- Research article
- Open Access
The efficacy of negative pressure wound therapy in treating sacroiliac joint tuberculosis with a chronic sinus tract: a case series
© Luo et al. 2015
- Received: 5 March 2015
- Accepted: 30 June 2015
- Published: 6 August 2015
Tuberculous sacroiliitis with abscess accounts for approximately 50 % of all sacroiliac joint tuberculosis cases. Tuberculous abscesses spread into the sacroiliac joint capsule, subcutaneous tissue, and the skin, and finally becomes a skin sinus. As there are no previous reports about sacroiliac joint tuberculosis with a chronic sinus, we evaluated its clinical characteristics and management by negative pressure wound therapy.
A retrospective analysis of 12 patients with sacroiliac joint tuberculosis with chronic sinuses treated between January 2005 and January 2010 was conducted. Patients were treated with negative pressure wound therapy (NPWT). Treatment was divided into three phases: control phase, standard dressing changes daily for 4 weeks; interphase washout period, dressing changes every 3 days for 1 week; and intervention phase, no dressing changes until minimal sinus tract drainage (<5 ml per 24 h). Outcomes including the sinus healing time and the drainage volume were evaluated.
The mean follow-up was 37.1 months. Sinus healing was observed at an average of 25.25 ± 7.23 (range, 20–42) days after initial treatment. The mean volume of drainage did not change during the control phase, but decreased from 29.17 ± 16.63 to 0.25 ± 0.87 ml in the intervention phase. The mean daily reduction of wound volume, erythrocyte sedimentation rate (ESR), and C-reactive protein (CRP) in the intervention phase was greater than in the control phase (P < 0.05). Anti-tubercular therapy was administered an average of 14.00 ± 2.95 (range, 12–18) months. ESR and CRP returned to normal within 3 months after the sinus closure. Bony fusion was observed in 5 (41.7 %) patients, and fibrous ankylosis in the other patients at last follow-up. All patients healed uneventfully.
Early diagnosis of sacroiliac joint tuberculosis with a chronic sinus can be difficult. NPWT provides better healing of sacroiliac joint tuberculosis with a chronic sinus than standard dressing changes.
- Sacroiliac joint
- Negative pressure wound therapy
Tuberculosis is a global problem, with an estimated 8.6 million new cases and 1.3 million related deaths in 2012. About 12 % of newly diagnosed cases are in China, making China the second largest tuberculosis country .
Skeletal tuberculosis accounts for 3 to 5 % of all tuberculosis cases. Sacroiliac joint tuberculosis accounts for approximately 10 % of skeletal tuberculosis cases [5, 13, 28]. The formation of paraspinal tuberculous abscesses is seen in 50 to 75 % of spinal tuberculosis cases [7, 18, 26]. Kim  and Gao  reported similar results in that almost 50 % of patients with sacroiliac joint tuberculosis had gluteal and inguinal abscesses. In the late stages of infection, sacroiliac joint abscesses destroyed the capsule, spread into the adjacent subcutaneous tissues, and finally form sinus tracts. Treatment can be challenging. Traditional surgeries include curettage, curettage plus arthrodesis, and the modified Smith-Petersen arthrodesis method [11, 17]. Negative pressure wound therapy (NPWT) is an advanced wound treatment protocol developed in recent years. However, there are no reports of NPWT used to treat sacroiliac joint tuberculosis with a chronic sinus.
The aim of this study was to evaluate the clinical characteristics and efficacy of NPWT in the management of sacroiliac joint tuberculosis with a chronic sinus tract.
The records of 12 patients with sacroiliac joint tuberculosis and a chronic sinus tract treated at our institution between January 2005 and January 2010 were retrospectively reviewed. The drainage volume and inflammatory markers were assessed before and after NPWT. Demographic data collected included age, sex, location of the sinus, and surgical history. Because the cases in this study were rare, the sample size was small. In addition, the disease was chronic and recurrent. Therefore, a self-control study of inpatients before and after intervention was used in order to reduce bias. There was a control period, a middle period, and intervention period. Erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), wound volume, and drainage were compared between the control period and the intervention period in order to evaluate the effects of NPWT.
