Endodontology
Postoperative pain after root-end resection and filling

https://doi.org/10.1016/j.tripleo.2005.01.010Get rights and content

Objective

To evaluate the pain experience following root-end resection and filling with Mineral Trioxide Aggregate or Intermediate Restorative Material.

Study design

Referred adult patients recruited using strict entry criteria were randomly allocated to receive either material. A standardized surgical technique was employed. Postoperative instructions and a pain questionnaire were given to each patient to record the severity of their pain at 3 time intervals—3-5 hours, 24 hours, and 48 hours after surgery—on a standard visual analog scale (VAS). Patients were also asked to record consumption of any self-prescribed analgesics, the type, and dosage.

Results

At 3-5 hours after surgery, regardless of the material used, 90% of all patients experienced some level of postoperative pain. Twenty-four hours after surgery 82% of patients experienced pain, as did 72% after 48 hours. Thirty-seven percent of patients did not take any analgesics at all. In order of popularity, the analgesics taken were ibuprofen, acetaminophen, and acetaminophen plus codeine phosphate. The VAS measurements were reduced over time in both treatment groups (P < .001). There was no statistically significant difference in the proportion of subjects taking analgesics in each treatment group. Patients who used analgesics showed higher median VAS measurements at all time periods (P < .05).

Conclusions

There was no significant difference in the pain experienced by both treatment groups. The postoperative pain was of a relatively short duration, at its maximum intensity early in the postoperative period but progressively decreased with time. Even if pain relief medication was needed, nonprescription analgesics were adequate and effective.

Section snippets

Material and methods

An account of the methods has been described previously11 but is repeated here. Adult patients who were referred for root-end resection and filling were invited to participate. Approval was obtained from the local ethical committee. Each patient was given written advice about the study and the follow-up care necessary; they were also given the opportunity to withdraw. A consent form was signed if they agreed to participate in the study. There was no financial inducement to participate. The

Results

A full breakdown on the flow of patients through this study is shown in Table I. The number of surgical procedures performed was 198. A total of 100 pain questionnaires (54 in IRM group, 46 in MTA group) were deemed correctly completed. Others were not returned or were excluded if the writing was illegible or the information entered was incomplete. No patient returned or telephoned because of severe pain. Because there was no difference in the male-to-female ratio and their related VAS

Discussion

The VAS, as used in this study, is a standard pain measurement technique based on the theory that pain intensity is continuous, without jumps or intervals. Other pain measurement techniques such as verbal rating or numerical descriptive scales may not adequately reflect the changes produced within this variable. Within the boundaries of the VAS line respondents can mark the extent of their pain providing a quantitative measurement. Thus respondents are presented with a rating system with

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    Nevertheless, this factor may also have contributed to the lower degree of postoperative pain and swelling reported in this study. The present study supports previous findings (7, 9–13) that, on average, maximum pain is experienced on the night of the surgery and maximum swelling is experienced on day 1 of the surgery and pain and swelling improve over time after the surgical procedure. Our results also show that patients are more likely to experience swelling than pain.

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This work received funding from DHSC–London, Research & Development, Responsive Funding Programme.

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