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ISSN 1011 - 4181

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TOMO 49
APIIO - IOYNIO 2005

hellenic
stomatological review
HELLENIC DENTAL ASSOCIATION
VOLUME 49, ISSUE 2, APRIL - JUNE 2005

ISSN 1011 - 4181

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TOMO 49, TEYXO 2


APIIO - IOYNIO 2005
ISSN 1011 - 4181

EPIEXOMENA

EPEYNHTIKH EPAIA

I

E. M, . Z M. ......................129-135
ENIAEPOYA EPITH

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TOMO 49, TEYXO 2


APIIO - IOYNIO 2005
ISSN 1011 - 4181

PAKTIKA EMATA

X

. , X. X A. K..........219-227
H


. K, . , M. B M. Bamber........229-233

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603

Hellenic Dental Association

Hellenic
Stomatological
Review
CONTENTS

PROPRIETOR:
Hellenic Dental Association
EDITOR -IN- CHIEF:
J. G. Tzoutzas
EDITORIAL BOARD:
G. Douvitsas
F. Zervou - Valvi
H. Karkazis
E. Katsavrias
G. Mountouris
L. Papagiannoulis
D. Tziafas
V. Topitsoglou - Themeli
COPY EDITOR:
Evelin Babai
PRODUCTION - PROMOTION:
TypeProduct
V. & E. Babai Ltd
32 Epikourou Str., Athens Hellas
Phone#: (3210) 32.14.904
Fax#: (3210) 32.14.991
ADVERTISEMENTS - PUBLIC
RELATIONS:
M. Morfoniou - S. Gogas
Phone#: (3210) 33.02.343
Fax: (3210) 38.34.385
E-mail: eoo@otenet.gr
Hellenic Stomatological Review is the
official publication of the Hellenic Dental
Association, published trimonthly.
Annual subscription

40 $ USD

PUBLISHER:
Panos Alexiou
President of the Hellenic Dental Association
HEADQUARTERS
38 Themistokleous Str., Athens, 106 78
Phone#: (3210) 38.13.380
Fax#: (3210) 38.34.385
E-mail: eoo@otenet.gr

VOLUME 49, ISSUE 2


APRIL - JUNE 2005
ISSN 1011 - 4181

RESEARCH PAPERS

Special characteristics of dental phobic patients treated under


general anesthesia
E. Boghossian, T. Zouridaki and M. Fragakis ............................129-135
CASE REPORT

Intraoral manifestations of resistant acute myelomonocytic


leukaemia. Therapeutic approach
M. Papadopoulou, J. Stergiopoulos,
D. Tzitiridis and N. Papanikolaou..............................................137-140
LITERATURE REVIEWS

Per os and intravenus sedation in oral surgery


E. Stavrou, N. Papachristou, L. Prezas and I. Stavrou...............141-146
The role of the dentist in the prevention of infective endocarditis
T. Almaghout, V. Karagkiozaki, I. Litsas and A. Zorbas .............147-154
Bleeding disorders and oral surgery
L. Hadjipetrou, D. Mangoudi and K. Antoniades ......................155-168
Guided bone regeneration adjacent to implants placed into
immediate extraction sockets
M. Manda, E. Dima, I. Karoussis and I. Fourmousis ..................169-178
Xerostomia and complete dentures
S. Yannikakis, A. Dimitriou and A. Zissis...................................179-187
Timing of performing Guided Bone Regeneration in Implant
Dentistry
E. Sinanioti and V. Piperias ......................................................189-198
Intrauterine preventive dentistry
A. Polychronopoulou, K. Divaris and K. Kavvadia ....................199-209
Behavioral sciences in Dentistry
H. Koletsi-Kounari, J. Avgeris ...................................................211-218

stomatologika exof.

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604

Hellenic Dental Association

Hellenic
Stomatological
Review
PROPRIETOR:
Hellenic Dental Association
EDITOR -IN- CHIEF:
J. G. Tzoutzas
EDITORIAL BOARD:
G. Douvitsas
F. Zervou - Valvi
H. Karkazis
E. Katsavrias
G. Mountouris
L. Papagiannoulis
D. Tziafas
V. Topitsoglou - Themeli
COPY EDITOR:
Evelin Babai
PRODUCTION - PROMOTION:
TypeProduct
V. & E. Babai Ltd
32 Epikourou Str., Athens Hellas
Phone#: (3210) 32.14.904
Fax#: (3210) 32.14.991
ADVERTISEMENTS - PUBLIC
RELATIONS:
M. Morfoniou - S. Gogas
Phone#: (3210) 33.02.343
Fax: (3210) 38.34.385
E-mail: eoo@otenet.gr
Hellenic Stomatological Review is the
official publication of the Hellenic Dental
Association, published trimonthly.
Annual subscription

40 $ USD

PUBLISHER:
Panos Alexiou
President of the Hellenic Dental Association
HEADQUARTERS
38 Themistokleous Str., Athens, 106 78
Phone#: (3210) 38.13.380
Fax#: (3210) 38.34.385
E-mail: eoo@otenet.gr

VOLUME 49, ISSUE 2


APRIL - JUNE 2005
ISSN 1011 - 4181

PRACTICAL NOTES

Usefulness of microbiological testing in Clinical Periodontology


D. Sakellari, C. Xatzigeorgiou and A. Konstantinidis .................219-227
The use of mini-comparator in the construction of an oculofacial
prosthesis
P. Kafas, S. Dalambiras, M. Vourvachis and M. Bamber ...........229-233

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SUMMARY

Special characteristics of dental phobic patients


treated under general anesthesia
E. Boghossian, T. Zouridaki, M. Fragakis
hellenic stomatological review 49: 129-135, 2005

Dental fear and anxiety is a world-wide problem and a


barrier to oral health care services. Fears acquired in
childhood through direct experiences or indirect through
parents, siblings or friends may persist into adulthood.
Phobia is a persisting and irrational fear for an object,
situation or activity, which results in avoidance behavior.
Dental phobia is a special phobia as well as Blood-InjuryInjection phobia. Corah's Dental Anxiety Scale is used
since 1969 in order to assess dental fear and anxiety. The
scale yields a score from 4 to 20. Score greater than 17
indicates dental phobia.
The purpose of this study is to record the special
characteristics and evaluate the experience that derives
from applying general anesthesia for treatment of dental
phobic patients.
The present study is a retrospective longitudinal evaluation
of 5.158 patients examined during the period 1991-2.000
in the Dental Clinic of University Hospital of Heraklion and
it showed that 946 (18,34%) presented anxiety for dental
procedures, 243 (4,71%) scored more than 17 points in
the Dental Anxiety Scale. 62 of them were treated with the
use of general anesthesia.
After completing the medical and dental history, all
patients completed the Corah Dental Anxiety Scale (DAS).
They all underwent basic preoperative control, including
clinical dental and x-ray examination.
Out of 62 patients 23 (37,1%) were male and 39 (62,9%)
female. The patients' age ranged from 6 to 63 years. Of the
62 patients 46 (82,25%) were 11-40 years old. All patients
scored at the Dental Anxiety Scale more than 17 points. 37
of them referred to previous traumatic dental experience, 8
suffered from Blood-Injury-Injection phobia, 8 presented
phobia for medical procedures and establishments
caused of severe chronic therapies. 9 patients presented
134

coexisting psychiatric conditions. The dental treatment


included 187 extractions, 40 surgical extractions, 29
extractions of impacted third molars, 31 fillings, 9
endodontic therapies, 8 apicectomies, 6 scaling
procedures and so on. All patients underwent treatment
without any problems or complications. The total time of
hospitalization was 130 days with an average of 2,1 days
per patient.
Dental fear and anxiety are common reasons why patients
fail to seek dental care. All dental patients have some fear
and anxiety. About 5% of dental patients suffer from severe
dental phobia. The majority of patients in this study were
female. This is in accordance with WHO and findings from
other studies indicating that fear and anxiety are more
prevalent among females. A great percentage of the
study's patients aged between 11-40 years. International
Classification of Diseases indicate that specific phobias
usually arise in childhood or early adult life and can persist
for decades if they remain untreated. That is in accordance
with related studies indicating that dental anxiety is less
prevalent among older adults. Corah's DAS is the most
widely used measure of dental anxiety. It has satisfactory
reliability, validity and it is easy to use. The most prevalent
cause of patients' fear was reported to be previous dental
traumatic experience especially in childhood. In addition
social, economical and educational factors and individual
personality traits seem to be associated with dental
phobia. Prevention of fear development through the use of
effective behavioral child management techniques
combined with preventive dentistry is possible to improve
the level of oral hygiene and the fear of dental treatment as
well. Blood-Injury-Injection phobia often co-exists with
dental phobia. The number of extractions illustrates the
patients' oral health status. It has been proved from several
studies that dental anxiety is positively correlated with
dental problems and it is likely to be a significant predictor
of dental caries experience. General anesthesia is a safe
and effective treatment tool for providing comprehensive
dental and oral surgical treatment for the dental phobic
patients. It is possible that phobic patients would seek oral
health care more regularly if general anesthesia was more
prevalent.
Conclusively dental phobia results in severe dental
problems for many patients. Using general anesthesia it is
possible not only to cope with this problem and improve
their oral health status but also to change their apprehension about dentistry.
Key words: Fear, dental anxiety, dental phodia, dental treatment,
general anesthesia

