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Endocarditis prophylaxis : new guidelines from the british cardiac society guidelines and medical practice committee and roya

DENTAL ASPECTS OF ENDOCARDITIS PROPHYLAXIS : New
recommendations from the British Cardiac Society Guidelines and
Medical Practice Committee and Royal College of Physicians Clinical
Effectiveness and Evaluation Unit. 2004 [18-04-03]
Graham J Roberts
David Ramsdale
Consultant and Professor of Paediatric
Consultant Cardiologist
Dentistry
Cardiothoracic Centre
Unit of Paediatric Dentistry
Thomas Drive
The Eastman Dental Hospital and
Liverpool
University College London
256 Gray's Inn Road
tel 0151 293 2388
fax 0151 293 2254
tel 020 7915 1022
fax 020 7915 2329
Victoria S Lucas
The British Cardiac Society Guidelines
Senior Clinical Research Fellow
Group Comprises:
Unit of Paediatric Dentistry
The Eastman Dental Institute
Lead author: David R Ramsdale
tel 020 7915 1263
fax 020 7915 2329
Advisory Group:
David R Ramsdale (Cardiology)
Tom SJ Elliott (Microbiology)
Paul Wright (Microbiology)
Graham J Roberts (Dentistry)
Peter Wallace (Cardiac Anaesthesia)
Brian Fabri (Cardiac Surgery)
Nicholas Palmer (Cardiology)
Petros Nihoyannopoulos
(Echocardiography)
Michael Pearson (Clinical Effectiveness
& Evaluation Unit)
Chris Mutton (Cardiac Nursing)
Douglas Broadbent (Cardiac Patients
Association)

It is over 10 years since the endocarditis guidelines of the British Society of Antimicrobial Chemotherapy were published.(1) Since that time there have been many advances in the understanding of the susceptibility of patients ‘at risk' of contracting infective (bacterial) endocarditis.(2) In addition, considerable advances have been made as regards the intensity, nature, and causes of bacteraemia of dental origin(3;4) Accompanying these developments there have been further advances in the formulation and use of antibiotics.(5) It is clear that knowledge and understanding has advanced to the stage where it is appropriate to revise and update the existing guidelines. It is fortunate that The British Cardiac Society Medical Practice Committee and the Royal College of Physicians Clinical Effectiveness and Evaluation Unit have combined resources to produce comprehensive recommendations on the diagnosis, prophylaxis, and treatment of Infective Endocarditis (IE).(6) This report is an extended excerpt of the main document and covers only the prophylaxis of IE in relation to clinical dental practice. It provides dental practitioners with advice on how to use the recommendations in the context of clinical dental practice with further help provided by a specially developed set of web pages that can be used to help practitioners decide, if, when, and what antibiotic prophylaxis is required. It is important to note that all the information in this report is derived from the master document of the British Cardiac Society and The Royal College of Physicians.(6) This is The Recommendaton Development Group
These recommendations were developed by a working group nominated by the Guidelines and Medical Practice Committee of the British Cardiac Society in collaboration with the Clinical Effectiveness Unit of the Royal College of Physicians (London). Contributors to the recommendation's formulation included representatives of the British Cardiac Society (BCS), the British Junior Cardiologist's Association (BJCA), the Faculty of Dental Surgery of the Royal College of Surgeons of England, the Society of Cardiothoracic Surgeons (SCTS), the British Society of Echocardiography (BSE), the Royal College of Pathologists (Microbiology), the Royal College of Anaesthetists (RCA), the British Association for Nursing in Cardiac Care (BANCC) and the British Cardiac Patients' Association (BCPA). Other bodies with a practical interest in this field such as the Faculty of General Dental Practice of the Royal College of Surgeons of England, The British Dental Association and The American Heart Association were also consulted. Individuals with a special clinical or research interest (informed opinion) were also invited to offer advice. Patients at Risk
Changes in approach It is now recognised that the susceptibility to IE varies with the underlying cardiac condition. This is especially so with congenital heart disease where there is differential susceptibility according to the haemodynamic severity of the condition and whether surgery has been palliative or definitive. (2) (7), This is often related to the turbulence of blood flow with more severe turbulence causing damage to the endothelium which in turn increases the likelihood of a non-bacterial thrombotic vegetation occurring. A bacteraemia from a dental procedure may lead to seeding of the vegetation. Further platelet aggregation covers the bacteria and prevents the body's normal blood borne defenses from killing the bacteria. In this relatively well protected microenvironment the bacteria proliferate and in time, the symptoms and signs of IE appear. This differential susceptibility is reflected in the document by classifying patients into three risk groups: Table 1 [Table 3 in the British Cardiac Society/ Royal College of
Physicians Recommendations] (6)

