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Histologic study of a human immature permanent premolar with chronic apical abscess after revascularization/revitalization

Becerra, Patricia; Ricucci, Domenico; Loghin, Simona; Gibbs, Jennifer L; Lin, Louis M
INTRODUCTION: Histologic studies of teeth from animal models of revascularization/revitalization are available; however, specimens from human studies are lacking. The nature of tissues formed in the canal of human revascularized/revitalized teeth was not well established. METHODS: An immature mandibular premolar with infected necrotic pulp and a chronic apical abscess was treated with revascularization/revitalization procedures. At both the 18-month and 2-year follow-up visits, radiographic examination showed complete resolution of the periapical lesion, narrowing of the root apex without root lengthening, and minimal thickening of the canal walls. The revascularized/revitalized tooth was removed because of orthodontic treatment and processed for histologic examination. RESULTS: The large canal space of revascularized/revitalized tooth was not empty and filled with fibrous connective tissue. The apical closure was caused by cementum deposition without dentin. Some cementum-like tissue was formed on the canal dentin walls. Inflammatory cells were observed in the coronal and middle third of revascularized/revitalized tissue. CONCLUSIONS: In the present case, the tissue formed in the canal of a human revascularized/revitalized tooth was soft connective tissue similar to that in the periodontal ligament and cementum-like or bone-like hard tissue, which is comparable with the histology observed in the canals of teeth from animal models of revascularization/revitalization.
PMID: 24332005
ISSN: 0099-2399
CID: 689302

Predictive factors in opioid administration for acute odontalgia; a pilot study [Meeting Abstract]

Levine, M H; Burlingame, S; Gibbs, J; Raphael, K
Purpose: The use of non-steroidal anti-inflammatory drugs (NSAIDs) after third molar surgery has been shown to be superior to the use of combination opioid narcotics (1). However, most oral surgeons frequently prescribe these narcotics to their patients. Unlike NSAIDs, opioids have significant addiction potential and prescription drug abuse has reached epidemic proportions (2). Prescribing patterns are often based on providers' preferences without clear scientific evidence as to which modality of postoperative pain management is best. A better understanding of the prescribing patterns after third molar surgery may help focus provider behavior and alter the management of acute odontalgia. Hypothesis: Patient, provider, and surgical factors are related to the prescribing of opioids analgesics by oral surgeons. Materials and Methods: Using a historical cohort study design, 300 charts were reviewed from patients who underwent mandibular third molar extractions in the New York University College of Dentistry's Oral and Maxillofacial Surgery Clinic in 2011. Ultimately, 260 charts were included in the study. The presence or absence of specific patient predictor risk factors and outcomes were identified and recorded. Patient predictors included: age, gender, ethnicity, and American Dental Association (ADA) procedure code. ADA code is related to the difficulty of extraction. Outcomes included: positive or negative combination opioid narcotic prescription, type of opioid prescribed, dosage of opioid prescribed, number of subsequent visits to the clinic for postoperative pain, number of additional combination opioid prescriptions given, type of additional opioid prescribed, and dosage of additional opioid prescribed. Provider experience was also recorded. 20 charts were reviewed by two independent examiners to calculate inter- examiner reliability. Results: Overall, 78.8% of the sample was prescribed a combination opioid narcotic. Risk ratios were calculated for the relationship between individual risk fa!
EMBASE:71166055
ISSN: 0278-2391
CID: 549492

Clinical, radiographic, and histological observation of a human immature permanent tooth with chronic apical abscess after revitalization treatment