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T B: A . E X 2003; 47:
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A E I. T O E.O.O. 1990: 148.
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T O E.O.O. 1991: 88-89.
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M.
. X 6,
H 71202
T: 2810-392473, 2810-392475

49: 129-135, 2005

135

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E
.
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25/2/2004 - 8/6/2004

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H N K.


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E. 2: M
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, ,
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49: 137-140, 2005

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,
. (9). H

, . T A-O
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SUMMARY
E. 5: M .

YZHTHH
O ,
18%
80%, 4%
. A
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A) .



, , (4). B )
. A ,
, ,


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. H
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, , 49: 137-140, 2005

Intraoral Manifestations of Resistant


Acute Myelomonocytic Leukaemia.
Therapeutic Approach
M. Papadopoulou, J. Stergiopoulos,
D. Tzitiridis, N. Papanikolaou
hellenic stomatological review 49: 137-140, 2005

This is a case report of resistant acute myelomonocytic


leukaemia in a 57 years old female patient. Clinical examination revealed refractory extramedullary infiltrations in the
gingivae and necrotic ulcerative lesions in the oral
mucosa. The patient had not received any antileukaemic
medication for the previous 5 months because of the
resistance of the disease. She had followed-up in Haematology Out-Patients while she was treated conservatively
(blood and platelet transfusions, management of
infections). The oral manifestations occurred as a result
not only of leukaemic cell infiltrates in the gingivae (white
blood cells 55,000 /mm with 95% myelomonoblasts) but
also from haemorrhagic diathesis and local infections by
fungi. The patient was subjected to combined therapy
comprising: chemotherapy with hydroxyurea per os (2gr
daily) for the systemic disease and local treatment by
gentle cleaning, mouthrinses with saline, chlorhexidine
digluconate 0.12% and locally-delivered antifungal and
analgesic drugs (nystatin oral suspension, xylocain gel).
Additionally itraconazole was administered systemically.
Finally platelets were given for the haemorrhagic diathesis.
One week later the patient showed marked local
improvement (chewing, deglutition and speech without
discomfort) while laboratory tests showed severe pancytopenia for which support with transfusions were given.
Hydroxyurea was stopped and systematic close dental
screening and care supplemented with circumstantial
management of her haematologic disorders were
implemented. The oral lesions disappeared while the
systemic disease persisted. Oral and perioral manifestations of acute leukaemia are reported to have a prevalence of 18% to 80%, whereas in about 4% of the cases
these are the first sign of the disease leading to the
139

137-140 SEL. PAPADOPOULOU*

3-10-08 13:11

140

diagnosis of leukaemia. They are more common in acute


monocytic or myelomonocytic leukaemias, and they
complicate the treatment of the disease. They can be
classified as: 1) Primary manifestations with generalised or
localised gingival overgrowth, odontalgia and tooth
mobility due to leukaemic infiltrates in soft tissues and
alveolar bone of the oral cavity.2) Secondary manifestations as a result of anaemia, leukopenia and thrombocytopenia resulting in paleness and aching necrotic lesions
due to superinfections and microhaemorrhages. 3)
Tertiary manifestations resulting from chemo - or radiotherapy toxicity and Graft versus Host Disease (GVHD). In
this reported case the patient exhibited primary as well as
secondary lesions which demanded the bi-disciplinary
Heamatologist-Dentist approach. Furthermore this emphasises the importance of dental care and stringent oral
hygiene measures in immuno-compromised patients
which substantially reduce the severity of intraoral lesions,
enhancing the quality of life for these patients.
Key words: acute myelomonocytic leukaemia (AMML), oral manifrstations, therapy

BIBIOPAIA
1. Miller BK: Clinical Manifestations of Acute Myeloid
Leukemia In Hoffman R. Hematology Basic Principal and
Practice, p: 997-1000. Churchill Livingstone Second Edition
NY, USA 1995.

2. Sklavounou-Andricopoulou A, Piperi E, Paikos S: Oral and


maxillofacial manifestations of malignant haemopoietic and
lymphoreticular disorders Part IIA Haema 2002; 5(4): 305319.
3. Sklavounou-Andricopoulou A, Piperi E, Paikos S: Oral and
maxillofacial manifestations of malignant haemopoietic and
lyphoreticular disorders Part IIB Haema 2003; 6 (1): 48-53.
4. X E, N- O, M M, N , K :
: . E
X 1998; 13 (3): 125-129.
5. BA, N , M I,
, X, K : A o
: . 2002;
59 (3): 120-124.
6. T E, NA: H . 1997; 11
(1): 30-36.
7. N- O, I, K K,
: : . 1997; 11 (4): 148-152.
8. Hou GL , Huang JS , Tsai CC: Analysis of oral manifestations
of leukemia: A retrospecive study. Oral Dis 1997; 3: 31-38.
9. Barrett AP: Oral changes as initial diagnostic indicators in
acute leukemia. J Oral Med 1986; 41(4): 234-238.

:
M.
K 16, K 60100
T: 23510-39475
E-mail: pepper 2@ otenet.gr.

140

49: 137-140, 2005

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H

E. *, N. **, . ***, I. ****

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) . . H
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142

BENZOIAZEINE: IAZEAMH KAI MIAZOAMH


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X H A 1989.
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144

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49: 141-146, 2005

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SUMMARY

Per os and intravenus sedation in oral surgery


E. Stavrou, N. Papachristou, L. Prezas, I. Stavrou
hellenic stomatological review 49: 141-146, 2005

Fear, pain, the inability of the patient (mainly children or


mentally retarded people) to co-operate with his doctor,
and special groups of patients (people with systemic
diseases) are common reasons for postponing oral
surgery. In order to deal with this situation conscious
sedation (CS) was developed. CS is a method of keeping
the patient relaxed, while the latter remains conscious. CS
is achieved by means of oral or -mainly- IV administration
of drugs. Even though per os sedation is the most simple
and desirable technique, it has some serious defects,
resulting to the prevalence of the IV sedation. Most
commonly benzodiazepines like diazepam and midazolam are used, with midazolam appearing to be more
safe and effective. Propofol is also a potent IV agent with
major pharmacokinetic benefits. CS is used for over
twenty years for dental purposes in many counties (not in
Greece). The safety and effectiveness of CS increases its
use and reduces the need for general anesthesia.
Therefore, it constitutes the ideal method for most dental
patients.
Key words: Conscious sedation, oral surgery, diazepam, midazolam, propofol
49: 141-146, 2005

BIBIOPAIA
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, 1 . E 1993:
75-80.
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B A

26. Valtonen M, Salonen M, Forssell H, Scheinin M, Viinamaki:


Propofol infusion for sedation in outpatient oral surgery.
Anaesthesia 1989; 44: 730-4.
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:
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49: 147-154, 2005

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INAKA 3
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EPITH

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E:2,0gr per os, : 50mg/kg


A per os

E: 2,0gr IM IV , :
50mg/kg IM IV

E: 600 mg, : 20 mg/kg


per os

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E:2,0gr per os, : 50mg/kg


A K

E: 500 mg, : 15 mg/kg


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A
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* T Dajani 1997 (20).


** O (,
) .
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49: 147-154, 2005

151

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,
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147-154 ZORBAS

3-10-08 13:12

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.

