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1.
Stem Cell Res Ther ; 15(1): 146, 2024 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-38764070

RESUMO

BACKGROUND: Based on previous in vivo studies and human trials, intrathecal cell delivery is a safe and relevant therapeutic tool for improving patient's quality of life with neurological conditions. We aimed to characterise the safety profile of intrathecally delivered Mesenchymal stem cells (MSCs). METHODS: Ovid MEDLINE, Embase, Scopus, Cochrane Library, KCI-Korean Journal Database, and Web of Science. Databases were searched from their inception until April 13, 2023. Randomised Controlled Trials (RCTs) that compared intrathecal delivery of MSCs to controls in adult populations were included. Adverse events (AEs) were pooled and meta-analysed using DerSimonian-Laird random effects models with a correction factor 0.5 added to studies with zero count cells. Pooled AEs were described using Risk ratio (RR) and 95% confidence intervals (95% CI). Then, a random-effects meta-regress model on study-level summary data was performed to explore the relationship between the occurrence of AEs and covariates thought to modify the overall effect estimate. Finally, publication bias was assessed. RESULTS: 303 records were reviewed, and nine RCTs met the inclusion criteria and were included in the quantitative synthesis (n = 540 patients). MSCs delivered intrathecally, as compared to controls, were associated with an increased probability of AEs of musculoskeletal and connective tissue disorders (categorised by Common Terminology Criteria for Adverse Events-CTCAE version 5.0) (RR: 1.61, 95% CI 1.19-2.19, I2 = 0%). The random-effects meta-regress model suggested that fresh MSCs increased the probability of occurrence of AEs compared to cryopreserved MSCs (RR: 1.554; p-value = 0.048; 95% CI 1.004-2.404), and the multiple-dose, decreased the probability of AEs by 36% compared to single doses (RR: 0.644; p-value = 0.048; 95% CI 0.416-0.996); however, univariate random effects meta-regression models revealed a not significant association between the occurrence of AEs from MSCs intrathecal delivery and each covariate. CONCLUSIONS: Intrathecal delivery of MSCs was associated with a slight increase in AEs associated with musculoskeletal and connective tissue disorders, albeit without serious AEs. We conclude that intrathecal MSCs delivery is safe for patients with neurological conditions. However, further high-quality, large-scale RCTs are needed to confirm these findings.


Assuntos
Injeções Espinhais , Transplante de Células-Tronco Mesenquimais , Células-Tronco Mesenquimais , Doenças do Sistema Nervoso , Ensaios Clínicos Controlados Aleatórios como Assunto , Humanos , Transplante de Células-Tronco Mesenquimais/efeitos adversos , Transplante de Células-Tronco Mesenquimais/métodos , Doenças do Sistema Nervoso/terapia , Células-Tronco Mesenquimais/citologia
2.
PLoS One ; 18(7): e0284828, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37498842

RESUMO

BACKGROUND AND OBJECTIVES: Some patients have insufficient treatment response to conventional disease-modifying antirheumatic drugs (cDMARD); although biologics have proven to be an effective treatment for RA, the effects that bDMARDs have on integumentary, cardiac, and immune systems and the high costs associated with these treatments, make that mesenchymal stem cell-based therapies (MSCs) for RA are being considered potential treatment methods. This work analyses the performance in safety and efficacy terms of MSCs techniques. METHODS AND FINDING: A literature search was performed in PubMed, EMBASE, Cochrane Library, Web of Science, and Open Grey databases from inception to October 28, 2022. Three randomized controlled trials (RCTs) and one non-randomized controlled trial (non-RCTs), including 358 patients met our inclusion criteria and were included in qualitative synthesis; only RCTs were eligible for quantitative synthesis (meta-analysis). Meta-analysis of adverse events (AE) in RCTs showed no significant differences in the incidence of AE in the MSCs group compared to the control group (Risk ratio: 2.35; 95% CI, 0.58 to 9.58; I2 = 58.80%). The pooled Risk ratio for non-serious and serious adverse events showed no statistical difference between intervention and control groups concerning the incidence of non-serious and serious adverse events (Risk ratio: 2.35; 95% CI, 0.58 to 9.51; I2 = 58.62%) and (Risk ratio: 1.10; 95% CI, 0.15 to 7.97; I2 = 0.0%) respectively. The Health Assessment Questionnaire (HAQ) and Disease Activity Score (DAS28) decreased in agreement with the decreasing values of C-reactive protein (CRP) and Erythrocyte sedimentation rate (ESR). Additionally, a trend toward clinical efficacy was observed; however, this improvement was not shown in the studies after 12 months of follow-up without continuous treatment administration. CONCLUSION: This Systematic review and meta-analysis showed a favorable safety profile, without life-threatening events in subjects with RA, and a trend toward clinical efficacy that must be confirmed through high-quality RCTs, considerable sample size, and extended follow-up in subjects with RA.


Assuntos
Antirreumáticos , Artrite Reumatoide , Humanos , Antirreumáticos/efeitos adversos , Artrite Reumatoide/tratamento farmacológico , Metotrexato/uso terapêutico , Resultado do Tratamento , Ensaios Clínicos Controlados como Assunto
3.
CES med ; 23(2): 63-71, jul.-dic. 2009. tab, ilus
Artigo em Espanhol | LILACS | ID: lil-565224

RESUMO

El tromboembolismo pulmonar (TEP) es una posibilidad diagnóstica que obliga a determinar una probabilidad a través del puntaje (score) de Wells, con el fin de evitar subdiagnósticos o realizar diagnósticos tardíos en el servicio de urgencias. En ocasiones el TEP se presenta como una condición amenazante de la vida que requiere intervención inmediata, siendo la trombolisis el tratamiento adecuado cuando se acompaña de inestabilidad hemodinámica y no hay contraindicaciones para su realización. Se presenta el caso de un hombre de 61 años que ingresa a un servicio de urgencias de alto nivel de complejidad, con diagnóstico de TEP masivo y se procede a trombolisis con Alteplase®, obteniéndose adecuada reperfusión de la circulación pulmonar y estabilidad cardiorrespiratoria luego de realizar el procedimiento.


Pulmonary thromboembolism (PTE) is a diagnosis possibility that implies determining a probability with Wells score in order to avoid subdiagnosis or late diagnosis in emergency services. In some occasions, it presents as a life threatening condition that requires immediate intervention. Thrombolysis is the adequate treatment when PTE is accompanied with hemodynamic instability and when there are no counter-indications. The following article describes the case of a 61 year old man who enters a high complexity level emergency service with a diagnosis of massive PTE and thrombolysis is carried out with Alteplase ®. Adequate reperfusion of pulmonary circulation is obtained as well as cardio respiratory stability following the procedure.


Assuntos
Diagnóstico , Embolia Pulmonar/cirurgia , Embolia Pulmonar/diagnóstico , Terapia Trombolítica , Hemodinâmica
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