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1.
Esophagus ; 17(3): 270-278, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32026048

RESUMO

BACKGROUND: In April 2017, we launched the multidisciplinary Hamamatsu Perioperative Care Team (HOPE) for all surgical patients. We developed a reinforced intervention strategy, particularly for esophagectomy. We herein report the outcomes of the HOPE at 2 years after commencement. METHODS: A total 125 patients underwent esophagectomy and gastric conduit reconstruction for esophageal or esophagogastric junction cancer between January 2014 and December 2018 at the Department of Surgery in Hamamatsu University School of Medicine. The patients were divided into the pre-HOPE group including 62 patients who underwent esophagectomy before the introduction of the HOPE and the HOPE group including 63 patients who underwent esophagectomy after the introduction of the HOPE. The outcomes of surgery were compared between the two groups. RESULTS: There were no significant differences in the clinicopathological characteristics between the two groups. The incidence rates of atrial fibrillation and pneumonia were significantly lower in the HOPE group than in the pre-HOPE group (6% vs. 19%, p = 0.027 and 14% vs. 29%, p = 0.037, respectively). The estimated calorie doses at the time of discharge were approximately 750 and 1500 kcal/day in the pre-HOPE group and the HOPE group, respectively. The body weight loss was significantly less in the HOPE group than the pre-HOPE group at 1, 3, 6, and 12 months postoperatively than that before the surgery (p < 0.001). CONCLUSIONS: The introduction of the multidisciplinary HOPE was associated with a significant reduction in the incidence of postoperative pneumonia and significantly less weight loss.


Assuntos
Neoplasias Esofágicas/cirurgia , Esofagectomia/efeitos adversos , Equipe de Assistência ao Paciente/normas , Pneumonia/prevenção & controle , Idoso , Fibrilação Atrial/epidemiologia , Estudos de Casos e Controles , Neoplasias Esofágicas/patologia , Junção Esofagogástrica/patologia , Junção Esofagogástrica/cirurgia , Feminino , Humanos , Incidência , Japão/epidemiologia , Masculino , Pessoa de Meia-Idade , Estadiamento de Neoplasias/métodos , Avaliação de Resultados em Cuidados de Saúde , Equipe de Assistência ao Paciente/estatística & dados numéricos , Assistência Perioperatória/normas , Pneumonia/epidemiologia , Complicações Pós-Operatórias/epidemiologia , Procedimentos de Cirurgia Plástica/métodos , Estudos Retrospectivos , Redução de Peso
2.
Eur Spine J ; 26(8): 2138-2145, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28190204

RESUMO

PURPOSE: To identify the effects of corrective long spinal fusion to the ilium on physical function in patients with adult spinal deformity (ASD). METHODS: Thirty patients who underwent corrective long spinal fusion to the ilium were prospectively analysed. Patients were divided into the ++ group [sagittal vertical axis (SVA) ≥ 95 mm and pelvic tilt (PT) ≥ 30°, 14 patients] and 0+ group (SVA <95 mm or PT <30°, 16 patients). Subjects' low back pain [visual analogue scale (VAS) (pain with motion)], muscle strength (knee extensors and hip flexors), balance [timed up and go (TUG)], gait performance [10-metre walking test (10MWT, maximum speed), and 6-minute walk test (6MWT)] were assessed before surgery, at discharge, and 6 and 12 months after the surgery. RESULTS: All study patients had a significant improvement in the VAS score between baseline and at discharge, 6 months postoperatively, and 12 months postoperatively. The values of the TUG and 6MWT significantly improved 12 months postoperatively. The values of the TUG, 10MWT, and 6MWT improved significantly more in the ++ group than in the 0+ group at 12 months. CONCLUSION: Corrective long spinal fusion contributed to improving back pain at discharge and gait ability at 12 months in patients with ASD.


