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Ann Thorac Surg 2006;82:902-907
© 2006 The Society of Thoracic Surgeons
Division of Cardiac Surgery, The Johns Hopkins Medical Institutions, Baltimore, Maryland
Accepted for publication April 20, 2006.
* Address correspondence to Dr Conte, Division of Cardiac Surgery, Department of Surgery, 600 N Wolfe St, Blalock 618, Baltimore, MD 21287-4618. (Email: jconte{at}csurg.jhmi.jhu.edu).
| Abstract |
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METHODS: Retrospective review of the cardiac surgery database identified 48 patients with noninfectious sternal dehiscence in a group of 12,380 median sternotomies between 1994 and 2004. The review included diagnosis, demographics, concomitant medical conditions, and surgical outcomes. Functional outcomes were assessed using the Short Form-12 questionnaire. One hundred fifty-six median sternotomy patients served as controls. Follow-up was 97.9% (47 of 48 patients) complete, for a total of 150.1 patient-years.
RESULTS: Mean age of patients at reoperation was 58.8 ± 12.8 years, with a male to female ratio of 45:3. Multivariate analysis determined that New York Heart Association class IV, obesity, and chronic obstructive pulmonary disease were preoperative risk factors for sternal dehiscence. The incidence of sternal dehiscence was 0.39% at a mean interval between initial operation and reoperation of 5.4 months. At a mean interval of 3.9 months, 14.6% (7 of 48) of patients required additional sternal procedures. Infectious complications after reoperation occurred in 12.5% (6 of 48). Functional outcomes demonstrated that 72.2% (26 of 36) had no or mild limitation of physical activities, with 90.5% (38 of 42) reporting no or mild sternal pain at follow-up.
CONCLUSIONS: Although patients undergoing surgical correction of noninfectious sternal dehiscence fare better than those with infectious complications, optimal sternal approximation during the initial procedure and sternal precautions during convalescence should be emphasized to prevent recurrent complications.
| Introduction |
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Certain patients are at a greater risk for experiencing sternal wound complications, and many studies have established both preoperative and operative risk factors. Previously reported preoperative risk factors for sternal dehiscence include obesity [2, 8], diabetes mellitus [9], chronic obstructive pulmonary disease [2, 9], chronic cough [10], smoking [2, 3], New York Heart Association functional class [11], osteoporosis [1, 2], use of angiotensin-converting enzyme inhibitors [10], use of ß-adrenergic drugs for respiratory problems [11], immunosuppression [2, 9], and previous sternotomy [9]. Operative risk factors include bilateral internal mammary artery harvest [9], excessive volumes of blood transfused [11], and prolonged cardiopulmonary bypass time [3].
Several previous studies have examined long-term outcomes of patients after muscle flap placement for mediastinal infection [1216]. However, no significant efforts have been made to address long-term functional outcomes of patients experiencing sternal dehiscence in the absence of infection, making the long-term morbidity of this complication relatively unknown. The purpose of this study was to conduct a retrospective review of all patients experiencing noninfectious sternal dehiscence after median sternotomy at our institution during a 10-year period.
| Patients and Methods |
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Medical records were used to obtain patient histories; demographics; preoperative, operative and postoperative data; and complications. Telephone interview with patients or family members was the primary mode of follow-up contact. Functional outcomes were evaluated using patient follow-up interviews and the Short Form-12 (SF-12) quality assessment tool. Institutional review board approval of the study was obtained on May 20, 2004, and each patient in the study gave informed consent before serving as a subject.
The SPSS statistical software (SPSS, Inc, Chicago, IL) was used to quantitatively analyze the collected data. Univariate analysis was done using
2 analysis or Fisher's exact test for categorical data and the Mann-Whitney U test for continuous data. Multivariate analysis was conducted using binomial logistic stepwise regression, confirmed by forward and backward conditional method. Descriptive statistics are presented as mean ± standard deviation. Event-free curves and at-risk patients for sternal infection and additional sternal revisions were calculated using KaplanMeier analysis. Statistical significance was defined as a probability less than or equal to 0.05.