Shimizu, Emi; Ricucci, Domenico; Albert, Jeffrey; Alobaid, Adel S; Gibbs, Jennifer L; Huang, George T-J; Lin, Louis M
INTRODUCTION: Revitalization procedures have been widely used for the treatment of immature permanent teeth with apical periodontitis. The treatment procedures appear to be capable of encouraging continued root development and thickening of the canal walls. The nature of tissues formed in the canal space and at the root apex after revitalization has been shown histologically in several animal studies; similar studies in humans were recently reported. METHODS: A 9-year-old boy had a traumatic injury to his upper anterior teeth. Tooth #9 suffered a complicated crown fracture with a pulp exposure, which was restored with a composite resin. The tooth developed a chronic apical abscess. Revitalization procedures were performed on tooth #9 because it was an immature permanent tooth with an open apex and thin canal walls. Twenty-six months after revitalization, the tooth had a horizontal crown fracture at the cervical level and could not be restored. The tooth was extracted and processed for routine histological and immunohistochemical examination to identify the nature of tissues formed in the canal space. RESULTS: Clinically and radiographically, the revitalization of the present case was successful because of the absence of signs and symptoms and the resolution of periapical lesion as well as thickening of the canal walls and continued root development. The tissue formed in the canal was well-mineralized cementum- or bone-like tissue identified by routine histology and immunohistochemistry. No pulp-like tissue characterized by the presence of polarized odontoblast-like cells aligning dentin-like hard tissue was observed. CONCLUSIONS: The tissues formed in the canal of revitalized human tooth are similar to cementum- or bone-like tissue and fibrous connective tissue.
PMID: 23880282
ISSN: 0099-2399
CID: 458762

Paradoxical surrogate markers of dental injury-induced pain in the mouse

Gibbs, Jennifer L; Urban, Rochelle; Basbaum, Allan I
Dental pain, including toothache, is one of the most prevalent types of orofacial pain, causing severe, persistent pain that has a significant negative effect on quality of life, including eating disturbances, mood changes, and sleep disruption. As the primary cause of toothache pain is injury to the uniquely innervated dental pulp, rodent models of this injury provide the opportunity to study neurobiological mechanisms of tissue injury-induced persistent pain. Here we evaluated behavioral changes in mice with a dental pulp injury (DPI) produced by mechanically exposing the pulp to the oral environment. We monitored the daily life behaviors of mice with DPI, including measures of eating, drinking, and movement. During the first 48hours, the only parameter affected by DPI was locomotion, which was reduced. There was also a significant short-term decrease in the amount of weight gained by DPI animals that was not related to food consumption. As cold allodynia is frequently observed in individuals experiencing toothache pain, we tested whether mice with DPI demonstrate an aversion to drinking cold liquids using a cold-sucrose consumption test. Surprisingly, mice with DPI increased their consumption of sucrose solution, to over 150% of baseline, regardless of temperature. Both the weight loss and increased sucrose intake in the first 2days of injury were reversed by administration of indomethacin. These findings indicate that enhanced sucrose consumption may be a reliable measure of orofacial pain in rodents, and suggest that alterations in energy expenditure and motivational behaviors are under-recognized outcomes of tooth injury.
PMCID:3743260
PMID: 23719574
ISSN: 0304-3959
CID: 361562

Histological findings of revascularized/revitalized immature permanent molar with apical periodontitis using platelet-rich plasma [Case Report]

Martin, Gabriela; Ricucci, Domenico; Gibbs, Jennifer L; Lin, Louis M
INTRODUCTION: An immature mandibular right first molar (#30) with apical periodontitis of a 9-year-old boy was treated with a revascularization/revitalization procedure using either a mixture of platelet-rich plasma (PRP) and a blood clot or a blood clot alone on the same tooth. METHODS: Tooth #30 fractured 2 years and 1 month after the revascularization/revitalization procedure and could not be saved. The tooth was extracted and processed for histologic examination to determine the nature of the tissues that formed in the canals. RESULTS: Clinically, the endodontic treatment of the case was successful based on the resolution of apical periodontitis and the absence of clinical signs and symptoms. Histologically, the tissues formed in the distal and mesial canals were mineralized tissue similar to cementoid/osteoid tissue and uninflamed fibrous connective tissue regardless of PRP or no PRP treatment. No pulp-like tissue characterized by the presence of odontoblast-like cells polarized along the dentin-like mineralized tissue was observed. CONCLUSIONS: The tissues formed in the canals were mineralized tissue and some fibrous connective tissue. No pulp-like tissue characterized by the presence of odontoblast-like cells was observed lining the dentin-like mineralized tissue.
PMID: 23228274
ISSN: 0099-2399
CID: 1070602

Acute and chronic orofacial and dental pain

Chapter by: Hargreaves, Kenneth; Gibbs, Jennifer
in: Wall and Melzack's textbook of pain by McMahon, S (Ed)
Philadelphia, PA : Elsevier/Saunders, 2013
pp. 803-814
ISBN: 0702053740
CID: 3899152

