| Literature DB >> 32983667 |
Barkat Ali1, Venus Barlas2, Anil K Shetty2, Christopher Demas2, Jess D Schwartz2.
Abstract
The treatment of sternoclavicular joint infection is a topic of controversy. This systematic review aims to evaluate the preferred treatment of sternoclavicular joint infections. A literature search using PubMed/MEDLINE®/Embase databases was conducted to identify publications on the surgical management of sternoclavicular joint infections. Case reports and studies without surgical management were excluded. The outcomes of interest included patient demographics, comorbidities, infectious etiologies, radiographic features, surgical management, and complications. Sixteen articles met the inclusion criteria. The mean age of the subjects was 53.4 years; there was a predominance of males (65%), and a minority of the subjects were obese (15%). The most common infectious etiology was methicillin-susceptible Staphylococcus aureus (MSSA) (48%). CT scan was reported in 46% of cases. The most common treatment was surgical resection of the joints (85%), followed by muscle flap closure of the wounds (54.2%). The complication rate ranged from 0-40%. Specifically, recurrence of infection was low with resection of the joint, followed by muscle flap closure. Given the heterogeneity of the methodology and inconsistency in the outcomes, a meta-analysis could not be performed. Overall, the current literature favors the resection of the sternoclavicular joint as the gold standard treatment. Closure of the wound using muscle flap seems to adequately treat this problem without any major untoward events.Entities:
Keywords: joint resection; muscle flap; sternoclavicular joint infection; surgical management
Year: 2020 PMID: 32983667 PMCID: PMC7510516 DOI: 10.7759/cureus.9963
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Classification of study design
| Level | Strength of evidence | Type of study design |
| I | Good | Meta-analysis of randomized controlled trials |
| II | Large-sample randomized controlled trials (n = ≧25 for each group) | |
| III | Good to fair | Small-sample randomized controlled trials (n = <25 for each group) |
| IV | Non-randomized controlled prospective trials | |
| V | Non-randomized controlled retrospective trials | |
| VI | Fair | Cohort studies |
| VII | Case-control studies | |
| VIII | Poor | Non-controlled clinical series; descriptive studies |
| IX | Anecdotes or case reports |
Mean Coleman methodology score
| Components of the Coleman score (maximum score) | Individual components (score) |
| Study size (10) | >60 (10) |
| 41-60 (7) | |
| 20-40 (4) | |
| <20, not stated (0) | |
| Mean duration of follow-up (5) | >24 (5) |
| 12-24 (2) | |
| <12, not stated or unclear (0) | |
| Number of different surgical procedures included in each reported outcome (10) | 1 surgical procedure only (10) |
| >1 surgical procedure, but >90% undergoing one procedure (7) | |
| Not stated, unclear, or <09% undergoing 1 procedure (0) | |
| Type of study (15) | Randomized control study (15) |
| Prospective cohort study (10) | |
| Retrospective study (0) | |
| Diagnostic certainty (5) | In all (5) |
| In >80% (3) | |
| In <80% (0) | |
| Description of surgical procedure (5) | Adequate (5) |
| Fair (3) | |
| Inadequate (0) | |
| Description of postoperative rehabilitation (10) | Well described, >80% complying (10) |
| Well described with 60%-80% complying (5) | |
| Protocol not reported or <60%-80% complying (0) |
Figure 1Origin of studies
Figure 2Flowsheet for study selection
Characteristics of studies
| Author | Number of patients | Country | Journal | Timeframe | Coleman methodology score | Total |
| Ali et al. (2019) [ | 50 | USA | Seminars in Thoracic and Cardiovascular Surgery | 2004-2018 | 7, 5, 10, 0, 5, 5, 10 | 42 |
