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PERIODONTA
L DRESSING
DR. THASLIM FATHIMA
SECOND YEAR POSTGRADUATE
DEPARTMENT OF PERIODONTOLOGY
1
CONTENTS
 Introduction
 History
 Uses
 Ideal requisites
 Rationale
 Types
 Substitutes for dressing
 Placement, retention and removal of the pack
 Physical properties
 Biological properties
 Periodontal dressing for all ?
 Conclusion
INTRODUCTIO
N
3
 One may thus infer that the environment in
which a wound heals plays a critical role.
 This favorable environment can be, in part,
created by a surgical dressing.
4
Factors that influence wound healing must be
addressed in a holistic fashion,
looking, as Pasteur suggested,
at the terrain in which the wound is found.
5
• They are applied to serve as a bandage over the surgical site with the objective of holding the flap
in place; protecting newly formed tissue; minimizing postoperative pain, infection and hemorrhage;
protecting the surgical site from trauma during eating and drinking and finally, supporting mobile
teeth during the healing process.
• Zentler in 1918 first reported the use of a periodontal dressing in the form of iodoform gauze.
• This marked the beginning of a trend toward using periodontal dressings after surgery.
Periodontal dressing is a surgical
dressing used post operatively to cover
and protect the surface of surgical
wound created by periodontal therapy.
Contoso
S u i t e s
• Wonderpak, consist
of - Zno Eugenol
mixed with -
Alcohol, pine oil,
Asbestos fibers
• use of Zno Eugenol
dressing to perform
chemical curettage
in treatment of NUG
– tannic acid was
included for
haemostasis and
astringency- thymol
was used as an
astringent.
• Zno Eugenol +
Paraformaldehyde to
perform Gingivectomy
by chemosurgery.
• This dressing caused
extensive necrosis of the
gingival and bone.
• for wound
protections.
HISTORY
1923 – Dr A W Ward 1942 – Box and Ham 1943 – Orban 1947 – Bernier and
Kaplan
Dr. A.W. Ward
1962 - Blanquie – control post operative bleeding- splint loose teeth – prevent re-
establishment of pocket – desensitize cementum
1964 – Gold – splint teeth, as it was cement dressing that set hard.
1964 - Weinreb and Shapiro - Zno Eugenol impregnated cords into periodontal
pockets ,but found to be less effective than gingivectomy.
USESOF PERIODONTAL DRESSING
Provide
mechanical
protection for the
surgical wound.
Enhancement of
patient comfort .
Prevents post
operative
bleeding.
Maintenance of
debris free area.
Control of
bleeding
Supports mobile
teeth during
healing
Helps in shaping
or molding the
newly formed
tissue
Richards, Caffesse RG. PERIODONTAL DRESSING. JIDENT2012
IDEALREQUISITESOF PERIODONTAL DRESSINGS
Soft, but still
have enough
plasticity and
flexibility.
Set within a
reasonable time.
Sufficient rigidity.
Smooth surface
after setting.
Bactericidal
properties.
IDEAL REQUISITES OF PERIODONTAL DRESSINGS
Not interfere
with healing.
Dimensional
stability
Not induce possible
systemic detrimental
effects and allergic
reactions
Acceptable
taste.
Economical and
easily available.
Good shelf life.
Shetty Neetha. Periodonatl dressings: An informed view. J Pharm Biomed Sci. 2013, January; 26(26): 269-272.
RATIONALE
Protection of the wound area
Enhancement of patient comfort
Maintenance of a debris free area
Control of bleeding: from trauma.
Protect newly exposed root surfaces from temperature changes
Protect sutures.
Protects surgical healing areas
H. A. Sachs, A. Farnoush. Current Status of Periodontal Dressings. J. Periodontol. December, 1984; 55; 689-696
TYPES OF PERIODONTAL
DRESSINGS
3
Those containing
zinc oxide and
eugenol
Those containing
zinc oxide without
eugenol and
Those containing
neither zinc oxide
nor eugenol
EUGENOLDRESSINGS
1. The Wondrpak was the first periodontal dressing introduced containing eugenol.
(Ward AW 1923)
• Powder - zinc oxide, powdered pine resin, talc, tannic acid and asbestos
• Liquid - isopropyl alcohol, clove oil, pine resin, pine oil, peanut oil, camphor and
colouring materials. (Haugen E1978)
A modified form of a eugenol dressing was introduced by Kirkland, called the Kirkland formula.
It consisted of zinc oxide, resin, zinc acetate, eugenol, tannic acid and olive oil.
Asbestos was found to have the potential to cause asbestosis, lung cancer and mesothelioma.
Tannic acid was found to cause potential liver damage, if absorbed systemically.
On the other hand, a few components were added to improve the properties – e.g., the addition of zinc
acetate as an accelerator to increase the working time
(Newman MG, Takei H 2006)
• Liquid and powder or paste.
• These are mixed together on a waxed paper pad
using a wooden tongue depressor or spatula. The
powder or paste is gradually incorporated into the
liquid until it reaches a dough- like consistency.
• The dressing may be used immediately or
wrapped in aluminium foil and refrigerated for use
for up to 1 week. (Newman MG, Takei H 2006)
• Setting time of Ward’s Wondrpak under oral
conditions was 24 minutes which was shown to be
less than its working time under room conditions
because both heat and moisture accelerate the
reaction of ZOE.
ZOE
16
ROLEOFEUGENOL
• Gingivectomy (Neil TC 1975)
• Waerhaug and Loe in 1957 - prevent or retard bacterial growth based on
their antiseptic properties.
• However, eugenol was found to irritate oral mucosal tissues, induce
allergic reactions and cause tissue necrosis, particularly of bone.
• Furthermore, it presents difficulties in manipulation and has a rough
surface after setting.
• Histological evidence - greater tissue destruction, with more
inflammatory cell infiltration and connective tissue response. (Kreth KK
1966)
• Eugenol has proven to be cytotoxic at higher concentrations and has an
adverse effect on fibroblasts and osteoblast-like cells.
• All of these reasons lead to the development of noneugenol dressings in
the late 1950s.
NON-EUGENOL DRESSINGS
COE-PAK
Base paste - zinc oxide
with added oils and
gums, and lorothidol
which is a fungicide
related to
hexachlorophene.
Most widely used non-eugenol intraoral dressing, and is
manufactured by Coe Laboratories (Alsip, IL, USA).
The catalyst paste -
fatty acids thickened
with colophony resin
or rosin and
chlorothymol as an
antibacterial agent.
CROSS PACK
• Cross Pack was formerly the powder part of a zinc oxide– eugenol dressing
in use in the late 1940s (W.G. Cross, personal communication, 1974).
• It consists of colophony powder, zinc oxide, tannic acid, bentonite and
powdered neomycin sulphate.