Public health surveillance of dental pain via Twitter

Heaivilin, N; Gerbert, B; Page, J E; Gibbs, J L
On Twitter, people answer the question, "What are you doing right now?" in no more than 140 characters. We investigated the content of Twitter posts meeting search criteria relating to dental pain. A set of 1000 tweets was randomly selected from 4859 tweets over 7 non-consecutive days. The content was coded using pre-established, non-mutually-exclusive categories, including the experience of dental pain, actions taken or contemplated in response to a toothache, impact on daily life, and advice sought from the Twitter community. After excluding ambiguous tweets, spam, and repeat users, we analyzed 772 tweets and calculated frequencies. Of the sample of 772 tweets, 83% (n = 640) were primarily categorized as a general statement of dental pain, 22% (n = 170) as an action taken or contemplated, and 15% (n = 112) as describing an impact on daily activities. Among the actions taken or contemplated, 44% (n = 74) reported seeing a dentist, 43% (n = 73) took an analgesic or antibiotic medication, and 14% (n = 24) actively sought advice from the Twitter community. Twitter users extensively share health information relating to dental pain, including actions taken to relieve pain and the impact of pain. This new medium may provide an opportunity for dental professionals to disseminate health information.
PMCID:3169887
PMID: 21768306
ISSN: 0022-0345
CID: 1070612

Nerve growth factor links oral cancer progression, pain, and cachexia

Ye, Yi; Dang, Dongmin; Zhang, Jianan; Viet, Chi T; Lam, David K; Dolan, John C; Gibbs, Jennifer L; Schmidt, Brian L
Cancers often cause excruciating pain and rapid weight loss, severely reducing quality of life in cancer patients. Cancer-induced pain and cachexia are often studied and treated independently, although both symptoms are strongly linked with chronic inflammation and sustained production of proinflammatory cytokines. Because nerve growth factor (NGF) plays a cardinal role in inflammation and pain, and because it interacts with multiple proinflammatory cytokines, we hypothesized that NGF acts as a key endogenous molecule involved in the orchestration of cancer-related inflammation. NGF might be a molecule common to the mechanisms responsible for clinically distinctive cancer symptoms such as pain and cachexia as well as cancer progression. Here we reported that NGF was highly elevated in human oral squamous cell carcinoma tumors and cell cultures. Using two validated mouse cancer models, we further showed that NGF blockade decreased tumor proliferation, nociception, and weight loss by orchestrating proinflammatory cytokines and leptin production. NGF blockade also decreased expression levels of nociceptive receptors TRPV1, TRPA1, and PAR-2. Together, these results identified NGF as a common link among proliferation, pain, and cachexia in oral cancer. Anti-NGF could be an important mechanism-based therapy for oral cancer and its related symptoms
PMCID:3375020
PMID: 21750223
ISSN: 1538-8514
CID: 155492

Differential TRPV1 and TRPV2 channel expression in dental pulp

Gibbs, J L; Melnyk, J L; Basbaum, A I
Hypersensitivity to thermal and mechanical stimuli can occur in painful pulpitis. To explore the neuro-anatomical basis of heat and mechanical sensitivity, we evaluated expression of TRPV1 (heat) and TRPV2 (heat/mechanical) channels in the cell bodies and terminal arborizations of neurons that innervate the dental pulp (DP) and periodontal tissues (PDL). We report that ~50% of trigeminal ganglion (TG) neurons retrogradely labeled from the DP express TRPV2, and this was significantly greater than the general expression of this channel in the TG (15%) and slightly more than what is expressed in the PDL by retrograde labeling (40%). The TRPV1 receptor, however, was less prevalent in neurons innervating the DP than their general expression in the TG (17% vs. 26%) and was more extensively expressed in neurons innervating the PDL (26%). Co-labeling studies showed that 70% of neurons that innervate the DP are myelinated. Approximately 1/3 of the retrogradely labeled neurons from the DP were calcitonin-gene-related-peptide-positive (peptide-expressing), but very few expressed the IB4 marker of non-peptidergic unmyelinated afferents. These findings suggest that the DP has a unique neurochemical innervation with regard to TRP receptor expression, which has significant implications for the mechanisms contributing to odontogenic pain and management strategies.
PMCID:3144115
PMID: 21406609
ISSN: 0022-0345
CID: 1070622

Commentary: a burning question of subgroup analysis in pain trials [Comment]

Gibbs, Jennifer
PMID: 20149536
ISSN: 0304-3959
CID: 160768