SUMMARY
The role of the dentist in the prevention
of infective endocarditis
T.P Almaghout, V. Karagkiozaki, I. Litsas, A. Zorbas
hellenic stomatological review 49: 147-154, 2005

Infective endocarditis (IE) is a disease characterized by


the microbial infection of the inner surface of the heart. It
is caused mainly by streptococci, staphylococci, gramnegative bacteria, fungi, and rarely by rickettsiae and
clamydiae. The entrance of these microorganisms in the
blood circulation is necessary for the development of
infective endocarditis, and it occurs usually via the oral
cavity (teeth extractions, periodontal diseases etc.), the
skin, the respiratory system and the system.
The possibility of inducing endocarditis after dental therapy should worry the dentist. Thorough and accurate
medical record of the patient along with the knowledge of
the diseases that predispose to the development of IE,
allow the prevention of IE mainly by providing the proper
antibiotic prophylaxis for every patient and by maintaining
good oral health.
This paper presents the reasons for IE, its symptoms, the
diseases that predispose the development of IE and
finally the dental procedures that can cause IE, as well as
the proper antibiotic regimens and treatment for the
patients in risk of developing IE.
Key words: Infective endocarditis, Bacteremia, Antibiotic prophylaxis

BIBIOPAIA
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5 . I E . 1997.
2. T : K. I E 1999.
3. Kayser FH, Bienz KA, Eckert J, Lindenmann J: I M, 8 , A, E E . ,
1995: 167.
4. MacMahon SW, Roberts JK, Kramer-Fox R, et al: Mitral valve
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153

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3-10-08 13:12

154

B A

5. Sandre MA, Lee BL, et al: Endocarditis in intravenous drug


users. In Kaye D. eds: Infective Endocarditis, 2nd ed., New
York, Raven Press, 1992: 345.
6. Van der Meer JTM, Thompson J, Valkenburg HA and Mitchel
MF: Epidimiology of infective endocarditis in the
Netherlands. Patient Characteristics. Arch Intern Med 1992;
152: 1863-1868.
7. Drangsholt MT: A new causal model of dental diseases
associated with endocarditis. Ann Periodontol 1998; 3: 184196.
8. K IK, M Z: .
O 1999; 53: 232-242.
9. Rice LB, Calderwood SB, Eliopoylos GM, et al: Enterococcal
endocarditis: A comparison of prosthetic and native valve
disease. Rev Infect Dis 1991; 13: 1-7.
10. Ugolini V, Pacifio A, Smitherman TC, Mackowiak PA:
Pneumococcal endocarditis updata: Analysis of 10 cases
diagnosed between 1974 and 1984. Am Heart J 1986; 112:
813-819.
11. Terpenning MS, Buggy BP and Kauffman CA: Infective
Endocarditis: Clinical features in young and elderly patients.
Am J Med 1987; 83: 626-634.
12. Whitener C, Caputo GM, Weitekamp MR and Karchmer AW:
Endocarditis due to coagulase-negative staphylococci:
Microbiologic, epidemiologic, and clinical considerations.
Infect Dis Clin North Am 1993; 7: 81-96.
13. Steckelberg JM, Melton LJ III, Iistrup DM, et al: Influence of
referral bias on the apparent clinical spectrum of infective
endocarditis. Am J Med 1990; 88: 582-588.
14. Troyillet JL: Early infective endocarditis on prosthetic valves
(ed): Infective Endocarditis. 2nd ed. New York, Raven Press,
Heart J, 1992.
15. Kanter MC, and Hart R.G: Neurological complications of
infective endocarditis. Neurology 1991; 41: 1015-1020.
16. Mansur AJ, Grinberg M, da Luz PL, and Belloti G: The
complications of infective endocarditis: A reappraisal in the
1980s. Arch Intern Med 1992; 152: 2428-2432.
17. Bush LM and Johnson, CC: Clinical syndrome and
diagnosis. In: Kaye D. ed. Infective Endocarditis, 2nd ed.
New York. 1992 Raven Press, p.99.
18. Braunwald Eugene, Zipes DP, Libby P: Heart disease, 6th
edition, 2001.
19. Durack DT: Prevention of infective endocarditis. N England J
Med1995; 332: 38-44.
20. Dajani AS, Taubert KA, Wilson W, Bulger AF, Bayer A, Femen
P et al: Prevention of bacterial endocarditis. Recommendations by the American Heart Association. J Am Med
Assoc1997; 277: 1794-1801.
21. Harvey RA, Champe PC: : 1 . A. E
E . . 1994: 263.
22. Brown AR, Papasian CJ, Shultz P, Theisen FC and Shultz RE:
Bacteremia and intraoral suture removal: can an antimicrobial
rinse help? J Am Dent Assoc 1998; 129: 1455-1461.
23. Seymour RA, Whitworth JM: Antibiotic prophylaxis for
endocarditis, prosthetic joints, and surgery. Dent Clin N Am
2002; 46: 635-651.
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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:
317-325.

25. American Academy of Periodontology: Periodontal disease


as a potential risk factor for systemic diseases. Position
paper. J Periodontol 1998; 69: 841-850.
26. Holten KB, Onusko EM: Appropriate prescribing of oral betalactam antibiotics. Am Fam Physician 2000; 62: 611-620.
27. Hall G, Nord CE, Heimdahl AJ: Elimination of bacteremia
after dental extraction: comparison of erythromycin and
clindamycin for prophylaxis of infective endocarditis. J
Antimicrob Chemother 1996; 37: 783-795.
28. Titsas A, Ferguson MM: Concepts for the prophylaxis of
infective endocarditis in dentistry. Aust Dent J 2001; 46:
220-225.
29. X E, NI, TH: A
. A. I . X. . 1997: 192, 194.
30. B : I . 5 . A.
E E . , 1987: 514.
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193: 525-527.
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review and practice recommendations. J Am Dent Assos
2000; 131: 366-374.
33. Cowper TR: Pharmacologic management of the patient with
disorders of the cardiovascular system. Infective endocarditis. Dent Clin North Am 1996; 40: 611-647.
34. Tomas Carmona I, Diz Dios P, Limeres Posse J, Gonzales
Quintela A, Martinez Vasquez C, Castro Iglesias A: An update
on infective endocarditis of dental origin. J Dent 2002; 30:
37-40.
35. Strom BL, Abrutyn E, Berlin JA, Kinman JL, Feldman RS,
Stoley PD et al: Risk factors for infective endocarditis: Oral
hygiene and nondental exposures. Circulation 2000; 102:
2842-2848.
36. Carmona IT, Diz Dios P, Scully C: An update on the
controversies in bacterial endocarditis of oral origin. Oral Surg
Oral Med Oral Pathol Oral Radiol Endod 2002; 93: 660-670.
37. Barreira JL, Baptista MJ, Moreira J, Azevedo A, Areias JC:
Understanding of endocarditis risk improves compliance
with prophylaxis. Rev Port Cardiol 2002; 21: 939-95.
38. Bate AL, Ma JK, Pitt Ford TR: Detection of bacterial virulence
genes associated with infective endocarditis in infected root
canals. Int Endod J 2001; 28: 194-203.
39. Daly CG, Mitchell DH, Highfield JE, Grossberg DE, Stewart D:
Bacteremia due to periodontal probing: a clinical and microbiological investigation. J Periodontol 2001; 72: 210-214.
40. Hall GE, Baddour LM: Apparent failure of endocarditis
prophylaxis caused by penicillin-resistant Streptococcus
mitis. Am J Med Sci 2002; 324: 51-53.
41. Seymour RA, Lowry R, Whitworth JM, Martin MV: Infective
endocarditis, dentistry and antibiotic prophylaxis; time for a
rethink? Br Dent J 2000; 189: 610-616.
42. Delahaye F, Hoen B, McFadden E, Roth O, de Gevigney G:
Treatment and prevention of infective endocarditis. Expert
Opin Pharmacother 2002; 3: 131-145.
43. Vergis EN, Demas PN, Vaccarello SJ, Yu VL: Topical antibiotic prophylaxis for bacteremia after dental extractions.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2001; 91:
162-165.
:
A. Z
A 18,
106 80 A

154

49: 147-154, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

155

B A

A
. X*, . M**, K. A***

O . H ,
, . H
. H
: ,
. /
/ , . ,
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. . .
49: 155-168, 2005
30/12/2003 - 11/6/2004

EIAH
H . ,
. H

: , , .
* X
** X, E
EY
*** X, K
A
A E X, O T A.