• filler to Coe-Pak
• Zinc oxide alone can be used instead of Cross Pack if desired . (Neil TC
1975)
PERIPAC
• Peripac (Dentsply, Konstanz, Germany) is a paste
containing calcium sulphate, zinc sulphate, zinc oxide,
polymethyl methacrylate,dimethoxy tetraethylene glycol,
ascorbic acid, flavor and iron oxide pigment.
• It reacts on exposure to air or moisture.
• Hardening of Peripac begins as soon as it comes into
contact with water and is complete in about 20 minutes.
Application of the dressing should not take more than
2-3 minutes. A correctly applied dressing remains with
no change for 8-10 days.
• Peripac is indicated as a dressing following gingivectomies and papillectomies,
deep curettage, reattachment surgery and gingival repositioning.
• It can also be used in treatment of necrotic gingivitis and ulcers; protection of
nonspecific lesions or sutured margins, fixation of desensitizing medicaments to
cervical areas and temporary rebasing of immediate dentures in periodontal
surgery. (Neil TC 1975)
SEPTO- PACK
• Septo-Pack (Septodont, Saint Maur-des-Fosses, France)
contains amyl acetate, dibutyl phthalate, butyl
polymetacrylate, zinc oxide and zinc sulphate.
• It is a self hardening plastic paste.
• Working time – 2 to 3 min
• Setting time – 30 min
• Neither Peripac nor Septopack contains any
specific antibacterial agent.
PERIOCARE
• PerioCare (Pulpdent Corp., Watertown, MA, USA) is a highly
elastic periodontal dressing and sets resiliently hard.
• It comes in a paste and gel system:
• 1 contains a paste of metal oxides in vegetable oil, and the
other contains a gel of rosin suspended in fatty acids.
• Equal amounts are dispensed, mixed and applied.
• Setting time of this product is 45-60 seconds and
the working time is 4-5 min.
PERIOPUTTY
• Perio Putty (Cadco Dental Products Inc., Los Angeles, CA USA) is another non-
eugenol dressing
• Methylparabens and propylparabens
• Benzocaine
(Sachs HA 1984)
PERIOGENIXTM
• PeriogenixTM is a noneugenol dressing manufactured by OroScience (New Line
Medical Inc., Lafayette, LA, USA).
• It contains perfluorodecalin, purified water, glycerin, hydrogenated
phosphatidylcholine, cetearyl alcohol, benzyl alcohol,polysorbate ,tocopheryl
acetate, methylparaben, propylparaben and oxygen.
• It has been said that this dressing accelerates healing of postoperative surgical
wounds. (Mulliken JB 1995)
• It was also observed that wounds treated with PeriogenixTM demonstrated an up-
regulation of vascular endothelial growth factors, collagens I and III, and matrix
metalloproteinase levels. (Mulliken JB 1995)
• PeriogenixTM allows for the exchange of oxygen and carbon dioxide into and out of
injured tissues.
• The main advantages of noneugenol dressings are :
 minimal irritation of the mucous membrane
 pleasant odor
 neutral taste
 ease of manipulation
pliability
 elimination of the objectionable taste of eugenol.
• Although they possess neither the analgesic nor antibacterial properties of eugenol
dressings, they are less irritating and form a closely adapted adhesive barrier to
saliva and oral bacteria.
DRESSINGSCONTAINING NEITHERZINC OXIDE NOR EUGENOL
Cyanoacrylate dressing
Light cure dressing
Collagen dressing
Mucoadhesive/stomahesive dressing
CYANOACRYLATE
• The cyanoacrylate alkyls were obtained for the first time in 1949 by A. E. Ardis.
• In 1959 Coover et al synthesized tissue adhesive materials and suggested their
possible use as surgical adhesives
• Only n-butyl cyanoacrylate was found to be biocompatible and therefore was
suggested to be used in surgical procedures (e.g., Histoacryl; B. Braun
Biosurgicals, Germany and PeriAcryl; Glustitch Inc, Delta, Canada).
• As a dressing it has been evaluated clinically and histologically following
procedures such as gingivectomy, mucoperiosteal flaps, excisional biopsies, free
mucosal grafts, frenectomies and for oral mucosal ulcers. (Richard PS 1988)
• Rapid hemostasis in the presence of moisture
• It accelerates initial healing and also possesses antimicrobial properties. (Sachs HA
1984)
LIGHTCURE DRESSINGS
• Light cure dressings (e.g., Bucrylate; Ethicon Inc.,
Somerville, NJ, USA) is a novel concept for the
protection of periodontal surgical sites.
• It is a single-component, light-activated dressing
material supplied in a syringe for direct placement.
• It is cured in increments with a visible light curing
unit and retains its elasticity on setting.
• It is tasteless and has a tinted pink
36
Barricaid placement
Light-cured resin “Barricaid” – An aesthetic and biocompatible dressing: A step ahead.Ellora Madan et al. J Indian Soc Periodontol
COLLAGEN DRESSINGS
• Collagen dressings (e.g., Colla products from Zimmer Dental, Carlsbad, CA, USA) are biological
dressings which create a physiologic interface between the wound and the environment and
enhances healing.
• The advantages over other dressings include :
 ease of application,
 non-immunogenic,
 non-pyrogenic,
 hypoallergenic properties.
• Moreover, an inherent property of native collagen is the ability to promote hemostasis by facilitating
aggregation of platelets and subsequently, the coagulation cascade.
• Additionally, the structure of absorbable collagen provides a 3-
dimensional matrix for strengthening the blood clot.
• Commercially available collagen dressings have three forms:
• tape (CollaTape; Zimmer Dental, Carlsbad, CA, USA),
• cote (CollaCote, Zimmer Dental, Carlsbad, CA, USA) and
• plug (CollaPlug; Zimmer Dental, Carlsbad, CA, USA).
(Steer PL 2002)
Tape is used for localized ridge defects,
socket grafting, Schneiderian
membrane tears, subantral
augmentations and protection of soft
tissue donor sites
Plug is used as a dressing
for biopsy sites
Cote is used in procedures
like soft tissue recontouring,
sinus graft containment,
guided bone regeneration
and sinus membrane
perforations
• Some surgeons reported the use of mucoadhesive/ stomahesive dressing
(CovaTec,UK), whenever mucosal coverage is required for a short period
of time.
• It is an adhesive, nonsensitizing wound dressing which was patented by
Peter L. Steer and Howard Mathew in 1982.
• It is a multilayered dressing including a layer of curative and absorbent
material which makes contact with the wounds, a layer of deodorizing
material and an outer layer which secures the bandage to the tissues.
Mucoadhesive/ Stomahesive dressing
• The contents include gelatin, pectin, sodium carboxymethyl cellulose and
polyisobutylene.
• The longevity of the dressing is minimal (dissolves in 8 - 2 4 hours).
• However, some surgeons find this short time adequate for protecting the donor
and recipient sites of a soft tissue graft or for gingivoplasty procedures. (Addy M
1975)
MODIFICATIO
NS
41
DRESSINGANDCHLORHEXIDINE
• Chlorhexidine is an established antibacterial agent.
