Search results for "Visual Analogue Scale"

showing 10 items of 232 documents

Efficacy of the photobiomodulation therapy in the treatment of the burning mouth syndrome

2019

Background This study aims to evaluate the efficacy of the photobiomodulation therapy (PBMT) - in terms of pain and of quality of life- in patients affected by burning mouth syndrome (BMS). Material and Methods This study was designed as a randomised double-blinded prospective study. Patients diagnosed with BMS in the period from June 2015 to June 2018 were recruited. The patients were randomised into two groups and each received treatment once a week for ten weeks: group A received laser therapy (K Laser Cube 3®) while group B was given sham therapy (placebo). Pain was evaluated through the Visual Analogue Scale (VAS) and quality of life was assessed with the short form of the Oral Health …

medicine.medical_specialtyVisual analogue scaleBurning Mouth SyndromeOral healthPlaceboGroup Blaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled trialQuality of lifelawSurveys and QuestionnairesInternal medicineHumansMedicineProspective StudiesLow-Level Light TherapyProspective cohort studyGeneral DentistryOral Medicine and Pathologybusiness.industryResearch030206 dentistryBurning mouth syndrome:CIENCIAS MÉDICAS [UNESCO]OtorhinolaryngologyUNESCO::CIENCIAS MÉDICASQuality of LifeSurgerymedicine.symptombusiness
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Photobiomodulation therapy for the management of recurrent aphthous stomatitis in children : clinical effectiveness and parental satisfaction

2020

Background This study aims to evaluate the effectiveness of the photobiomodulation therapy (PBMT) in the treatment of minor recurrent aphthous stomatitis (MiRAS) in children, in terms of pain relief, lesion size reduction and the parental satisfaction of the therapy. Material and Methods This randomized controlled study was carried out on 60 children with clinical diagnosis of MiRAS. Patients were randomized into two groups: group A receiving laser therapy and group B receiving sham therapy (placebo). Laser therapy (diode laser, λ: 645 nm) was administered on day 1 (T0) for three consecutive days. Patients were evaluated also on day 4 (T1), on day 7 (T2) and on day 10 (T3). Oral aphthous le…

medicine.medical_specialtyVisual analogue scaleChildren; Lasers; UlcersPersonal SatisfactionPlaceboRecurrent aphthous stomatitisPeriodontal probeGroup Blaw.inventionLesion03 medical and health sciences0302 clinical medicineRandomized controlled triallawInternal medicinemedicineHumansLow-Level Light TherapyChildChildrenGeneral DentistryStomatitisPain MeasurementUlcersOral Medicine and Pathologybusiness.industryResearchLasers030206 dentistrymedicine.disease:CIENCIAS MÉDICAS [UNESCO]Treatment OutcomeOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASStomatitis AphthousSurgerymedicine.symptombusiness
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Immunoadsorption with tryptophan columns: A therapeutic option for the treatment of rheumatoid arthritis with septic complications

2009

Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune disease affecting multiple organs and tissues. Although there is a wide range of therapeutic applications, the coexistence of severe side effects and contraindications outlines the necessity of new therapeutic options in the treatment of severe RA. We report on the case of a 71-year-old patient with successful treatment of a complicated RA with tryptophan immunoadsorption combined with low-dose steroids. Bacterial spondylitis developed in this patient during long-term treatment with infliximab and methotrexate. Weekly immunoadsorption sessions with tryptophan columns resulted in continuous suppression of RA activity over a perio…

medicine.medical_specialtyVisual analogue scaleGastroenterologyArthritis RheumatoidRefractorySepsisInternal medicineHumansMedicineImmunoadsorptionSpondylitisImmunosorbent TechniquesAgedAutoimmune diseasebusiness.industryTryptophanBacterial InfectionsHematologyGeneral Medicinemedicine.diseaseInfliximabSurgeryTreatment OutcomeRheumatoid arthritisSteroidsMethotrexatebusinessSpondylitismedicine.drugJournal of Clinical Apheresis
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Translation and validation of the Finnish version of the Fear-Avoidance Beliefs Questionnaire (FABQ)