| Results |
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Surgical treatment of sternal dehiscence included simple debridement and rewire; debridement, rewire, and placement of bilateral muscle flaps; debridement, rewire, and placement of sternal plates; debridement, rewire, and placement of sternal plates with bilateral muscle flaps; and sternal wire removal (Table 4). Rewire closure of the sternum, when uncomplicated, generally involved the use of a Robicsek weave as described by Robicsek and colleagues [2] using no. 5 or no. 6 wire. When bilateral pectoralis muscle flaps were used, both the pectoralis and rectus muscles were elevated off of the ribs to create a bipedicle flap. The flaps were then mobilized to cover the region of the sternal repair and sutured into place. Synthes sternal plate fixation systems (Synthes, Inc, West Chester, PA) were used in patients requiring sternal plates to stabilize the sternum. The types of plates varied in each of the patients, from parallel 2.7 mm or 3.0 mm, depending on the clinical situation.
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All patients were cultured for examination of infection at the time of reoperation and received standard antibiotic prophylaxis, which included 24-hour administration of a first-generation cephalosporin or vancomycin (in penicillin-allergic patients). At that time, all cultures were negative for infective microorganisms. In patients who experienced infectious complications after the initial reapproximation procedure, antibiotics were administered according to culture sensitivities for 6 weeks and only continued beyond that time if the wound remained frankly purulent.
Most patients were free from further sternal revisions and wound infections at the time of follow-up. However, 7 patients required further sternal revisions, and 6 patients exhibited wound infections confirmed by culture (Fig 1). As seen in Figure 2, freedom from additional sternal revisions was 86.6% ± 5.1%, 83.9% ± 5.6%, and 83.9% ± 5.6% at 1, 4, and 9 years, respectively, with a mean interval between revisions of 3.9 months. Figure 3 demonstrates an 85.6% ± 5.5% freedom from wound infection at 1, 4, and 9 years.
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| Comment |
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Technical errors and misapproximation of the sternal halves often result in inadequate coaptation of the sternum [6, 7, 9, 18]. Despite a technically sound sternal approximation, mechanical analysis of median sternotomy closures demonstrates that the application of simple physiologic forces to the thorax can lead to significant sternal motion. In this cohort, 45.8% (22 of 48) of the patients experienced mechanical stresses on their wound that likely contributed to their sternal dehiscence, including premature overexertion, chest reexploration, intubation greater than 7 days, chronic ventilator dependence, and respiratory symptoms [3, 4, 12, 18]. Of note, 25 patients in this cohort experienced sternal dehiscence of undetermined causes.
Because of these physical problems, many studies describe the use of reinforced closure techniques to decrease the incidence of sternal dehiscence [7, 9, 19, 20]. Although these techniques are potentially effective in reducing the incidence of sternal dehiscence, they are more invasive, more technically cumbersome, and carry an increased risk of bleeding, making them less attractive options for use during routine closure of the initial midline sternotomy [2]. No studies have clearly identified a population of patients who are likely to benefit from a prophylactic sternal weave over standard sternal closure technique on a routine basis. The standard closure of the initial median sternotomy at our hospital from 1994 to 2002 involved the use of six to seven single sternal wires (no. 5 or no. 6) with a multitwist closure. In 2002, the use of double wires became standard, and closure then involved the use of three or four double wires in the sternum and two single wires placed in the manubrium with a multitwist closure of all wires. In general, this standard technique is replaced with a Robicsek sternal weave during the rewire procedure, in which peristernal single wire loops are placed around a continuous vertical pericostal weave [2]. Additionally, some patients with dehiscence and multiple sternal fractures received bilateral pectoralis muscle flaps both with and without sternal plates to further reinforce the sternum when clinically necessary. Allograft bone, Opteform (Exatech, Gainesville, FL) was used between the two sternal halves in 1 patient to help promote bone healing in the setting of chronic nonunion.