HIGH RISK: CLASS I
Prosthetic heart valves
Previous infective endocarditis
Complex cyanotic congenital heart disease
Transposition of great arteries
Fallot's tetralogy
Gerbode's defect
Surgically constructed systemic pulmonary shunts or conduits Mitral valve prolapse with mitral regurgitation or thickened valve leaflets MODERATE RISK: CLASS II
Acquired valvular heart disease eg: rheumatic heart disease Aortic regurgitation Mitral regurgitation Other structural cardiac defects eg: ventricular septal defect Bicuspid aortic valve Primum atrial sepal defect Patent Ductus Arteriosus Aortic root replacement Coarctation of aorta Atrial septal aneurysm/patent foramen ovale Ventricular septal defect Hypertrophic obstructive cardiomyopathy Subaortic membrane LOW RISK: CLASS III (NOT REQUIRING ANTIBIOTIC PROPHYLAXIS)
Isolated secundum atrial septal defect Pulmonary stenosis Surgically-repaired atrial septal defect, Surgically repaired ventricular septal defect, Surgically repaired patent ductus arteriosus, Post Fontan or Mustard procedure without residual defect/murmur Previous coronary artery bypass surgery Isolated secundum atrial septal defect Mitral valve prolapse without regurgitation Innocent heart murmurs@ Cardiac pacemakers/defibrillators*$ Coronary artery stent implantation* Heart / Heart and Lung Transplant** Pulmonary stenosis Antibiotic prophylaxis is recommended for up to 12 months after ASD/PFO catheter-based closure procedures * Unless these procedures are being performed in patients at moderate or high risk of endocarditis when antibiotic prophylaxis is advisable. Antibiotic prophylaxis is not required for patients with previous pacemaker, defibrillator or coronary stent implantation. $ Pre and post procedure antibiotics are generally used routinely (see Table 10 in original document) @ If unsure as to the exact nature of the murmur and the need for prophylaxis, an opinion should be sought from a cardiologist. In an emergency or when it is difficult to obtain specific advice then antibiotic prophylaxis should be given prior to dental or surgical treatment **Within the first 6 months after heart/heart-lung transplantation, patients should receive antibiotic prophylaxis