2015

Abstract Background and aim Low back pain (LBP) is a debilitating problem worldwide causing disability and reducing quality of life. The Fear Avoidance Beliefs Questionnaire (FABQ) was developed on the basis of the assumption that fear-avoidance beliefs play a major role in LBP-related disability. It comprises 16 items scored by the patient and includes sub-scores for fear-avoidance beliefs regarding work and physical activity. This study aimed to translate and validate the Finnish version of the FABQ and to measure its properties among Finnish patients with LBP. Material and methods A forward-backward translation procedure was used based on modified recommended guidelines. The FABQ was app…

medicine.medical_specialtyVisual analogue scaleIntraclass correlation03 medical and health sciences0302 clinical medicineQuality of lifeCronbach's alphaSurveys and QuestionnairesmedicineHumans030212 general & internal medicineFinlandbusiness.industryquestionnaireChronic painReproducibility of ResultsMean ageta3141Fearmedicine.diseaseLow back painOswestry Disability IndexAnesthesiology and Pain Medicinefear-avoidance beliefsPhysical therapyQuality of LifeNeurology (clinical)medicine.symptombusinessLow Back Pain030217 neurology & neurosurgeryScandinavian Journal of Pain
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Local Formula with Mucoadhesive Property: A Randomized Clinical Trial of a Therapeutic Agent for the Treatment of Oral Aphthous Ulcers

2020

Background Recurrent or occasional aphthous lesions represent a painful oral condition with high prevalence. Since the etiology is still unclear and most likely related to a dysfunction in the local immune system, several treatment strategies have been proposed, including systemic agents, local agents, and laser therapy, to reduce the pain and discomfort for the patient without acting on the causes. Materials and methods The purpose of the present randomized study was to assess the clinical efficacy of a new topical gel with mucoadhesive property to reduce the pain and the dimension of the aphthosis lesions. Fifty patients presenting at least one minor ulcer were randomized to a control gro…

medicine.medical_specialtyVisual analogue scalePainPlacebolaw.invention03 medical and health sciencesOral aphthous ulcers0302 clinical medicineRandomized controlled triallawAdjuvant therapyHumansMedicineClinical significanceMedical prescriptionGeneral DentistryWound Healingbusiness.industry030206 dentistryDermatologyTreatment Outcome030220 oncology & carcinogenesisEtiologyStomatitis AphthousbusinessGelsThe Journal of Contemporary Dental Practice
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Efficacy and tolerability of a plant-based, multi-component cream (Ginetrox®) in vulvovaginal disorders of the genitourinary syndrome during menopaus…

2017

BACKGROUND Genitourinary syndrome of menopause (GSM) is a symptomatic condition including vaginal dryness, irritation, dyspareunia and recurrent urinary tract infections which affects 40-54% of post-menopausal women. Although several estrogen-based therapies are available, it is generally preferable to avoid hormonal therapy, particularly in women with mild symptoms or at risk for estrogen-responsive neoplasia. Therefore, the most common treatment options are over-the-counter vaginal creams for symptomatic relief. METHODS Thirty-three postmenopausal women suffering from GSM were enrolled in this observational study. A multi-component cream (Ginetrox®, Indena, Milan, Italy) was applied on th…

medicine.medical_specialtyVisual analogue scaleVaginal DiseasesPainmedicine.disease_causeMedication AdherenceInternal medicinemedicineHumansAgedbusiness.industryGenitourinary systemObstetrics and GynecologySyndromeMiddle Agedmedicine.diseaseSymptomatic reliefMenopauseAdministration Intravaginalmedicine.anatomical_structureDyspareuniaTreatment OutcomeTolerabilityItalyVaginaVaginal Creams Foams and JelliesHormonal therapyFemalePlant PreparationsVulvar DiseasesIrritationMenopausebusinessMinerva ginecologica
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Vulvo-vaginal atrophy: A new treatment modality using thermo-ablative fractional CO2 laser.