, ,
(1, 2).
H .

. H
(),
(),

. H
,
155

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

156

B A

(3, 4).

, ,
,
.
H
: , (5). E


.

.
IATPIKO ITOPIKO KAI YIKH EETAH
(. 1). H , ,
. H
. O ,

. O
, . H
/ (2, 3, 4).
H
(T:150,000-450,000/mm3),

(PT) (T:12-13sec. X
+/- 1 sec), INR (T:1-1,3),
(APTT)
(T:25-38sec),
(T:200-400mg/dl)
(Ivy:2-7min).
EIO ANAIHIA KAI AIMOPPAIKH IAEH
,
,

. H
(6).
(.. ),
1:100,000,
1:50,000(5). A ,
- , ,

2-, (7).
A , (.. ), , .
,

, .
NOHMATA ME AIMOPPAIKH IAEH
H
, 2.

1: I



M
"A" (atypical bruising)
A
E
M-Y
O

T X
E
I
A
A

156

A
K
M (NSAIDs)
49: 155-168, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

157

2: A

N
-N von Willebrand
-A A
-A B
-
-

:
-VWF
-VIIIF
-IXF
-I, II, V, VII, X, XI, XII, XIII

-A
-A Fanconi,
- Alport,
- Wiskott-Aldrich
-A May-Hegglin

- :
A

- Bernard-Soulier
- Glanzmann

-
- Chediak-Higashi
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- K
-H
-:

K A:

( , , , , ), , , B12 , , ,
, )

A:

, , , , , , ), , ,
, , ,

-M ( ,
, )
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-
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-: ,
, , ,
49: 155-168, 2005

157

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

158

B A

H

, . M ,
. O

, ,
HIV, HBV
HCV ( ) (8).
N Von Willebrand (VWD)
O Von Willebrand (VWF)
. ,
VIII
. H VWD

VWF VIII . H VWD
( 1% ). T VWD
(9, 10).
H VWD :
I=
(VWF>5 IU/dL). E 80% .
II= VWF
( IIa IIb)
III= VWF<5
IU/dL). E
1:1,000,000
A A B
H A ( VIII)
B ( IX)
. T 30% de novo ( ) (8, 9, 11).
H ,

, , . H , , , .
. K 158


(8, 9).
O A B

(FVIII FIX) :
A/B: (
FVIII FIX>5 IU/dL)
M A/B: (
FVIII FIX 1 5 IU/dL)
B A/B: (
FVIII FIX<1 IU/dL)

O ( , , V, VII, X, XI, XII, XIII) , XII, . , , , VII
(12, 13).

H
,
. T

, 2. H
. T
.

H
( 2). O . E ,

, , ,
. , , ,
.
A K
H K II, VII, IX X . H
K , -, .
49: 155-168, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

159

B A

A
A ,
. H , .
E ,
,
,

. O ,
(14). B , , . (15)
M
) , ) (,
) ) (16). T
. . H
,
(15). H A2
. A

. H

36 ,
. (16, 17). H .
, 20 (15).
H (Ticlid) (Plavix)

ADP. M 49: 155-168, 2005

, . H
. O
2
, 4 . M .
GpIIb-IIIa .
tirofiban
(Aggrastat), , abciximab (ReoPro), eptifibatide (Integrilin)(16).
H . T
. A
, , (16, 17). O

(1-2 ). H :
A ( ) .

.
A , , .
E (bypass).
A.

. E
(15).
O (HXMB) ,
. H (Lovenox)
HXMB, HXMB : (Normiflo), (Fragmin), (Fraxiparine), (Clivarin), (Innohep). H ,

. , (2-4 ) , PT APTT(16, 17).
T (Sintrom), 159

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

160

B A


,
(18-20, 21, 22). H
K : VII, IX, X, (17, 23). H INR (International
Normalized Ratio)=PTISI, PT ISI (International Sensitivity Index)

. ,
, INR
(17, 21, 24, 25).
O
(26-29),
(30, 31).

,
(30, 32-35).
T (, , rt-PA,
APSAC)
,
, (16).
POEXEIPHTIKH POETOIMAIA
/
/ ,
. E .
H
VWD, , ,
( ) . H ( )
, . T ,
. VWF 160

50IU/dL(36).
VWD ( II III
VWD), , ( I VWD)
,
(9, 10, 36-38). T
, ( ) VWF 30%,
. VWF 40-50%
3-4
VWF 60-100% 7
7 VWF (16, 39). E

VWF ,
.
H VWD. O VWF , 12
24 . O
(39):
A (IU)=B (kg) x (%) x 0,5
H
FVIII VWF (
VWD A). H

(37, 40). H .
,
.

,

(10).
H

(Desmopressin acetate 0.3g/kg) 30 0.3g/kg 50 ml 30-60 . H


12 24 (36,
41)
. M
(36, 38, 40). O , , , , , (39, 42).
, , VWD,
(
). FVIII FIX>50 IU/dL(36).
49: 155-168, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

161

B A

, A B(41). A (Desmopressin
acetate 0.3g/kg) (37, 38, 40, 41).
, ,
,
VWD.
A B,
, ( ) FVIII FIX 30%,
(8, 9,
37)
. E
FVIII FIX
,
. 4050% 3-4 ( A) 30-50% 3-4
( B).
60100% 7 7
( A) 50-75% 7
( B)(39). H
(plasma-derived
products) 250, 500, 1000 1500 IU
FVIII 250, 500 580 IU FIX. E A B : KOATE-HP ( ), RECOMBINATE, MONOCLATE-P ( )
FACTOR IX. O (16, 39):
A FVIII (IU)=B (kg) x
(%) x 0,5
A FIX (IU)=B (kg) x
(%) x 1
H plasma-derived products A B
, 12 24
.
A B
,
VIII IX. T
,
.
, ,
. O , A,
VIII, 49: 155-168, 2005

, , , , (43). ,

(activated prothrombinase complex concentrates) 30
50 U/kg,
75 100 U/kg. , VIII, VIII, VIIa
(43).
H ,
. , , , .
H
. O 100,000/mm3
30,000/mm3 . ,
100,000/mm3 ,
(6).
50,000/mm3
100,000/mm3 (11). O ,
, (11). Y 5,000-8,000/mm3
. I
,
,
. , , , ( )
.

. H 0.3g/kg, A
VWD. H 3-4g/kg(11).
H , (17). A

, 161

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

162

B A

. H . H ,
.
M (PT) (APTT)

K . H
K (Konakion) 10-20
mg IV IM(1-3, 16, 44, 45). H

K
. H ,
K, 8-10
. E
( ) .
, ,
(46). 3-5
(2). T , 20 ,
, 0.3g/kg,
(47). E
(.. ) , .
,
. O
COX-2 (16).

, . (.. ).

, 2-3
(16).
O
162

HXMB
. O .
, HXMB,
HXMB (15). E

HXMB.

( -Sintrom), (35, 48-53)
, PT INR (PT 1,5 )(2, 44) (45)
. E (34, 54-57). H (ADA)
, PT ( , ) (PT 2 )(27).

(PT 2,5 (3, 35, 58)
INR (INR 4)(49).
A

(26, 28, 29, 59, 60),
,
,
(28, 31, 49).

(61, 62). E (31, 63). ,
, (64-67).
T PT 2,5 INR 3,5(15). O
Evans .(48) , INR
4,1. H ,
49: 155-168, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

163

B A

.

, per os ,
, 3. INR,
PT INR 3-5 . O
,
(23).
, .
O (16).
, , , , COX-2(68, 69). , , , T3 T4.

, , , , , , (68, 69).

. T



(70-72). O
(59, 68, 73, 74).