HOW TO PROCEED: STEP 1
When assessing a patient for dental treatment the medical history will reveal the
existence of a cardiac problem. The above table should be consulted to determine the cardiac risk category of the patient. For example, the patient may report that he/she has mitral valve prolapse with mitral regurgitation. It is clear that the patient is in the High Risk group and that antibiotic prophylaxis against IE is required for any bacteraemia inducing procedures. Patients who are known to be at risk should carry a Warning Card. This should 1. The precise type of cardiac lesion present. 2. The degree of risk of developing Infective Endocarditis. 3. Whether or not the patient is allergic to Penicillin and the antibiotic prophylaxis that would normally be given to that patient. 4. The name and telephone number of the Cardiologist who can be contacted for The full British Cardiac Society recommendations for diagnosis and treatment of Infective Endocarditis are given at Significant Bacteraemia
Changes in Approach The term significant bacteraemia has been used loosely and without satisfactory definition for many years. In the new recommendations the term has been interpreted in a specific and unambiguous way. 1. The use of the term ‘…procedures that cause significant bleeding…' has been abandoned. This is because it has been shown in a detailed study that bleeding following dental treatment procedures is a poor predictor of odontogenic bacteraemia.(3) Consequently, the criterion of ‘significant bleeding' has been discarded as an indication for antibiotic prophylaxis in cardiac patients at risk of developing IE. 2. The term significant bacteraemia has been newly defined as ‘Dental bacteraemia following a dental procedure that is ‘statistically significantly different from the pre- procedure bacteraemia'. That is to say Post Procedure Bacteraemia is statistically significantly greater than the Pre Procedure Bacteraemia. The term procedure covers surgical procedures such as dental extractions and mucoperiosteal flaps but also procedures such as matrix band and wedge placement, placement of gingival retraction cord or rubber dam placement. Using this definition it has been possible to review the literature (back to the 1930's) on odontogenic bacteraemia and exclude those reports where the investigators did not take a pre-operative blood sample. In this way, only studies that reported statistically significant differences have been included for antibiotic prophylaxis of IE. An additional refinement of these data is to list both significant bacteraemia and non significant bacteraemia side by side in related groups and procedures. (Table 2) HOW TO PROCEED: STEP 2.
If the cardiac condition requires that antibiotic prophylaxis is administered to eliminate
odontogenic bacteraemia the clinician should look at the following table and determine which dento-gingival procedures are likely to be used when providing care. The details below will assist with this. TABLE 2. [Table 4 in the British Cardiac Society Document] DENTAL
PROCEDURES AND ENDOCARDITIS PROPHYLAXIS FOR HIGH AND
MODERATE AT-RISK CASES
Preliminary Considerations
Dental treatment is often made up of a series of Dento Gingival Manipulative Procedures. For example, a dental extraction may comprise an Intra Ligamentary Injection, Pre-Extraction Scaling, and Extraction of the tooth with forceps. Thus clinicians should consider the planned dental care, check with the list below, and if one of the procedures requiring prophylaxis is to be used then antibiotic prophylaxis should be administered. There are some difficulties which may be resolved with some thought. An example of a treatment procedure that may be carried out ‘without and ‘with antibiotic prophylaxis is endodontic treatment confined to the root canal. When the table is consulted it is clear that antibiotic prophylaxis is not required. If rubber dam is to be used then even if the endodontic procedure is confined to the root canal antibiotic prophylaxis should be used because of the significant bacteraemia caused by the placement of the rubber dam. RECOMMENDED FOR ANTIBIOTIC
NOT RECOMMENDED FOR
PROPHYLAXIS
ANTIBIOTIC PROPHYLAXIS
Examination Procedures
Examination Procedures
Periodontal probing (8) Dental examination with mirror & probe (9) Investigation Procedures
Investigation Procedures
Sialography (10) Intra oral radiographs Extra oral radiographs Preventive Procedures
Preventive Procedures
Fissure Sealants Fluoride treatments Professional Cleaning Procedures
Professional Cleaning Procedures
Polishing teeth with a Rubber Cup(11) Air polishing (12) Oral irrigation with water jet (13) , (14) Light scaling (15) Deep scaling (15) Scaling teeth with hand instrument (11),(16) Scaling with ultrasonic instrument (16) Anaesthetic Procedures