• In 1989, most commercial periodontal dressings claiming to have initially
good antimicrobial activity.
• Thus the addition of chlorhexidine to dressings to improve their properties
was proposed
• Pluss et al in 1975 incorporated 15- 20 mg of chlorhexidine dihydrochloride in a
periodontal dressing (Peripac) and documented a significant reduction in the
amount of plaque formation.
• In another similar study, Othman et al found that surgical dressings containing
antimicrobial agents, having high retention and slow release properties are
advantagious.
• In a study by Zyskind et al- chlorhexidine varnish.
• Significantly less plaque was found on teeth pre-coated with the slow-release
varnish.
• A review of the literature seems to suggest that the addition of
chlorhexidine is a valuable asset in postsurgical care.
• However, since the use of chlorhexidine mouth rinses is preferred by
patients, the practice of direct incorporation of chlorhexidine powder in
the dressing seems to have waned.
• Additionally, mouth rinses have a rinsing and washing off effect against
the bacteria from the potential infection site and can reach more surfaces
compared with any hard or semirigid materials.
DRESSINGAND ANTIBACTERIAL AGENTS
• To enhance healing and prevent infections.
• The earliest reports outlining the use of tetracycline are by Fraleigh and of zinc
bacitracin, by Baer et al.
• Though the addition of these agents is beneficial, there are a few authors who
claim that their addition may be harmful.
• Heaney et al suggested the removal of the dressing within 7 days of application.
• Two possible problems may occur: emergence of resistant organisms and
opportunistic infections.
Antibacterial Properties of Packs
 Improved healing and patient comfort with less odor and taste have been obtained by
incorporating antibiotics into the pack.
 Bacitracin,oxytetracycline (Terramycin), neomycin, and nitrofurazone have been tried,
but all of these may produce hypersensitivity reactions.
 The emergence of resistant organisms and opportunistic infections has been reported.
 The incorporation of tetracycline powder into the Coe-Pak is generally recommended,
particularly when long and traumatic surgeries are performed.
OTHERMEDICAMENTSAND DRESSINGS
• The addition of noneugenol phenol derivatives such as chlorothymol and
oil of bergamot was described by Molnar and by Schach, respectively.
• To improve postoperative healing, Saad and Swenson and Swann et
al added steroids and Dilantin to dressings.
• Such agents had been previously reported to increase the rate of healing
in skin wounds of rats and humans, but neither agent showed any
advantage in these periodontal studies.
SUBSTITUTESFORDRESSINGS
• In 1975, the modification of a methacrylic gel for use as a periodontal
dressing was attempted, and the results suggested that the modified
methacrylic gel fulfilled the requirements of a periodontal dressing.
• However, further research was proposed for the use of this gel
as a dressing.
• In 1990, a study was carried out with the aim of evaluating the healing of the gingival grafts
covered with dental adhesive paste in comparison with the grafts covered with Peripac.
• The results indicated the use of adhesive pastes as a substitute for conventional
dressings.
(Steer PL 1990)
APPLICATION
OF THE PACK
51
Inserting the periodontal pack.
A, Strip of pack is hooked around the last molar and
pressed into place anteriorly.
B, Lingual pack is joined to the facial strip at the
distal surface of the last molar and fitted into place
anteriorly.
C, Gentle pressure on the facial and lingual surfaces joins
the pack interproximally.
53
The pack should cover the gingiva, but overextension onto uninvolved mucosa
should be avoided.
Excess pack irritates the mucobuccal fold and the floor of the mouth, and it
interferes with the tongue.
The excess tends to break off and to take pack from the operated area with it.
Pack that interferes with the occlusion should be trimmed away before the
patient is dismissed.
The operator should ask the patient to move the tongue forcibly out and to
each side, and the cheek and lips should be displaced in all directions to mold
the pack while it is still soft.
After the pack has set, it should be trimmed to eliminate all excess.
RETENTIONOF PACKS
In the 1950s, numerous splints and stents were used to stabilize the periodontal dressings.
The materials used were acrylic resin, advocated by McKenzie and later by Munns.
In 1953, Waerhaug and Anerud described interproximal use of spiral saws and lengthwise cotton thread
In 1952, Castenfelt mentioned the use of cotton tapes with interdental sutures.
Cowan advocated the inclusion of wiring to increase the retention.
Subsequently, in 1970,Smith reported preliminary trials with polyacrylate dressing materials.
 Periodontal dressings are usually kept in place mechanically by interlocking in interdental spaces
and joining the lingual and facial portions of the pack.
 In isolated teeth or when several teeth in an arch are missing, retention of the pack may be
difficult.
• Retention of dressing over palatal wounds has always gained extra
attention.
• In 1992, Ferguson described a technique which utilized a light- cured
periodontal dressing – i.e., Barricaid in conjunction with the surgical
exposure of palatally displaced maxillary canines.
• The procedure was very quick and simple to perform.
• It was noted that a composite intraoral dressing remained secure for
days if incorporated with various appliances in the anterior palate (e.g.,
quad-helix coil for maxillary expansion, orthodontic brackets or a
retainer wire).
• The placement of dental floss tied loosely around the teeth enhances retention
of the pack.
REMOVALOFTHE PACK
• Insert a scaler or plastic instrument under the border of the dressing and apply
lateral pressure.
• Watch for sutures that can get lodged in the dressings.
• Remove fragments of dressing gently with cotton pliers to avoid scratching the thin
epithelial covering of the healing tissue.
• Use a scaler for removal of fragments adhering to tooth surfaces.
• Use a curet for particles near the gingival surface.
• Syringe with a gentle stream of warm water.
PHYSICALPROPERTIES
• Two chemically cured (Coe- Pakand PerioCare) and 1 photocured dressing
(Barricaid) were examined by von Fraunhofer and Argyropoulos.
• All materials absorbed water, both Coe-Pak and PerioCare acted in a similar
manner at 23˚C, but PerioCare absorbed far more water at 37˚C.
• For Barricaid, it was shown that increased light exposure had little effect on its water
sorption or solubility.
• The adhesion of different dressings was also tested.
• Adhesion of Coe-Pak to a single tooth at 1 hour was about 7 kg, but this
decreased to about 6.5 kg at 24 hours and to 5 kg at 7 days.
• The adhesion of PerioCare was 2 kg at 1 hour and 8.5 kg at 24 hours, but
it decreased to 7.5 kg at 7 days.
• The adhesion of Barricaid was about 5 kg at 1 hour, which decreased to 3.5
kg at 24 hours and 1.5 kg at 7 days.
• The mechanis of adhesion of Barricaid appeared to involve mechanical
locking, which differs from that of Coe-Pak and PerioCare
Von Fraunhofer JA, Argyropoulos DC. Properties of periodontal dressings. Dent
Mater. 1990; 6(1): 51-55.
• Eugenol-free dressings were developed to offset the
irritant and toxic properties of liquid eugenol.