IEXEIPHTIKO TAIO AIMOTAH


, ,
,
(6).
T ( ), ,
. H
10-15 . H
,
(4).
. E
,
7 , ,
(36).
H

. T

,
.
,
(75).
T
(76):

3: per os
X K

M K
A

Y K
A

-Y
-A

-Y
-A

-E
-A
-

>

>T

> >M INR


.
> 4-5
>T >K HXMB

49: 155-168, 2005

-M
-A
-
-

163

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

164

B A

) M
O Horsley (Bone wax)
. M
,
,
. H
Horsley . ,
,

. (6).
) X
T
, . T 1:50,000
, (5). , ,
.
O (ferric sulfate) ,
. E
. E in situ
. H .
) B
H (Thrombostat, Thrombogen) . B
(78). . H
(Gelfoam), (Surgicel). H
(fibrin glue) (,
, , XIII) .

(8).

(77), (13, 41, 78),

(78).
164

) A
: T ,
(6). B
,
.
A : O
. (Gelfoam, Spongostan),
(Calgitex) (Hemofibrin) . ,
. T
. X , . K
. O
4-6 (4).
H (12, 66, 73, 74, 79, 80). E Gelfoam - (EACA),
(6).
A : T

. B
. E
(36). To M (Microfibrillar
collagen hemostats) (Avitene(r)) ,
(6, 69). X .
O (Oxycell) O (Surgicel). H o . H ,
. H
,
,
(69, 81). A
(48, 69, 81).
METEXEIPHTIKO TAIO AIMOTAH

.
H 24/
49: 155-168, 2005

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

165

B A

. T
, . O

.

.
O
.
15-20 , . K . E ,
24/ , (
, ) ,
. O

,
, (82).
H 1- (5), .
, . (tranexamic) -
(EACA). T , 7-10 EACA . T
per os, , . H per os
20 mg/kg 8
7-10 (36, 41).
, 10 gr
1g/h(11). A
.
10ml 5% 2 , 4-6
. H
49: 155-168, 2005


(83).
B

, ,
. O
,
(68, 83-87),
(6).
M ( )

, . ,

. H MA ( ) , COX2, .


. H
.
O
. B , , :
1) 1h.
2) E ,
,
, 3/0 silk.
3) E , .
4) E ,

(Fresh Frozen Plasma, , K,
Platelets) (19,68,69,72-74,80,83,85).
YMEPAMATA
1) T ,
. H

.
165

155-168 SEL. - HADJIPETROU*

3-10-08 13:12

166

B A

2) H
,
. ,
, .
3) )
/
/ , ) .

.
4) H , , , , .

SUMMARY

Bleeding disorders and oral surgery


L. Hadjipetrou, D. Mangoudi, K. Antoniades
hellenic stomatological review 49: 155-168, 2005

Hemorrhage is an inevitable consequence to surgical


incisions and dissections. Hemostasis, the arrest of
bleeding from an injured blood vessel, requires the
combined activity of vascular, platelet, and plasma factors.
Hemostatic abnormalities can lead to prolonged or
excessive bleeding. Hemostasis in a surgical procedure
should be considered in three stages: presurgical,
surgical and postsurgical. The presurgical stage
highlights the importance of any medical intervention
dealing with the correction of defective hemostasis before
surgery. A thorough medical and dental history and
comprehensive clinical and laboratory examinations are
the basis of preventative care and should be an essential
component of the oral and maxillofacial care of all patients
with a bleeding disorder. In addition to that, the presurgical stage involves the use of local anesthetic with vasoconstrictor or hypotensive anesthesia. The management
of hemostasis involves the use of any local measures
essential to contribute to the control of any bleeding
during surgery. In most instances it is vital that dental
extractions or other surgical procedures should only be
done under the care of a hospital dental or oral and
166

maxillofacial surgery department. Postoperatively, the


surgeon should be able to control any bleeding and
ensure that hemostasis is permanently achieved.
Key words: hemorrhage, hemostasis, bleeding disorders, oral
surgery

BIBIOPAIA
1. Catalano PM: Introduction to hemostasis. In: Rose LF, Kaye
D, eds. Internal medicine for dentistry. 2nd ed. St Louis, CV
Mosby 1990: 346.
2. Peterson LJ: Prevention and management of surgical
complications. In: Peterson L.J., Ellis E., Hupp J.R., Tucker
M.R., eds. Contemporary Oral and Maxillofacial Surgery. 2nd
ed. St Louis, CV Mosby 1993: 269-288.
3. Little JW, Falace DA, eds: Bleeding disorders. In: Dental
management of the medically compromised patient. 5th ed.
St Louis, CV Mosby 1997: 466-494.
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SUMMARY

Guided bone regeneration adjacent to implants


placed into immediate extraction sockets
M. G. Manda, El. G. Dima, I. K. Karoussis, I. Fourmousis

NEA EOMENA THN OTIKH ANAAH


hellenic stomatological review 49: 169-178, 2005

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Extensive research has demonstrated through clinical and


histological studies that guided bone regeneration is a
regenerative procedure used for ridge augmentation prior
to or in conjuction with dental implants placement.
Guided bone regeneration, using membrane barriers, has
enabled implant placement in sites compromised by
insufficient bone volume, including immediate extraction
sites.
This review evaluates the combination of guided bone
regeneration and immediate implant placement by
presenting the available experimental and human studies,
which have shown great rates of success both for onestage and two-stage endosseous dental implant systems.
Different kinds of membranes, absorbable and nonabsorbable, have been used for this purpose, both
resulting in similar success rates.
The possibility of incorporation of bone grafts and bone
substitutes with or without the use of membranes along
with the immediate implant installation, is also discussed.
Key words: guided bone regeneration, submerged, transmucosal, immediate

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SUMMARY

Xerostomia and complete dentures


S. Yannikakis, A. Dimitriou, A. Zissis
hellenic stomatological review 49: 179-187, 2005

Saliva serves many physiologic needs and is critical in


maintaining oral health and promoting normal function of
the stomatognathic system. Oral mucosa, covered by a
considerably thin saliva layer, exerts a deficient resistance
against exogenous influences such as toxins, acids,
bacterial metabolic products, and allergic and mechanical
irritants. Moreover, saliva is a lubricant for the oral mucosa
and the tongue and it is necessary for the microbiologic
balance of the oral cavity. Factors involved in the quantity
and quality of saliva can cause not only a significant
discomfort, but may also have a negative effect on the oral
tissues, called xerostomia or dry mouth.
Many systematic diseases (e.g. Sjogrens syndrome), dehydration conditions (e.g. diabetic acidosis), depression,
aging etc. can cause xerostomia. Furthermore, a dramatic
decrease in the saliva secretion is performed when the
salivary glands are exposed to high doses of radiation, as
it may occur in the radiotherapy treatment of head and
neck cancer.
Xerostomia is appeared to be one of the most common
side effects of drugs intake, particularly caused by those
with an atropinic action. Atropine, bella donna, chlorpromazine, anti-hypertensives, anti-spasmodies, skeletal
muscle relaxants, cardiac antiarrhythmics, anti-neoplastic
agents, anxiolytics, tranquilizers, sedatives, general
anesthetics are some of the drugs that can induce in a
light, moderate or severe xerostomia.
Saliva is particularly important for the removable denture
wearers by protecting the underlying oral mucosa from
mechanical irritation and infections, and promoting the
retention of complete dentures.
The aim of this review paper was to present the salivary
glands malfunction problem and associate it with the
complete dentures. A number of treatment methods, such
as a specific diet, use of special toothpaste and mouth
rinse wash, sialogogue drugs or artificial saliva, are
described and discussed. Emphasis has been given on
the construction characteristics applied on a complete
denture for the xerostomic patient. Maxillary complete
dentures made of a metal base instead of an acrylic one,
seems to be more comfortable to the patient. Mandibular
complete dentures, relined by a permanent soft liner seem
to improve the denture-altered mucosa contact. On the
other hand, construction of an artificial saliva reservoir in a
denture, despite the laboratory difficulties, might be an
effective way of minimizing the problem.
Early diagnosis of xerostomia and its cause is of primary
importance. The treatment plan must be based on the real
needs of each one patient.
Key words: xerostomia, dry mouth, burning mouth, complete
dentures, saliva, artificial saliva, salivary glands
186

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:

N 6, 106 80 A
T: 210-7715814, 210-3600005
Fax: 210-7715814
E-mail: yannista@otenet.gr

49: 179-187, 2005

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T E E K
O A (K.O.A.) E
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49: 189-198, 2005
20/4/2004 - 19/1/2005

EIAH
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.
K O A (K.O.A.) E
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A. ANAKOHH BIBIOPAIKN EOMENN
A1. YXPONA YIKA OY XPHIMOOIOYNTAI IA
K.O.A.
Y
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(12).
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A2. XPONIKH TOOETHH TH TEXNIKH TH K.O.A.
E XEH ME THN TOOETHH OTEOENMATOYMENN EMYTEYMATN
K.O.A.
(1): ( 2)
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placement + GBR).
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, (2, 3, 4, 5, 7) .