Anaesthetic Procedures
Intraligamental local anaesthesia (17) Infiltration local anaesthesia (17) Nerve block local anaesthesia Oral airway for GA (18),(19) Nasal airway for GA {(18),(20) Laryngeal mask airway for GA (21),(22) Comprehensive Dental Treatment under
Comprehensive Dental Treatment under
General Anaesthesia
General Anaesthesia
Extractions and Filling (23) ,(24) Conservation (Restorative) Procedures [δ] Conservative (Restorative) Procedures
Rubber dam placement (25),(26) Slow & Fast drilling of teeth(without rubber dam) (25),(26) Matrix band and wedge placement (25),(26) Gingival retraction cord placement (26) Periodontal Procedures
Periodontal Procedures
Root planning (15) [similar to scaling] Antibiotic fibres or strips placed subgingivally [ά]
Gingivectomy (15)
Periodontal Surgery (27) Endodontic Procedures
Endodontic Procedures
Root canal instrumentation beyond the root Root canal instrumentation within canal (15),(28) Pulpotomy of primary molar (29),(30) Pulpotomy of permanent tooth [β] Avulsed tooth reimplantation [γ] Orthodontic Procedures
Orthodontic Procedures
Tooth separation (31) Alginate Expose OR Expose and Bond of Tooth or Band placement and cementation Adjustment of fixed appliances (31) Surgical Procedures
Surgical Procedures
Incision and drainage of an abscess (40) Extraction of a single tooth (15),(38),(39),(9),(9) Extraction of multiple teeth (9),(39),(9),(15),(32) Mucoperiosteal flap to gain access to tooth or Lesion. (33),(32) Dental Implants (as for Mucoperiosteal Dental Implants Transmucosal fixture (as flap) Post Surgical Procedures
Post Surgical Procedures
None – as at July 2002 Suture removal (41),(42),(43) Removal of Surgical Packs (as for suture removal) Other Events (Daily or Physiological Other Events
Events)
Antibiotic prophylaxis not recommended as it is impractical despite presence of bacteraemia following some of these events. This is largely because of the significant risk of development of bacteria resistant to the antibiotics used Exfoliation of primary teeth [ά] no data but the procedure is very similar to that of gingival retraction cord placement[β] no data but the procedure is similar to pulpotomy of a primary molar [γ] the avulsed tooth can be quickly washed and re-implanted immediately by a parent or other responsible person and the antibiotic prophylaxis administered when the child attends the dental surgery provided this is within 2 hour of the reimplantation. This is because antibiotic prophylaxis is still successful if administered after the bacteraemic episode. (44) [δ] it is common for a course of dental treatment to take place over several visits to the dentist. For patients at high or moderate risk of developing infective endocarditis as much treatment as possible should be carried out at each visit. The antibiotic should be changed at alternate visits e.g. Amoxicillin – Clindamycin – Amoxicillin and so on. For young children the sequence would be Amoxicillin – Azithromycin – Amoxicillin and so on. If penicillin or penicillin related antibiotics are used as one of the antibiotics
then a period of 1 month must be allowed between visits when a penicillin antibiotic is
used. (45),(46) Dentists can help further by planning dental care to minimize the number
of times that patients are exposed to antibiotics by carrying out as much treatment as is
feasible at each visit.
In an emergency when treatment needs to be carried out urgently the dental surgeon
should make an assessment as to whether or not the patient is significantly at risk from
IE. If the answer is affirmative, the patient's clinical records should then be marked
appropriately and consideration given to the risk of bacteraemia associated with the
dental procedures to be carried out on the patient. If there is a risk of a significant
bacteraemia then antibiotic prophylaxis should be given.
HOW TO PROCEED: STEP 3
If it has been decide that antibiotic prophylaxis is required then the choice of antibiotic,
the dosage and the mode of administration should be made after scrutinising Tables 3
and 4.
Current Antibiotic Advice
Developments in Antibiotics The wider use of newer antibiotics and changes in formulation of other antibiotics has led to a re-appraisal of antibiotics suitable for prophylaxis in children and adults. These are presented as regimens suitable for use with Local Anaesthesia (LA) or no anaesthesia.(Table 3 [Table 6 in the BCS recommendations]) Where the treatment is to be carried out under General Anaesthesia (GA) or Intravenous Sedation (IVS) then alternative drug regimens are recommended. (Table 4 [Table 6 in the BCS recommendations]). DENTAL TREATMENT UNDER LOCAL ANAESTHESIA (OR PROCEDURES
WITHOUT LOCAL ANAESTHESIA)