• Numerous reports have outlined the adverse tissue
effects and intensity of inflammatory reaction with
the use of a eugenol based dressing. (Sarrami N
2002)
• At the same time, in vitro studies have revealed that
eugenol- based dressings may cause less growth
inhibition of permanent cells and primary human
leukocytes than some noneugenol products. (Wyan
VJ 1977)
BIOLOGICAL
PROPERTIES-
EFFECTS ON
WOUND
HEALING
60
• It has been established that dressings such as WondrPak produce greater
tissue destruction, with more inflammatory cell infiltration and connective
tissue response, involving a much wider reaction area in the adjacent
tissues. (Wyan VJ 1977)
• Comparative evaluation of different noneugenol dressings has shown
conflicting results. Coe-Pak, in a few studies, showed a severe tissue
reaction as compared with Peripac and PerioPutty, (Nezwek RA 1980) which
elicited the least inflammatory response, whereas in others, Coe-Pak was
also seen to cause least damage. (Wennberg A 1983)
• Light-cured periodontal dressings were not cytotoxic in cell cultures and
different cell types.
• With the development of collagen-based dressings, products such as
CollaCote had better clinical and histological effects on palatal wound
healing than Coe-Pak. (Shanmugam M 2010)
• The literature thus seems to suggest that in comparison, non- eugenol
dressings are more biocompatible than their eugenol counterparts.
• Furthermore, dressings falling in other categories including light cure
dressing, Barricaid and collagen-based dressing CollaCote are better than
the conventional noneugenol based dressings.
• One of the purposes of periodontal dressings is to
aid in reducing postoperative discomfort.
• In earlier reports, measuring the degree of pain
experienced by the patient was done based on
the consumption of analgesic tablets.
• Such studies reported that the experience of pain
was significantly more frequent after the use of
Peripac than Coe-Pak and Wondrpak, based on
higher tablet consumption in the Peripac group.
• Also, when sensitivity was observed, it was seen
that the highest proportion of sensitive teeth was
found after the use of Coe-Pak, and the lowest
with Peripac
POSTOPERATIV
E PAIN AND
DRESSING
64
• Pain measurements using visual analogue scale (VAS) studies have reported
that pain scores with Coe-Pak were higher than with Wondrpak after a
gingivectomy procedure. (Jorkjend L 1990)
• The same authors, in another study, compared pain experience after
gingivectomy when using a local anesthetic agent.
• They reported that pain was masked when using a eugenol-based
periodontal dressing, thus proving that eugenol dressings cause less pain
than non-eugenol ones. (Jorkjend L 1991)
PERIODONTALDRESSINGSFORALL?
• The fact that complete healing can take place even without a dressing,
provided the surgical area is kept clean, and that there is no difference in
healing between dressed and non-dressed wounds, lends support to the
theory that not all surgical areas need to be “packed” . (Loe H 1961)
• Other factors such as the presence of inflammation seemed to influence
the rate of wound healing to a larger extent than the use of a dressing.
(Stahl SS1969)
• A number of clinical trials have proposed that the use of a dressing
accumulates plaque-causing inflammation, irritates the healing tissues,
produces transient bacteremia during postoperative dressing change and
causes more pain and swelling but less sensitivity and difficulty in eating.
(Henry TG 1976, Newman PS1982)
• Despite these drawbacks, it appears that healing is slightly more rapid in
the dressed segments.
• The use of periodontal dressings from the patients’ preference and comfort
point of view has also been elaborated.
• Conflicting reports exist in the literature, as these factors are based on
patient responses and thus are not objectively evaluated, because of the
subjective criteria usually employed.
• The use of chlorhexidine mouth rinse instead of a dressing has been found
to reduce postoperative plaque accumulation and surgical inflammation
and is considered to be roughly equivalent to professional plaque control
in postsurgical healing, thus providing a viable alternative regime for plaque
control. (Westfelt E1983)
• Moreover, many patients experience discomfort when a periodontal
dressing was used and preferred to use a mouth rinse.
• Conversely, some patients exhibit a psychological feeling of protection and
well- being when a periodontal dressing was put in place.
• The answer to this controversy, though still open to debate, is probably
that the choice of use of a periodontal dressing is a matter of individual
preference and the judgment of the operator.
• It is, however, the use of a dressing for stabilization of free gingival grafts
and protection of donor site, retention of an apically positioned flap,
protection of the denuded bone from further injury, protection of the graft
site in periodontal regeneration and to facilitate retention of drugs
delivered locally in the subgingival sites.
CONCLUSION
REFERENCES
• Carranza’s clinical periodontology 11th edition.
• Clinical periodontology and implant dentistry. Jan Lindhe 5th edition.
• Text book of Clinical practice of the dental hygienist . Wilkins 10th edition
• Rahul Kathariya, Hansa Jain, Tanya Jadhav. To pack or not to pack: the current status of periodontal
dressings. JAppl Biomater Funct Mater 2015.
• Zahra Baghani, Mahdi Kadkhodazadeh. Periodontal Dressing: A Review Article. JDent Res Dent Clin
Dent Prospect 2013.
• K. David,Shetty Neetha J.& Pralhad Swati. Periodontal Dressings: An Informed View. Journal of
pharmaceutical and biomedical sciences (JPharm Biomed Sci.) 2013.
• Muthukumarasamy, Nazargi Mahabob. PERIODONTAL DRESSING. JIDENT 2012.
• Triveni Kale, Nitin Dani, Tejas Patange . Periodontal Dressing. IOSR Journal of Dental and Medical
Sciences 2014.
Thank You
74

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Periodontal dressing

  • 1. PERIODONTA L DRESSING DR. THASLIM FATHIMA SECOND YEAR POSTGRADUATE DEPARTMENT OF PERIODONTOLOGY 1
  • 2. CONTENTS  Introduction  History  Uses  Ideal requisites  Rationale  Types  Substitutes for dressing  Placement, retention and removal of the pack  Physical properties  Biological properties  Periodontal dressing for all ?  Conclusion
  • 4.  One may thus infer that the environment in which a wound heals plays a critical role.  This favorable environment can be, in part, created by a surgical dressing. 4 Factors that influence wound healing must be addressed in a holistic fashion, looking, as Pasteur suggested, at the terrain in which the wound is found.
  • 5. 5 • They are applied to serve as a bandage over the surgical site with the objective of holding the flap in place; protecting newly formed tissue; minimizing postoperative pain, infection and hemorrhage; protecting the surgical site from trauma during eating and drinking and finally, supporting mobile teeth during the healing process. • Zentler in 1918 first reported the use of a periodontal dressing in the form of iodoform gauze. • This marked the beginning of a trend toward using periodontal dressings after surgery. Periodontal dressing is a surgical dressing used post operatively to cover and protect the surface of surgical wound created by periodontal therapy.