| Jang et al. (2019) [ | 22 | Korea | Infectious Diseases (London, England) | 2009-2016 | 4, 5, 10, 0, 5, 5, 0 | 29 |
| Von Glinski et al. (2019) [ | 13 | USA/Germany | Journal of Clinical Orthopaedics and Trauma | 2008-2015 | 0, 0, 10, 0, 5, 3, 0 | 18 |
| Murga et al. (2017) [ | 15 | USA | The Journal of Thoracic Disease | 2001-2014 | 0, 0, 10, 0, 5, 3, 0 | 18 |
| Kachala et al. (2016) [ | 40 | USA | The Annals of Thoracic Surgery | 1992-2012 | 4, 0, 10, 0, 5, 5, 10 | 34 |
| Muesse et al. (2014) [ | 12 | USA | Surgery Research and Practice | 2002-2012 | 0, 0, 0, 0, 5, 3, 0 | 8 |
| Chun et al. (2012) [ | 10 | Korea | Journal of Shoulder and Elbow Surgery | 1996-2008 | 0, 5, 10, 0, 5, 5, 10 | 35 |
| Song et al. (2012) [ | 7 | USA | The Annals of Thoracic Surgery | 0, 5, 10, 0, 5, 5, 0 | 25 | |
| Abu Arab et al. (2011) [ | 14 | Canada/Egypt | The European Journal of Cardio-Thoracic Surgery | 2003-2009 | 0, 0, 0, 0, 5, 0, 0 | 5 |
| Puri et al. (2011) [ | 20 | USA | The Annals of Thoracic Surgery | 2002-2009 | 4, 0, 10, 0, 5, 3, 0 | 22 |
| Nusselt et al. (2011) [ | 5 | Germany | Archives of Orthopaedic and Trauma Surgery | 1992-2007 | 0, 0, 0, 0, 5, 0, 0 | 5 |
| Bakaeen et al. (2008) [ | 5 | USA | The American Journal of Surgery | 1998-2006 | 0, 0, 0, 0, 5, 0, 0 | 5 |
| Kendrick et al. (2007) [ | 7 | USA | The American Surgeon | 1997-2006 | 0, 0, 10, 0, 5, 3, 10 | 28 |
| Ross et al. (2004) [ | 10 | USA | Medicine (Baltimore) | 0, 0, 0, 0, 5, 0, 0 | 5 | |
| Burkhart et al. (2003) [ | 26 | USA | The Journal of Thoracic and Cardiovascular Surgery | 1998-2001 | 4, 5, 7, 0, 5, 5, 10 | 36 |
| Carlos et al. (1997) [ | 8 | USA | The Journal of Thoracic and Cardiovascular Surgery | 1994-1997 | 0, 5, 10, 0, 5, 5, 0 | 25 |
Quality of studies and their conclusions
SCJ: sternoclavicular joint; MCF: myocutaneous flap; DWVT: deep wound vacuum therapy; MRSA: methicillin-resistant Staphylococcus aureus
| Study | Coleman methodology aggregate score | Conclusions |
| Ali et al. (2019) [ | 42 | Wound closure with an MCF (primary or delayed) is associated with less recurrence of infections compared with DWVT closure. Radical resection of the entire SCJ with MCF (primary or delayed) should be considered the preferred management strategy in patients with SCJ infections |
| Burkhart et al. (2003) [ | 36 | If no evidence of abscess or bone destruction is found, parenteral antibiotics should be initiated. When doubt persists as to the diagnosis, incision and drainage can be performed. However, when either abscess or bone destruction exists, advocate resection of the SCJ. Surgical resection combined with muscle transposition provides effective long-term outcome |
| Chun et al. (2012) [ | 35 | Curative resection arthroplasty should be preferentially considered for patients with pyogenic infection of the SCJ |
| Kachala et al. (2016) [ | 34 | Perform joint resection on all patients who can tolerate surgical intervention. Limited surgical intervention or joint aspiration may be warranted when the diagnosis is in question; however, once the joint infection is documented, believe resection is warranted to achieve optimal source control. Primary closure with a muscle flap can achieve similar outcomes to secondary intention in selected patients |
| Jang et al. (2019) [ | 29 | Medical treatment alone or accompanied by limited surgery would appear to be successful therapeutic strategies for the complicated sternoclavicular septic arthritis caused by Staphylococcus aureus in selected patients that do not suffer from major complications. Surgery should be considered in patients with chest wall and/or neck abscesses |
