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1.
Med Oral Patol Oral Cir Bucal ; 29(2): e211-e218, 2024 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-37823292

RESUMO

BACKGROUND: The transcutaneous electrical nerve stimulation (TENS) stimulus inhibits the activity of nociceptive neurons of the central nervous system. Pain relief is achieved by increasing the pulse amplitude of TENS to induce a non-painful paranesthesia beneath the electrodes. This study aimed to assess the effect of TENS on acute pain, edema, and trismus after surgical removal of impacted third molars. MATERIAL AND METHODS: This randomized, double blind, split-mouth clinical trial was conducted on 37 patients with bilaterally impacted mandibular third molars. The angle and body of mandible at the site of surgery in one randomly selected quadrant underwent TENS immediately after surgery (50 Hz, 100-µs short pulse, 15 minutes for 6 days). The TENS stimulator device was used in off mode for the placebo quadrant. The pain score (primary outcome) was measured for 7 days postoperatively, and edema and trismus (secondary outcomes) were assessed at 2, 4 and 7 days, postoperatively. The results were analyzed by repeated measures ANOVA using R software (alpha=0.05). RESULTS: The overall mean pain score was significantly lower in the TENS than the placebo group (P<0.05). The number of taken analgesics in the first 3 days was significantly lower in the TENS group (P<0.001). Postoperative edema in the TENS group was lower than the placebo group but only the difference was not statistically significant (P>.05). The inter-incisal distance, as an index to assess trismus, was not significantly different between the two group at day 2, but it was significantly higher in the TENS group after the second day (P<0.001). CONCLUSIONS: TENS effectively decreased pain and trismus following impacted third molar surgery, and may be recommended as a non-pharmaceutical method to relieve postoperative symptoms.


Assuntos
Dente Impactado , Estimulação Elétrica Nervosa Transcutânea , Humanos , Trismo/etiologia , Trismo/prevenção & controle , Dente Serotino/cirurgia , Boca , Dente Impactado/cirurgia , Dor , Edema/etiologia , Edema/prevenção & controle
2.
Bone Marrow Transplant ; 52(5): 689-696, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28067872

RESUMO

Allogeneic stem cell transplantation (allo-SCT) following a non-myeloablative (NMA) or reduced-intensity conditioning (RIC) is considered a valid approach to treat patients with refractory/relapsed Hodgkin lymphoma (HL). When an HLA-matched donor is lacking a graft from a familial haploidentical (HAPLO) donor, a mismatched unrelated donor (MMUD) or cord blood (CB) might be considered. In this retrospective study, we compared the outcome of patients with HL undergoing a RIC or NMA allo-SCT from HAPLO, MMUD or CB. Ninety-eight patients were included. Median follow-up was 31 months for the whole cohort. All patients in the HAPLO group (N=34) received a T-cell replete allo-SCT after a NMA (FLU-CY-TBI, N=31, 91%) or a RIC (N=3, 9%) followed by post-transplant cyclophosphamide. After adjustment for significant covariates, MMUD and CB were associated with significantly lower GvHD-free relapse-free survival (GRFS; hazard ratio (HR)=2.02, P=0.03 and HR=2.43, P=0.009, respectively) compared with HAPLO donors. In conclusion, higher GRFS was observed in Hodgkin lymphoma patients receiving a RIC or NMA allo-SCT with post-transplant cyclophosphamide from HAPLO donors. Our findings suggest they should be favoured over MMUD and CB in this setting.