  • 6. Contoso S u i t e s • Wonderpak, consist of - Zno Eugenol mixed with - Alcohol, pine oil, Asbestos fibers • use of Zno Eugenol dressing to perform chemical curettage in treatment of NUG – tannic acid was included for haemostasis and astringency- thymol was used as an astringent. • Zno Eugenol + Paraformaldehyde to perform Gingivectomy by chemosurgery. • This dressing caused extensive necrosis of the gingival and bone. • for wound protections. HISTORY 1923 – Dr A W Ward 1942 – Box and Ham 1943 – Orban 1947 – Bernier and Kaplan Dr. A.W. Ward
  • 7. 1962 - Blanquie – control post operative bleeding- splint loose teeth – prevent re- establishment of pocket – desensitize cementum 1964 – Gold – splint teeth, as it was cement dressing that set hard. 1964 - Weinreb and Shapiro - Zno Eugenol impregnated cords into periodontal pockets ,but found to be less effective than gingivectomy.
  • 8. USESOF PERIODONTAL DRESSING Provide mechanical protection for the surgical wound. Enhancement of patient comfort . Prevents post operative bleeding. Maintenance of debris free area. Control of bleeding Supports mobile teeth during healing Helps in shaping or molding the newly formed tissue Richards, Caffesse RG. PERIODONTAL DRESSING. JIDENT2012
  • 9. IDEALREQUISITESOF PERIODONTAL DRESSINGS Soft, but still have enough plasticity and flexibility. Set within a reasonable time. Sufficient rigidity. Smooth surface after setting. Bactericidal properties.
  • 10. IDEAL REQUISITES OF PERIODONTAL DRESSINGS Not interfere with healing. Dimensional stability Not induce possible systemic detrimental effects and allergic reactions Acceptable taste. Economical and easily available. Good shelf life. Shetty Neetha. Periodonatl dressings: An informed view. J Pharm Biomed Sci. 2013, January; 26(26): 269-272.
  • 11. RATIONALE Protection of the wound area Enhancement of patient comfort Maintenance of a debris free area Control of bleeding: from trauma. Protect newly exposed root surfaces from temperature changes Protect sutures. Protects surgical healing areas H. A. Sachs, A. Farnoush. Current Status of Periodontal Dressings. J. Periodontol. December, 1984; 55; 689-696
  • 12. TYPES OF PERIODONTAL DRESSINGS 3 Those containing zinc oxide and eugenol Those containing zinc oxide without eugenol and Those containing neither zinc oxide nor eugenol
  • 13.
  • 14. EUGENOLDRESSINGS 1. The Wondrpak was the first periodontal dressing introduced containing eugenol. (Ward AW 1923) • Powder - zinc oxide, powdered pine resin, talc, tannic acid and asbestos • Liquid - isopropyl alcohol, clove oil, pine resin, pine oil, peanut oil, camphor and colouring materials. (Haugen E1978)
  • 15. A modified form of a eugenol dressing was introduced by Kirkland, called the Kirkland formula. It consisted of zinc oxide, resin, zinc acetate, eugenol, tannic acid and olive oil. Asbestos was found to have the potential to cause asbestosis, lung cancer and mesothelioma. Tannic acid was found to cause potential liver damage, if absorbed systemically. On the other hand, a few components were added to improve the properties – e.g., the addition of zinc acetate as an accelerator to increase the working time (Newman MG, Takei H 2006)
  • 16. • Liquid and powder or paste. • These are mixed together on a waxed paper pad using a wooden tongue depressor or spatula. The powder or paste is gradually incorporated into the liquid until it reaches a dough- like consistency. • The dressing may be used immediately or wrapped in aluminium foil and refrigerated for use for up to 1 week. (Newman MG, Takei H 2006) • Setting time of Ward’s Wondrpak under oral conditions was 24 minutes which was shown to be less than its working time under room conditions because both heat and moisture accelerate the reaction of ZOE. ZOE 16
  • 17. ROLEOFEUGENOL • Gingivectomy (Neil TC 1975) • Waerhaug and Loe in 1957 - prevent or retard bacterial growth based on their antiseptic properties. • However, eugenol was found to irritate oral mucosal tissues, induce allergic reactions and cause tissue necrosis, particularly of bone. • Furthermore, it presents difficulties in manipulation and has a rough surface after setting.
  • 18. • Histological evidence - greater tissue destruction, with more inflammatory cell infiltration and connective tissue response. (Kreth KK 1966) • Eugenol has proven to be cytotoxic at higher concentrations and has an adverse effect on fibroblasts and osteoblast-like cells. • All of these reasons lead to the development of noneugenol dressings in the late 1950s.
  • 20. COE-PAK Base paste - zinc oxide with added oils and gums, and lorothidol which is a fungicide related to hexachlorophene. Most widely used non-eugenol intraoral dressing, and is manufactured by Coe Laboratories (Alsip, IL, USA). The catalyst paste - fatty acids thickened with colophony resin or rosin and chlorothymol as an antibacterial agent.
  • 21.
  • 22.
  • 23. CROSS PACK • Cross Pack was formerly the powder part of a zinc oxide– eugenol dressing in use in the late 1940s (W.G. Cross, personal communication, 1974). • It consists of colophony powder, zinc oxide, tannic acid, bentonite and powdered neomycin sulphate. • filler to Coe-Pak • Zinc oxide alone can be used instead of Cross Pack if desired . (Neil TC 1975)
  • 24. PERIPAC • Peripac (Dentsply, Konstanz, Germany) is a paste containing calcium sulphate, zinc sulphate, zinc oxide, polymethyl methacrylate,dimethoxy tetraethylene glycol, ascorbic acid, flavor and iron oxide pigment. • It reacts on exposure to air or moisture. • Hardening of Peripac begins as soon as it comes into contact with water and is complete in about 20 minutes. Application of the dressing should not take more than 2-3 minutes. A correctly applied dressing remains with no change for 8-10 days.
  • 25. • Peripac is indicated as a dressing following gingivectomies and papillectomies, deep curettage, reattachment surgery and gingival repositioning. • It can also be used in treatment of necrotic gingivitis and ulcers; protection of nonspecific lesions or sutured margins, fixation of desensitizing medicaments to cervical areas and temporary rebasing of immediate dentures in periodontal surgery. (Neil TC 1975)
  • 26. SEPTO- PACK • Septo-Pack (Septodont, Saint Maur-des-Fosses, France) contains amyl acetate, dibutyl phthalate, butyl polymetacrylate, zinc oxide and zinc sulphate. • It is a self hardening plastic paste. • Working time – 2 to 3 min • Setting time – 30 min • Neither Peripac nor Septopack contains any specific antibacterial agent.
  • 27. PERIOCARE • PerioCare (Pulpdent Corp., Watertown, MA, USA) is a highly elastic periodontal dressing and sets resiliently hard. • It comes in a paste and gel system: • 1 contains a paste of metal oxides in vegetable oil, and the other contains a gel of rosin suspended in fatty acids. • Equal amounts are dispensed, mixed and applied. • Setting time of this product is 45-60 seconds and the working time is 4-5 min.
