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Microflora of normal maxillary sinuses: does it justify perioperative antibiotic treatment in sinus augmentation procedures

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Clinical Oral Investigations
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Objectives To investigate bacterial flora of normal maxillary sinuses in order to facilitate perioperative antibiotic management in sinus augmentation procedures. Materials and methods Specimens of maxillary sinus mucosa were harvested during planned orthognatic surgery in 18 patients with no evidence of rhinosinusitis. The samples were processed according to hospital routine for aerobic and anaerobic cultures. Results Ten maxillary sinuses were found sterile. Twenty-six (72%) maxillary mucosa specimens were culture-positive. Aerobes were recovered in 21 sinus samples (58%), predominantly as polymicrobial flora (18 cultures, 50% of all specimens), S. aureus in 2 sinuses of the same patient (6% of the samples), and Bacillus sp. in 1 sinus (3%). Anaerobes were isolated in 20 of 26 culture-positive specimens (56% of all sinus samples). They were recovered alone in 5 samples. Fifteen anaerobic cultures were polymicrobial (42% of all samples). Propionibacterium acnes was isolated from another 5 sinuses (14%) of 3 patients. Conclusions Our data support the policy of perioperative antibiotic prophylaxis in sinus augmentation procedures where Schneiderian membrane is perforated. Clinical relevance Evaluating the need of a perioperative antibiotic therapy in sinus augmentation procedures.
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ORIGINAL ARTICLE
Microflora of normal maxillary sinuses: does it justify perioperative
antibiotic treatment in sinus augmentation procedures
Oren Peleg
1
&Danielle Blinder
1,2
&Keren Yudovich
3
&Arkadi Yakirevitch
4,5
Received: 2 August 2017 /Accepted: 25 September 2018 /Published online: 2 October 2018
#Springer-Verlag GmbH Germany, part of Springer Nature 2018
Abstract
Objectives To investigate bacterial flora of normal maxillary sinuses in order to facilitate perioperative antibiotic management in
sinus augmentation procedures.
Materials and methods Specimens of maxillary sinus mucosa were harvested during planned orthognatic surgery in 18 patients
with no evidence of rhinosinusitis. The samples were processed according to hospital routine for aerobic and anaerobic cultures.
Results Ten maxillary sinuses were found sterile. Twenty-six (72%) maxillary mucosa specimens were culture-positive. Aerobes
were recovered in 21 sinus samples (58%), predominantly as polymicrobial flora (18 cultures, 50% of all specimens), S. aureus in
2 sinuses of the same patient (6% of the samples), and Bacillus sp. in 1 sinus (3%). Anaerobes were isolated in 20 of 26 culture-
positive specimens (56% of all sinus samples). They were recovered alone in 5 samples. Fifteen anaerobic cultures were
polymicrobial (42% of all samples). Propionibacterium acnes was isolated from another 5 sinuses (14%) of 3 patients.
Conclusions Our data support the policy of perioperative antibiotic prophylaxis in sinus augmentation procedures where
Schneiderian membrane is perforated.
Clinical relevance Evaluating the need of a perioperative antibiotic therapy in sinus augmentation procedures.
Keywords Maxillary sinus .Microflora .Tissue culture .Sinus augmentation
Introduction
The routine use of antibiotics in oral implant treatment seems to
be widespread. Antibiotic therapy in conjunction with implant
surgery and its correlation with failure and success rates remain
poorly documented, however. The debate regarding overpre-
scription of antibiotics raises the need for a critical evaluation of
proper antibiotic coverage in association with implant treat-
ment and sinus augmentation procedures. In the setup of dental
implantology, knowledge of the bacterial flora of normal max-
illary sinuses is important for planning the perioperative man-
agement. However, the knowledge of presence and nature of
the sinus flora is not clear. According to some studies, healthy
paranasal sinuses are sterile [1,2]. Nonetheless, others have
found bacteria in normal sinuses [35].
Additionally, possible correlation between the microflora
of nasal cavity and maxillary sinus could guide the choice of
postoperative antibiotic prophylaxis. So far, research on this
correlation lacks. In attempt to shed some light on these issues,
we conducted a study of nasal cavity and maxillary sinus
mucosa cultures obtained during elective orthognatic surgery
for maxillary deformities. The tissue culture was chosen as it
is deemed the most reliable method of sampling [6,7].
