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1.
Artigo em Inglês | MEDLINE | ID: mdl-36266177

RESUMO

OBJECTIVES: To determine the types of products used to treat dry mouth and their perceived effectiveness, the relationship between salivary function and xerostomia symptoms, and whether salivary function predicts response to management strategies. STUDY DESIGN: Cross-sectional study of 87 patients with dry mouth and documented unstimulated whole salivary (UWS) and stimulated whole salivary (SWS) flow rates. Participants completed a questionnaire assessing dry mouth complaints and symptoms and effectiveness of specific dry mouth products. RESULTS: Mean (SD) age was 61.7 (12.9) years including 78 (90%) females. 47 (54%) participants had Sjögren's disease. Oral dryness symptoms (0-10 scale) rated highest with a mean (SD) of 7.2 (2.17); other symptoms scored from 3.4 to 5.1. Lower levels of UWS and SWS were associated with worse dry mouth and difficulty speaking, while lower levels of SWS flow alone were associated with greater difficulty swallowing and a decline in taste. More than half of the participants (55%, n = 48) reported using ≥4 dry mouth products. Participants with normal SWS flow had significantly better responses to lozenges and prescription products. CONCLUSIONS: Patients with dry mouth and normal stimulated flow rates (i.e., residual salivary capacity) respond better to stimulatory products (parasympathomimetic and lozenges). Salivary flow rate assessments may help with recommendations of dry mouth products.


Assuntos
Síndrome de Sjogren , Xerostomia , Feminino , Humanos , Pessoa de Meia-Idade , Masculino , Satisfação do Paciente , Estudos Transversais , Síndrome de Sjogren/complicações , Inquéritos e Questionários , Saliva
2.
Oral Dis ; 18(7): 661-6, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22458329

RESUMO

OBJECTIVES: The aims of this study were to determine the frequency of bleeding complications following dental procedures in patients with known or suspected chronic liver disease and whether international normalized ratio (INR) determination could aid in predicting bleeding complications in these patients. PATIENTS AND METHOD: We identified 90 patients (mean age: 51 ± 9 years) in this retrospective chart review. Sixty-nine patients had a known history of chronic liver disease and 21 had suspected chronic liver disease. Descriptive statistics were determined. Independent sample t-test and one-way variance test were utilized for continuous variables and chi-square test for dichotomous variables. RESULTS: The mean INR value for all patients was 1.2 ± 0.3. The INR value was significantly associated with the diagnosis of liver cirrhosis, the diagnoses of Hepatitis B and C together, the presence of ascites alone, and the number of clinical signs and symptoms (i.e. ascites, jaundice and encephalopathy) present. Nine patients with INR values between 1.5 and 2 underwent invasive dental procedures without postoperative bleeding complications. CONCLUSION: There were no episodes of postoperative bleeding in patients. The findings suggest that clinicians should not rely solely on an INR value to predict post-procedure bleeding in patients with liver disease.


Assuntos
Assistência Odontológica para Doentes Crônicos , Profilaxia Dentária/efeitos adversos , Hepatite/complicações , Cirrose Hepática/complicações , Hemorragia Bucal/etiologia , Hemorragia Pós-Operatória/etiologia , Extração Dentária/efeitos adversos , Adulto , Idoso , Análise de Variância , Distribuição de Qui-Quadrado , Feminino , Hepatite B Crônica/complicações , Hepatite C Crônica/complicações , Humanos , Coeficiente Internacional Normatizado , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Estudos Retrospectivos
3.
Br Dent J ; 211(12): E24, 2011 Dec 16.
Artigo em Inglês | MEDLINE | ID: mdl-22193507

RESUMO

OBJECTIVE: The aim of this audit was to investigate complex chronic facial pain patients' satisfaction after an initial, comprehensive, 45-60 minute consultation visit. DESIGN: Prospective audit using a post-visit satisfaction survey. SETTING: Specialised outpatient facial pain unit. METHODS: A convenience sample of 50 consecutive new patients were recruited. History, pain and psychosocial functioning were assessed through standard, validated pre-visit questionnaires. A post-visit satisfaction questionnaire was sent (twice if necessary) to patients by mail, and non-responders were contacted by telephone. MAIN OUTCOME MEASURES: Patients' satisfaction scores on pain management processes were evaluated. RESULTS: Response rate for the questionnaire was 63% (32/50) and 12 additional patients who did not respond to the questionnaire replied by telephone. Among questionnaire respondents, mean overall patient satisfaction was 8.1 ± 2.2 on an 11-point scale (best score 10), with no differences based on age, gender, diagnosis, length of symptoms and treatment. There was a trend of higher overall satisfaction among patients referred by dentists and specialists. Patients who had seen at least one specialist before their visit reported higher scores in understanding the reasons for their condition and what to do to treat their condition. CONCLUSIONS: A consultation with adequate time for history taking, addressing patients' goals and thorough explanation accompanied by written information, results in high satisfaction among patients with chronic facial pain.