The diagnosis of sacroiliac joint tuberculosis was based on clinical history and symptoms, physical signs, laboratory tests, imaging studies, and pathologic examination. Tuberculin skin testing, acid-fast bacilli (AFB) smear, culture results, ESR, and CRP were used as conventional markers of infection. Plain X-ray, ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI) were performed to detect bone-marrow edema, sequestrum, sclerosis, abscesses, sinus tracts, and bony fusion. Laboratory and imaging testing were routinely performed during follow-up.
Pathologic specimens of sinus tract caseous necrosis were evaluated before NPWT. Neutral Lowenstein-Jensen culture medium was used for Mycobacterium tuberculosis culture. Drug susceptibility testing was performed on Lowenstein-Jensen medium using the proportion method. Routine bacterial cultures and sensitivity testing were performed.
Patients received standard anti-tuberculosis therapy before and after admission, and the anti-tuberculosis therapy was not modified during admission. Systemic antibiotics were administered when mixed infection was diagnosed. The results of common bacterial susceptibility testing were reported after 1 week, and antibiotic treatment was initiated according to bacterial susceptibility testing.
The treatment was divided into three phases: control phase, standard dressing changes daily for 4 weeks; interphase washout period, dressing changes every 3 days for 1 week; and intervention phase, no dressing changes until minimal sinus tract drainage (<5 ml per 24 h). All patients underwent the whole treatment process.
After discharge, all patients continued anti-tuberculosis medications. Usually, the results of tuberculosis drug susceptibility testing were available after more than 2 months; drug therapy was modified according to the susceptibility result [19, 22].
Healing criteria included lack of pain or tenderness over the affected area, no discomfort during working, normal ESR, no abscess or sinus tract drainage, clearance and sclerosis of the joint margin, fusion of the sacroiliac joint, and the presence of fibrous ankylosis .
Clinical findings, imaging studies, ESR, CRP, and hepatic and renal function were routinely evaluated and recorded during and after admission. Fusion of the sacroiliac joint was assessed using plain X-ray, and CT and MRI were used to confirm bony fusion.
Statistical analyses were performed using SPSS 13.0 (SPSS Inc., Chicago, IL). Data were presented as number (%) and mean ± standard deviation (SD). Matched-pair t tests was used to evaluate significant differences between two phases. A two-tailed value of P < 0.05 was considered statistically significant.
There were seven female and five male patients included in the study. The average patient age was 32.8 years (range, 21 to 63 years), and the average length of follow-up was 37.1 months (range, 24 to 54 months).
All 12 patients complained of persistent buttock or low back pain, a chronic sinus tract, and difficulty walking. Ten (83.3 %) patients had typical symptoms of tuberculosis infection including weight loss, poor appetite, fever, and sleep hyperhidrosis. The pelvic compression test and Gaenslen’s test was positive on the affected side of all patients. Pain of the hip can be induced by hip over flexion and over extension. Four (33.3 %) patients had undergone abscess drainage or curettage before admissions. One (8.3 %) patient had bilateral sacroiliac joint tuberculosis, and seven (58.3 %) patients had left and four (33.3 %) had right sacroiliac involvement.
Other sites affected
All patients were treated with NPWT according to the site and the size of the sinuses. The average duration of symptoms was 12.41 ± 4.36 months (range, 9 to 24 months). The average time interval between onset of low back pain and sinus tract formation was 8.50 ± 4.56 months (range, 3 to 20 months). The average duration of sinus tract drainage was 3.92 ± 1.08 months (range, 3 to 6 months). Patients received regular anti-tuberculosis therapy for a mean of 4.67 ± 1.37 months (range, 2 to 7 months) before admission. Patients were treated with NPWT for an average of 18.33 ± 6.97 days (range, 14–35 days). Sinus tract closure was observed after the initiation of NPWT at an average of 25.25 ± 7.23 days (range, 2042 days).
Culture in one (8.3 %) patient was positive for methicillin-resistant Staphylococcus aureus (MRSA) resistant to ampicillin, pefloxacin, ceftazidime, gentamicin, and ciprofloxacin. Vancomycin was used to treat this patient. One sinus culture revealed Staphylococcus epidermidis, and appropriate antibiotic treatment was initiated.
