis. 2015;21(3):535–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Rodge G, Nagvekar V, Jhala D, George A. Mycobacterium abscessus causing native valve endocarditis due to peripherally inserted central catheter line. J Clin Tuberc Other Mycobact Dis. 2017;9:19–20.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Beatty N, Brown C, Zangeneh T, Al Mohajer M. A rare case of Mycobacterium abscessus subspecies abscessus prosthetic valve endocarditis and the clinical importance of inducible erm(41) gene testing. BMJ Case Rep. 2017;2017:bcr2017219618.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Sharma A, Mundi I, Behal K, Kaur N, Singh P, Mahant M. Fever work-up unfolds a rare diagnosis of native valve endocarditis caused by Mycobacterium abscessus. Indian J Pathol Microbiol. 2019;62(4):589–91.

    Article  PubMed  Google Scholar 

  16. Rahi MS, Reyes SP, Parekh J, Gunasekaran K, Amoah K, Rudolph D. Disseminated Mycobacterium abscessus infection and native valve endocarditis. Respir Med Case Rep. 2021;32:101331.

    PubMed  PubMed Central  Google Scholar 

  17. Maheshwarappa HM, Machanalli G, Thilakchand KR, Tejaswini DD. Story of an abscess: a case of Mycobacterium abscessus infection in an Immunocompetent patient. Indian J Crit Care Med. 2022;26(4):533–4.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Habib G, Hoen B, Tornos P, et al. Guidelines on the prevention, diagnosis, and treatment of infective endocarditis (new version 2009): the Task Force on the Prevention, diagnosis, and treatment of infective endocarditis of the European Society of Cardiology (ESC). Endorsed by the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) and the International Society of Chemotherapy (ISC) for infection and Cancer. Eur Heart J. 2009;30(19):2369–413.

    Article  PubMed  Google Scholar 

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Contributions

MJB conceived and designed this study. OAO collected the data. OAO, SHS, and KY drafted the initial manuscript with critical feedback from MJB. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kanhua Yin.

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Olatidoye, O.A., Samat, S.H., Yin, K. et al. Pulmonary valve infective endocarditis caused by Mycobacterium abscessus. J Cardiothorac Surg 18, 221 (2023). https://doi.org/10.1186/s13019-023-02336-9

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