Research Article
Prevalence and Antibiotic Resistance Profile of Streptococcus Mutans Isolated from Dental Caries in Iraqi Children Using the VITEK® 2 System
Zainab Jawad Abo-Tbeak, Rusul Hamza AL-Hilali, Roqaya Hussein Abeid, Hiba Hamed Zidan, Zahraa Jawad Majeed
Middle East Research Journal of Medical Sciences; 94-101.
https://doi.org/10.36348/merjms.2026.v06i02.004
Background: Dental caries is still a major public health issue across the globe, especially in the case of rich regions, where the school-aged children of the poor families suffer most. Streptococcus mutans is the bacteria that causes dental decay, and that is the reason for its great adhesion, biofilm formation, and acid production. The increase of antibiotic-resistant oral streptococci may make it difficult to treat such infections in the teeth. Aim: The study was to extract and classify S. mutans from children with dental cavities and also create the profile of the isolates' antibiotic susceptibility using the automated VITEK® 2 system. Methods: A cross-sectional study was carried out on 40 swab specimens taken from carious teeth of children aged 5–13 years who were visiting the Specialized Dental Center in Al-Diwaniyah and the College of Dentistry, University of Al-Qadisiyah, between 28 January 2024 and 20 April 2024. The samples were then cultured on blood agar and Mitis Salivarius agar (MSA) for primary isolation; the isolates were characterized by their colony morphology, Gram stain, and biochemical features and confirmed using the VITEK® 2 identification system. Furthermore, antibiotic susceptibility testing was done with VITEK® 2 AST cards (AST-ST01) as per the manufacturer’s instructions. Results: Out of the total of 40 specimens, 20 specimens (50%) were determined to be S. mutans; the remaining isolates consisted of S. anginosus (4; 10%), S. sanguinis (2; 5%), S. mitis (1; 2%), and other organisms (13; 32%) (Table 1). The antibiotic resistance patterns that were determined by VITEK® 2 showed high resistance rates among S. mutans strains to many of the commonly used antibiotics such as benzylpenicillin, ampicillin, cefotaxime, ceftriaxone, levofloxacin, and erythromycin; however, the strains were still sensitive to linezolid, teicoplanin, tigecycline, tetracycline, and chloramphenicol (the representative MIC data are in Table 2). Conclusion: The study revealed that S. mutans was the most prevalent isolate from dental caries in children and at the same time alarming presence of multidrug resistance due toβ-lactams, macrolides, and fluoroquinolones. The highlights of these facts are the necessity of dental practitioners adopting the practice of antimicrobial stewardship accompanied by the monitoring of oral streptococcal resistance patterns.
Research Article
Evaluation of the Relationship between Base Excess Value and Mortality in Multiple Trauma Patients Admitting to the Emergency Medical Clinic
Semih Sozen, Ozlem Guneysel, Gözde Sımsek, Burcu Ozdemır
Middle East Research Journal of Medical Sciences; 102-108.
https://doi.org/10.36348/merjms.2026.v06i02.005
Background: Early identification of severe injury and patients at risk of death remains a core challenge in the emergency management of multiple trauma. Base excess (BE), obtained rapidly from venous blood gas analysis, reflects metabolic derangement and may support early risk stratification. To evaluate the association between admission venous BE and mortality/clinical disposition in adult multiple-trauma patients, and to assess the discriminative performance of absolute BE for predicting trauma severity using the New Trauma Severity Score (NTSS). Methods: This prospective observational study included 307 adult (≥16 years) multiple-trauma patients presenting to the emergency department between 1 June 2012 and 1 February 2013. Venous blood gas samples were obtained within the first hour of arrival, and BE was measured using a blood gas analyzer. BE values were compared across comorbidity strata and disposition/outcome groups (death, ICU admission, ward admission, discharge). The ability of |BE| to discriminate NTSS ≤15 vs NTSS>15 was evaluated using ROC analysis and agreement metrics at predefined cut-offs. Results: Admission BE did not differ significantly according to the presence of comorbidity, including coronary artery disease, diabetes mellitus, hypertension, congestive heart failure, or chronic kidney disease (all p>0.05). In contrast, BE differed significantly across disposition/outcome categories, demonstrating a stepwise increase with clinical severity: death 16.35±0.92, ICU 9.57±4.79, ward 4.48±2.07, and discharge 1.70±1.23 (overall p<0.001). |BE| showed excellent discrimination for YTCS >15 (AUC 0.959). At |BE|>2, discrimination was moderate (AUC 0.810) with high sensitivity (98.8%) and negative predictive value (99.3%), whereas |BE|>4 improved overall classification balance (AUC 0.887; sensitivity 84.5%, specificity 92.9%, PPV 82.6%, NPV 93.8%). Conclusions: Early venous BE, particularly |BE|, is strongly associated with adverse disposition and mortality in multiple-trauma patients and demonstrates high performance for identifying patients with YTCS >15. BE may serve as a rapid, practical adjunct for early emergency department triage and severity assessment.
Review Article
The S100A8/A9 Axis in Acute Myocardial Infarction: Connecting Innate Inflammation to Myocardial Damage and Clinical Risk
Elham F. Hamzah, Abdulsamie Hassan Alta'ee, Ameer Aljubawi
Middle East Research Journal of Medical Sciences; 109-117.
https://doi.org/10.36348/merjms.2026.v06i02.006
Acute myocardial infarction (AMI) is a predominant cause of morbidity and mortality globally, with post-infarction heart failure serving as a significant factor in long-term prognosis. In addition to myocardial ischemia and necrosis, the early onset of sterile inflammation significantly affects infarct expansion, ventricular remodeling, and ensuing cardiac dysfunction. The identification of biomarkers that indicate these upstream inflammatory pathways is still an unresolved clinical necessity. AMI initiates a swift innate immune response marked by neutrophil activation and the release of the S100A8/A9 heterodimer comprising the calcium-binding proteins S100A8 and S100A9, which has surfaced as a pivotal pro-inflammatory mediator in cardiovascular disease. Subsequent to cardiac ischemia, S100A8/A9 is facilitating ischemia-reperfusion damage via innate immune signaling pathways. S100A8/A9, besides its role in acute myocardial injury, modulates leukocyte recruitment, cytokine synthesis, and fibroblast activation, therefore influencing post-infarction scar formation and ventricular remodeling. Recent clinical findings suggest that circulating S100A8/A9 provides predictive information that exceeds conventional biomarkers by reflecting the intensity of inflammation-driven pathological processes. S100A8/A9 levels increase promptly during acute myocardial infarction (AMI), frequently occurring before BNP elevation and supplementing troponin I by elucidating inflammation-mediated mechanisms that contribute to ventricular remodeling and the risk of heart failure, rather than solely indicating myocardial injury or wall stress. These characteristics facilitate its developing function as a prognostic biomarker and a prospective therapeutic target in the treatment of patients post-AMI.
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