Fifty percent (6/12) of patients had positive cultures for M. tuberculosis. Of them, 33 % (2/6) were multi-drug resistant tuberculosis (MDR-TB). Of the six positive tuberculosis cultures, 33.3 % (2/6) were resistant to isoniazid, 33.3 % (2/6) to rifampicin, 16.7 % (1/6) to streptomycin, 16.7 % (1/6) to pasiniazid, and 16.7 % (1/6) were resistant to rifapentine. Resistance to three drugs was found in one case, and resistance to four drugs was found in one case. Anti-tubercular drugs were modified in two patients based on sensitivity testing after their wounds healed.
During the control phase, the duration of dressing changes was 30 days. The average daily drainage volume, wound volume, ESR, and CRP changed from 21.75 ± 8.86 to 21.33 ± 7.90 ml, 37.75 ± 33.80 to 35.17 ± 37.44 cm3, 40.16 ± 23.99 to 38.25 ± 21.63 mm/h, and 32.33 ± 12.09 to 33.33 ± 13.36 mg/dl, respectively. The average reduction of wound volume following treatment was 6.45 %.
During the 7 days of the interphase, the average daily drainage volume, wound volume, ESR, and CRP changed from 20.75 ± 6.94 to 22.33 ± 7.28 ml, 35.17 ± 37.44 to 34.08 ± 33.91 cm3, 38.25 ± 21.63 to 38.33 ± 20.82 mm/h, and 33.33 ± 13.36 to 33.67 ± 11.72 mg/dl, respectively. There was no significant difference of the change in the drainage volume, wound volume, ESR, and CRP in the control phase and interphase (P > 0.05).
Wound volume, ESR, and CRP of patients who received dressing changes or NPWT
Control phase (dressing changes)
Intervention phase (NPWT)
Length of the treatment (days)
18.33 ± 6.97
Pre-treatment wound volume (cm3)
37.75 ± 33.80
34.08 ± 33.91
Post-treatment wound volume (cm3)
35.17 ± 37.44
25.50 ± 26.04
Reduction of wound volume (cm3)
2.58 ± 2.74
8.58 ± 8.53
Pre-treatment ESR (mm/h)
40.16 ± 23.99
38.33 ± 20.82
Post-treatment ESR (mm/h)
38.25 ± 21.63
25.50 ± 11.72
Reduction of ESR (mm/h)
1.92 ± 6.04
17.75 ± 28.82
Pre-treatment CRP (mg/dl)
32.33 ± 12.09
33.67 ± 11.72
Post-treatment CRP (mg/dl)
33.33 ± 13.36
13.00 ± 8.01
Reduction of CRP (mg/dl)
−1 ± 2.77
19.75 ± 32.56
Sacroiliac joint tuberculosis is rare. The diagnosis of tuberculosis of the sacroiliac joint in the early stages is difficult due to the vague presenting symptoms, and thus the diagnosis is delayed in many cases [3, 11, 28].
Typical symptoms of the sacroiliac joint tuberculosis included groin or buttock pain, posterior thigh pain, and lower limb radiculopathy associated with walking. These findings may results in a misdiagnosis of arthritis or neurologic disease [14, 17, 24, 27, 28]. Radiographic imaging can be normal in the early stage of the disease. As the disease progresses, erosion of the sacroiliac joint becomes more distinct and abscesses appear.
The diversity of abscesses is always confusing and misleading. In addition to spontaneous abscess rupture, incision and drainage of an abscess can also lead to sinus tract formation. Gluteal or perineal sinuses formed spontaneously in eight (66.7 %) of our patients, and postoperative sinuses were found in four (33.3 %) patients; three after incision and drainage and one after curettage. We believe simple incision and drainage of tubercular abscesses puts patients at risk for sinus tract formation, and is therefore not recommended. Of our patients, 91.7 % (11/12) had gluteal sinuses and 8.3 % (1/12) inguinal sinuses. Gluteal sinuses were most commonly spontaneous because the gluteus muscle is compressed during sitting and lying down, thus facilitating local spread. Inguinal sinuses usually occurred after abscess incision and drainage.