I. TAYTOXPONH EAPMOH
I. TAYTOXPONH EAPMOH K.O.A. KAI TOOETHH OTEOENMATOYMENN EMYTEYMATN
AMEA META THN EAH TN ONTIN
(Immediate Implant Placement +GBR) (IN. 3)
INAKA 3: B
K.O.A. (1)
* T .
* E .
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).
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,
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I. TAYTOXPONH EAPMOH K.O.A. KAI TOOETHH OTEOENMATOYMENN EMYTEYMATN


4 E 8 EBOMAE META THN EAH TN
ONTIN
(Early Implant Placement +GBR)
4 8

. H

(1).
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12 (1).




(1).

B. ANAYTIKH APOYIAH KINIKN EPITEN

II. TAIAKH EAPMOH


APXIKA K.O.A. KAI TOOETHH OTEOENMATOYMENN EMYTEYMATN E EYTEPO XPONO
(Staged Approach)
H 192

1 KINIKH EPITH. TAYTOXPONH EAPMOH


K.O.A. KAI AMEH TOOETHH OTEOENMATOYMENN EMYTEYMATN (SIMULTANEOUS
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.

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100% .

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. (22)
.
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7
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3),
.
.
( +
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24) 0.12% (Chlorexil, Intermed) 7 .

E.7: .

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6
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laser (Biolitec) 12 Watt.
194

T 5 100%

(E. 4)
.

(24)
laser (Biolitec) 12 Watt (E. 5, 6). (E. 7) 3 (E. 8).
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B A

.

. T 3 (E 9).
2 KINIKH EPITH: TAIAKH EAPMOH
K.O.A. KAI OTEOENMATOYMENN EMYTEYMATN (SIMULTANEOUS APPROACH).
A 40 , , , .
.
H :
A. 1. A
2. A
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.
.
10 A . , .
A2. O . A (E. 10).


(E. 11, 12).

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E.12: .

B. 1. K
2.
B1. A
K.O.A.
6
.
B2. O .
. E

E.10: H
.
49: 189-198, 2005

K
( (E. 13) (Geistlich Biomaterials) . Maiorana .25
.
195

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196

B A

E 13: T (

(Geistlich Biomaterials)
.

( +
625mg per os 6, 500mg per os 12) (
24) 0.12% (Chlorexil, Intermed) 7 .
.
,
(
) (E. 14). (Chlorexil, Intermed).
(
10 ) , (E. 15) 6 (E. 16).

E 15: ( 10 )
.

E. 16: T .

E 17: Y 10
K.O.A.

E 14: .
,
( ). (Chlorexil, Intermed).
196

H 10 K.O.A. (E. 17). H 10 (E.18).


.

49: 189-198, 2005

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B A

YMEPAMATA

E. 18:
( 10 )

,
, .
T 4
(E. 19). H 4 (E. 20).

A
:
H K.O.A ,
.
A
K.O.A. .
K.O.A. 6 8
, .
H K.O.A.
.

.
M , .
H .
A
.
SUMMARY

Timing of performing Guided Bone


Regeneration in Implant Dentistry
E. 19: T 4 .

E. Sinanioti, V. Piperias
hellenic stomatological review 49: 189-198, 2005

E. 20: Y 4 ( ).
49: 189-198, 2005

Ideal architectural structure of the alveolar crest facilitate


ideal prosthetic placement of dental implants from the
aesthetic and functional point of view. The reconstruction
of deficient alveolar ridges through Guided Bone
Regeneration (GBR) is capable of promoting new bone
formation in horizontal or vertical dimensions or both.
GBR has been successfully used in Implant Dentistry with
high predictability(1, 2, 3, 4, 5, 6, 7). GBR procedures are reported
as being performed prior (staged approach) to or during
(simultaneous approach) dental implant placement. The
regenerative activity can take place at the time of
extraction (immediate implant placement), 4 to 8 weeks
after extraction (early implant placement), after gingival
healing, or after 3 to 6 months or later, when the bony
197

189-198 SEL. - SINANIOTI*

3-10-08 13:14

198

B A

extraction vault has healed. In cases of early implant


placement the sockets are partially healed, implant bed
preparation is less difficult and if present infections have
cleared so the long term success of therapy is
improving(1). The primary stability of the dental implants is
of paramount importance for successful results of GBR in
cases of simultaneous approach.
The timing of GBR may be the dictating factor influencing
the end point when extensive bone damage is observed in
the presence of a tooth that will be extracted. Performing
GBR in large osseous defects is a demanding surgery
which requires clinical experience and technical capabilities.
Key words: Dental implants, guided bone regeneration (GBR),
timing, clinical experience

EIIKH HMEIH
O
K A .
K T
. E
. I. N E. K
A . A. .
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2005; 25: 19-25.
:
E
K 12, N. 154 51
T.: 210-6756691
email: efisin@otenet.gr, www.periodontics.gr

198

49: 189-198, 2005

199-209 SEL.-POLYXRONOPOULOU

3-10-08 13:17

199

B A

O
A. *, K. **, K. K***

: ) ,
, ) ,
, .
M , , ,
, .
M , , mutans ,
. E 5,5 , .
T , , OM
.
,
.
49: 199-209, 2005
16/9/2004 - 9/12/2004

EIAH
O O . O ,
: , , , .
* E K, E K O, O A
** O A
*** , E , O
A
M
34 , K 7-9
M 2004.

. K

, , .
: )
, , )
, .
ENOMHTPIOI APAONTE KINYNOY IA THN
EKHH NON TOY TOMATO TO AII
A , 199

199-209 SEL.-POLYXRONOPOULOU

3-10-08 13:17

200

B A

1A: E .
, , , .

IATPOH
(3)

Y , ,
RR=2-5(4).
M , , (3).

A,C,D
(3)

Y , ,
RR=2-5(4).
A (-/
), RR=1,7(8).

HH OYIN
T(3)

X 4 9
(9,10).

A,
(9-12)

M ,
(-/)(8).
Y , ,
RR=2-5(4) .

YNHEIE MHTEPA
K(1,3,14,15)

A
(15).
X/X-: RR=1,9 Y: RR=2,3.

K (1,3,8,16,17)

A , RR=3(16) .

OIMEI MHTEPA
CMV(1,19), (18,19),
,
(18)

Y , ,
RR=2-5(4).

RR:
,
(1). , ,
, ( 1A).
,
, ,
, ,
(2, 3). E,
200

2-5 (4),
(5, 6).
Milgrom .(7), .
E

(3). E 49: 199-209, 2005

199-209 SEL.-POLYXRONOPOULOU

3-10-08 13:17

201

B A

, ,
(8). A
,
,
(9-13).
T ,
, ,
,
(1, 3).
O
, (14, 15). A ,

(8, 16, 17). Werler .(16) ,

. E,
(18, 19),

(20)
, , (4-7).

,
( 1B). ,


. O mutans (S. mutans S. sobrinus)
, (21-24). H
, (25-27) . O Kohler .(28) ,
mutans
23 ,
. A , ,

2 , Zanata .(29)
H
49: 199-209, 2005

, 7 (30-36). H
(PG, TNF, IL,
CRP) (37). (38).
M mutans (39). E,

,
(40-44). Wan .(39) , 2 , 26
.
A (45),

mutans , , .
AOTEEMATIKOTHTA OONTIATPIKN
POPAMMATN APEMBAH TI MHTPIKE
NOOY TOY TOMATO
H
,
mutans . Kohler .(28, 46). O
,
( 2).
Gunay .(47) 3
, ,
.
T
4 mutans . H Brambilla .(48) mutans
. A
201

202

i.

(PG, TNF, IL,CRP)(37)
ii. A (38).

O :

EPIOONTITIA


,
(43):
i. Ca
()
ii.
iii. A

A ( 2
)

RR=4,4(39)

O
(7,40,44).

M (2 )
, DMFS
' : 4,5.
(p<0,001)(29)

M (2 )
,
DMFS
2 :9,4.

