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. 2009 Jun 29:9:104.
doi: 10.1186/1471-2334-9-104.

Role of pathogenic oral flora in postoperative pneumonia following brain surgery

Affiliations

Role of pathogenic oral flora in postoperative pneumonia following brain surgery

Kinga Bágyi et al. BMC Infect Dis. .

Abstract

Background: Post-operative pulmonary infection often appears to result from aspiration of pathogens colonizing the oral cavity. It was hypothesized that impaired periodontal status and pathogenic oral bacteria significantly contribute to development of aspiration pneumonia following neurosurgical operations. Further, the prophylactic effects of a single dose preoperative cefazolin on the oral bacteria were investigated.

Methods: A matched cohort of 18 patients without postoperative lung complications was compared to 5 patients who developed pneumonia within 48 hours after brain surgery. Patients waiting for elective operation of a single brain tumor underwent dental examination and saliva collection before surgery. Bacteria from saliva cultures were isolated and periodontal disease was scored according to type and severity. Patients received 15 mg/kg cefazolin intravenously at the beginning of surgery. Serum, saliva and bronchial secretion were collected promptly after the operation. The minimal inhibitory concentrations of cefazolin regarding the isolated bacteria were determined. The actual antibiotic concentrations in serum, saliva and bronchial secretion were measured by capillary electrophoresis upon completion of surgery. Bacteria were isolated again from the sputum of postoperative pneumonia patients.

Results: The number and severity of coexisting periodontal diseases were significantly greater in patients with postoperative pneumonia in comparison to the control group (p = 0.031 and p = 0.002, respectively). The relative risk of developing postoperative pneumonia in high periodontal score patients was 3.5 greater than in patients who had low periodontal score (p < 0.0001). Cefazolin concentration in saliva and bronchial secretion remained below detectable levels in every patient.

Conclusion: Presence of multiple periodontal diseases and pathogenic bacteria in the saliva are important predisposing factors of postoperative aspiration pneumonia in patients after brain surgery. The low penetration rate of cefazolin into the saliva indicates that its prophylactic administration may not be sufficient to prevent postoperative aspiration pneumonia. Our study suggests that dental examination may be warranted in order to identify patients at high risk of developing postoperative respiratory infections.

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Figures

Figure 1
Figure 1
Clinical parameters of patients. Patients that developed pneumonia had comparable age, weight and duration of operation to controls that had no postoperative pneumonia. (A): Patients demographic data in a table format. (B-C): The patients who developed postoperative pneumonia were matched according to sex, age, weight and length of brain surgery. Data were compared using the non-parametric Mann-Whitney test and expressed as "box and whiskers: 10–90 percentile".
Figure 2
Figure 2
Relative risk for postoperative pneumonia in relation to periodontal diseases. Presence of periodontal diseases and disease severity were significantly greater in patients with postoperative pneumonia. (A-B): Data were expressed as "box and whiskers: 10–90 percentile" and compared using the non-parametric Mann-Whitney test (A): Disease score: periodontal diseases in every patient were evaluated. A score number was ordered to each diagnose, and the sum of the scores appears as "disease score". * = p = 0.0018 (B): Severity score is the number of co-existing periodontal diseases in each patient. * = p = 0.031; (C): Analysis of Relative Risk: "High score" patients had a Disease Score of ≥ 15 and a Severity Score of ≥ 3. Number of patients is shown in each groups. Chi-square test was performed, one-sided p value was calculated. *p < 0.0001; Relative risk: 3.5; confidence interval (95%): 1.085 to 11.29.
Figure 3
Figure 3
Minimal inhibitory concentrations (MIC) of cefazolin and its concentration in serum. Neither cefazolin sensitivity of the bacteria isolated from the saliva/bronchial secretions nor serum cefazolin levels were different between control and pneumonia patients. Bacteria were isolated from the saliva pre- and postoperatively. Bronchial secretion and serum were obtained post-operatively for bacterial culture and determination of cefazolin levels. (A): Distribution of isolated bacteria according to their MIC values. The antibiotic level of all the saliva and bronchial secretion samples fell below 0.5 mg/L; marked by the vertical dashed line. (B): Distribution of isolated bacteria according to percentage of patients with that particular species in each group. (C): Serum cefazolin levels are expressed as "box and whiskers: 10–90 percentile" and compared using the non-parametric Mann-Whitney test between control and pneumonia patients (n = 18 and 5, respectively).
Figure 4
Figure 4
Comparison of the minimal inhibitory concentration (MIC) of cefazolin regarding the bacteria isolated preoperatively from the saliva and postoperatively from the sputum. Cefazolin resistant pathogenic, Gram negative bacteria isolated from the saliva pre-operatively, were also grown from the sputum of the postoperative pneumonia patients. The vertical axis of the graphs crosses the x axis at 0.5 mg/L. The antibiotic level of all the sputum samples fell below 0.5 mg/ml. The bars indicate the MIC value of bacteria obtained pre-operative from the saliva. Black bars denote the bacteria that were cultured from both the sputum and the saliva of the same patient.

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