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CASE REPORT Interactive CardioVascular and Thoracic Surgery 14 (2012) 872–874 doi:10.1093/icvts/ivs084 Advance Access publication 14 March 2012 Candidal mediastinitis successfully treated using vacuum-assisted closure following open-heart surgery Hiroaki Osada*, Hiroyuki Nakajima, Manabu Morishima and Takamitsu Su Department of Cardiovascular Surgery, Mitsubishi Kyoto Hospital, Kyoto, Japan * Corresponding author. Department of Cardiovascular Surgery, Mitsubishi Kyoto Hospital, 1 Katsuragoshomachi, Nishikyo-ku, Kyoto 615-8087, Japan. Tel: +81-75-3812111; fax: +81-75-3927952; e-mail: [email protected] (H. Osada). Received 28 November 2011; received in revised form 26 January 2012; accepted 14 February 2012 Abstract Deep sternal wound infections (DSWIs) are an uncommon but serious complication after open-heart surgery. The reported incidence of DSWIs due to Candida albicans is 0.4%, but these infections have an extremely high mortality of 56%. We herein report a rare case of a 79-year old woman who suffered from Candidal DSWI after repeated open-heart surgeries. We treated her with negative pressure wound therapy (NPWT). This is the rare case report that provides evidence that NPWT is a safe and suitable technique for the management of Candidal DSWIs. Keywords: Antibiotics • Mediastinal infection • Postoperative care • Candidal infection • Surgical site infection INTRODUCTION Deep sternal wound infection (DSWI) including osteomyelitis and mediastinitis due to Candida albicans following open-heart surgery is relatively rare. Once it occurs, however, extremely high mortality and morbidity are unavoidable. MATERIALS AND METHODS A 79-year old woman was admitted to our hospital with a diagnosis of recent myocardial infarction of the inferior wall. Coronary angiography showed total occlusion of the proximal right coronary artery and severe stenosis of the proximal left anterior descending and left circumflex arteries. Severe tricuspid regurgitation was also evaluated by echocardiography. We performed coronary artery bypass grafting and tricuspid annuloplasty with a 30-mm MC3 annuloplasty ring (Edwards Lifesciences, Irvine, CA, USA) under a standard cardiopulmonary bypass. Because the inferior wall appeared to have undergone haemorrhagic infarction, we avoided anastomosis to the right coronary artery. The postoperative course was good, but a left ventricular aneurysm with a diameter of 20 mm × 14 mm at the basal inferior wall was revealed by transthoracic echocardiography 10 days after the initial operation. Three months later, because echocardiography revealed a gradually increasing size of ventricular aneurysm, she underwent a second open-heart surgery involving left ventricular aneurysmectomy. The left ventricular aneurysm was closed with a bovine pericardial patch from the left atrium. There was no mitral regurgitation. The posterior mitral leaflet was incised for visualization, and mitral valvuloplasty and annuloplasty with a 26-mm Physio annuloplasty ring (Edwards Lifesciences) were performed. Two weeks after the closure of aneurysm, mitral regurgitation suddenly worsened. Mitral valve replacement was performed urgently with a 25-mm Mosaic porcine bioprosthesis (Medtronic, Inc., Minneapolis, MN, USA) under inotropic support. On the 9th postoperative day after mitral valve replacement, laboratory tests showed a sudden elevation of C-reactive protein 3.65 to 8.25 mg/dl without elevation of white blood cells or high fever. A purulent exudate from the midline skin incision was increased. Chest computed tomography (CT) revealed an abscess forming behind her sternal bone. Therefore, sternal exploration was performed. Her retrosternal space was filled with purulent exudate. Candida albicans was isolated from the sternal bone and mediastinum, and antifungal therapy with micafungin (150 mg, intravenously, once daily) was started. Blood cultures were negative for C. albicans. We initiated negative pressure wound therapy (NPWT) as delivered by the vacuum-assisted closure (VAC) Therapy System (KCI USA, San Antonio, TX, USA) following surgical debridement and irrigation (Fig. 1). Five layers of non-adhesive silicone-coating sheets TREX-C (Fuji Systems Corp., Tokyo, Japan) were placed on the epicardium and aorta, the second and the third layers of polyurethane foam was placed between the sternal edges and between the pectoral muscle edges. The wound was sealed with a drape, and an evacuation tube was connected to a continuous vacuum source (Fig. 2). Continuous negative pressure was maintained at −50 mmHg. She was able to walk around with the device for rehabilitation. The wound filler was changed every 2–4 days under general anaesthesia with debridement, partial sternectomy and irrigation before a definitive secondary wound closure could be performed. After 13 debridements and irrigations (six weeks from sternal exploration), we confirmed a negative fungal culture in the wound swab. © The Author 2012. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved. H. Osada et al. / Interactive CardioVascular and Thoracic Surgery Figure 1: Frequent debridement of necrotic tissue and irrigation were required. Figure 2: The wound was sealed with a drape, and an evacuation tube was connected to a continuous vacuum source. Therefore, we performed the transposition of the greater omentum and closed the chest wall using a major pectoral muscle. Because of a skin rash, micafungin was discontinued in 3 weeks. Intravenous fluconazole (200 mg once daily) was administered for 8 weeks and was then converted to oral therapy (100 mg twice daily). She developed acute heart failure and required inotropes to control the condition twice during hospitalization. 873 multifactorial. In 2009, Modrau et al. [1] stated that the risk factors of Candidal DSWI were Candidal colonization in tracheal secretions or urine and reoperation before the diagnosis of DSWI. Risnes et al. [3] reported that diabetes, obesity, chronic obstructive pulmonary disease and age are important independent risk factors for mediastinitis. For this patient, age and Candidal colonization in urine seemed to be significant risk factors for DSWI. Moreover, frequent sternotomy procedures should have been avoided. In a randomized trial, Armstrong and Lavery [4] introduced the effectiveness of NPWT with a VAC therapy system for a diabetic foot in 2005. Several management techniques have been discussed in patients with DSWI [5, 6]. Tocco et al. [7] and Petzina et al. [8] reported the effectiveness of NPWT for poststernotomy mediastinitis that reduces the mortality rate and sternal reinfection compared with conventional treatment. Generally, the initiation of NPWT is a contraindication for wounds in which the cardiac surface directly touches the device because of the fear of haemorrhage. We initiated NPWT with a non-adhesive silicone-coating sheet on the cardiac surface and minimum low negative pressure of −50 mmHg. Major complications, such as active haemorrhage and impairment of cardiac function, were not seen. Malani et al. reported 11 cases of DSWI due to C. albicans. They stated that azole therapy must be provided for at least six months and longer if CT reveals bone destruction [9]. Based on this recommendation, we have used micafungin for three weeks and fluconazole for eight weeks intravenously and will continue oral fluconazole therapy even after discharge. A combination of NPWT with a VAC therapy system and conventional treatment, including surgical debridement, transposition of the greater omentum and intravenous antifungal therapy, led to this patient’s favourable outcome. This is preferable for the management of DSWI due to C. albicans. Although the device we used probably allowed for better patient performance during hospitalization, further study is needed to discuss if the secondary wound closure have been actually shortened. In summary, this case report provides evidence that our technique for DSWI may represent a viable therapeutic approach for patients with C. albicans infection. Conflict of interest: none declared. RESULTS DISCUSSION Although the most commonly isolated pathogens in primary DSWI are Staphylococcus epidermidis, S. aureus and gramnegative bacteria, Candidal DSWI is clinically rare. Although the incidence is estimated to be 0.4% in open-heart surgery patients [1], Candidal DSWI has an extremely high mortality rate of 56% [2] during perioperative care. The incidence of Candidal DSWI is [1] Modrau IS, Ejlertsen T, Rasmussen BS. Emerging role of Candida in deep sternal wound infection. Ann Thorac Surg 2009;88:1905–9. [2] Clancy CJ, Nguyen MH, Morris AJ. Candidal mediastinitis: an emerging clinical entity. Clin Infect Dis 1997;25:608–13. [3] Risnes I, Abdelnoor M, Almdahl SM, Svennevig JL. Mediastinitis after coronary artery bypass grafting risk factors and long-term survival. Ann Thorac Surg 2010;89:1502–10. [4] Armstrong DG, Lavery LA. Negative pressure wound therapy after partial diabetic foot amputation: a multicentre, randomized controlled trial. Lancet 2005;366:1704–10. [5] Gustafsson RI, Sjogren J, Ingemansson R. Deep sternal wound infection: a sternal –sparing technique with vacuum-assisted closure therapy. Ann Thorac Surg 2003;76:2048–53. [6] Sjogren J, Nilsson J, Gustafsson R, Malmsjo M, Ingemansson R. The impact of vaccum-assisted closure on long-term survival after post-sternotomy mediastinitis. Ann Thorac Surg 2005;80:1270–5. CARDIAC GENERAL REFERENCES After rehabilitation and treatment for several comorbidities, she recovered completely with no sequelae. She was discharged after six weeks of VAC therapy and 11 weeks of antifungal therapy. 874 H. Osada et al. / Interactive CardioVascular and Thoracic Surgery [7] Tocco MP, Costantino A, Ballardini M, D’Andrea C, Masala M, Mosillo L et al. Improved results of the vacuum assisted closure and Nitinol clips sternal closure after postoperative deep sternal wound infection. Euro J Cardiothorac Surg 2009;35:833–8. [8] Petzina R, Hoffmann J, Navasardyan A, Malmsjo M, Stamm C, Unbehaun A et al. Negative pressure wound therapy for post-sternotomy mediastinitis reduces mortality rate and sternal re-infection rate compared to conventional treatment. Euro J Cardiothorac Surg 2010; 38:110–3. [9] Malani PN, McNeil SA, Bradley SF, Kauffman CA. Candida albicans sternal wound infections: a chronic and recurrent complication of median sternotomy. Clin Infect Dis 2001;35:1316–20.