Elsevier

Journal of Endodontics

Volume 40, Issue 12, December 2014, Pages 1958-1960
Journal of Endodontics

Clinical Research
Does Acetaminophen/Hydrocodone Affect Cold Pulpal Testing in Patients with Symptomatic Irreversible Pulpitis? A Prospective, Randomized, Double-blind, Placebo-controlled Study

https://doi.org/10.1016/j.joen.2014.09.008Get rights and content

Abstract

Introduction

The purpose of this prospective randomized, double-blind, placebo-controlled study was to determine the effects of a combination dose of 1000 mg acetaminophen/10 mg hydrocodone on cold pulpal testing in patients experiencing symptomatic irreversible pulpitis.

Methods

One hundred emergency patients in moderate to severe pain diagnosed with symptomatic irreversible pulpitis of a mandibular posterior tooth randomly received, in a double-blind manner, identical capsules of either a combination of 1000 mg acetaminophen/10 hydrocodone or placebo. Cold testing with Endo-Ice (1,1,1,2 tetrafluoroethane; Hygenic Corp, Akron, OH) was performed at baseline and every 10 minutes for 60 minutes. Pain to cold testing was recorded by the patient using a Heft-Parker visual analog scale. Patients' reaction to the cold application was also rated.

Results

Cold testing at baseline and at 10 minutes resulted in severe pain for both the acetaminophen/hydrocodone and placebo groups. Although pain ratings decreased from 20–60 minutes, the ratings still resulted in moderate pain. Patient reaction to cold testing showed that 56%–62% had a severe reaction. Although the reactions decreased in severity over the 60 minutes, 20%–34% still had severe reactions at 60 minutes. Regarding pain and patients' reactions to cold testing, there were no significant differences between the combination acetaminophen/hydrocodone and placebo groups at any time period.

Conclusions

A combination dose of 1000 mg of acetaminophen/10 mg of hydrocodone did not statistically affect cold pulpal testing in patients presenting with symptomatic irreversible pulpitis. Patients experienced moderate to severe pain and reactions to cold testing.

Section snippets

Materials and Methods

One hundred adult patients participated in this study. All were emergency patients of the College of Dentistry, The Ohio State University, Columbus, OH, and were in good health as determined by a health history and oral questioning. Exclusion criteria were as follows: subjects who were younger than 18 years, had a history of significant medical problem, had taken central nervous system depressants or any analgesic medication within the last 6 hours, were pregnant or lactating, or were unable to

Results

For the acetaminophen/hydrocodone group, 31 women and 19 men ranging in age from 20–67 with a mean age of 35 ± 12 years participated in this study. For the placebo, 23 women and 27 men ranging in age from 18–61 with a mean age of 36 ± 13 years participated. There was no significant difference between the 2 groups regarding sex (P = .1085) or age (P = .7750).

The initial preoperative pain, mean Corah Dental Anxiety Scale ratings, and tooth type are presented in Table 1. There were no significant

Discussion

There were no statistically significant differences for the effect of age, initial pain, Corah Dental Anxiety Scale ratings, sex, or tooth type so these variables would be minimized between the 2 groups. Cold testing with Endo-Ice at baseline (minute 0) and at 10 minutes resulted in severe pain for both groups (Table 2). Although the pain ratings decreased from 20 minutes to 60 minutes, the ratings still resulted in moderate pain. It is likely that patients adapted to the cold testing procedure

Acknowledgments

Sara Fowler compiled the data, analyzed the results, and helped write the manuscript. Spencer Fullmer completed a portion of this study for a Master of Science degree. Melissa Drum and Al Reader contributed to the study design, institutional review board submission, statistical analysis, and served on the Masters Examination Committee.

The authors thank Dr Mike Beck for the statistical analysis of the data.

The authors deny any conflicts of interest related to this study.

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    Patients were excluded if they had a systemic disease including other types of diabetes, uncontrolled diabetes, prediabetes, or any diseases that could affect the results (eg, hypertension [patients were considered to be hypertensive if their blood pressure was ≥140 mm Hg systolic or 90 mm Hg diastolic]7, hyperparathyroidism, hyperthyroidism, chronic renal disease, or hepatic disease). In addition, patients were excluded if they had diseases that could cause injury to the head and neck nervous system (stroke, multiple sclerosis, and so on)3,4,6,7,11,21 as well as other conditions that might affect the results such as cancer; pregnancy; or taking corticosteroids, ibuprofen, opium, or other medications such as gabapentin or phenytoin22. Further reasons for exclusion were trauma history, severe periodontal disease, orthodontic brackets or recent history of orthodontic treatment, extensive caries or restorations, apical periodontitis, teeth that had root canal treatment, and teeth with crowns5,14,23,24.

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