Class I. High Risk of Developing Infective Endocarditis
and
Class II Moderate Risk of Developing Infective Endocarditis

Clinical Situation
Drug
Patients not allergic to Penicillin
Amoxicillin
Oral Amoxicillin 2g administered Patients who have not received
1 hour before the procedure more than a single dose or course of penicillin in the previous Children
< 5 years: Oral Amoxicillin 250mg administered 1 hour before the 5-10 years: Oral Amoxicillin 500mg administered 1 hour before the procedure > 10 years: use adult dose Patients allergic to Penicillin or
Clindamycin
who have had more than a single Oral Clindamycin 600mg 1 hour dose or course of Penicillin (or other Beta Lactam antibiotic) within the last month Children
< 5 years: Oral Clindamycin 150 mg
administered 1 hour before the
procedure
5-10 years: Oral Clindamycin 300 mg administered 1 hour before the procedure > 10 years: use adult dose [The oral suspension of Azithromycin
Clindamycin is no longer (as a suspension) 500 mg administered 1 hour before the available in the United Kingdom. If children are unwilling or unable to swallow tablets or Children
capsules, or patients are < 5 years: Oral Azithromycin suffering with dysphagia, then 200mg administered 1 hour before the Azithromycin is a suitable alternative.] 5-10 years: Oral Azithromycin 300mg administered 1 hour before the procedure > 10 years: use adult dose of 500mg 1 hour before the procedure Class III. Low Risk of Developing Infective Endocarditis
No Antimicrobial Prophylaxis Required Special Considerations:
Multiple Visits for Treatment Using Local (or no) Anaesthesia
For a care plan that will require several visits then a period of 1 month should elapse before the
second dose of the same antibiotic. If treatment is planned to extend over more than two visits
then Amoxicillin should be used one visit and Clindamycin (or Clarithromycin) for the next
visit. This alternating sequence can be continued until treatment is complete and the time
interval between different types of antibiotics does not need to exceed one month.
For Those at Highest of IE eg: Patients with Prosthetic Heart Valves or Previous IE

Adults - Intravenous Amoxicillin 2G within the 30 minutes before the procedure
plus Intravenous Gentamicin 1.5mg/kg within the same time period
Followed post-operatively by Intravenous Amoxicillin 1G
or Oral Amoxicillin 1G 6 hours post procedure
Children < 5 years as for < 10years
< 10 years Intravenous Amoxicillin 1G within the 30 minutes before the procedure
plus Intravenous Gentamicin 1.5 mg/kg within the same time period
Followed postoperatively by Oral Amoxicillin at 6 hours post procedure
For Patients Allergic to Penicillin
Adults - Intravenous Vancomycin 1G infused over the 2 hours before the procedure
plus Intravenous Gentamicin 1.5mg/kg within the same time period
Children < 5 years as for < 10years
< 10 years Intravenous Vancomycin 20mg/Kg over the 2 hours before the procedure
plus Intravenous Gentamicin 1.5 mg/kg within the same time period
> 10 years, use the adult dose
Not in the current recommendations but recently it has been shown to be as effective
as IV Ampicillin(47) as been used for several years as part of an antibiotic policy at Great
Ormond Street Hospital. This regimen should be reserved for use in hospitals or areas
where there is a special antibiotic policy to help cope MRSA

Adults- & Intravenous Teicoplanin 6mg/Kg and
Children -
plus Intravenous Amikacin 15mg/Kg immediately before the procedure


The need for a General Anaesthesia (GA) or Intra Venous Sedation (IVS) requires a modification to the drug regimen particularly with regard to dosage. (Table 4 [Table 6 in the BCS recommendations]). Table 4. DENTAL TREATMENT UNDER GENERAL ANAESTHESIA,
INTRAVENOUS SEDATION, OR PATIENTS UNABLE TO TAKE
ORAL MEDICATIONS

Clinical Situation
Drug
Patients not allergic to Penicillin Amoxicillin or
or Patients who have not Ampicillin
IV Amoxicillin 2g administered upon received more than a single dose attainment of GA and immediately or course of penicillin in the before the dental procedure
Children
< 5 years: IV Amoxicillin 250mg
administered upon attainment of GA
and immediately before the procedure
5-10 years: IV Amoxicillin 500 mg administered upon attainment of GA and immediately before the procedure > 10 years: use adult dose 2g administered immediately before the procedure Patients allergic to Penicillin or Clindamycin
who have had more than a single IV Clindamycin 300 mg infused over dose or course of Penicillin (or at least 10 minutes upon attainment of other Beta Lactam antibiotic) GA and commenced before the start of within the last month the dental surgery. This is followed by oral or IV Clindamycin 150 mg 6 hours later Children
< 5 years: IV Clindamycin
75 mg infused over at least 10 minutes
upon attainment of GA and
commenced before the start of the
dental procedure
5-10 years: IV Clindamycin 150mg infused over at least 10 minutes upon attainment of GA and commenced before the start of the dental procedure > 10 years: use adult dose Special concern :
for those at highest risk of IE eg: Prosthetic Heart Valve or Previous Infective Endocarditis see
Table 3.

