pulp capping

About this set

Created by:

pedohong  on February 22, 2012

Log in to favorite or report as inappropriate.
Pop out
No Messages

You must log in to discuss this set.

pulp capping

reason to control pulpal bleeding
1) increased bleeding--> indication of inflammation
2) difficult to obtain and adequate seal b/c of mositre & contamination of dentin from bleeding
1/33
Preview our new flashcards mode!

Study:

Cards

Speller

Learn

Test

Scatter

Games:

Scatter

Space Race

Tools:

Export

Copy

Combine

Embed

Order by

Terms

Definitions

reason to control pulpal bleeding 1) increased bleeding--> indication of inflammation
2) difficult to obtain and adequate seal b/c of mositre & contamination of dentin from bleeding
direct pulp cap medicament is placed directly over exposed pulp
Indirect pulp cap cavity liner/sealer is placed over residual caries to maintain pulp vitality
some restorative matierals if placed directly on the pulp can cause cytotoxicity & immunosupression
if they are LC, can raise pulp temp
Mechanical exposure better outcome than bacterial exposure
asymptomatic teeth of pulp capping fare better than w/ pathology (Rad, inflammation)
ability to control bleeding before placing cap influences outcome 1. more bleeding= worse exposure/infection
2. bleeding leads to moist dentin which id difficult to obtain a seal
agent to help control bleeding saline: easiest on tissue
NaHClO2: some inflammation, but anti-bacterial & hemorrhage contorl
Chlorohexidine: antibcaterial but not effective for hemorrahge
ferric sulfate : increased post op pain
ferric sulfate increase post op pain
Chlorohexidine ntibcaterial but not effective for hemorrahge
Direct pulp capping materials ZOE (zinc oxide eugenol)
adhesive system
GI/RMGI
CaOH
MTA (mineral trixoxide aggregate)
ZOE eugenol is cytotoxic
release eugenol in coc that are cytotoxic
effeciveness of ZOE to exclude bactiera is reduced in the mouth over time
high interfacial leakagye
chronic inflammation, no pulp healing, no dentin bridge formation after 12wks, while control CaOH healed in 4wks
RMGI cytotoxic but less than ZOE
chronic inflammation
Good biocompatibility if not directly on pulp (close approximation)
Good seal formation (precludes cavities and toxins from pulp)
Human study: chronic inflammation, no dentin bridge formation after 300 days, CaOH better healing
Adhesive system cytotoxic to pulp cells (esp unpolymerized components)
Animal study: mechanical exposure had healing similar to CaOH, bacterial had poor healing
Etch/prime are vasodilators (more bleeding, less polymerization, less seal, more cytotoxic polymer)
CaOHgold standard of direct pulp capping
excellent antibacterial propertieis
highly soluble
Advantages: antibacterial, high pH stimulates healing, long term clinical success record
Solubilize BMP (bone morphogenic protein) & TGF-B1 (transforming growth factor beta 1) from dentin, which stimulate pulp repair
Disadvantages: highly soluble, dissolution over time, no adhesive qualities, poor seal, tunnel defects in reparative dentin
MTA Mineral trioxide aggregate
Mostly CaO, which reacts w/ H2O to form CaOH
advantage of MTA similar to CaOH; antibacterial, biocompatible, high pH, radiopacity, aids release of bioactive dentin matrix proteins
Differences of MTA white & gray (Fe added) colors, able to provide some seal to tooth structure
Disadvantages of MTA high solubility, Fe can darken tooth, prolonged setting (~3hrs; pulp capping needs 2 procedures w/ a temporary or GI/RMGI sealer), 24xs as expensive as CaOH
the reason MTA is more successful than Ca OH serve as a reservoir for Ca OH : antibacteria
provide seal at the site of pulp exposure
however, GI or RMGI will be needed as a liner over either pulp cap material (MTA or CaOH)
MTA vs CaOH (similarity) antibacterial and biocompatiblity
high pH
radiopacity
can release bioactive dentin matrix proteins
MTA vs CaOH (difference) MTA can provide some seal to tooth structure
disadvantage of MTA prolonged setting time
less cost effective
MTA over exuberance? MTA > Ca OH for pulp capping mechanically exposed human teeth
Does CaOH provide any benefits over MTA CaOH shows long term clinical success
Tunnel defect patency from the site of pulp exposure through the reparative dentin to the pulp
sometimes having fibroblasts & capillaries present in the defect
Avoid exposing pulp survavial chances are good if tooth is asymptomatic & well sealed
How to control hemorrage H2O, saline, sodium hypochlorite
H2O and saline for hemorrage benign to pulp
Sodium hypochlorite for hemorrage best at controlling hemorrhage & disinfecting
ZOE, GI/RMGI poor direct pulp capping against
avoid
MTA comparable to CaOH in short term data
CaOH gold standard
longest record
cost-effective
probably the effective component in MTA
The best way for pulp capping provide well sealed restoration after pulp capping
to portect from leakage & bacterial contamination

First Time Here?

Welcome to Quizlet, a fun, free place to study. Try these flashcards, find others to study, or make your own.

Set Champions

There are no high scores or champions for this set yet. You can sign up or log in to be the first!