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PURPOSE OF REVIEW: This review investigates the roles of artificial intelligence (AI) and virtual reality (VR) in enhancing cognitive pain therapy for chronic pain management. The work assesses current research, outlines benefits and limitations and examines their potential integration into existing pain management methods. RECENT FINDINGS: Advances in VR have shown promise in chronic pain management through immersive cognitive therapy exercises, with evidence supporting VR's effectiveness in symptom reduction. AI's personalization of treatment plans and its support for mental health through AI-driven avatars are emerging trends. The integration of AI in hybrid programs indicates a future with real-time adaptive technology tailored to individual needs in chronic pain management. Incorporating AI and VR into chronic pain cognitive therapy represents a promising approach to enhance management by leveraging VR's immersive experiences and AI's personalized tactics, aiming to improve patient engagement and outcomes. Nonetheless, further empirical studies are needed to standardized methodologies, compare these technologies to traditional therapies and fully realize their clinical potential.
Subject(s)
Artificial Intelligence , Cognitive Behavioral Therapy , Pain Management , Virtual Reality , Humans , Pain Management/methods , Cognitive Behavioral Therapy/methods , Chronic Pain/therapy , Chronic Pain/psychology , Virtual Reality Exposure Therapy/methodsABSTRACT
El tratamiento del dolor crónico severo es una meta histórica de la medicina. Los opioides naturales (como la morfina) se han usado por muchos años y la aparición reciente de opioides sintéticos se ha sumado a esta opción terapéutica, sin embargo, el potencial adictivo de estas sustancias obliga a la reglamentación de su uso. Las agencias médicas internacionales recomiendan prudencia en el uso terapéutico de opioides.The treatment of chronic and severe pain is a principal goal of medicine. Natural opioids have been used for several years, and the recent development of synthetic opioids has increased therapeutic options; however, the addictive potential of these substances obliges the regulation of their use. International agencies recommend prudent rules in the therapeutic use of opioids.
Subject(s)
Analgesics, Opioid/administration & dosage , Chronic Pain/drug therapy , Opioid-Related Disorders/prevention & control , Analgesics, Opioid/adverse effects , Chronic Pain/physiopathology , Drug and Narcotic Control , Humans , International Agencies , Severity of Illness IndexABSTRACT
INTRODUCTION: IL-33 signals through ST2 receptor and promotes inflammation by activating downstream pathways culminating in the production of pro-inflammatory mediators such as IL-1ß, TNF-α, and IL-6 in an NF-κB-dependent manner. In fact, compelling evidence has demonstrated the importance of IL-33/ST2 in both innate and adaptive immune responses in diseases presenting pain as an important clinical symptom. Areas covered: IL-33 is a pleiotropic cytokine with varied immune functions. Dysregulation of this pathway has been described as a key step in varied immune responses. Further, IL-33 contributes to peripheral and spinal cord nociceptor neuron sensitization in innate and adaptive inflammatory immune responses as well as in neuropathic and cancer pain. In this sense, targeting IL-33/ST2 signaling is a promising therapeutic approach. Expert opinion: The modulation of IL-33/ST2 signaling represents a possible approach in regulating immune functions. In addition to immune function, strategies targeting IL-33/ST2 signaling pathway display a favorable preclinical analgesic profile in both acute and chronic models of pain. Therefore, IL-33-targeting therapies represent a potential target for the development of novel analgesic drugs given that IL-33 activates, for instance, neutrophils, mast cells, macrophages, astrocytes, and microglia that are important cells in the induction and maintenance of chronic pain states.
Subject(s)
Acute Pain/drug therapy , Chronic Pain/drug therapy , Interleukin-33/metabolism , Acute Pain/immunology , Analgesics/pharmacology , Animals , Chronic Pain/immunology , Cytokines/immunology , Drug Design , Humans , Inflammation/drug therapy , Inflammation/immunology , Inflammation Mediators/metabolism , Interleukin-1 Receptor-Like 1 Protein/metabolism , Interleukin-33/immunology , Molecular Targeted Therapy , Signal Transduction/drug effectsABSTRACT
INTRODUCTION: In Colombia, 40% of the population has used acupuncture services for the treatment of chronic diseases; however, there is lack of evidence on the effectiveness of this treatment. OBJECTIVE: To evaluate the effect of acupuncture in the treatment of patients with low back pain treated at a health center in Bogotá. MATERIALS AND METHODS: We analyzed 150 medical records of patients treated for low back pain from January, 2014, to May, 2016, at a health center in Bogotá. From these, we selected 48 records basedon the inclusion criteria previously defined. We then used the Friedman test to establish the effect of acupuncture on the pain among the patients selected, and an unstructured measurement instrument to measure the impact of adherence to the therapy on its effectiveness. RESULTS: The results of the Friedman test (95% confidence interval), showed that there was a positive impact on pain reduction among patients with low back pain treated with acupuncture and that adherence to the treatment was a key factor for its effectiveness. DISCUSSION: As acupuncture was effective among these patients, and adherence proved to be a fundamental part of the process, it would be important to include this type of therapy in the mandatory health plan in Colombia.