Summary of the New Approach:

Consult the BCS recommendations (paper document) or the abstracted dental
recommendations in the current web pages (http://www.bcs.com) or

1. Assessment of Cardiac Risk - Determine the cardiac risk from Table 1. If the risk is
Moderate or High then the patient requires antibiotic prophylaxis for procedures that
produce a significant bacteraemia. If the risk is deemed to be Low then no antibiotic is
required for prophylaxis against Infective Endocarditis.
2. Assessment of Risk of Significant Bacteraemia - If the cardiac risk is Moderate
Risk or High Risk then the dentist should consider the details of the dental procedure.
If any planned dento-gingival manipulative procedure causes a significant bacteraemia
then it is clear that antibiotic prophylaxis is needed. The dental surgeon must undertake
a careful appraisal of all dento gingival manipulative procedures listed in Table 2 at the
planning stage of the operation to ensure that all bacteraemia inducing procedures are
included in the appraisal. If the dental bacteraemia risk is ‘non-significant' then
antibiotic prophylaxis is not required even if the patient is moderate or high risk as
regards the cardiac lesion.
3. Assessment of Antibiotic Prophylaxis - The choice of antibiotic regimen needs to
be made by first identifying whether treatment is to be carried out under no or local
anaesthesia. Table 3 provides the information required. If treatment is to be carried
out under general anaesthesia or intravenous sedation then the required information is in
Table 4. For Special concern patients, that is those with a prosthetic valve and/or
previous endocarditis it is important to remember to use IV Amoxicillin and
Gentamicin or IV Vancomycin and Gentamicin. This applies to patients treated under
No anaesthesia or Local Anaesthesia as well as patients receiving treatment under
Intravenous sedation or General Anaesthesia.
The information can be obtained from web pages on the Royal College of Surgeons of
England, ( ) or The Eastman Dental Institute and Hospital website.
)
Finally, it is important to write down the reasons for giving the antibiotic prophylaxis
and the choice of antibiotics. For a patient ‘at risk' of developing endocarditis it is
important that he/she understand the need to consult the doctor if any symptoms
develop which may possibly be related to the onset of infective endocarditis. For
example an unexplained fever or general malaise.
Adherence to the recommendations whenever possible is recommended but it is
recognised that there may be occasional circumstances where the clinician is required to
adapt the recommendations to fit a particular clinical scenario. The reasons for the
choices made must be recorded in the patient's notes.

Acknowledgements
Our thanks to the many colleagues who have offered advice and encouragement. It is
not possible to mention them individually but their contribution is duly acknowledged.