2015

a b s t r a c t Objective: To evaluate the efficacy and feasibility of thermo-ablative fractional CO2 laser for the treatment of symptoms related to vulvo-vaginal atrophy (VVA) in post-menopausal women. Methods: From April 2013 to December 2013, post-menopausal patients who complained of one or more VVA-related symptoms and who underwent vaginal treatment with fractional CO2 laser were enrolled in the study. At baseline (T0) and 30 days post-treatment (T1), vaginal status of the women was evaluated using the Vaginal Health Index (VHI), and subjective intensity of VVA symptoms was evaluated using a visual analog scale (VAS). At T1, treatment satisfaction was evaluated using a 5-point Likert …

medicine.medical_specialtyVisual analogue scaleVaginal DiseasesPilot ProjectsGeneral Biochemistry Genetics and Molecular BiologyVulvaAtrophyQuality of lifeLaser treatmentAblative casemedicineHumansAdverse effectbusiness.industryObstetrics and GynecologyMiddle Agedmedicine.diseaseSettore MED/40 - Ginecologia E OstetriciaSurgeryMenopausePostmenopauseAdministration IntravaginalDyspareuniaTreatment OutcomeLasers GasQuality of LifeItchingFemaleVaginal atrophyLaser Therapymedicine.symptomAtrophyMenopausebusinessVulvo-vaginal atrophy
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Preventive Analgesia with Pregabalin in Neuropathic Pain from “Failed Back Surgery Syndrome”: Assessment of Sleep Quality and Disability

2015

Objective. Pregabalin group (PGB) is an antiepileptic used to treat neuropathic pain. We evaluated analgesic efficacy and safety for postoperative/chronic pain, disability, and sleep quality in patients who underwent spine surgery administered with PGB, or not, during the presurgical and postsurgical periods. Design. Retrospective cohort study of 60 patients (two groups with 30 patients) with full information on 50 (29 with PGB and 21 without PGB). Ten patients were dismissed as information was lacking. The PGB group (P) (29 patients) received 75 mg/12 hours before surgery, 150 mg 10 hours after surgery, and 150 mg/12 hours 3 days after surgery. The control group (C; 21 patients) took no PG…

medicine.medical_specialtyVisual analogue scalebusiness.industryAnalgesicChronic painPregabalinGeneral Medicinemedicine.diseaseSurgeryPreventive analgesiaOswestry Disability IndexAnesthesiology and Pain MedicineAnesthesiaNeuropathic painmedicineNeurology (clinical)businessAdverse effectmedicine.drugPain Medicine
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Standardisiertes postoperatives Schmerztherapieschema in der Orthopädie

2006

In order to treat patients with postoperative acute pain effectively, we have developed a standardised algorithm for analgesia. This process includes three levels and the appropriate supply of medication. The therapy level is defined based on the scale of the operation. Accordingly, the prescription and handling of the pain medication is simplified for the attending physician and nurses. The pain level has to be measured by the nursing staff sing a visual analogue scale (VAS). Thus, the efficiency of the analgesics will be continuously evaluated and controlled. The standardised supply medication can be applied in those cases with pain levels > or = 4 (VAS). It is possible to up- or down-gra…

medicine.medical_specialtyVisual analogue scalebusiness.industryPain medicationAnalgesicGuidelinePain levelOrthopedic surgeryPhysical therapymedicineOrthopedics and Sports MedicineSurgeryMedical prescriptionbusinessPain therapyZeitschrift für Orthopädie und ihre Grenzgebiete
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Effects of Adding Motor Imagery to Early Physical Therapy in Patients with Knee Osteoarthritis who Had Received Total Knee Arthroplasty

2020

Abstract Objective To investigate the effects of the inclusion of motor imagery (MI) principles into early physical therapy on pain, disability, pressure pain thresholds (PPTs), and range of motion in the early postsurgical phase after total knee arthroplasty (TKA). Methods A randomized clinical trial including patients with knee osteoarthritis who have received TKA was conducted. Participants were randomized to receive five treatment sessions of either physical therapy with or without MI principles in an early postsurgical phase after a TKA (five days after surgery). Pain intensity (visual analog scale [VAS], 0–100), pain-related disability (short-form Western Ontario McMaster Universities…

medicine.medical_specialtyWOMACVisual analogue scaleTotal knee arthroplastyOsteoarthritislaw.invention03 medical and health sciences0302 clinical medicineMotor imageryRandomized controlled triallawThreshold of painmedicineHumans030212 general & internal medicineRange of Motion ArticularArthroplasty Replacement KneePhysical Therapy ModalitiesOntariobusiness.industryGeneral MedicineOsteoarthritis Kneemedicine.diseaseTreatment OutcomeAnesthesiology and Pain MedicinePhysical therapyNeurology (clinical)Range of motionbusiness030217 neurology & neurosurgery
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