NPWT is a non-invasive therapy applied to acute or chronic wounds of different etiologies. The concept of NPWT was first proposed by Fleischmann in 1993 . NPWT was performed in our patients using a suction tube wrapped in foam, a fluid-impermeable transparent film, and a vacuum pump. This device is widely used in the treatment of acute and chronic wounds . This method has also been used in the treatment of tuberculous mid-palmar abscesses, and tuberculous osteomyelitis of the sternum [10, 16]. However, there have been no studies examining NPWT in tuberculous wounds. All patients we treated with NPWT had a satisfactory outcome with no recurrence.
Advantages of NPWT may be the exhaustive debridement of pus, local improvement in tissue perfusion, mechanical traction and stimulation with negative pressure, decrease in bacterial levels , and reduction in local edema . One reason for using NPWT to treat a tuberculous sinus tract is the decrease in the load of M. tuberculosis after applying NPWT. Some author considered the promotion of wound healing by NPWT may be explained by decreasing the bacterial load. One of the primary uses of NPWT therapy is the management of infected wounds.
Fleischmann et al. who was the earliest to propose NPWT therapy have also used the technique for the management of infected wounds . Morykwas et al. constructed an animal model infected by a human isolate of S. aureus and a swine isolate of S. epidermidis and treated the infection with either NPWT or controlled moist saline dressing changes and found that NPWT resulted in a significant reduction in the wound bacterial load . A similar result has also been seen in human wounds . Many other studies have shown that NPWT assists in healing infected wound [6, 12, 15].
Although NPWT has been used to manage infected wounds successfully, some studies suggest that healing of contaminated acute and chronic wounds cannot be explained by a significant reduction in bacterial load . In our study, all sinus tracts healed without recurrence after the initiation of NPWT at an average of 25.25 ± 7.23 days (range, 20–42 days). Wound volume and daily drainage volume decreased significantly after the application of NPWT. Thus, our results suggest that the positive effect of NPWT on tuberculous wound healing may be explained by a reduction of the bacterial load. However, the M. tuberculosis load was not determined because it was difficult to evaluate by with existing detection methods. Whether NPWT can reduce the M. tuberculosis load requires further study.
In this study, we evaluated wound healing during different stages of treatment, and tried to demonstrate the effective treatment of tuberculous sinus tracts using NPWT. There were no significant changes in drainage volume or wound volume during the control phase and interphase. However, in the intervention phase, drainage volume decreased significantly. This may be explained by exhaustive removal of pus, and the control of disease progression. In the intervention phase, the pre-treatment wound volume was not significantly different from that in the control phase (P > 0.05). But in the intervention phase, the post-treatment wound volume was 25.50 ± 26.04 cm3, and the reduction of wound volume was 26.98 %. These results were significantly different from the control phase (P < 0.05). Thus, NPWT can improve mechanical traction and granulation tissue proliferation in the tuberculous sinus tract. The mechanisms whereby NPWT promotes healing of the tuberculous sinus tract may include (1) reduction in the mycobacterium load to slow the progression of the wound and stop transmission, (2) persistent removal of the pus and necrotic tissue, and (3) promotion of granulation tissue proliferation. Moreover, NPWT decreased the hospitalization time and the number of daily dressing changes. In this study, all sinus tracts healed without recurrence. Thus, we believe the use of NPWT in tuberculous sinus tracts can also prevent relapse.
The ESR test determines the rate of fall of red blood cells in a column of anti-coagulated blood in 1 h . CRP, an acute phase protein, is synthesized by hepatocytes in response to pro-inflammatory cytokines, in particular interleukin (IL)-6 . ESR and CRP, which will initially be elevated significantly, and normalize over time on therapy, in patients with active tuberculosis have been used to predict disease severity and curative effects for several decades. Normalization of the ESR and CRP level are associated with resolution of the systemic inflammatory process and clinical response [2, 17, 25]. In our study, the pre-treatment ESR and CRP in the intervention phase were not significantly different from the control phase (P > 0.05). This study also showed that reductions of ESR and CRP in the intervention phase were significantly higher than those in control phase, and that NPWT for an average of 18.33 ± 6.97 days was associated with significant reductions of ESR and CRP.