Reference List

(1) Simmons NA. Recommendations for endocarditis prophylaxis. J Antimicrob Chemother. 1993; 31: 427-38. (2) Li W, Somerville J. Infective endocarditis in the grown-up congenital heart (GUCH) population. Eur Heart J. 1998; 19: 166-73. (3) Roberts GJ. Dentists Are Innocent! "Everyday" Bacteremia Is the Real Culprit: A Review and Assessment of the Evidence That Dental Surgical Procedures Are a Principal Cause of Bacterial Endocarditis in Children. Pediatr Cardiol. 1999; 20: 317-25. (4) Lucas VS, Lytra V, Hassan T, Tatham H, Wilson M, Roberts GJ. Comparison of lysis filtration and an automated blood culture system (bactec) for detection, quantification, and identification of odontogeneic bacteraemia in children. J Clin Microbiol. 2002; 40: 3416-20. (5) Pallasch TJ, Slots J. Antibiotic prophylaxis and the medically compromised patient. Periodontol 2000. 1996: 10: 107-38. (6) Ramsdale DR, Elliott TSJ, Wright P, Roberts GJ, Wallace P, Fabri B, et al. Guidelines for the prophylaxis and treatment of infective endocarditis in adults. 2004:1-106 (7) Dajani AS, Taubert KA, Wilson W, Bolger AF, Bayer A, Ferrieri P, et al. Prevention of bacterial endocarditis. Recommendations by the American Heart Association. JAMA. 1997; 277: 1794-801. (8) Daly CG, Mitchell DH, Highfield JE, Grossberg DE. Bacteremia due to periodontal probing: a clinical and microbiological investigation. Periodontol 2000. 2001; 72: 210-14. (9) Roberts GJ, Holzel H, Sury MRJ, Simmons NA, Gardner P, Longhurst P. Dental bacteraemia in children. Pediatr Cardiol. 1997; 18: 24-7. (10) Lamey PJ, MacFarlane TW, Patton DW, Samaranayake LP, Ferguson MM. Bacteraemia consequential to sialography. BDJ 1985; 158: 218-20. (11) Lucas VS, Roberts GJ. Odontogenic bacteremia following tooth cleaning procedures in children. Pediatr Dent. 2000; 22: 96-100. (12) Hunter KM, Holborow DW, Kardos TB, Lee-Knight CT, Ferguson MM. Bacteraemia and tissue damage resulting from air polishing. BDJ 1989; 167: 275-8. (13) Berger SA, Weitzman S, Edberg SC, Casey JI. Bacteraemia after the use of an oral irrigation device. Ann Intern Med. 1974; 80: 510-1. (14) Felix JE, Rosen S, App GR. Detection of bacteremia after the use of an oral irrigation device in subjects with periodontitis. J Periodontol. 1971; 42: 785-89. (15) Bender IB, Seltzer S, Tashman S, Meloff G. Dental procedures in patients with rheumatic heart disease. Oral Surg Oral Med and Oral Path. 1963; 16: 466-73. (16) Bandt CL, Korn NA, Schaffer EM. Bacteremias from ultrasonic and hand instrumentation. J Periodontol 1964; 35: 214-5. (17) Roberts GJ, Simmons NB, Longhurst PB, Hewitt PB. Bacteraemia following local anaesthetic injections in children. BDJ. 1998; 185: 295-98. (18) Ali MT, Tremewen DR, Hay AJ, Wilkinson DJ. The occurrence of bacteraemia associated with the use of oral and nasopharyngeal airways. Anaesthesia 1992; 47: 153-5. (19) Gerber MA, Gastanaduy AS, Buckley J, Kaplan EL. Risk of Bacteremia after endotracheal intubation for general anesthesia. South Med J. 1980; 73: 1478-80. (20) Dinner M, Tjeuw M, Artusio JF. Bacteremia as a complication of nasotracheal intubation. Anesth Analg 1987; 66: 460-2. (21) Stone JM, Karalliedde LD, Carter ML, Cumerland NS. Bacteraemia and insertion of laryngeal mask airways. Anaesthesia 1992; 47: 77. (22) Brimacombe J, Shorney N, Swainston R, Bapty G. The incidence of bacteraemia following laryngeal mask insertion. Anaesthesia and Intensive Care 20, 484-490. 1992. Ref Type: Journal (Full) (23) Berry FA, Yarbrough S, Yarbrough N, Russell CM, Carpenter MA, Hendley JO. Transient bacteremia during dental manipulation in children. Pediatrics 1973;51 No3:476-9. (24) Roberts GJ, Radford P, Holt R. Prophylaxis of dental bacteraemia with oral amoxycillin in children. BDJ 1987;162:179-82. (25) Roberts GJ, Gardner P, Longhurst P, Black A, Lucas VS. Intensity of bacteraemia associated with conservative dental procedures in children. BDJ. 2000; 188: 95-8. (26) Sonbol H, Spratt D, Roberts GJ, Lucas VS. Bacteraemia from conservative (restorative) procedures. 2003. Proceedings of the 7th International Symposium on Modern Concepts in Endocarditis. (27) Lineberger LT, De Marco TJ. Evaluation of transient bacteraemia following routine periodontal procedures. J Periodontol. 