| Kendrick et al. (2007) [ | 28 | Initial treatment usually consists of antibiotics appropriate to the source of infection and results of blood cultures or needle aspirations, and control of the primary site of infection. Septic arthritis of the SCJ may be successfully treated in this fashion; however, the development of osteomyelitis necessitates surgical intervention. Failure of antibiotics to control fever and cellulitis leading to progression of the SCJ phlegmon or radiographic findings of osteomyelitis are evidence of refractory SCJ infection best managed surgically |
| Song et al. (2012) [ | 25 | Aggressive surgical management including resection of the SCJ and involved ribs with pectoralis flap closure would appear to be the preferred treatment for all but the most minor infections of the SCJ. This approach has minimal impact on upper extremity function |
| Carlos et al. (1997) [ | 25 | Most cases of early SCJ infections will respond to conservative measures. However, when radiographic evidence of infection beyond the SCJ is present, en bloc resection, although seemingly aggressive, results in immediate eradication of all infection with negligible functional morbidity. Prolonged antibiotic therapy or continued local drainage procedures appear to have little value in these cases, adding only to patient care costs and the potential sequelae of chronic infections |
| Puri et al. (2011) [ | 22 | For SCJ infection, a single-stage resection and muscle advancement flap lead to a higher incidence of complications. Debridement with open wound care provides satisfactory outcomes with minimal perioperative complications but requires prolonged wound care |
| Von Glinski et al. (2019) [ | 18 | Conservative management alone may suffice in early disease stages, knowing that a significant number of these patients will progress and require surgical intervention. However, recommend a thorough debridement plus SCJ resection followed by antibiotics (as soon as possible adapted to bacterial sensitivity) |
| Murga et al. (2017) [ | 18 | Debridement of the joint is key to early diagnosis for cultures and early treatment. The sooner the patient can get to the operating room for debridement, the sooner the infection can be adequately treated to prevent a worsening infection. Early start of broad-spectrum antibiotics that provide coverage against MRSA infections and early surgical intervention is the ideal treatment. Surgical management should include incision, drainage, and joint resection. The joint should be resected in all cases |
| Muesse et al. (2014) [ | 8 | Treat all patients who need surgical debridement for osteomyelitis of the SCJ with initial incision and debridement followed by two to three weeks of wound care along with antibiotic treatment followed by delayed resection of infected bone and pectoralis major muscle flap advancement into the acquired defect |
| Abu Arab et al. (2011) [ | 5 | Surgery is indicated in cases of SCJ infections after the failure of an antibiotic therapy trial. The type of operation depends on the general condition of the patient and the presence or absence of osteomyelitis. SCJ resection is indicated when there is a recurrence of infection, sinus formation, severe osteomyelitis, and when there is no response to the other forms of surgical treatment |
| Nusselt et al. (2011) [ | 5 | For sufficient infection control, surgical debridement of infected tissue combined with suitable antibiotic therapy is essential. The early stages of infection can be managed by simple incision, debridement, and drainage. In advanced stages of infection, a more radical intervention is preferable |
| Bakaen et al. (2008) [ | 5 | SCJ infections in cirrhotic patients tend to be advanced and extensive in nature and pose a high surgical risk. Clinicians should have a high index of suspicion when a cirrhotic patient presents with SCJ pain in an effort to achieve an earlier diagnosis. Surgical drainage with adequate debridement may be better tolerated than a radical en bloc resection |