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ABSTRACT Etodolac is a non-steroidal anti-inflammatory drug (NSAID) and approved by USFDA as a COX2 inhibitor. Although etodolac therapy provides clinical benefits, it is associated with upper gastrointestinal (GI) tract complications also. Etodolac loaded gum Katira microsphere (ELGKM) was prepared by W1/O/W2 emulsion solvent evaporation technique. The gastric irritation properties of orally administered pure etodolac, ELGKM and blank microspheres (without etodolac) were evaluated in experimental rats treated for 6 days. The stomach examination and biochemical investigation of stomach tissue of treated rats indicated that ELGKM formulation remarkably reduced ulcerogenecity as compared to pure etodolac. The anti-inflammatory activities of pure etodolac and ELGKMs were ascertained by the implantation of cotton pellets in rats for 6 days. Based on the results, ELGKMs showed significant anti-inflammatory activities (P<0.01) as compared to control group. The cotton pellets test suggested that ELGKM formulation retained more anti-inflammatory properties among the groups. The hematological changes, biochemical analysis and histopathological studies of subacute toxicity in rats revealed that ELGKM were the effective sustained release formulation in the treatment of chronic pain and inflammation. In conclusion, the physicochemical characterization, pharmacological and toxicological studies suggest that ELGKMs may represent as a potential candidate for sustained drug delivery (10-12 hours) in chronic joint pain related diseases with remarkably diminished gastrointestinal side effects.
Subject(s)
Animals , Male , Rabbits , Rats , Tragacanth/therapeutic use , Evaporation/methods , Etodolac/analysis , Etodolac/therapeutic use , Microspheres , Upper Gastrointestinal Tract/pathologyABSTRACT
Objective: To determine the level of knowledge and attitudes of physicians in Tijuana based on Clinical Practice Guidelines (CPG) for the prevention, diagnosis and treatment of Nonspecific Low Back Pain (NLBP). Methods: Prospective, cross-sectional, descriptive study. Data were obtained from doctors who practice in clinics, private surgeries, and/or government institutions. Results: Of a total of 56 doctors surveyed, 37 were men and 19 women. None of the doctors said they had not seen a patient with Back Pain. 49% knew the GPC, and 51% did not know of its existence. Conclusions: Although some physicians reported knowledge of the GPC, according to the results, there was a lack of full knowledge of, and adherence to these guidelines. Not knowing the GPC did not make it impossible to complete the questionnaire. The doctors felt more connected to the health system, but with less confidence in the management of cases of NLBP.
Objetivo: Determinar o nível de conhecimentos e a conduta dos médicos de Tijuana, com base nas Diretivas de Prática Clínica (DPC) para prevenção, diagnóstico e tratamento da dor lombar não específica (DLNE). Métodos: Estudo prospectivo, transversal e descritivo. Os dados foram obtidos junto a médicos que prestam serviços em clínicas, consultórios particulares e/ou instituições governamentais. Resultados: Atingiu-se um total de 56 médicos entrevistados, dos quais 37 eram homens e 19 mulheres. Nenhum médico disse que não atende um paciente com dor lombar. Do total, 49% conhecem as DPC e 51% não sabiam da sua existência. Conclusões: Apesar de alguns médicos relatarem conhecer as DPC, de acordo com os resultados obtidos, falta-lhes maior domínio e conformidade com relação a essas diretivas. Não conhecer as DPC não impossibilita responder ao questionário. Os médicos sentem-se mais conectados ao sistema de saúde, mas com menos confiança na conduta em casos DLI.