Assuntos
Dor Crônica/terapia , Auditoria Odontológica , Dor Facial/terapia , Unidades Hospitalares , Clínicas de Dor , Satisfação do Paciente , Adulto , Assistência Ambulatorial , Ansiedade/classificação , Dor Crônica/diagnóstico , Dor Crônica/psicologia , Assistência Odontológica Integral , Aconselhamento , Relações Dentista-Paciente , Depressão/classificação , Dor Facial/diagnóstico , Dor Facial/psicologia , Feminino , Humanos , Masculino , Anamnese , Pessoa de Meia-Idade , Medição da Dor , Planejamento de Assistência ao Paciente , Educação de Pacientes como Assunto , Estudos Prospectivos , Encaminhamento e Consulta , Inquéritos e Questionários
4.
Support Care Cancer ; 18(8): 1061-79, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20333412

RESUMO

PURPOSE: This systematic review aimed to assess the literature for management strategies and economic impact of salivary gland hypofunction and xerostomia induced by cancer therapies and to determine the quality of evidence-based management recommendations. METHODS: The electronic databases of MEDLINE/PubMed and EMBASE were searched for articles published in English since the 1989 NIH Development Consensus Conference on the Oral Complications of Cancer Therapies until 2008 inclusive. For each article, two independent reviewers extracted information regarding study design, study population, interventions, outcome measures, results, and conclusions. RESULTS: Seventy-two interventional studies met the inclusion criteria. In addition, 49 intensity-modulated radiation therapy (IMRT) studies were included as a management strategy aiming for less salivary gland damage. Management guideline recommendations were drawn up for IMRT, amifostine, muscarinic agonist stimulation, oral mucosal lubricants, acupuncture, and submandibular gland transfer. CONCLUSIONS: There is evidence that salivary gland hypofunction and xerostomia induced by cancer therapies can be prevented or symptoms be minimized to some degree, depending on the type of cancer treatment. Management guideline recommendations are provided for IMRT, amifostine, muscarinic agonist stimulation, oral mucosal lubricants, acupuncture, and submandibular gland transfer. Fields of sparse literature identified included effects of gustatory and masticatory stimulation, specific oral mucosal lubricant formulas, submandibular gland transfer, acupuncture, hyperbaric oxygen treatment, management strategies in pediatric cancer populations, and the economic consequences of salivary gland hypofunction and xerostomia.


Assuntos
Neoplasias/terapia , Doenças das Glândulas Salivares/etiologia , Xerostomia/etiologia , Humanos , Guias de Prática Clínica como Assunto , Radioterapia de Intensidade Modulada/efeitos adversos , Radioterapia de Intensidade Modulada/métodos , Doenças das Glândulas Salivares/economia , Doenças das Glândulas Salivares/terapia , Xerostomia/economia , Xerostomia/terapia
5.
Support Care Cancer ; 18(8): 1039-60, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20237805

RESUMO

PURPOSE: This systematic review aimed to assess the literature for prevalence, severity, and impact on quality of life of salivary gland hypofunction and xerostomia induced by cancer therapies. METHODS: The electronic databases of MEDLINE/PubMed and EMBASE were searched for articles published in English since the 1989 NIH Development Consensus Conference on the Oral Complications of Cancer Therapies until 2008 inclusive. Two independent reviewers extracted information regarding study design, study population, interventions, outcome measures, results and conclusions for each article. RESULTS: The inclusion criteria were met by 184 articles covering salivary gland hypofunction and xerostomia induced by conventional, 3D conformal radiotherapy or intensity-modulated radiotherapy in head and neck cancer patients, cancer chemotherapy, total body irradiation/hematopoietic stem cell transplantation, radioactive iodine treatment, and immunotherapy. CONCLUSIONS: Salivary gland hypofunction and xerostomia are induced by radiotherapy in the head and neck region depending on the cumulative radiation dose to the gland tissue. Treatment focus should be on optimized/new approaches to further reduce the dose to the parotids, and particularly submandibular and minor salivary glands, as these glands are major contributors to moistening of oral tissues. Other cancer treatments also induce salivary gland hypofunction, although to a lesser severity, and in the case of chemotherapy and immunotherapy, the adverse effect is temporary. Fields of sparse literature included pediatric cancer populations, cancer chemotherapy, radioactive iodine treatment, total body irradiation/hematopoietic stem cell transplantation, and immunotherapy.


Assuntos
Neoplasias/terapia , Doenças das Glândulas Salivares/etiologia , Xerostomia/etiologia , Medicina de Emergência Baseada em Evidências , Humanos , Guias de Prática Clínica como Assunto , Prevalência , Qualidade de Vida , Doenças das Glândulas Salivares/epidemiologia , Doenças das Glândulas Salivares/fisiopatologia , Índice de Gravidade de Doença , Xerostomia/epidemiologia , Xerostomia/fisiopatologia
6.
J Dent Res ; 87(8): 740-4, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18650545

RESUMO

Aspirin is a common, chronically administered preventive treatment for cardiovascular disease, but is often discontinued prior to invasive dental procedures because of concern for bleeding complications. We hypothesized that aspirin does not cause increased bleeding following a single tooth extraction. Thirty-six healthy persons requiring a tooth extraction were randomized to receive 325 mg/day aspirin or placebo for 4 days. Cutaneous bleeding time (BT) and platelet aggregation tests were obtained prior to extraction. The primary outcome measure, oral BT, and secondary bleeding outcomes were evaluated during and following extraction. No significant baseline differences, except for diastolic blood pressure, were found between groups. There were no differences in oral BT, cutaneous BT, secondary outcome measures, or compliance. Whole-blood aggregation results were significantly different between the aspirin and placebo groups. These findings suggest that there is no indication to discontinue aspirin for persons requiring single-tooth extraction.


Assuntos
Aspirina/efeitos adversos , Hemorragia Bucal/etiologia , Inibidores da Agregação Plaquetária/efeitos adversos , Hemorragia Pós-Operatória/etiologia , Extração Dentária/efeitos adversos , Adulto , Anti-Inflamatórios não Esteroides/efeitos adversos , Tempo de Sangramento , Feminino , Hemostasia/efeitos dos fármacos , Humanos , Masculino , Pessoa de Meia-Idade , Hemorragia Bucal/prevenção & controle , Agregação Plaquetária/efeitos dos fármacos , Valores de Referência , Resultado do Tratamento
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