| Ross et al. (2004) [ | 5 | If extensive bony destruction, chest wall phlegmon or abscess, retrosternal abscess, mediastinitis, or pleural extension is seen on imaging, en bloc joint resection, with debridement of bone and soft tissues until they appear healthy, is indicated. Small wounds can be allowed to heal by secondary intention. Larger wounds may require the involvement of the plastic surgeon to advance an ipsilateral pectoralis major muscle flap |
Patient characteristics
The outcome measure was not reported in the corresponding article for any cell without data
DM: diabetes mellitus; IVDU: intravenous drug user; HTN: hypertension; CRF: chronic renal failure; CT: computed tomography; MSSA: methicillin-sensitive Staphylococcus aureus; MRSA: methicillin-resistant Staphylococcus aureus
| Study | Sample | Mean age | Male | Obesity | Comorbidities | Symptoms | Imaging | Microbiology | |||||||
| DM | IVDU | HTN | CRF | Pain | Swelling | Fever | CT | MSSA | MRSA | Strep | |||||
| Ali et al. (2019) [ | 50 | 49 | 37 | 14 | 25 | 17 | 20 | 2 | 50 | 50 | 22 | 50 | 25 | 5 | 6 |
| Jang et al. (2019) [ | 22 | 61 | 17 | 3 | 5 | 2 | - | - | - | - | - | - | - | - | - |
| Von Glinski et al. (2019) [ | 13 | 38 | 8 | - | 8 | 2 | - | 2 | - | - | - | - | 12 | 1 | - |
| Murga et al. (2017) [ | 15 | 55 | 12 | - | 8 | - | 9 | 1 | 13 | - | 2 | 15 | 11 | - | 1 |
| Kachala et al. (2016) [ | 40 | 57 | 28 | 14 | 11 | 4 | - | 4 | 37 | 30 | 18 | 37 | 23 | 6 | 4 |
| Muesse et al. (2014) [ | 12 | 58 | 8 | 7 | 6 | - | 8 | 2 | - | - | - | - | 8 | - | 1 |
| Chun et al. (2012) [ | 10 | 53 | 6 | - | 1 | - | - | - | 6 | 3 | 2 | - | 1 | - | 2 |
| Song et al. (2012) [ | 7 | 53 | 5 | - | 2 | - | - | - | 7 | 7 | - | - | 1 | - | 1 |
| Abu Arab et al. (2011) [ | 14 | 49 | 12 | - | 6 | 3 | - | 5 | - | - | - | - | 11 | - | - |
| Puri et al. (2011) [ | 20 | 57 | - | 2 | 6 | - | - | - | 17 | 19 | 7 | 17 | - | 6 | - |
| Nusselt et al. (2011) [ | 5 | 60 | 5 | - | - | - | - | - | - | - | - | - | 1 | 2 | 1 |
| Bakaeen et al. (2008) [ | 5 | 57 | 5 | - | 2 | - | - | - | - | - | - | 5 | - | 1 | 3 |
| Kendrick et al. (2007) [ | 7 | 59 | 5 | - | 4 | - | 5 | - | - | - | - | - | 7 | - | - |
| Ross et al. (2004) [ | 10 | 45 | 9 | - | 2 | 3 | - | - | - | - | - | - | 6 | 2 | 1 |
| Burkhart et al. (2003) [ | 26 | - | - | - | - | - | - | - | 21 | 14 | - | - | 17 | - | - |
| Carlos et al. (1997) [ | 8 | 51 | 7 | - | 2 | - | 2 | - | - | - | - | 4 | - | - | |
| Total = 16 studies | 264 | 801/15 (53.4) | 164/264 (65%) | 40/264 (15%) | 88/264 (33.3%) | 31/264 (11.7%) | 42/264 (15.9%) | 18/264 (6.8%) | 151/264 (57.2%) | 123/264 (46.6%) | 51/264 (19.3%) | 124/264 (46.9%) | 127/264 (48.1%) | 23/264 (8.7%) | 20/264 (7.5%) |
Figure 3Treatment methods
Complications
The outcome measure was not reported in the corresponding article for any cell without data
| Study (n = sample size) | Overall complications | Muscle flap-related complications | Recurrence of infection | Deaths (30 days) | Follow-up (months) |
| Ali et al. (2019) [ | 11 (22%) | 5 (10%) | 6 (12%) | 0 | 36 |
| Jang et al. (2019) [ | 0 | - | 0 | 1 (5%) | 53 |
| Von Glinski et al. (2019) [ | - | - | 3 (23%) | 2 (15%) | 3 |
| Murga et al. (2017) [ | - | - | - | 2 (13%) | - |
| Kachala et al. (2016) [ | 7 (17.5%) | - | 4 (10%) | 0 | 6.3 |
| Muesse et al. (2014) [ | - | - | - | - | - |
| Chun et al. (2012) [ | 1 (10%) | - | 0 | 0 | 35.4 |
| Song et al. (2012) [ | 0 | - | - | - | 28 |
| Abu Arab et al. (2011) [ | - | - | - | - | - |
| Puri et al. (2011) [ | 8 (40%) | - | - | 1 (5%) | - |
| Nusselt et al. (2011) [ | 0 | - | 0 | - | - |
| Bakaeen et al. (2008) [ | 2 (40%) | - | - | 2 (40%) | - |
| Kendrick et al. (2007) [ | - | - | - | 0 | 5.2 |
| Ross et al. (2004) [ | - | - | 1 (10%) | 1 (10%) | - |
| Burkhart et al. (2003) [ | 2 (7.7%) | - | - | 1 (3.8%) | 25 |
| Carlos et al. (1997) [ | 0 | - | - | - | - |