Objetivo: Determinar el nivel de conocimientos y las actitudes de los médicos en Tijuana, con base en la Guía de Práctica Clínica (GPC) para la prevención, diagnóstico y tratamiento del Dolor Lumbar Inespecífico (DLI). Métodos: Estudio prospectivo, transversal y descriptivo. Los datos fueron obtenidos de los médicos que prestan sus servicios en clínicas, consultorios privados y/o instituciones de gobierno. Resultados: Se obtuvo un total de 56 médicos encuestados, 37 hombres y 19 mujeres. Ningún médico contestó que no atiende un paciente con dolor lumbar. El 49% conocen la GPC y el 51% no saben de su existencia. Conclusiones: A pesar de que algunos médicos refieren conocer la GPC, según los resultados obtenidos falta mayor dominio y apego de la misma. El no conocer la GPC no hace imposible contestar el cuestionario. Los médicos se sienten más conectados con el sistema de salud, pero con menor autoconfianza en el manejo del DLI.
Subject(s)
Practice Guidelines as Topic/standards , Clinical Diagnosis , Low Back Pain/diagnosis , Low Back Pain/prevention & controlABSTRACT
La dexmedetomidina es un fármaco agonista de los receptores alfa-2 adrenérgicos, altamente selectivo, utilizado para sedación en unidades de cuidados críticos. Posee también, efectos analgésicos importantes que pueden atribuirle un rol en el manejo clínico del dolor. Diversas comunicaciones científicas han estudiado su utilidad en el manejo del dolor agudo, crónico y en cuidados paliativos, tanto en adultos como en niños. En este artículo de revisión se analiza la evidencia científica disponible hasta la fecha con el objeto de dilucidar cuál es el real aporte de este fármaco en el tratamiento de las diversas formas de dolor...
Dexmedetomidine is a highly selective alpha-2 adrenergic agonist commonly used in the critical care units for sedation therapy. It has analgesic effects that may be used in pain treatment. Many scientific reports have studied its utility in the management of acute and chronic pain and palliative care. In this review we analyze the scientific evidence in relation to the real role of dexmedetomidine in pain therapy...
Subject(s)
Humans , /therapeutic use , Dexmedetomidine/therapeutic use , Pain/drug therapyABSTRACT
Esta revisão se propõe analisar os estudos que utilizaram a glicose como recurso terapêutico em neonatologia durante procedimentos que resultam em dor de intensidade leve a moderada apontando os benefícios e limitações de sua utilização. Os recém-nascidos internados em unidades neonatais são submetidos a inúmeros procedimentos dolorosos sem abordagem terapêutica adequada, apesar de a literatura recomendar de maneira enfática a necessidade de tratamento e ressaltar as repercussões neurológicas deletérias para esses pacientes. A maior parte destas intervenções constitui procedimentos frequentemente realizados nas unidades e necessários à manutenção da estabilidade clínica, nos quais a analgesia sistêmica não está indicada. A administração de solução oral de glicose parece ser eficaz e segura no controle da dor durante procedimentos que geram dor de intensidade leve a moderada nas unidades de terapia intensiva neonatais, os efeitos adversos são raros e o mecanismo de ação ainda não está descrito de maneira consistente na literatura. A indicação da solução oral de glicose durante punções venosas é bem descrita e durante punções de calcanhar parece ser o método mais eficaz de controle da dor especialmente quando associado à sucção não nutritiva, com resultados favoráveis na maior parte dos estudos.
This article aims to review the main studies evaluating glucose as a therapeutic alternative during mildly to moderately painful procedures in neonatology, highlighting its benefits and limitations. During their stay in neonatal intensive care units, neonates are constantly subjected to a number of painful procedures without proper therapeutic management, although the medical literature emphatically recommends this type of management, highlighting the deleterious neurological consequences of pain. Most of these interventions are frequently necessary in neonatal intensive care units to maintain clinical stability in these children; the use of systemic analgesia, however, is not considered to be a good option. The administration of oral glucose solution is apparently effective and safe for pain control during procedures causing mild-to-moderate pain in neonate intensive care units, with rare adverse effects; however, its mode of action has not yet been described clearly in the literature. The administration of oral glucose solution is well described for use in venous punctures; it is apparently effective also for heel punctures, especially when associated with nonnutritive sucking, with most studies showing favorable results.