Our patient cohort demonstrated that the majority of patients were free from further sternal revisions and sternal wound infections at the time of follow-up. Cultures were routinely obtained at the time of sternal revision to ensure that infection did not cause the dehiscence, and all cultures were negative. However, 7 of 48 patients required additional sternal revisions, and 6 of 48 patients experienced wound infections after their initial sternal revision (Fig 1). Of the 7 patients who required an additional sternal procedure, 4 also experienced sternal infections. This means that of the 48 patients undergoing additional sternal reoperation procedures, 9 had long-term complications associated with their repeat procedure. Although this number is favorable compared with outcomes of patients after infectious sternal dehiscence and pectoralis flap reconstructions [14], it emphasizes the importance of adequate reapproximation of the sternum after the initial procedure. Despite patients with noninfectious sternal dehiscence faring better than those with infections, patient outcomes can be maximized by avoiding sternal rewire procedures.
The retrospective nature of this study leads to some limitations when analyzing our data. First, because this complication is rare and the study evaluated patients from one institution during a 10-year period, data could only be analyzed for a relatively small number of patients. In addition, our follow-up data were also somewhat subjective as they were based on individual patients reporting their postoperative experiences. We obtained consistency in our methods by having a single investigator interview all patients using a standard set of questions with the SF-12 quality assessment tool. One technical aspect that we could not specifically address was the role of opening of the sternum off-center. Although this would make intuitive sense to be a risk factor for dehiscence, we could not study this. It has been our practice to perform a partial weave on the thin side if there seems to be a significant disparity in the size of sternal bone on opposite sides. We did not find any patients who had such a partial weave who experienced a dehiscence. Despite the limitations of this study, these findings provide new insight into patient outcomes after noninfectious sternal dehiscence and support the hypothesis that patients generally do better than those experiencing infectious sternal dehiscence.
In conclusion, risk factors for noninfectious sternal dehiscence identified include obesity, chronic obstructive pulmonary disease, and New York Heart Association functional class IV. Patients undergoing surgical correction of noninfectious sternal dehiscence fared better than those patients who experienced complications after infectious sternal dehiscence. Although the majority was free from infectious complications and further sternal revisions, approximately 19% still experienced long-term complications, emphasizing the importance of adequate sternal reapproximation after the initial median sternotomy procedure to avoid recurrent complications. Our current recommendation is for patients who are morbidly obese (body mass index greater than 36), those with a chronic cough, or those with a sternum not divided in the midline to undergo a prophylactic sternal weave.
| Requirements for Recertification/Maintenance of Certification in 2006 |
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The American Board of Thoracic Surgery will no longer publish the names of individuals who have not recertified in the American Board of Medical Specialties directories. The Diplomate's name will be published upon successful completion of the recertification/maintenance of certification process.
The CME requirements are 70 Category I credits in either cardiothoracic surgery or general surgery earned during the 2 years prior to application. SESATS and SESAPS are the only self-instructional materials allowed for credit. Category II credits are not allowed. The Physicians Recognition Award for recertifying in general surgery is not allowed in fulfillment of the CME requirements. Interested individuals should refer to the Booklet of Information for a complete description of acceptable CME credits.
Diplomates should maintain a documented list of their major cases performed during the year prior to application for recertification. This practice review should consist of 1 year's consecutive major operative experiences. If more than 100 cases occur in 1 year, only 100 should be listed.
Candidates for recertification/maintenance of certification will be required to complete all sections of the SESATS self-assessment examination. It is not necessary for candidates to purchase SESATS individually because it will be sent to candidates after their application has been approved.
Diplomates may recertify the year their certificate expires, or if they wish to do so, they may recertify up to two years before it expires. However, the new certificate will be dated 10 years from the date of expiration of their original certificate or most recent recertification certificate. In other words, recertifying early does not alter the 10-year validation.
Recertification/maintenance of certification is also open to Diplomates with an unlimited certificate and will in no way affect the validity of their original certificate.
The deadline for submission of applications for the recertification/maintenance of certification process is May 10 each year. A brochure outlining the rules and requirements for recertification/maintenance of certification in thoracic surgery is available upon request from the American Board of Thoracic Surgery, 633 N St. Clair St, Suite 2320, Chicago, IL 60611; telephone: (312) 202-5900; fax: (312) 202-5960; e-mail: info{at}abts.org. This booklet is also published on the website: www.abts.org.
| Acknowledgments |
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