RR: , I: , ms: mutans

E : I=40,9%
: I=17,4%
(p<0,05)(41)

: I=42,1%
T : I=17,6% (p<0,05)(41)

A ( 2 )
RR=26,2 (p<0,05)(39)

3-10-08 13:17



RR=3,5-7,07
(p<0,05)(30-36)


ms>106 CFU
23: I=65%
(p<0,05)(28)

1.
2. (,
)

S. mutans
S. sobrinus

M mutans
(ms):


ms<3x105 CFU
23:
I=35%

M
(21-24), :

TEPHONA

A ms

NOHMA
TOMATO
MHTEPA

1B: E .
N .

199-209 SEL.-POLYXRONOPOULOU
202

49: 199-209, 2005

O: 86 ( 3-4 )
OE: 110 ( 3-4 )

O: 33 ( 2 )
OE: 32 ( 2 )

O: 180 ( 1-3.5 )
OE: 180
- ( 1-3,5
)

O: 199 ( 5-6 )
OE: 75 ( 5-6 )

O: 43 ( 2 )
OE: 38 ( 2 )

Gunay .,
1998(47)

Brambilla
., 1998(48)

Gomez
., 2001(51)

49: 199-209, 2005

Gomez
., 2001(52)

Zanata .,
2003(29)

203

O (2 ): 14,7%
OE (2 ): 33,3%

O (5 ): 86.7%

OE (5 ): 50%
(p<0.05)

O (1-3.5 ): 97%

OE (1-3.5 ): 77%

O (4 ): 91,5%

OE (4 ): 57,7%

(p<0,001)

O: 100% ms<103CFU
OE: 81,5% ms<103CFU
(p<0,001)

O: A ms:
22,5
OE: A ms:
18,2
(p<0,005)

T
(dft)

ms

AOTEEMATA TO AII

O: , OE: , ms: mutans

i. E, OY
ii. A IRM
.P
iii. T NaF
/Iodine*
iv. ,

2-3
2

i. E, OY
ii. A,
iii. 1mgF per os (6 . )
iv. NaF 0.05% (6 . )
v. 0,12% (6 .
)
vi.

3 2

i. E, OY ( triclosan
2 )
ii. A,
iii. A (Listerfluor)
iv. E
v.

i. E, OY
ii. A
iii. T

iv.
v.

3
3-4

4 5-6

EPIEXOMENO POHTIKOY
POPAMMATO

ENAPH & IAPKEIA


APEMBAH

3-10-08 13:17

*(1g KI + 1,2g NaF + 53ml Glyc. + H2O/100ml : pH=4,5)

EIMA MEETH

EPEYNHTE

2: A .

199-209 SEL.-POLYXRONOPOULOU
203

199-209 SEL.-POLYXRONOPOULOU

3-10-08 13:17

204

B A

1mg F ,
(49), , (1, 50).
T
Gomez .(51, 52) Zanata .(29)
NaF-Iodine (1g KI + 1,2g NaF + 53ml Glyc. +
H2O/100ml: pH=4,5), . K ,
, 5 .
M , ,(34, 35, 52) 3. A


. Mitchell-Lewis
.(53) , , ,
. Lopez .(34)
Jeffcoat .(35) 0,12% 250mg, . T

, 5,5 .
POTEINOMENH APEMBAH TH MHTEPA
M ,
.
4A, ,
. ,
, NaF 0,05%
16 (48). E ,

0,12%(34, 48). E, , , (35).
O

(54). K

204

,
. A (55). E , (11, 54, 56).
, (13).
, , , , (12). E,
(13).
H , ( 4B).
A Lydon-Rochelle
.(57), (58% ) 26
. K ,

,
,
(58). E, ,
, /(54). ,
(1, 3, 57). ,
, , .
YMEPAMATA
A :
1) O ,
.
2) O .
3) H
mutans , .
49: 181-189, 2005

28
E 2-3

O:200
OE: 200

O: 366
OE: 723

Lopez .,
2002(34)

Jeffcoat
., 2003(35)

49: 181-189, 2005

O..Y
A
P
0,12%

O..Y
A,
P

A

O A :4,9%
O B: 0,8%
O : 3,3%
OE: 6,3%

O: 2,5%
OE: 8,6%
RR=5,49 (p<0,05)

O: 13,5%
OE: 18,9%

AOTEEMATA TO AII
( /
)

O: , OE: , RR:

Y- :
i. A,
ii. P
iii. X 250mg (3
1 )

Y- B:
i. A,
ii. P
iii. X placebo (3 )

Y- A:
i. A
ii.
iii. X placebo (3 )

i.
ii.
iii.
iv.

i.
ii.
iii.
iv.
v.

EPIEXOMENO POHTIKOY
POPAMMATO

3-10-08 13:17

21 - 25

XPONO & IAPKEIA


APEMBAH

O:74
OE: 90

EIMA MEETH

Mitchell-Lewis
., 2001(53)

EPEYNHTE

3: A M .

199-209 SEL.-POLYXRONOPOULOU
205

205

206

, K, K, E.

* , **

A ().

: ,
, ( 1:100.000).

A .
A .

A .

A

.

AOKATATAH

3-10-08 13:17

OY
A

* NaF 0,05%
** 0,12%

OY
A

**P
** 0,12%
* NaF 0,05%
**X (M)

OY
A

>28 .

POHH

2
16<. <28

1
<16 .

TPIMHNO KYHH

4A: .
.

199-209 SEL.-POLYXRONOPOULOU
206

49: 181-189, 2005

49: 199-209, 2005

E

:

E
-


:

CMV, , ,
.

, ,
N2O.

O, , .

E (, , Rh, / ).

K, , , (, )
(, , ).

, & .Y .
.Y. .

>28 .

3-10-08 13:17

A:

E
:

, , . .

2
16<. <28

1
<16 .

TPIMHNO KYHH

4B: .
.

199-209 SEL.-POLYXRONOPOULOU
207

207

199-209 SEL.-POLYXRONOPOULOU

3-10-08 13:17

208

B A

4) O mutans .
5) H ,
mutans ,
.
6) H , .
7) H

.

SUMMARY

Intrauterine preventive dentistry


A. Polychronopoulou, K. Divaris, K. Kavvadia
hellenic stomatological review 49: 199-209, 2005

The aim of this study was a) to review in utero risk factors for
offspring oral disease, as well as dental intervention
programs applied to expectant mothers, and b) to develop a
comprehensive intrauterine oral disease prevention
program by pregnancy semester.
Health problems during pregnancy, medication use,
malnutrition, deleterious habits, and presence of caries and
periodontitis constitute the main maternal risk factors for
child oral disease. Intervention studies in pregnant women
to control their cariogenic flora, show delayed colonization
with mutans streptococci and significant decrease in caries
occurrence both in primary and permanent dentition.
Furthermore, treatment of maternal periodontal disease
reduces the risk for premature or low birth weight child, by
5.5 times. Noteworthingly, premature and low weight birth,
increases the risk for enamel hypoplastic defects development.
In a comprehensive program of intrauterine preventive
dentistry, the pregnant mother must be informed regarding
the etiology and pathogenesis of oral diseases and the
possible consequences to the offspring. Furthermore, a
preventive program must be followed to control dental
plaque, both qualitatively and quantitatively, as well as
periodontal disease. Controlling dental plaque should be
facilitated by meticulous oral hygiene, during all three
pregnancy semesters. Periodontal therapy should not be
postponed; curettage can be performed, if indicated,
during the 2nd semester and may be supplemented with
antimicrobial agent administration. Elective dental treatment
should be performed between the 16th and 28th week of
gestation, whereas consulting with the physician in charge
must precede emergency treatment.
In conclusion, intrauterine preventive dentistry is feasible and
has proved to be effective in maintaining child oral health
Key words: prevention, pregnancy, oral diseases, offspring
208

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49: 199-209, 2005

209

211-218 SEL.- KOLETSH-KOYNARH

3-10-08 13:17

211

B A

E O
X. K - K*, I. A**

,
,
. H , , / , (, )
. O / E . O
, . O , .
49: 211-218, 2005
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211-218 SEL.- KOLETSH-KOYNARH

3-10-08 13:17

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211-218 SEL.- KOLETSH-KOYNARH

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, 14.
OI EITHME YMEPIOPA TO POTYXIAKO
OONTIATPIKO EKAIEYTIKO POPAMMA
I, ,
1950
.
1960,
,
1970 1980,

34.
H
, , . A O O (American Association of
Dental Schools), 1991 ,
O 198421.

O
,


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,
213

211-218 SEL.- KOLETSH-KOYNARH

3-10-08 13:17

214

B A


:
1.N , .
2.N
.
3.N

,
. O , , ,
- .