  • 28. PERIOPUTTY • Perio Putty (Cadco Dental Products Inc., Los Angeles, CA USA) is another non- eugenol dressing • Methylparabens and propylparabens • Benzocaine (Sachs HA 1984)
  • 29. PERIOGENIXTM • PeriogenixTM is a noneugenol dressing manufactured by OroScience (New Line Medical Inc., Lafayette, LA, USA). • It contains perfluorodecalin, purified water, glycerin, hydrogenated phosphatidylcholine, cetearyl alcohol, benzyl alcohol,polysorbate ,tocopheryl acetate, methylparaben, propylparaben and oxygen. • It has been said that this dressing accelerates healing of postoperative surgical wounds. (Mulliken JB 1995)
  • 30. • It was also observed that wounds treated with PeriogenixTM demonstrated an up- regulation of vascular endothelial growth factors, collagens I and III, and matrix metalloproteinase levels. (Mulliken JB 1995) • PeriogenixTM allows for the exchange of oxygen and carbon dioxide into and out of injured tissues.
  • 31. • The main advantages of noneugenol dressings are :  minimal irritation of the mucous membrane  pleasant odor  neutral taste  ease of manipulation pliability  elimination of the objectionable taste of eugenol. • Although they possess neither the analgesic nor antibacterial properties of eugenol dressings, they are less irritating and form a closely adapted adhesive barrier to saliva and oral bacteria.
  • 32. DRESSINGSCONTAINING NEITHERZINC OXIDE NOR EUGENOL Cyanoacrylate dressing Light cure dressing Collagen dressing Mucoadhesive/stomahesive dressing
  • 33. CYANOACRYLATE • The cyanoacrylate alkyls were obtained for the first time in 1949 by A. E. Ardis. • In 1959 Coover et al synthesized tissue adhesive materials and suggested their possible use as surgical adhesives • Only n-butyl cyanoacrylate was found to be biocompatible and therefore was suggested to be used in surgical procedures (e.g., Histoacryl; B. Braun Biosurgicals, Germany and PeriAcryl; Glustitch Inc, Delta, Canada).
  • 34. • As a dressing it has been evaluated clinically and histologically following procedures such as gingivectomy, mucoperiosteal flaps, excisional biopsies, free mucosal grafts, frenectomies and for oral mucosal ulcers. (Richard PS 1988) • Rapid hemostasis in the presence of moisture • It accelerates initial healing and also possesses antimicrobial properties. (Sachs HA 1984)
  • 35. LIGHTCURE DRESSINGS • Light cure dressings (e.g., Bucrylate; Ethicon Inc., Somerville, NJ, USA) is a novel concept for the protection of periodontal surgical sites. • It is a single-component, light-activated dressing material supplied in a syringe for direct placement. • It is cured in increments with a visible light curing unit and retains its elasticity on setting. • It is tasteless and has a tinted pink
  • 36. 36 Barricaid placement Light-cured resin “Barricaid” – An aesthetic and biocompatible dressing: A step ahead.Ellora Madan et al. J Indian Soc Periodontol
  • 37. COLLAGEN DRESSINGS • Collagen dressings (e.g., Colla products from Zimmer Dental, Carlsbad, CA, USA) are biological dressings which create a physiologic interface between the wound and the environment and enhances healing. • The advantages over other dressings include :  ease of application,  non-immunogenic,  non-pyrogenic,  hypoallergenic properties. • Moreover, an inherent property of native collagen is the ability to promote hemostasis by facilitating aggregation of platelets and subsequently, the coagulation cascade.
  • 38. • Additionally, the structure of absorbable collagen provides a 3- dimensional matrix for strengthening the blood clot. • Commercially available collagen dressings have three forms: • tape (CollaTape; Zimmer Dental, Carlsbad, CA, USA), • cote (CollaCote, Zimmer Dental, Carlsbad, CA, USA) and • plug (CollaPlug; Zimmer Dental, Carlsbad, CA, USA). (Steer PL 2002) Tape is used for localized ridge defects, socket grafting, Schneiderian membrane tears, subantral augmentations and protection of soft tissue donor sites Plug is used as a dressing for biopsy sites Cote is used in procedures like soft tissue recontouring, sinus graft containment, guided bone regeneration and sinus membrane perforations
  • 39. • Some surgeons reported the use of mucoadhesive/ stomahesive dressing (CovaTec,UK), whenever mucosal coverage is required for a short period of time. • It is an adhesive, nonsensitizing wound dressing which was patented by Peter L. Steer and Howard Mathew in 1982. • It is a multilayered dressing including a layer of curative and absorbent material which makes contact with the wounds, a layer of deodorizing material and an outer layer which secures the bandage to the tissues. Mucoadhesive/ Stomahesive dressing
  • 40. • The contents include gelatin, pectin, sodium carboxymethyl cellulose and polyisobutylene. • The longevity of the dressing is minimal (dissolves in 8 - 2 4 hours). • However, some surgeons find this short time adequate for protecting the donor and recipient sites of a soft tissue graft or for gingivoplasty procedures. (Addy M 1975)
  • 42. DRESSINGANDCHLORHEXIDINE • Chlorhexidine is an established antibacterial agent. • In 1989, most commercial periodontal dressings claiming to have initially good antimicrobial activity. • Thus the addition of chlorhexidine to dressings to improve their properties was proposed
  • 43. • Pluss et al in 1975 incorporated 15- 20 mg of chlorhexidine dihydrochloride in a periodontal dressing (Peripac) and documented a significant reduction in the amount of plaque formation. • In another similar study, Othman et al found that surgical dressings containing antimicrobial agents, having high retention and slow release properties are advantagious.
  • 44. • In a study by Zyskind et al- chlorhexidine varnish. • Significantly less plaque was found on teeth pre-coated with the slow-release varnish.
  • 45. • A review of the literature seems to suggest that the addition of chlorhexidine is a valuable asset in postsurgical care. • However, since the use of chlorhexidine mouth rinses is preferred by patients, the practice of direct incorporation of chlorhexidine powder in the dressing seems to have waned. • Additionally, mouth rinses have a rinsing and washing off effect against the bacteria from the potential infection site and can reach more surfaces compared with any hard or semirigid materials.
  • 46. DRESSINGAND ANTIBACTERIAL AGENTS • To enhance healing and prevent infections. • The earliest reports outlining the use of tetracycline are by Fraleigh and of zinc bacitracin, by Baer et al. • Though the addition of these agents is beneficial, there are a few authors who claim that their addition may be harmful. • Heaney et al suggested the removal of the dressing within 7 days of application. • Two possible problems may occur: emergence of resistant organisms and opportunistic infections.