Assuntos
Marcha , Ílio/cirurgia , Equilíbrio Postural , Recuperação de Função Fisiológica , Curvaturas da Coluna Vertebral/cirurgia , Fusão Vertebral/métodos , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Curvaturas da Coluna Vertebral/fisiopatologia , Curvaturas da Coluna Vertebral/reabilitação , Fusão Vertebral/reabilitação , Resultado do Tratamento
3.
Sci Rep ; 13(1): 21905, 2023 12 11.
Artigo em Inglês | MEDLINE | ID: mdl-38081947

RESUMO

Rheumatoid arthritis (RA) causes significant physical disability. We comprehensively investigated the relationship between RA disease activity (Disease Activity Score 28-C-reactive protein [DAS28-CRP], Simplified Disease Activity Index [SDAI], and Clinical Disease Activity Index [CDAI]), physical function (10-Meter Walk Test [10 MWT], Timed Up and Go test [TUG], Functional Reach Test [FRT], and Disabilities of the Arm, Shoulder, and Hand [DASH]), and quality of life (QOL) (Short-Form 36 [SF-36®]). We also investigated the relationship between van der Heijde's modified Total Sharp Score (mTSS), modified Health Assessment Questionnaire (mHAQ), and physical function and QOL assessments. Among 35 female patients with RA, DAS28-CRP correlated solely with DASH (r = 0.376), while SDAI and CDAI did not correlate with physical function. The mTSS-hand roentgenographic evaluation correlated with TUG (r = 0.359), FRT (r = - 0.415), and DASH (r = 0.533) among physical function assessments. The mHAQ correlated with 10 MWT (r = 0.347), TUG (r = 0.356), FRT (r = - 0.420), and DASH (r = 0.646). DAS28-CRP correlated with six of the eight subscales of SF-36®, and mTSS and mHAQ correlated with only one subscale. RA disease activity assessments may not reflect all physical functions and QOL domains of female patients with RA. Evaluating physical function and QOL in female patients with RA is essential.


Assuntos
Artrite Reumatoide , Qualidade de Vida , Humanos , Feminino , Equilíbrio Postural , Estudos de Tempo e Movimento , Exame Físico , Índice de Gravidade de Doença
4.
Global Spine J ; 13(8): 2245-2254, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-35192405

RESUMO

STUDY DESIGN: Prospective single-center study. OBJECTIVE: This study aimed to investigate the muscle activity of the trunk, pelvis, and lower limb, which are used to maintain a standing posture in elderly patients with spinal deformities. We also elucidated the mechanism of compensation against spinal deformity in terms of muscle activity. METHODS: Any patient scheduled to undergo surgery for adult spinal deformity was included. Surface electromyography and radiography were performed preoperatively. The following four representative alignments were defined as compensations: 1. pelvic retroversion, 2. reduction in thoracic kyphosis, 3. hyperextension of the lumbosacral junction, and 4. knee flexion. Individual muscle activity was compared with and without compensation. The patients were stratified into three groups according to the severity of spinal compensation, and differences in muscle activity were compared. RESULTS: This study included 76 patients (7 men and 69 women, average age 69.4 years). Our results revealed that pelvic retroversion and knee flexion were compensations that required trunk muscle activity. In contrast, reduction of thoracic kyphosis and hyperextension of the lumbosacral junction did not require much trunk muscle activity. There was a significant difference in the muscle activity of the pelvis and lower limbs according to the severity of the deformity. CONCLUSIONS: In terms of muscle activity, compensation for regional alignment changes in the adjacent spine is economical. However, extra-spinal compensations, such as pelvic retroversion and knee flexion, are non-economical. According to compensation recruitment, the muscle activity of the pelvis and lower limbs increased with the severity of the spinal deformity.

