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Gingivitis and periodontitis are the
two major forms of in-
flammatory diseases affecting the periodontium. Their primary
etiology is bacterial plaque, which can initiate destruction of
the gingival tissues and periodontal attachment apparatus.
1,2
Gingivitis is inflammation of the gingiva that does not result
in clinical attachment loss. Periodontitis is inflammation of the
gingiva and the adjacent attachment apparatus and is character-
ized by loss of connective tissue attachment and alveolar bone.
Each of these diseases may be subclassified based upon etiol-
ogy, clinical presentation, or associated complicating factors.
3
Gingivitis is a reversible disease. Therapy is aimed primarily
at reduction of etiologic factors to reduce or eliminate inflam-
mation, thereby allowing gingival tissues to heal. Appropriate
supportive periodontal maintenance that includes personal and
professional care is important in preventing re-initiation of
inflammation.
Therapeutic approaches for periodontitis fall into two major
categories: 1) anti-infective treatment, which is designed to halt
the progression of periodontal attachment loss by removing
etiologic factors; and 2) regenerative therapy, which includes
anti-infective treatment and is intended to restore structures
destroyed by disease. Essential to both treatment approaches is
the inclusion of periodontal maintenance procedures.
4
Inflammation of the periodontium may result from many
causes (eg, bacteria, trauma). However, most forms of gingivitis
and periodontitis result from the accumulation of tooth-
adherent microorganisms.
5-7
Prominent risk factors for devel-
opment of chronic periodontitis include the presence of
specific subgingival bacteria,
8-10
tobacco use,
9-13
diabetes,
9,10,14
age,
9,10
and male gender.
9,10
Furthermore, there is evidence that
other factors can contribute to periodontal disease pathogenesis:
environmental, genetic, and systemic (eg, diabetes).
14,15
This paper primarily reviews the treatment of plaque-
induced gingivitis and chronic periodontitis, but there might
be some situations where the described therapies will not
resolve disease or arrest disease progression. Furthermore, the
treatments discussed should not be deemed inclusive of all
possible therapies, or exclusive of methods of care reasonably
directed at obtaining good results. The ultimate decision re-
garding the appropriateness of any specific procedure must be
made by the practitioner in light of the circumstances pre-
sented by an individual patient.
Plaque-induced gingivitis
Therapy for individuals with chronic gingivitis is initially
directed at reduction of oral bacteria and associated calcified
and noncalcified deposits. Patients with chronic gingivitis, but
without significant calculus, alterations in gingival morphology,
or systemic diseases that affect oral health, may respond to a
therapeutic regimen consisting of improved personal plaque
control alone.
16
The periodontal literature documents the short-
and long-term effects following self-treatment of gingivitis by
personal plaque control.
16-20
However, while it may be possible
under controlled conditions to remove most plaque with a
variety of mechanical oral hygiene aids, many patients lack the
motivation or skill to attain and maintain a plaque-free state
for significant periods of time.
21-23
Clinical trials also indicate
that self-administered plaque control programs alone, without
periodic professional reinforcement, are inconsistent in provi-
ding long-term inhibition of gingivitis.
19,24,25
Many patients with gingivitis have calculus or other associa-
ted local factors (eg, defective dental restorations) that interfere
with personal oral hygiene and the ability to remove bacterial
plaque. An acceptable therapeutic result for these individuals
is usually obtained when personal plaque control measures are
performed in conjunction with professional removal of plaque,
calculus, and other local contributing factors.
26,27
Removal of dental calculus is accomplished by scaling
and root planing procedures using hand, sonic, or ultrasonic
instruments. The therapeutic objective of scaling and root
planing is to remove plaque and calculus to reduce subgingival
bacteria below a threshold level capable of initiating clinical
Originating Group
American Academy of Periodontology - Research, Science, and Therapy Committee
Endorsed by the American Academy of Pediatric Dentistry
2004
Copyright © 2004 by the American Academy of Periodontology; all rights reserved. Copyrighted and reproduced with permission from the American Academy of
Periodontology. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photo-
copying, or otherwise without written permission of the publisher. Treatment of Plaque-induced Gingivitis, Chronic Periodontitis, and Other Clinical Conditions. J
Periodontol 2001;72:1790-1800. Available through the American Academy of Periodontology, Department of Scientific, Clinical and Educational Affairs, 737 North
Michigan Avenue, #800, Chicago, Ill., 60611-2690, Phone: (312) 787-5518, Fax: (312) 787-3670.