  • 47. Antibacterial Properties of Packs  Improved healing and patient comfort with less odor and taste have been obtained by incorporating antibiotics into the pack.  Bacitracin,oxytetracycline (Terramycin), neomycin, and nitrofurazone have been tried, but all of these may produce hypersensitivity reactions.  The emergence of resistant organisms and opportunistic infections has been reported.  The incorporation of tetracycline powder into the Coe-Pak is generally recommended, particularly when long and traumatic surgeries are performed.
  • 48. OTHERMEDICAMENTSAND DRESSINGS • The addition of noneugenol phenol derivatives such as chlorothymol and oil of bergamot was described by Molnar and by Schach, respectively. • To improve postoperative healing, Saad and Swenson and Swann et al added steroids and Dilantin to dressings. • Such agents had been previously reported to increase the rate of healing in skin wounds of rats and humans, but neither agent showed any advantage in these periodontal studies.
  • 49. SUBSTITUTESFORDRESSINGS • In 1975, the modification of a methacrylic gel for use as a periodontal dressing was attempted, and the results suggested that the modified methacrylic gel fulfilled the requirements of a periodontal dressing. • However, further research was proposed for the use of this gel as a dressing.
  • 50. • In 1990, a study was carried out with the aim of evaluating the healing of the gingival grafts covered with dental adhesive paste in comparison with the grafts covered with Peripac. • The results indicated the use of adhesive pastes as a substitute for conventional dressings. (Steer PL 1990)
  • 52. Inserting the periodontal pack. A, Strip of pack is hooked around the last molar and pressed into place anteriorly. B, Lingual pack is joined to the facial strip at the distal surface of the last molar and fitted into place anteriorly. C, Gentle pressure on the facial and lingual surfaces joins the pack interproximally.
  • 53. 53 The pack should cover the gingiva, but overextension onto uninvolved mucosa should be avoided. Excess pack irritates the mucobuccal fold and the floor of the mouth, and it interferes with the tongue. The excess tends to break off and to take pack from the operated area with it. Pack that interferes with the occlusion should be trimmed away before the patient is dismissed. The operator should ask the patient to move the tongue forcibly out and to each side, and the cheek and lips should be displaced in all directions to mold the pack while it is still soft. After the pack has set, it should be trimmed to eliminate all excess.
  • 54. RETENTIONOF PACKS In the 1950s, numerous splints and stents were used to stabilize the periodontal dressings. The materials used were acrylic resin, advocated by McKenzie and later by Munns. In 1953, Waerhaug and Anerud described interproximal use of spiral saws and lengthwise cotton thread In 1952, Castenfelt mentioned the use of cotton tapes with interdental sutures. Cowan advocated the inclusion of wiring to increase the retention. Subsequently, in 1970,Smith reported preliminary trials with polyacrylate dressing materials.  Periodontal dressings are usually kept in place mechanically by interlocking in interdental spaces and joining the lingual and facial portions of the pack.  In isolated teeth or when several teeth in an arch are missing, retention of the pack may be difficult.
  • 55. • Retention of dressing over palatal wounds has always gained extra attention. • In 1992, Ferguson described a technique which utilized a light- cured periodontal dressing – i.e., Barricaid in conjunction with the surgical exposure of palatally displaced maxillary canines. • The procedure was very quick and simple to perform.
  • 56. • It was noted that a composite intraoral dressing remained secure for days if incorporated with various appliances in the anterior palate (e.g., quad-helix coil for maxillary expansion, orthodontic brackets or a retainer wire). • The placement of dental floss tied loosely around the teeth enhances retention of the pack.
  • 57. REMOVALOFTHE PACK • Insert a scaler or plastic instrument under the border of the dressing and apply lateral pressure. • Watch for sutures that can get lodged in the dressings. • Remove fragments of dressing gently with cotton pliers to avoid scratching the thin epithelial covering of the healing tissue. • Use a scaler for removal of fragments adhering to tooth surfaces. • Use a curet for particles near the gingival surface. • Syringe with a gentle stream of warm water.
  • 58. PHYSICALPROPERTIES • Two chemically cured (Coe- Pakand PerioCare) and 1 photocured dressing (Barricaid) were examined by von Fraunhofer and Argyropoulos. • All materials absorbed water, both Coe-Pak and PerioCare acted in a similar manner at 23˚C, but PerioCare absorbed far more water at 37˚C. • For Barricaid, it was shown that increased light exposure had little effect on its water sorption or solubility.
  • 59. • The adhesion of different dressings was also tested. • Adhesion of Coe-Pak to a single tooth at 1 hour was about 7 kg, but this decreased to about 6.5 kg at 24 hours and to 5 kg at 7 days. • The adhesion of PerioCare was 2 kg at 1 hour and 8.5 kg at 24 hours, but it decreased to 7.5 kg at 7 days. • The adhesion of Barricaid was about 5 kg at 1 hour, which decreased to 3.5 kg at 24 hours and 1.5 kg at 7 days. • The mechanis of adhesion of Barricaid appeared to involve mechanical locking, which differs from that of Coe-Pak and PerioCare Von Fraunhofer JA, Argyropoulos DC. Properties of periodontal dressings. Dent Mater. 1990; 6(1): 51-55.
  • 60. • Eugenol-free dressings were developed to offset the irritant and toxic properties of liquid eugenol. • Numerous reports have outlined the adverse tissue effects and intensity of inflammatory reaction with the use of a eugenol based dressing. (Sarrami N 2002) • At the same time, in vitro studies have revealed that eugenol- based dressings may cause less growth inhibition of permanent cells and primary human leukocytes than some noneugenol products. (Wyan VJ 1977) BIOLOGICAL PROPERTIES- EFFECTS ON WOUND HEALING 60
  • 61. • It has been established that dressings such as WondrPak produce greater tissue destruction, with more inflammatory cell infiltration and connective tissue response, involving a much wider reaction area in the adjacent tissues. (Wyan VJ 1977) • Comparative evaluation of different noneugenol dressings has shown conflicting results. Coe-Pak, in a few studies, showed a severe tissue reaction as compared with Peripac and PerioPutty, (Nezwek RA 1980) which elicited the least inflammatory response, whereas in others, Coe-Pak was also seen to cause least damage. (Wennberg A 1983)
  • 62. • Light-cured periodontal dressings were not cytotoxic in cell cultures and different cell types. • With the development of collagen-based dressings, products such as CollaCote had better clinical and histological effects on palatal wound healing than Coe-Pak. (Shanmugam M 2010) • The literature thus seems to suggest that in comparison, non- eugenol dressings are more biocompatible than their eugenol counterparts. • Furthermore, dressings falling in other categories including light cure dressing, Barricaid and collagen-based dressing CollaCote are better than the conventional noneugenol based dressings.
  • 63.