5.
Commun Med (Lond) ; 3(1): 78, 2023 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-37280319

RESUMO

BACKGROUND: Patient motivation is an important determinant of rehabilitation outcomes. Differences in patients' and clinicians' perceptions of motivational factors can potentially hinder patient-centered care. Therefore, we aimed to compare patients' and clinicians' perceptions of the most important factors in motivating patients for rehabilitation. METHODS: This multicenter explanatory survey research was conducted from January to March 2022. In 13 hospitals with an intensive inpatient rehabilitation ward, 479 patients with neurological or orthopedic disorders undergoing inpatient rehabilitation and 401 clinicians, including physicians, physical therapists, occupational therapists, and speech-language-hearing therapists, were purposively selected using inclusion criteria. The participants were asked to choose the most important factor motivating patients for rehabilitation from a list of potential motivational factors. RESULTS: Here we show that realization of recovery, goal setting, and practice related to the patient's experience and lifestyle are the three factors most frequently selected as most important by patients and clinicians. Only five factors are rated as most important by 5% of clinicians, whereas nine factors are selected by 5% of patients. Of these nine motivational factors, medical information (p < 0.001; phi = -0.14; 95% confidence interval = -0.20 to -0.07) and control of task difficulty (p = 0.011; phi = -0.09; 95% confidence interval = -0.16 to -0.02) are selected by a significantly higher proportion of patients than clinicians. CONCLUSIONS: These results suggest that when determining motivational strategies, rehabilitation clinicians should consider individual patient preferences in addition to using the core motivational factors supported by both parties.


Rehabilitation is the interventions needed to restore the abilities required for daily life following illness or injury. Patients and clinicians who provide these interventions may have different ideas about what encourages patients to engage in rehabilitation. It is important to understand what motivates patients and any differences in opinion between patients and clinicians. We asked patients and clinicians about the most important motivational factors. All agreed that realizing recovery is possible, setting goals or targets for the stages of recovery, and targeting interventions relevant to the patient's experience and lifestyle were the most important motivational factors. The patients also found access to medical information and being able to control the difficulty of tasks required during rehabilitation motivating. These findings could help clinicians provide rehabilitation care that is more specifically tailored to each patient's needs and preferences.

6.
Rheumatol Int ; 28(3): 245-51, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17661050

RESUMO

This study was performed to evaluate the effects of the TNF-alpha inhibitor etanercept on oxidation stress markers representing DNA damage, lipid peroxidation, and protein glycosylation. Twenty-two rheumatoid arthritis (RA) patients underwent etanercept treatment. The levels of serum total, urinary total, and urinary free pentosidine, which is an advanced glycation end-product (AGE), of urinary N(epsilon)-hexanoyl lysine (N(epsilon)-HEL), and of 8-hydroxy-deoxy guanosine (8-OHdG) were measured at baseline and at 3 and 6 months after the initial treatment with etanercept. Serum total and urinary total pentosidine levels were reduced at 6 months after the initial treatment with etanercept, and urinary free pentosidine levels were reduced at 3 and 6 months. Urinary N(epsilon)-HEL levels were also reduced at 3 and 6 months, and urinary 8-OHdG levels were reduced at 6 months. Serum total and urinary total pentosidine levels in RA patients correlated with the number of swelling joints and tender joints, and urinary total pentosidine levels correlated with the Disease Activity Score using 28 joints (DAS28). This study demonstrated that etanercept acts as a regulator against pentosidine formation, oxidative DNA damage, and lipid peroxidation in RA patients.


Assuntos
Antirreumáticos/metabolismo , Antirreumáticos/uso terapêutico , Artrite Reumatoide/tratamento farmacológico , Imunoglobulina G/metabolismo , Imunoglobulina G/uso terapêutico , Estresse Oxidativo/efeitos dos fármacos , Receptores do Fator de Necrose Tumoral/metabolismo , Receptores do Fator de Necrose Tumoral/uso terapêutico , 8-Hidroxi-2'-Desoxiguanosina , Idoso , Arginina/análogos & derivados , Arginina/sangue , Arginina/urina , Artrite Reumatoide/sangue , Artrite Reumatoide/metabolismo , Biomarcadores/sangue , Biomarcadores/metabolismo , Biomarcadores/urina , Estudos de Casos e Controles , Cromatografia Líquida de Alta Pressão , Reagentes de Ligações Cruzadas/metabolismo , Desoxiguanosina/análogos & derivados , Desoxiguanosina/urina , Ensaio de Imunoadsorção Enzimática , Etanercepte , Feminino , Produtos Finais de Glicação Avançada/urina , Humanos , Lisina/análogos & derivados , Lisina/sangue , Lisina/metabolismo , Lisina/urina , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento
7.
Clin Rheumatol ; 26(4): 505-9, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16680388