Assuntos
Ciclofosfamida/uso terapêutico , Doença de Hodgkin/terapia , Transplante de Células-Tronco/métodos , Condicionamento Pré-Transplante/métodos , Transplante Haploidêntico , Adulto , Transplante de Células-Tronco de Sangue do Cordão Umbilical , Intervalo Livre de Doença , Feminino , Seguimentos , Doença Enxerto-Hospedeiro , Antígenos HLA , Histocompatibilidade , Doença de Hodgkin/mortalidade , Humanos , Masculino , Estudos Retrospectivos , Transplante de Células-Tronco/normas , Transplante Homólogo , Doadores não Relacionados/provisão & distribuição
3.
Pathol Biol (Paris) ; 61(4): 171-3, 2013 Aug.
Artigo em Francês | MEDLINE | ID: mdl-24011963

RESUMO

In the attempt to harmonize clinical practices between different French transplantation centers, the French Society of Bone Marrow Transplantation and Cell Therapy (SFGM-TC) set up the third annual series of workshops which brought together practitioners from all member centers and took place in October 2012 in Lille. Here we report our results and recommendations regarding the management of short and long-term endocrine dysfunction following allogeneic stem cell transplantation. The key aim of this workshop was to give an overview on secondary adrenal insufficiency and osteoporosis post-transplant.


Assuntos
Insuficiência Adrenal/terapia , Doenças do Sistema Endócrino/etiologia , Doenças do Sistema Endócrino/terapia , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Osteoporose/terapia , Insuficiência Adrenal/etiologia , Adulto , Densidade Óssea , Criança , Suplementos Nutricionais , Difosfonatos/uso terapêutico , Glucocorticoides/efeitos adversos , Humanos , Imunossupressores/efeitos adversos , Osteoporose/etiologia , Transplante Homólogo , Vitaminas/uso terapêutico
4.
Leukemia ; 24(11): 1867-74, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20882046

RESUMO

This retrospective report assessed the impact of rabbit antithymocyte globulins (ATG), incorporated within a standard myeloablative conditioning regimen prior to allogeneic stem cell transplantation (allo-SCT) using human leukocyte antigen-matched unrelated donors (HLA-MUD), on the incidence of acute and chronic graft-vs-host disease (GVHD). In this series of leukemia patients, 120 patients (70%) did not receive ATG ('no-ATG' group), whereas 51 patients received ATG ('ATG' group). With a median follow-up of 30.3 months, the cumulative incidence of grade 3-4 acute GVHD was 36% in the no-ATG group and 20% in the ATG group (P = 0.11). The cumulative incidence of extensive chronic GVHD was significantly lower in the ATG group as compared to the no-ATG group (4 vs 32%, respectively; P = 0.0017). In multivariate analysis, the absence of use of ATG was the strongest parameter associated with an increased risk of extensive chronic GVHD (relative risk) = 7.14, 95% CI: 1.7-33.3, P = 0.008). At 2 years, the probability of nonrelapse mortality, relapse, overall and leukemia-free survivals was not significantly different between the no-ATG and ATG groups. We conclude that the addition of ATG to GVHD prophylaxis resulted in decreased incidence of extensive chronic GVHD without an increase in relapse or nonrelapse mortality, and without compromising survival after myeloablative allo-SCT from HLA-MUD.


Assuntos
Soro Antilinfocitário/uso terapêutico , Doença Enxerto-Hospedeiro/etiologia , Leucemia Mieloide Aguda/cirurgia , Leucemia-Linfoma Linfoblástico de Células Precursoras/cirurgia , Transplante de Células-Tronco/métodos , Adolescente , Adulto , Idoso , Animais , Feminino , Doença Enxerto-Hospedeiro/epidemiologia , Doença Enxerto-Hospedeiro/prevenção & controle , Antígenos HLA/imunologia , Teste de Histocompatibilidade , Humanos , Incidência , Leucemia Mieloide Aguda/imunologia , Masculino , Pessoa de Meia-Idade , Síndromes Mielodisplásicas/imunologia , Síndromes Mielodisplásicas/cirurgia , Leucemia-Linfoma Linfoblástico de Células Precursoras/imunologia , Coelhos , Estudos Retrospectivos , Transplante de Células-Tronco/efeitos adversos , Doadores de Tecidos , Transplante Homólogo/métodos , Resultado do Tratamento
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