  • 64. • One of the purposes of periodontal dressings is to aid in reducing postoperative discomfort. • In earlier reports, measuring the degree of pain experienced by the patient was done based on the consumption of analgesic tablets. • Such studies reported that the experience of pain was significantly more frequent after the use of Peripac than Coe-Pak and Wondrpak, based on higher tablet consumption in the Peripac group. • Also, when sensitivity was observed, it was seen that the highest proportion of sensitive teeth was found after the use of Coe-Pak, and the lowest with Peripac POSTOPERATIV E PAIN AND DRESSING 64
  • 65. • Pain measurements using visual analogue scale (VAS) studies have reported that pain scores with Coe-Pak were higher than with Wondrpak after a gingivectomy procedure. (Jorkjend L 1990) • The same authors, in another study, compared pain experience after gingivectomy when using a local anesthetic agent. • They reported that pain was masked when using a eugenol-based periodontal dressing, thus proving that eugenol dressings cause less pain than non-eugenol ones. (Jorkjend L 1991)
  • 66. PERIODONTALDRESSINGSFORALL? • The fact that complete healing can take place even without a dressing, provided the surgical area is kept clean, and that there is no difference in healing between dressed and non-dressed wounds, lends support to the theory that not all surgical areas need to be “packed” . (Loe H 1961) • Other factors such as the presence of inflammation seemed to influence the rate of wound healing to a larger extent than the use of a dressing. (Stahl SS1969)
  • 67.
  • 68.
  • 69. • A number of clinical trials have proposed that the use of a dressing accumulates plaque-causing inflammation, irritates the healing tissues, produces transient bacteremia during postoperative dressing change and causes more pain and swelling but less sensitivity and difficulty in eating. (Henry TG 1976, Newman PS1982) • Despite these drawbacks, it appears that healing is slightly more rapid in the dressed segments.
  • 70. • The use of periodontal dressings from the patients’ preference and comfort point of view has also been elaborated. • Conflicting reports exist in the literature, as these factors are based on patient responses and thus are not objectively evaluated, because of the subjective criteria usually employed. • The use of chlorhexidine mouth rinse instead of a dressing has been found to reduce postoperative plaque accumulation and surgical inflammation and is considered to be roughly equivalent to professional plaque control in postsurgical healing, thus providing a viable alternative regime for plaque control. (Westfelt E1983) • Moreover, many patients experience discomfort when a periodontal dressing was used and preferred to use a mouth rinse. • Conversely, some patients exhibit a psychological feeling of protection and well- being when a periodontal dressing was put in place.
  • 71. • The answer to this controversy, though still open to debate, is probably that the choice of use of a periodontal dressing is a matter of individual preference and the judgment of the operator. • It is, however, the use of a dressing for stabilization of free gingival grafts and protection of donor site, retention of an apically positioned flap, protection of the denuded bone from further injury, protection of the graft site in periodontal regeneration and to facilitate retention of drugs delivered locally in the subgingival sites.
  • 73. REFERENCES • Carranza’s clinical periodontology 11th edition. • Clinical periodontology and implant dentistry. Jan Lindhe 5th edition. • Text book of Clinical practice of the dental hygienist . Wilkins 10th edition • Rahul Kathariya, Hansa Jain, Tanya Jadhav. To pack or not to pack: the current status of periodontal dressings. JAppl Biomater Funct Mater 2015. • Zahra Baghani, Mahdi Kadkhodazadeh. Periodontal Dressing: A Review Article. JDent Res Dent Clin Dent Prospect 2013. • K. David,Shetty Neetha J.& Pralhad Swati. Periodontal Dressings: An Informed View. Journal of pharmaceutical and biomedical sciences (JPharm Biomed Sci.) 2013. • Muthukumarasamy, Nazargi Mahabob. PERIODONTAL DRESSING. JIDENT 2012. • Triveni Kale, Nitin Dani, Tejas Patange . Periodontal Dressing. IOSR Journal of Dental and Medical Sciences 2014.

Editor's Notes

  1. Similarly, a surgical dressing is also utilized after periodontal surgical procedures. These dressings are applied around the necks of the teeth and adjacent tissue to cover and protect the surgical wound after periodontal surgery (3).
  2. A. W. Ward in 1923 invented the Wondrpak, using the word pack in this context for the first time.
  3. It was a 2-component system comprising a powder with zinc oxide…
  4. A modified form of a eugenol dressing was introduced by Kirkland, called the Kirkland formula. It consisted of zinc oxide, resin, zinc acetate, eugenol, tannic acid and olive oil.
  5. Zinc oxide and eugenol dressings are supplied as a liquid and powder or paste. These are mixed together on a waxed paper pad using a wooden tongue depressor or spatula. The powder or paste is gradually incorporated into the liquid until it reaches a dough-like consistency. The dressing may be used immediately or wrapped in aluminum foil and refrigerated for use for up to 1 week (9).
  6. Eugenol-based dressings were formerly popular, especially following gingivectomy (11), due to their property of obtunding pain and rendering sites less sensitive. Waerhaug and Löe in 1957
  7. Commercially available non-eugenol dressings include
  8. The Coe-Pak is prepared by mixing equal lengths of paste from tubes that contain the accelerator and the base until the resulting paste is a uniform color (Figure 55-1, A to C). A capsule of tetracycline powder can be added at this time. The pack is then placed in a cup of water at room temperature3 minutes, the paste loses its tackiness, and it can be handled and molded; The pack is then rolled into two strips that are approximately the length of the treated area. The end of one strip is bent into a hook shape and fitted around the distal surface of the last tooth to approach that tooth from the distal surfaceThe remainder of the strip is brought forward along the facial surface to the midline and gently pressed into place along the gingival margin and interproximally.
  9. The third group of periodontal dressings consists of
  10. The photocured dressing was dispensed at the juncture of the cervical one-third of the teeth and the margin of the surgical site on the facial aspect. It was exposed to a visible light-curing unit for 10 seconds per site per tooth until the entire dressing was cured. Same procedure was repeated for the lingual side. Occlusal clearance over the dressing coverage was checked prior to dismissing the patient.. It may be concluded than visible light-cured periodontal dressing Barricaid is easily applied, offers a perfect color match with no unpleasant taste or smell; hence, the patient is not hesitant to carry out his routine activities. It is biocompatible, offers good retentivity, and only a thin layer is required to be applied.
  11. , Many attempts have been made to enhance the properties of dressings as described in the following section.
  12. , Many attempts have been made to enhance the properties of dressings as described in the following section.
  13. When split flaps have been performed, the area should be covered with tinfoil to protect the sutures before the pack is placed
  14. Having discussed at length the biologic and therapeutic benefits of a periodontal dressing, the question of whether we need to use a dressing for all surgical procedures remains open.
  15. There appears to be no consensus regarding the absolute indication for the use of periodontal dressings after a surgical procedure. However, the literature does elaborate on the benefits of application of a dressing post-surgically. Moreover, no periodontal dressing material has been shown to exhibit all of the ideal properties – both physical and biologic. Further research to improve biomaterial properties may lead to a more universal applicability. As for now, periodontal dressings for all? – maybe, not yet!