RESUMO

The aim of this study was to analyze the change of serum cytokines and pentosidine levels in patients with rheumatoid arthritis (RA) by infliximab treatment. Twenty-three patients with RA were studied for 30 weeks on the effects of infliximab treatment. Serum levels of IL-15, IL-16, IL-17, and granulocyte-macrophage colony-stimulating factor (GM-CSF) were measured with ELISA methods and pentosidine levels were determined using high-performance liquid chromatography, both at baseline and at 14 and 30 weeks after the initial treatment with infliximab. In addition, the patients also underwent physical and routine blood examinations. The higher levels of serum IL-15 in RA patients before treatment with infliximab significantly decreased at 14 and 30 weeks after the initial treatment with infliximab, but serum IL-16, IL-17, GM-CSF, and pentosidine levels did not decrease. The serum IL-17 and GM-CSF levels remained to be a limited detectable level at the pre- and posttreatment with infliximab. Infliximab treatment significantly lowered the serum levels of IL-15 in patients with RA. IL-15 is one of the crucial cytokines affected by infliximab.


Assuntos
Anticorpos Monoclonais/farmacologia , Artrite Reumatoide/tratamento farmacológico , Fatores Imunológicos/farmacologia , Interleucina-15/metabolismo , Arginina/análogos & derivados , Arginina/sangue , Feminino , Humanos , Infliximab , Interleucina-15/sangue , Interleucina-16/sangue , Interleucina-17/sangue , Lisina/análogos & derivados , Lisina/sangue , Masculino , Pessoa de Meia-Idade , Fator de Necrose Tumoral alfa/antagonistas & inibidores
8.
Rheumatol Int ; 28(2): 137-43, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17619881

RESUMO

The purpose of this study was to analyze the effect of the soluble TNF-alpha receptor etanercept on the serum levels of IL-16, IL-17, IL-23, and macrophage inflammatory protein-3alpha (MIP-3alpha) in rheumatoid arthritis (RA) patients. Twenty-two patients with RA were administered etanercept once or twice a week for more than 6 months, and we evaluated clinical and laboratory parameters and serum levels of IL-16, IL-17, IL-23, and MIP-3alpha at the baseline and at 3 and 6 months. Additionally, the production of IL-23 and MIP-3alpha of cultured synovial cells stimulated with TNF-alpha from RA patients was determined by ELISA. We also used ELISA kits to determine synovial fluid (SF) levels of IL-17, IL-23, and MIP-3alpha in patients with RA, osteoarthritis (OA), pseudogouty arthritis (PGA), and gouty arthritis (GA). A significant decrease in serum levels of IL-23 and MIP-3alpha was observed at 3 and 6 months after initial treatment of etanercept. TNF-alpha induced MIP-3alpha but not IL-23 production in cultured synovial cells from RA patients. SF levels of IL-17, IL-23, and MIP-3alpha in RA patients showed significantly higher levels than those of OA, PGA, and GA patients. This study demonstrated that the reduction of IL-23 and MIP-3alpha production in RA patients was a newly determined function of etanercept.


Assuntos
Antirreumáticos/farmacologia , Artrite Reumatoide/sangue , Quimiocina CCL20/sangue , Imunoglobulina G/farmacologia , Interleucina-23/sangue , Idoso , Antirreumáticos/administração & dosagem , Artrite Gotosa/sangue , Artrite Gotosa/imunologia , Artrite Reumatoide/imunologia , Biomarcadores/sangue , Sedimentação Sanguínea , Proteína C-Reativa/análise , Estudos de Casos e Controles , Células Cultivadas , Etanercepte , Feminino , Fibroblastos/metabolismo , Humanos , Imunoglobulina G/administração & dosagem , Injeções Subcutâneas , Interleucina-16/sangue , Interleucina-17/sangue , Masculino , Pessoa de Meia-Idade , Osteoartrite/sangue , Osteoartrite/imunologia , Receptores do Fator de Necrose Tumoral/administração & dosagem , Líquido Sinovial/química , Líquido Sinovial/efeitos dos fármacos , Membrana Sinovial/química , Membrana Sinovial/citologia , Membrana Sinovial/efeitos dos fármacos
9.
Mod Rheumatol ; 17(5): 398-402, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17929132