NPWT helped to make the treatment and nursing care simple, easy, and effective. The mechanisms whereby NPWT promotes healing of the tuberculous sinus tract may include (1) reduction in the mycobacterium load to slow the progression of the wound and stop transmission, (2) persistent removal of the pus and necrotic tissue, and (3) promotion of granulation tissue proliferation. The use of NPWT assists in the healing of sacroiliac joint tuberculosis and sinus tracts more effectively that dressing changes. Further studies are needed to confirm this conclusion.
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- Argenta LC, Morykwas MJ. Vacuum-assisted closure: a new method for wound control and treatment: clinical experience. Ann Plast Surg. 2007;38:563–76. discussion 577.View ArticleGoogle Scholar
- Baynes RD, Flax H, Bothwell TH, Bezwoda WR, MacPhail AP, Atkinson P, et al. Haematological and iron related measurements in active pulmonary tuberculosis. Scand J Haematol. 1986;36:280–7.PubMedView ArticleGoogle Scholar
- Benchakroun M, El Bardouni A, Zaddoug O, Kharmaz M, Lamrani MO, El Yaacoubi M, et al. Tuberculous sacroiliitis. Four cases. Joint Bone Spine. 2004;71:150–3.PubMedView ArticleGoogle Scholar
- Brigden ML. Clinical utility of the erythrocyte sedimentation rate. Am Fam Physician. 1999;60:1443–50.PubMedGoogle Scholar
- Davies PD, Humphries MJ, Byfield SP, Nunn AJ, Darbyshire JH, Citron KM, et al. Bone and joint tuberculosis. A survey of notifications in England and Wales. J Bone Joint Surg Br. 1984;66:326–30.PubMedGoogle Scholar
- Demaria RG, Giovannini UM, Teot L, Frapier JM, Albat B. Topical negative pressure therapy. Avery useful new method to treat severe infected vascular approaches in the groin. J Cardiovasc Surg (Torino). 2003;44:757–61.Google Scholar
- Dinç H, Ahmetoğlu A, Baykal S, Sari A, Sayil O, Gümele HR. Image-guided percutaneous drainage of tuberculous iliopsoas and spondylodiskitic abscesses: midterm results. Radiology. 2002;225:353–8.PubMedView ArticleGoogle Scholar
- Fleischmann W, Becker U, Bischoff M, Hoekstra H. Vacuum sealing: indication technique and results. Eur J Orthop Surg Trauma. 1995;5:37–40.View ArticleGoogle Scholar
- Fleischmann W, Strecker W, Bombelli M, Kinzl L. Vacuum sealing as treatment of soft tissue damage in open fractures. Unfallchirurg. 1993;96:488–92.PubMedGoogle Scholar
- Ford SJ, Rathinam S, King JE, Vaughan R. Tuberculous osteomyelitis of the sternum: successful management with debridement and vacuum assisted closure. Eur J Cardio-Thorac. 2005;28:645–7.View ArticleGoogle Scholar
- Gao F, Kong XH, Tong XY, Xie DH, Li YG, Guo JJ, et al. Tuberculous sacroiliitis: a study of the diagnosis, therapy and medium-term results of 15 cases. J Int Med Res. 2011;39:321–35.PubMedView ArticleGoogle Scholar
- Giovannini UM, Demaria R, Teot L. Benefits of negative pressure therapy in infected surgical wounds after cardiovascular surgery. Wounds. 2001;13:82–7.Google Scholar
- Goldberg J, Kovarsky J. Tuberculous sacroiliitis. South Med J. 1983;76:1175–6.PubMedView ArticleGoogle Scholar
- Gupta R, Bienenstock H, Morano P, Gupta A. Tuberculosis of sacroiliac joint: an unusual presentation. J Natl Med Assoc. 2005;97:1174–6.PubMed CentralPubMedGoogle Scholar
- Gustafsson R, Johnsson P, Algotsson L, Blomquist S, Ingemansson R. Vacuum assisted closure therapy guided by C-reactive protein level in patients with deep sternal wound infection. J Thorac Cardiovasc Surg. 2002;123:895–900.PubMedView ArticleGoogle Scholar