O , , , O (General Dentistry
Council) A33, 35.
H
1980

. T 1990, O E O,
. ,

. H

.
, 33.
T , , ,
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SUMMARY

Behavioral sciefnces in dentistry


H. Koletsi - Kounari, J. Avgeris
hellenic stomatological review 49: 211-218, 2005

The aim of this article is to determine the factors that make


Behavioral Sciences an indispensable component of
dental undergraduate curricula and to present the trends
in teaching Behavioral Sciences in Dental Schools
worldwide.
In modern societies the main goal of dentistry is oral health
promotion of the populations according to the holistic
definition of health. This view of oral health recognizes that
a range of social and behavioral factors affect oral
conditions, hence dental care cannot be isolated from the
psychological makeup and social background of the
person receiving it and the person providing it. However,
this approach requires additional professional skills from
dentists, which go beyond the traditional biological and
mechanistic framework of the profession. It requires
developing a foundation of sociological and psychological
skills.
The practice of dentistry rests on the basic tenets of
appropriate communicative and ethical relationships
between dentist and patients. Not only is there the
relationship between dentist and patient, but also the
interface between dentist and community. Psychology and
sociology can aid the dental professionals to develop their
work both in the dental practice and, if they choose, in the
wider community. Behavioral sciences study the ways in
which people behave and the reasons for this behavior and
while they primarily describe the combination of the
subjects of psychology and sociology, other areas such as
ethics, communication, economics, and epidemiology are
also included. Behavioral sciences in dentistry may be
defined as the study to understand or explain the behavior
of people in relation to oral health. The appropriate setting
for behavioral dentistry, in theory and application, is in
clinical practice or within community oral health care
delivery systems. The concern is with intrapersonal,
interpersonal and social processes that occur while oral
health care is being discussed or delivered.
The inclusion of behavioral sciences in the graduate
dental curricula can help dental practitioners to deliver
optimal health care, since behavioral dentistry adapts and
integrates theory, empirical findings and practical skills
49: 211-218, 2005

from the social and behavioral sciences. Behavioral


sciences should be taught throughout the dental course
with careful integration so that that the subject matter
assumes its proper relevance to the care of the patients.
Instruction should provide students with an awareness of
the social and psychological aspects of patient care, in
order to appreciate the patient as an individual whose
response to dental care is determined by personality,
experience, and social and cultural influences. The core
behavioral dentistry curriculum aims to develop in dental
students an understanding of basic conceptualizations
that describe the causes of patient, dentist, and
community behavior and enhance students competence
in responding to the challenges involved in delivery of oral
health care.
Professional organizations, councils and associations
have had a pivotal role in developing guidelines for
teaching behavioral sciences in Dental Schools as well in
advising and making recommendations on this matter.
These documents promote the inclusion of behavioral
sciences in dental curricula and nowadays a considerable
number of Dental Schools have added the study of
behavioral sciences as a comprehensive part of their
curricula in the USA, Canada and Europe. Many variations
remain in the teaching that makes comparison between
schools difficult and it is recommended that more specific
guidance to be given to teachers of behavioral sciences in
dentistry. However, many Dental Schools have not
developed teaching of behavioral sciences in their
curricula and there is an urgent need to raise awareness of
the serious deficiency in this most important area of dental
education.
Key words: Behavioral Sciences, Dental Education, Oral Health
Promotion

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T.: 210 6725313
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SUMMARY

Usefulness of microbiological testing


in Clinical Periodontology
D. Sakellari, C. Xatzigeorgiou, A. Konstantinidis
hellenic stomatological review 49: 219-227, 2005

Although the microbial aetiology and the specific


subgingival flora of various forms of periodontal diseases
are well documented in the literature, microbial testing is not
yet officially incorporated in clinical practice and diagnosis
is still based on clinical recordings and radiological
findings. Microbiological testing does not affect the initial
treatment phase of various forms of periodontitis which
always includes oral hygiene instructions, supragingival and
subgingival scaling and root planing. Data in the literature
suggest that, certain categories of patients such as
aggressive periodontitis benefit from microbial testing,
especially after the initial healing phase, when the outcomes
of therapy are not satisfactory. Microbial testing can
determine residual pathogens and serve to guide further
therapy.The application of cultural techniques allows for
antibiograms,the recommended approach for correct
assesment of proper administration of antimicrobials.
Cultural techniques are considered the "gold standard" for
investigation of the complex subgingival flora, but can be
applied in well-organized, specialized laboratories and
require technical expertise. During the last years,molecular
biology techniques are widely used in periodontal research
mainly due to their ability to overcome technical problems of
anaerobic cultures and their specificity. These techniques
as well as immunofluorescence do not require viable
bacterial cells and are proven to be more rapid and sensitive
than culture.In clinical practice, the molecular biology
approach is more convenient although it does not allow the
determination of antibiotic susceptibility. Polymerase chain
reaction (PCR), whole genomic, synthetic oligonucleotide
and 16srRNA probes are examples of molecular techniques
applied in clinical periodontology. The Department of
Preventive Dentistry, Periodontology and Implant Biology,
Dental School, Aristotle University of Thessaloniki routinely
uses the checkerboard DNA-DNA hybridization technique
which allows the simultaneous processing of up to 30
clinical samples for up to 45 bacterial species or up to 90
samples for 4 species. This technique is used to monitor
226

periodontal patients and determine antibiotic regimens for


aggressive periodontitis patients or recurrency of disease in
chronic periodontitis patients. Systemic administration of
antibiotics is considered after the initial healing phase, in an
effort to limit overusage of antimicrobials which can lead to
development of resistant strains.
Key words: Microbiological testing, periodontitis, antimicrobials.

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:
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SUMMARY

The use of mini-comparator in the construction


of an oculofacial prosthesis
P. Kafas, S. Dalambiras, M. Vourvachis, M.A. Bamber
hellenic stomatological review 49: 229-233, 2005

Maxillofacial prosthetic rehabilitation after extensive tumor


resection constitutes a serious medical problem, especially when the post-surgical defect is wide.
The positive psychological effect created by a successful
prosthesis is essential for such a patient to confront - apart
from a biological problem - a radical treatment that results
in a large defect.
Radical treatment is usually required for Neurifibromatosis
type- 1 or von Recklinghausen disease. This is particularly
difficult when the affected facial area is extensive. The
surgical treatment of such a disease usually causes a
broad post-surgical defect that requires rehabilitation.
Prosthetic rehabilitation methods of facial defects, and
particularly of the peri-orbital region, set up a various range
of techniques used for the retention of such prosthesis.
Usually, such techniques are the mechanical retention, the
retention using the anatomical undercuts, the medical
adhesion and the modern use of osseointegrated implants.
This case report presents a post-surgical oculofacial defect
of the middle right facial third with orbital exenteration and
critical reduction of bone in the zygomatico-orbital complex.
The use of extra-oral osseointegrated implants for the
rehabilitation of this area was excluded due to inadequate

bone availability, after assessing this area using 3D-CT scan


and fusing deposition modeling (FDM). The estimation of
the soft tissues was performed using the surface Laser
assisted simulation and computer tomography (CT).
The options of mechanical and anatomical retentions were
excluded. Alternatively, retention of the prosthesis was
achieved using medical adhesion. This case report
presents the rehabilitation technique of medical adhesion
significantly improved for the construction of such a
prosthesis using the mini- comparatr for assessment of
the orbital characteristics.
This device assessed the orbital area dimensions giving
the ability to the clinicians to achieve high standards of
aesthetics.
Key words: Oculofacial prosthesis, von Recklinghausen disease, 3D-CT scan, mini comparatr, fused deposition modeling
(FDM), surface laser simulation.

BIBIOPAIA
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K
K 3, T.. 1353
K 654 03, T- 2510-223294
E-mail: panos@kafas.gr
49: 228-232, 2005

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