» Articles » PMID: 33447627

The STAPH Score: A Predictor of As the Causative Microorganism of Native Vertebral Osteomyelitis

Overview
Date 2021 Jan 15
PMID 33447627
Authors
Affiliations
Soon will be listed here.
Abstract

Background: (SA) is the most common causative microorganism in native vertebral osteomyelitis (NVO). Few studies have compared the clinical features of NVO due to SA (SA-NVO) and NVO due to other organisms (NSA-NVO). This study was conducted to validate a predictive score for SA-NVO to facilitate NVO treatment without broad-spectrum antimicrobial agents.

Methods: This retrospective study compared the clinical features of patients with SA-NVO and NSA-NVO who were diagnosed from 2004 to 2019. Univariate associations were assessed using χ , Fisher's exact, or Mann-Whitney test. Multivariable analysis was conducted using logistic regression. The optimal age cutoff point was determined by classification and regression tree analysis.

Results: Among 155 NVO patients, 98 (63.2%) had a microbiologically confirmed diagnosis: 40 (25.8%) with SA-NVO and 58 (37.4%) with NSA-NVO. Six predictors, either independently associated with SA-NVO or clinically relevant, were used to develop the STAPH prediction score: atopic dermatitis (Skin) (3 points); recent Trauma (2 points); Age < 67 years (1 point); Abscess (1 point); central venous Port catheter (2 points); and History of puncture (2 points). In a receiver operating characteristic analysis, the area under the curve was 0.84 (95% confidence interval, 0.76-0.91). The best cutoff point was 3. A score ≥3 had a sensitivity, specificity, positive predictive value, and negative predictive value of 58%, 84%, 84%, and 73%, respectively.

Conclusions: The STAPH score has relatively high specificity for use by clinicians to predict SA as the causative microorganism in patients with NVO until results of a confirmatory culture are available.

References
1.
Giai C, Gonzalez C, Ledo C, Garofalo A, Di Genaro M, Sordelli D . Shedding of tumor necrosis factor receptor 1 induced by protein A decreases tumor necrosis factor alpha availability and inflammation during systemic Staphylococcus aureus infection. Infect Immun. 2013; 81(11):4200-7. PMC: 3811831. DOI: 10.1128/IAI.00593-13. View

2.
Brauweiler A, Bin L, Kim B, Oyoshi M, Geha R, Goleva E . Filaggrin-dependent secretion of sphingomyelinase protects against staphylococcal α-toxin-induced keratinocyte death. J Allergy Clin Immunol. 2012; 131(2):421-7.e1-2. PMC: 3742335. DOI: 10.1016/j.jaci.2012.10.030. View

3.
Graham S, Fishlock A, Millner P, Sandoe J . The management gram-negative bacterial haematogenous vertebral osteomyelitis: a case series of diagnosis, treatment and therapeutic outcomes. Eur Spine J. 2013; 22(8):1845-53. PMC: 3731498. DOI: 10.1007/s00586-013-2750-4. View

4.
Horino T, Sato F, Hosaka Y, Hoshina T, Tamura K, Nakaharai K . Predictive factors for metastatic infection in patients with bacteremia caused by methicillin-sensitive Staphylococcus aureus. Am J Med Sci. 2014; 349(1):24-8. PMC: 4281166. DOI: 10.1097/MAJ.0000000000000350. View

5.
Shorr A . Epidemiology of staphylococcal resistance. Clin Infect Dis. 2007; 45 Suppl 3:S171-6. DOI: 10.1086/519473. View