Materials and methods
Patient selection
The study was performed at the tertiary medical center, from
2007 to 2013. Recruited patients were planned for orthognathic
*Oren Peleg
orenpeleg@gmail.com
1
Department of Oral and Maxillofacial Surgery, Sheba Medical
Center, Tel Hashomer, Israel
2
Maurice and Gabriela Goldschleger School of Dental Medicine, Tel
Aviv University, Tel Aviv-Yafo, Israel
3
Department of Oral and Maxillofacial Surgery, Rambam Medical
Center, Haifa, Israel
4
Department of Otolaryngology-Head & Neck Surgery, Sheba
Medical Center, Ramat Gan, Israel
5
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Clinical Oral Investigations (2019) 23:21732177
https://doi.org/10.1007/s00784-018-2662-0
Content courtesy of Springer Nature, terms of use apply. Rights reserved.
... Zinser et al. [42] evaluated risk factors in sinus lifts with 1-or 2-stage DI placement, showing that prescribing PAT does not significantly influence DI or graft failure rates compared to not prescribing PAT (LoE 2+). Some authors only recommend prescribing PAT if Schneider's membrane perforation occurs because of the high failure rate due to graft infection [45] (LoE 2+) (OR = 16.82 [46]). The rate of sinus membrane perforation in these procedures has been estimated at 18.3% [46]-23.5% [47]. ...
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CONFLICT-OF-INTEREST STATEMENT: Marco Esposito is the first author of two of the included studies; however, he was not involved in the quality assessment of these trials. This review is based on a Cochrane systematic review entitled 'Interventions for replacing missing teeth: antibiotics at dental implant placement to prevent complications' published in The Cochrane Library (see http://www.cochrane.org for more information). Cochrane systematic reviews are regularly updated to include new research, and in response to comments and criticisms from readers. If you wish to comment on this review, please send your comments to the Cochrane website or to Marco Esposito. The Cochrane Library should be consulted for the most recent version of the review. The results of a Cochrane Review can be interpreted differently, depending on people's perspectives and circumstances. Please consider the conclusions presented carefully. They are the opinions of the review authors, and are not necessarily shared by the Cochrane Collaboration. To assess the beneficial or harmful effects of systemic prophylactic antibiotics at dental implant placement versus no antibiotic/placebo administration and, if antibiotics are of benefit, to find which type, dosage and duration is the most effective. The Cochrane Oral Health Group's Trials Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE and EMBASE were searched up to 2 June 2010 for randomised controlled clinical trials (RCTs) with a follow-up of at least 3 months comparing the administration of various prophylactic antibiotic regimens versus no antibiotics to patients undergoing dental implant placement. Outcome measures were prosthesis failures, implant failures, postoperative infections and adverse events (gastrointestinal, hypersensitivity, etc.). Screening of eligible studies, assessment of the methodological quality of the trials and data extraction were conducted in duplicate and independently by two review authors. Meta-analyses were conducted. Four RCTs were identified: three comparing 2 g of preoperative amoxicillin versus placebo (927 patients) and the other comparing 1 g of preoperative amoxicillin plus 500 mg four times a day for 2 days versus no antibiotics (80 patients). The meta-analyses of the four trials showed a statistically significantly higher number of patients experiencing implant failures in the group not receiving antibiotics: risk ratio=0.40 (95% confidence interval (CI) 0.19 to 0.84). The number needed to treat (NNT) to prevent one patient having an implant failure is 33 (95% CI 17-100), based on a patient implant failure rate of 5% in patients not receiving antibiotics. The other outcomes were not statistically significant, and only two minor adverse events were recorded, one in the placebo group. There is some evidence suggesting that 2 g of amoxicillin given orally 1 h preoperatively significantly reduce failures of dental implants placed in ordinary conditions. No significant adverse events were reported. It might be sensible to suggest the use of a single dose of 2 g prophylactic amoxicillin prior to dental implant placement. It is still unknown whether post-operative antibiotics are beneficial, and which is the most effective antibiotic.
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