Treatment of Plaque-induced Gingivitis, Chronic
Periodontitis, and Other Clinical Conditions
AMERICAN ACADEMY OF PEDIATRIC DENTISTRY
ENDORSEMENTS 367
inflammation. The success of instrumentation is determined
by evaluating the periodontal tissues following treatment and
during the maintenance phase of therapy.
The use of topical antibacterial agents to help reduce
bacterial plaque may be beneficial for the prevention and treat-
ment of gingivitis in some patients.
28-30
A number of these agents in oral rinses and dentifrices
have been tested in clinical trials.
28
However, to be accepted by
the American Dental Association ( ADA) Council on Dental
Therapeutics as an effective agent for the treatment of gingivitis,
a product must reduce plaque and demonstrate effective reduc-
tion of gingival inflammation over a period of at least 6 months.
The agent must also be safe and not induce adverse side effects.
Three medicaments have been given the ADA Seal of
Acceptance for the control of gingivitis. The active ingredients
of one product are thymol, menthol, eucalyptol, and methyl
salicylate.
29
Active ingredients in the other two are chlorhexi-
dine digluconate and triclosan.
29
If properly used, the addition
of a topical anti-plaque agent to a gingivitis treatment regimen
for patients with deficient plaque control will likely result
in reduction of gingivitis.
30
However, experimental evidence
indicates that penetration of topically applied agents into the
gingival crevice is minimal.
31
Therefore, these agents are useful
for the control of supragingival, but not subgingival plaque.
Among individuals who do not perform excellent oral hy-
giene, supragingival irrigation with and without medicaments
is capable of reducing gingival inflammation beyond that
normally achieved by toothbrushing alone. This effect is likely
due to the flushing out of subgingival bacteria.
32
If gingivitis remains following the removal of plaque and
other contributing local factors, thorough evaluation should be
undertaken of systemic factors (eg, diabetes, pregnancy, etc.).
If such conditions are present, gingival health may be attained
once the systemic problem is resolved and plaque control is
maintained.
Acute periodontal diseases
Necrotizing ulcerative gingivitis (NUG) is associated with
specific bacterial accumulations occurring in individuals with
lowered host resistance.
1
NUG usually responds rapidly to the
reduction of oral bacteria by a combination of personal plaque
control and professional debridement. If lymphadenopathy or
fever accompanies oral symptoms, administration of systemic
antibiotics may be indicated. The use of chemotherapeutic
rinses by the patient may be beneficial during the initial treat-
ment stages. After the acute inflammation of the NUG lesion
is resolved, additional intervention may be indicated to prevent
disease recurrence or to correct resultant soft tissue deformities.
Necrotizing ulcerative periodontitis (NUP) manifests as
rapid necrosis and destruction of the gingiva and periodontal
attachment apparatus. It may initiate gingival bleeding and pain,
and it usually represents an extension of necrotizing ulcerative
gingivitis in individuals with lowered host resistance. NUP has
been reported among both HIV-positive and negative indi-
viduals, but its true prevalence is unknown.
33-38
Management
of NUP involves debridement which may be combined with
irrigation with antiseptics (eg, povidone iodine), antimicrobial
mouth rinses (eg, chlorhexidine), and administration of sys-
temic antibiotics.
39
There is also evidence that HIV-immune
deficiency may be associated with severe loss of periodontal
attachment that does not necessarily present clinically as an
ulcerative lesion.
40
Although not an acute disease, linear gin-
gival erythema (LGE) occurs in some HIV-infected individuals
and does not appear to respond to conventional scaling, root
planing, and plaque control.
39
Antibiotic therapy should be
used in HIV-positive patients with caution due to the pos-
sibility of inducing opportunistic infections.
39,40
The oral manifestations of a primary herpes simplex virus
type I infection often include gingivitis. By the time gingivitis
is present, patients are usually febrile, in pain, and have lymph-
adenopathy. Diagnosis is generally made from the clinical
appearance of the oral soft tissues. Although not performed
routinely, a viral culture may provide definitive identification
of the infective agent. In otherwise healthy patients, treatment
for herpetic gingivitis consists of palliative therapy. The infec-
tion is self-limiting and usually resolves in seven to 10 days.