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Advances in knowledge regarding the pathophysiology of pain among patients with knee osteoarthritis suggest that the central nervous system is involved as a source that maintains and amplifies the painful condition such that it is refractory to conventional orthopedic and rheumatological treatment. Initially, hyperalgesia is observed only at the affected site. However, when the pain becomes refractory, peripheral and central sensitization mechanisms contribute towards maintaining and amplifying the painful conditions, regardless of the peripheral process that originated the pain. At this stage, even removal of the etiological agent may no longer be enough to relieve the painful symptoms. It then becomes necessary to envisage that other factors, distant from the affected joint, may be responsible for the disabling painful condition in such patients. At present, osteoarthrosis does not have any known cure, and the aim of treatment is to lessen the pain while improving function and health-related quality of life, and whenever possible, to minimize the toxicity of the therapy. In the light of emerging evidence suggesting that the central nervous system has a role in the physiopathology of pain in patients with knee arthrosis, the central nervous system should be taken into consideration as a therapeutic target, instead of only administering local treatment using ordinary analgesics, anti-inflammatory drugs and non-pharmacological measures. Thus, methods that modulate the spinal cord and cerebral cortex, including the use of antidepressants, may have a role in managing these patients.
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Este é um estudo clínico, prospectivo, aleatório, e duplamente encoberto realizado em 80 doentes hansênicos de ambos os sexos e com idade variando entre 18 e 65 anos, portadores de dor neuropática. Os pacientes foram divididos em 4 grupos: Grupo G: pacientes tratados com gabapentina na dose de 400mg diários, Grupo C: pacientes tratados com carbamazepina na dose de 200 mg diários, Grupo GA: pacientes tratados com a associação de gabapentina 400 mg e amitriptilina 25 mg diários e Grupo CA: pacientes tratados com a associação de carbamazepina 200 mg e amitriptilina 25 mg diários e avaliados durante 4 meses quanto a intensidade da dor, consumo de prednisona, necessidade do uso de talidomida, queixa de queimação, parestesia, sensação de choque e alteração da sensibilidade, bem como da necessidade de realização de neurólise e eventos adversos relacionados ao tratamento. Os resultados permitiram verificar que o valor médio de intensidade de dor foi semelhante em todos os grupos no momento da inclusão e no momento de encerramento do estudo, e a diminuição da dor foi semelhante em todos os grupos, não havendo superioridade de nenhum dos esquemas terapêuticos sobre o outro, portanto a carbamazepina isolada ou associada a amitriptilina e a gabapentina isolada ou associada a amitriptilina foram igualmente eficientes na redução da dor que os pacientes apresentavam no momento de inclusão no estudo, porém a duração da dor, em dias, foi maior no grupo medicado com a gabapentina isolada, foi menor e igual nos grupos medicados com a carbamazepina e com a gabapentina associada a amitriptilina e teve uma duração intermediária no grupo medicado com a carbamazepina associada a amitriptilina, embora a diferença não tenha sido significativa pela análise estatística. Todos os fármacos foram igualmente eficazes na redução do consumo da prednisona e na necessidade do uso de talidomida. A queixa de queimação, de parestesia, de sensação de choque e de alteração da sensibilidade...
This study is a clinical trial. During the present study a prospective controlled four-way crossover double-blind randomized protocol was followed. Eighty hansen's patients, male and female, aged 18 to 65, with neuropathic pain took part. The patients were divided into 4 groups as follows: Group G -patients treated with a gabapentin 400 mg dose daily; Group C - patients treated with a carbamazepine 200 mg dose daily; Group GA - patients treated with a gabapentin 400 mg dose in association with an amitriptyline 25 mg daily, Group CA - patients treated with a carbamazepine 200 mg dose in association with an amitriptyline 25 mg daily. All four groups were assessed for four months taking into account pain intensity, prednisone consumption, the amount of thalidomide needed, burn sensation complaints, paresthesia, numbness, shock sensitivity and alterations to sensitivity, as well as neurolysis and side effects related to the treatment. The results of the study demonstrated that intensity of pain was similar in patients belonging to all four groups, both at the moment of inclusion and at the end of the study, and the reduction in the intensity of pain was also similar in all groups, without any report of superior effectiveness in any of the four groups studied. Therefore, the gabapentin and the carbamazepine, alone or in association with amitriptyline, proved to be equally effective in the reduction of the pain the patients felt at the moment of their inclusion to the present study. On the other hand, during the assessment of the duration of pain in days we noticed that it lasted longer in the group treated only with gabapentin, it was shorter or the same in the groups treated with carbamazepine and with gabapentin in association with an amitriptyline, and was considered intermediary in the group treated with carbamazepine in association with an amitriptyline, even though the difference was not considered significant in terms of statistical analysis...