- Kang GC, Yam A. Vacuum-assisted closure of a large palmar defect after debriding a midpalmar tuberculous abscess. Int Wound J. 2008;5:45–8.PubMedView ArticleGoogle Scholar
- Kim NH, Lee HM, Yoo JD, Suh JS. Sacroiliac joint tuberculosis. Classification and treatment. Clin Orthop Relat Res. 1999;358:215–22.PubMedView ArticleGoogle Scholar
- Lindahl S, Nyman RS, Brismar J, Hugosson C, Lundstedt C. Imaging of tuberculosis. IV. Spinal manifestations in 63 patients. Acta Radiol. 1996;37:506–11.PubMedGoogle Scholar
- Loddenkemper R, Sagebiel D, Brende A. Strategies against multi-drug resistant tuberculosis. Eur Respir J. 2002;36:66–77.View ArticleGoogle Scholar
- Morykwas MJ, Argenta LC, Shelton-Brown EI, McGuirt W. Vacuum-assisted closure: a new method for wound control and treatment: animal studies and basic foundation. Ann Plast Surg. 1997;38:553–62.PubMedView ArticleGoogle Scholar
- Mouës CM, Vos MC, van den Bemd GJ, Stijnen T, Hovius SE. Bacterial load in relation to vacuum-assisted closure wound therapy: a prospective randomized trial. Wound Repair Regen. 2004;12:11–7.PubMedView ArticleGoogle Scholar
- Mukherjee JS, Rich ML, Socci AR, Joseph JK, Alcántara Virú F, Shin SS, et al. Programmes and principles in treatment of multi-drug resistant tuberculosis. Lancet. 2004;363:474–81.PubMedView ArticleGoogle Scholar
- Pachowsky M, Gusinde J, Klein A, Lehrl S, Schulz-Drost S, Schlechtweg P, et al. Negative pressure wound therapy to prevent seromas and treat surgical incisions after total hip arthroplasty. Int Orthop. 2012;36:719–22.PubMed CentralPubMedView ArticleGoogle Scholar
- Papagelopoulos PJ, Papadopoulos EC, Mavrogenis AF, Themistocleous GS, Korres DS, Soucacos PN. Tuberculous sacroiliitis. A case report and review of the literature. Eur Spine J. 2005;14:683–8.PubMed CentralPubMedView ArticleGoogle Scholar
- Peresi E. Cytokines and acute-phase serum proteins as markers of inflammatory regression during pulmonary tuberculosis treatment. J Venom Anim Toxins Incl Trop Dis. 2008;14:190.View ArticleGoogle Scholar
- Pieri S, Agresti P, Altieri AM, Ialongo P, Cortese A, Alma MG, et al. Percutaneous management of complications of tuberculous spondylodiscitis: short- to medium-term results. Radiol Med. 2009;114:984–5.PubMedView ArticleGoogle Scholar
- Pouchot J, Vinceneux P, Barge J, Boussougant Y, Grossin M, Pierre J, et al. Tuberculosis of the sacroiliac joint: clinical features, outcome and evaluation of closed needle biopsy in 11 consecutive cases. Am J Med. 1988;84:622–8.PubMedView ArticleGoogle Scholar
- Ramlakan RJ, Govender S. Sacroiliac joint tuberculosis. Int Orthop. 2007;31:121–4.PubMed CentralPubMedView ArticleGoogle Scholar
- Ribeiro MA. Levels of C-reactive protein in serum samples from healthy children and adults in Sao Paulo, Brazil. Braz J Med Biol Res. 1997;30:1055–9.PubMedView ArticleGoogle Scholar
- Thompson JT, Marks MW. Negative pressure wound therapy. Clin Plast Surg. 2007;34:673–84.PubMedView ArticleGoogle Scholar
- Van Wicjck R, Manicourt D, Feruzi-Lukina G. Biological monitoring of wounds treated by negative pressure. Nice, France: ETRS New technologies Focus Group Meeting; 2002.Google Scholar
- World Health Organization. Global tuberculosis report 2012. Geneva, Switzerland: World Health Organization; 2012.Google Scholar