1973; 44: 757-63. (28) Debelian GJ, Olsen I, Tronstad L. Bacteremia in conjunction with endodontic therapy. Endod Dent Traumatol. 1995; 11: 142- 49. (29) Farrington FH. The incidence of transient bacteremia following pulpotomies on primary teeth. ASDC J Dent Child. 1973; 40:175-84. (30) Beechen II, Laston DJ, Garbarino VE. Transitory bacteremia as related to the operation of vital pulpotomy. Oral Surg 1956; 9: 902-5. (31) Lucas VS, Omar J, Vieira A, Roberts GJ. The relationship between odontogenic bacteraemia and orthodontic treatment procedures. Eur J Orth. 2002; 24: 293-301. (32) Roberts GJ, Watts R, Longhurst.P, Gardner P. Bacteraemia of dental origin and antimicrobial sensitivity following oral surgical procedures in children. Pediatric Dent. 1998; 20: 28-36. (33) Heimdahl A, Hall G, Hedberg M, Sandberg H, Soder PO, Tuner K, et al. Detection and quantitation by lysis-filtration of bacteraemia after different oral surgical procedures. J Clin Microbiol 1990; 28:2205-9. (34) Everdi N, Kadir T, Ozkan H, Acur A. Investigation of bacteremia after orthodontic banding. Am J Orthod Dentofacial Orthop. 1999; 116: 687-90. (35) McLaughlin JO, Coulter WA, Coffey A, Burden DJ. The incidence of bacteremia after orthodontic banding. Am J Orthod Dentofacial Orthop. 1996; 109: 639-44. (36) Erverdi N, Biren.S., Kadir T, Acar A. Investigation of bacteremia following orthodontic debanding. Angle Orthod. 2000; 70, 11-14. (37) Kyriazidou A, Lucas VS, Gelbier M, Roberts GJ. Bacteraemia following removal of orthodontic bands. Proceedings of the 7th Internatinal Symposium on Modern Concepts in Endocarditis . 2003. (38) Peterson LJ, Peacock R. The incidence of bacteremia in pediatric patients following tooth extraction. Circulation 1976; 53: 676-9. (39) Burket LW, Burn CG. Bacteremias following dental extraction. Demonstration of source of bacteria by means of a non pathogen (Serratia marcesens). J Dent Res. 1937; 16: 521-30. (40) Flood TR, Samaranayake LP, MacFarlane TW, McLennan A, MacKenzie D, Carmichael F. Bacteraemia following incision and drainage of dento-alveolar abscesses. BDJ 1990; 169: 51-3. (41) Giglio JA, Rowland RW, Dalton HP, Laskin DM. Suture removal induced bacteremia: a possible endocarditis risk. JADA. 1992; 123: 65-70. (42) King RC, Crawford JJ, Small EW. Bacteraemia following intraoral suture removal. Oral Surg. 1988; 65: 23-8. (43) Brown AR, Papasian J, Shultz P, Theisen D, Shultz RE. Bacteremia and Intraoral Suture Removal: Can an antimicrobial rinse help? JADA.1998; 129: 1455-461. (44) Blatter M, Francioli P. Endocarditis prophylaxis: from experimental models to human recommendation. Eur Heart J. 1995; 16(Supplement B): 107-09. (45) Woodman AJ, Vidic J, Newman HN, Marsh PD. Effect of repeated high dose prophylaxis with amoxycillin on the resident oral flora of adult volunteers. J Med Microbiol. 1985; 19: 15-23. (46) Fleming P, Feigal RJ, Kaplan EL, Liljemark WF, Little JW. The development of penicillin-resistant oral streptococci after repeated penicillin prophylaxis. Oral Surg. 1990; 70: 440-4. (47) Roberts GJ. The efficacy of intravenous antibiotics in reducing bacteraemia following extractions and restorations in children with severe congenital heart disease. BDJ. 2002; 193: 525-7.

Source: http://scts.org/_userfiles/resources/634343180320524595_SBEfromBCS.pdf

privateessex.ac.uk

Relating morphology to syntax Relating Morphology to Syntax Louisa Sadler and Rachel Nordlinger Relatively little attention in theoretical work in LFG has focussed on the nature ofthe interface between morphology and syntax, or indeed on the role of morphologyproper.1 2 While the contribution of morphology to the definition of f-structures isfirmly established, and the separation of external structures by the principle of lexicalintegrity is the backbone of LFG's lexicalist outlook, the internal operation of the mor-phological component, and how words come to contribute the relevant f-descriptionshave not generally been at the forefront of theoretical work.

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