RESUMO

This study was performed to investigate whether methotrexate (MTX) affects the levels of oxidative stress markers, including pentosidine one of the glycation end products (AGEs) or 8-hydroxy-deoxy guanosine (8-OHdG). These stress markers represent DNA damage; 19 rheumatoid arthritis (RA) patients underwent MTX treatment. The levels of serum total, urinary total, urinary-free pentosidine and also urinary 8-OHdG, as well as clinical parameters, including disease activity scores for 28 joints (DAS28) were measured at baseline and at 3 and 6 months after the initial treatment with MTX. After the initial treatment with MTX, serum total and urinary total pentosidine levels were reduced at 6 months, and urinary-free pentosidine levels were reduced at 3 and 6 months. Urinary 8-OHdG levels also were significantly reduced at 6 months after the initial treatment with MTX. This study demonstrated that MTX plays a role as a regulator against pentosidine formation and oxidative DNA damage in RA patients.


Assuntos
Arginina/análogos & derivados , Artrite Reumatoide/tratamento farmacológico , Artrite Reumatoide/metabolismo , Desoxiguanosina/análogos & derivados , Lisina/análogos & derivados , Metotrexato/farmacologia , 8-Hidroxi-2'-Desoxiguanosina , Antirreumáticos/farmacologia , Arginina/biossíntese , Arginina/sangue , Creatinina/urina , Dano ao DNA , Desoxiguanosina/biossíntese , Desoxiguanosina/urina , Humanos , Articulações/patologia , Lisina/biossíntese , Lisina/sangue , Estresse Oxidativo , Oxigênio/metabolismo , Espécies Reativas de Oxigênio , Fatores de Tempo , Resultado do Tratamento
10.
Arthritis Rheum ; 50(3): 968-75, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15022341

RESUMO

OBJECTIVE: To evaluate the therapeutic effect of the administration of plasmid encoding interleukin-4 (IL-4) via gene-gun delivery and via intradermal injection on collagen-induced arthritis (CIA). METHODS: IL-4 plasmid was administered by gene-gun delivery and intradermal injection to DBA/1 mice immunized with type II collagen (CII). The therapeutic effect on the development of CIA was evaluated clinically with a visual scoring method for arthritis and serologically by enzyme-linked immunosorbent assays and polymerase chain reaction. RESULTS: Treatment with IL-4-expressing plasmid significantly reduced the incidence and severity of CIA, including a reduction in the anti-CII antibody level. In particular, gene-gun delivery had a higher immunosuppressive effect on CIA compared with intradermal injection. As shown by in vitro stimulation assay, the spleen cells from mice immunized with CII and treated with IL-4 plasmid via gene gun exhibited higher Th2 cytokine responses compared with cells treated with control plasmid after in vitro stimulation with CII. CONCLUSION: The results of this study suggest that treatment with IL-4 plasmid may constitute a new clinical use of cytokine gene therapy for rheumatoid arthritis.


Assuntos
Artrite Experimental/fisiopatologia , Artrite Experimental/terapia , Terapia Genética , Interleucina-4/genética , Plasmídeos/genética , Animais , Artrite Experimental/prevenção & controle , Biolística , Colágeno Tipo II/imunologia , Citocinas/metabolismo , Imunização , Imunossupressores/administração & dosagem , Técnicas In Vitro , Injeções Intradérmicas , Interleucina-4/administração & dosagem , Interleucina-4/metabolismo , Linfonodos/citologia , Linfonodos/metabolismo , Camundongos , Camundongos Endogâmicos DBA , Índice de Gravidade de Doença , Baço/citologia , Baço/efeitos dos fármacos , Baço/imunologia , Baço/metabolismo , Células Th2/metabolismo
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