Systemic antiviral therapy with acyclovir is appropriate for
immuno-compromised patients with herpetic gingivitis.
41
Gingival enlargement
Chronic gingival inflammation may result in gingival enlarge-
ment. This overgrowth of gingiva may be exaggerated in patients
with genetic or drug-related systemic factors (eg, anticonvul-
sants, cyclosporine and calcium channel blocking drugs).
42-46
Among individuals taking phenytoin, gingival overgrowth
may be minimized with appropriate personal oral hygiene and
professional maintenance.
47,48
However, root debridement in
patients with gingival overgrowth often does not return the
periodontiumto normal contour. The residual overgrowth may
not only complicate the patient’s ability to adequately clean
the dentition, but it may also present esthetic and functional
problems.
49
For patients with gingival overgrowth, the modification
of tissue topography by surgical recontouring may be under-
taken to create a maintainable oral environment.
47,50
Postoper-
ative management following tissue resection is important.
The benefits of surgical reduction may be lost due to rapid
proliferation of the tissues during the post-therapy phase.
51
Recurrence is common in many patients with drug-induced
gingival overgrowth.
51
For these patients, consultation with the
patient’s physician is advisable to determine if it is possible to
use an alternative drug therapy that does not induce gingival
overgrowth. If not, then repeated surgical and/or non-surgical
intervention may be required.
Chronic periodontitis
Appropriate therapy for patients with periodontitis varies
considerably with the extent and pattern of attachment loss,
local anatomical variations, type of periodontal disease, and
therapeutic objectives. Periodontitis destroys the attachment
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apparatus of teeth resulting in periodontal pocket formation
and alteration of normal osseous anatomy. The primary ob-
jectives of therapy for patients with chronic periodontitis
are to halt disease progression and to resolve inflammation.
Therapy at a diseased site is aimed at reducing etiologic factors
below the threshold capable of producing breakdown, thereby
allowing repair of the affected region. Regeneration of lost
periodontal structures can be enhanced by specific procedures.
However, many variables responsible for complete regeneration
of the periodontium are unknown and research is ongoing in
this area.
Scaling and root planing
The beneficial effects of scaling and root planing combined
with personal plaque control in the treatment of chronic peri-
odontitis have been validated.
52-65
These include reduction
of clinical inflammation, microbial shifts to a less pathogenic
subgingival flora, decreased probing depth, gain of clinical
attachment, and less disease progression.
52-65
Scaling and root planing procedures are technically de-
manding and time-consuming. Studies show that clinical
conditions generally improve following root planing; nonethe-
less, some sites still do not respond to this therapy.
62,63,66,67
The
addition of gingival curettage to root planing in the treatment
of generalized chronic periodontitis with shallow suprabony
pockets does not significantly reduce probing depth or gain
clinical attachment beyond that attained by scaling and root
planing alone.
68,69
The following factors may limit the success
of treatment by root planing: root anatomy (eg, concavities,
furrows etc.), furcations,
66
and deep probing depths.
70-72
Several weeks following the completion of root planing
and efforts to improve personal plaque control, re-evaluation
should be conducted to determine the treatment response.
Several factors must be considered at sites that continue to
exhibit signs of disease. If the patient’s daily personal plaque
control is not adequate to maintain gingival health, then
additional instruction and motivation in personal plaque
control and/or the use of topical chemotherapeutics (eg,
mouthrinses, local drug delivery devices) may be indicated.
Anatomical factors that can limit the effectiveness of root
instrumentation or limit the patient’s ability to perform per-
sonal plaque control (eg, deep probing depths, root concavities,
furcations) may require additional therapy including surgery.
Host response may also have an effect on treatment outcome
and patients with systemic conditions (eg, diabetes, pregnancy,
stress, AIDS, immunodeficiencies, and blood dyscrasias) may
not respond well to therapy that is directed solely at con-
trolling local factors. In such patients, it is important that
attempts be made to control the contributing systemic factors.
Pharmacological therapy
Pharmacotherapeutics may have an adjunctive role in the
management of periodontitis in certain patients.
73
These ad-
junctive therapies are categorized by their route of adminis-
tration to diseased sites: systemic or local drug delivery.
Systemic drug administration
Numerous investigations
73
have assessed the use of systemic
antibiotics to halt or slow the progression of periodontitis or to
improve periodontal status. The adjunctive use of systemically
delivered antibiotics may be indicated in the following situa-
tions: patients with multiple sites unresponsive to mechanical
debridement, acute infections, medically compromised patients,
presence of tissue-invasive organisms and ongoing disease
progression.
74-77
The administration of antibiotics for the
treatment of chronic periodontitis should follow accepted
pharmacological principles including, when appropriate, iden-
tification of pathogenic organisms and antibiotic sensitivity
testing.
Considerable research efforts have focused on systemic
application of host modulating agents such as non-steroidal
anti-inflammatory drugs (NSAIDS)
78-80
and subantimicrobial
dose doxycycline.
81-84
Investigators have reported some benefit
when these medications are incorporated into treatment proto-
cols.
78,81-84
Recently [year 2000], the United States Food and
Drug Administration (FDA) approved the use of a systemically
delivered collagenase inhibitor consisting of a 20-mg capsule of
doxycycline hyclate as an adjunct to scaling and root planing
for the treatment of periodontitis. Benefits included a statisti-
cally significant reduction in probing depths, a gain in clinical
attachment levels and a reduction in the incidence of disease
progression.
82-84
Overall, the data suggest that use of subantimi-
crobial dose doxycycline as an adjunct to scaling and root planing
provides defined but limited improvement in periodontal status.
It is important to consider the potential benefits and
side effects of systemic pharmacological therapy. Benefits may
include the ability to treat patients unresponsive to conventional
therapy or an individual with multiple sites experiencing
recurrent periodonitits. In contrast, potential risks associated
with systemically administered antibiotics include development
of resistant bacterial strains,
85
emergence of opportunistic in-
fections, and possible allergic sensitization of patients.
73
With
regard to the prolonged administration of NSAIDS, harmful
effects may include gastrointestinal upset and hemorrhage,
renal and hepatic impairment, central nervous system
disturbances, inhibition of platelet aggregation, prolonged
bleeding time, bone marrow damage, and hypersensitivity
reactions.
73
At present, the incidence of negative side effects
reported after root planing with or without administration
of subantimicrobial dose doxy-cycline has been similar. In
general, since patients with chronic periodontitis respond to
conventional therapy, it is unnecessary to routinely admin-
ister systemic medications such as antibiotics, NSAIDS, or
subantimicrobial dosing with doxycycline.
Local delivery
Controlled delivery of chemotherapeutic agents within peri-
odontal pockets can alter the pathogenic flora and improve
clinical signs of periodontitis.
86-94
Local drug delivery systems
provide several benefits; the drug can be delivered to the site
of disease activity at a bactericidal concentration and it can
AMERICAN ACADEMY OF PEDIATRIC DENTISTRY
ENDORSEMENTS 369
facilitate prolonged drug delivery. The FDA has approved the
use of an ethylene vinyl acetate fiber that contains tetracy-
cline,
86-91
a gelatin chip that contains chlorhexidine
93
and a
minocycline polymer formulation
92
as adjuncts to scaling and
root planing. The FDA has also approved doxycycline hyclate
in a bioabsorbable polymer gel as a stand-alone therapy for the
reduction of probing depths, bleeding upon probing, and gain
of clinical attachment.
94
Local delivery systems have potential limitations and
benefits. If used as a monotherapy, problems associated with
local delivery can include allergic reaction, possible inability to
disrupt biofilms, and failure to remove calculus.
95
The benefits
include the ease of application, selectively targeting a limited
number of diseased sites that were unresponsive to conventional
therapy, and possibly enhanced treatment results at specific
locations. Local delivery modalities have shown beneficial clini-
cal improvements with regard to probing depth reduction and
gain in clinical attachment.
91-94
Furthermore, there are limited
data to suggest that local delivery of antibiotics may also be
beneficial in preventing recurrent attachment loss in the ab-
sence of maintenance therapy.
90
Utilization of antibiotics at an individual site will depend
on the discretion of the treating therapist after consultation
with the patient. The greatest potential of local delivery devices
may be to enhance therapy at sites that do not respond to
conventional treatment. Ultimately, the results of local drug
delivery must be evaluated with regard to the magnitude of
improvement that can be attained relative to disease severity. A
more complete review of local drug delivery can be found in
the American Academy of Periodontology position paper “The
Role of Controlled Drug Delivery for Periodontitis”.
87
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