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1.
Zhonghua Jie He He Hu Xi Za Zhi ; 45(6): 602-608, 2022 Jun 12.
Artículo en Zh | MEDLINE | ID: mdl-35658385

RESUMEN

Pulmonary aspergilloma (PA) is usually secondary to pulmonary cavities. The main purpose of PA treatment is to prevent life-threatening hemoptysis. Many patients cannot tolerate surgical resection, which is considered the preferred treatment. Oral or intravenous antifungal therapy is less effective because PA usually does not invade the blood vessels of the pulmonary cavity. In this case, arterial embolization, local injection with drugs, and radiation therapy can be considered. This article will summarized various non-surgical local treatments for PA (hemoptysis) to refer clinical decision-making.


Asunto(s)
Embolización Terapéutica , Aspergilosis Pulmonar , Antifúngicos/uso terapéutico , Embolización Terapéutica/efectos adversos , Hemoptisis/etiología , Humanos , Pulmón/cirugía , Aspergilosis Pulmonar/terapia , Resultado del Tratamiento
2.
Nano Lett ; 14(7): 4036-43, 2014 Jul 09.
Artículo en Inglés | MEDLINE | ID: mdl-24956434

RESUMEN

Tuning the metal insulator transition (MIT) behavior of VO2 film through the interfacial strain is effective for practical applications. However, the mechanism for strain-modulated MIT is still under debate. Here we directly record the strain dynamics of ultrathin VO2 film on TiO2 substrate and reveal the intrinsic modulation process by means of synchrotron radiation and first-principles calculations. It is observed that the MIT process of the obtained VO2 films can be modulated continuously via the interfacial strain. The relationship between the phase transition temperature and the strain evolution is established from the initial film growth. From the interfacial strain dynamics and theoretical calculations, we claim that the electronic orbital occupancy is strongly affected by the interfacial strain, which changes also the electron-electron correlation and controls the phase transition temperature. These findings open the possibility of an active tuning of phase transition for the thin VO2 film through the interfacial lattice engineering.

3.
Zhonghua Xue Ye Xue Za Zhi ; 41(11): 890-895, 2020 Nov 14.
Artículo en Zh | MEDLINE | ID: mdl-33333690

RESUMEN

Objective: To evaluate the safety and efficacy of eltrombopag combined with immunosuppressive therapy in patients with aplastic anemia (AA) in China. Methods: We investigated and analyzed the clinical data of AA patients from 14 hematological treatment centers who were treated with oral eltrombopag for at least 3 mon. Results: We enrolled 56 AA patients, including 19 treatment-naïve patients and 37 IST-refractory patients. The median administration period for eltrombopag was 7 (3-31) months, and the median maximum stable dosage was 75 mg/d (50-150 mg/d) . The 3-month hematological response (HR) rate was 60%, and the complete response (CR) rate was 30% in 10 SAA patients who were treated with first-line eltrombopag and standard IST (ATG+CsA) . Eight of 9 eltrombopag and CsA ± androgen first-line treated SAA patients responded (8/9, 89%) and 4 (44%) gave CR. The overall HR and CR rates were 79% and 52.6%, respectively, among these 19 patients by the end of the follow-up period. Of the 19 AA patients who were refractory to CsA ± androgen, 11 achieved HR (57.9%) at 3 mon, and the best HR rate was 44% in standard IST (ATG+CsA) refractory 18 patients after eltrombopag treatment. Fifty-one percent of the patients experienced mild or moderate adverse events, and gastrointestinal discomfort was the most common adverse effect reported by the study subjects. Conclusion: Adding Eltrombopag in first-line IST can accelerate the acquisition and improve the quality of hematological responses in AA patients. AA with relatively more residual hematopoietic cells may be well treated with eltrombopag and non-ATG IST. Eltrombopag can be used as salvage therapy for CsA±androgen refractory patients. Eltrombopag was generally safe and well tolerated by AA patients in China.


Asunto(s)
Anemia Aplásica , Benzoatos/uso terapéutico , Hidrazinas/uso terapéutico , Pirazoles/uso terapéutico , Anemia Aplásica/tratamiento farmacológico , Suero Antilinfocítico , China , Ciclosporina , Humanos , Inmunosupresores , Encuestas y Cuestionarios , Resultado del Tratamiento
4.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi ; 54(12): 894-901, 2019 Dec 07.
Artículo en Zh | MEDLINE | ID: mdl-31887814

RESUMEN

Objective: By use of Meta analysis to compare efficacy, safety and compliance of subcutaneous immunotherapy (SCIT) and sublingual immunotherapy (SLIT) on allergic rhinitis (AR). Methods: Cochrane Library, Pubmed, Embase, CNKI Database, Wan Fang and Chinese Sci-tech Journal Database (from established time to May of 2018) were searched for trials about the AR treated by SCIT and SLIT. The relevant literatures were screened, and the randomized controlled studies were chosen. Nasal symptom scores, visual analogue scale (VAS) scores, adverse reactions and compliance were used as the outcome indicators, and the methodological quality of the literatures was evaluated strictly. The extracted data were analyzed by RevMan 5.3 and Stata 14 software. Results: A total of 20 randomized controlled studies were included, the overall quality of which was relatively high. No publication bias was found. There was no significant difference in nasal symptom scores, VAS scores and compliance between SCIT and SLIT (SMD value was 0.03, 0.14, respectively, RR=1.12; 95%CI value was -0.17-0.23, -0.03-0.31, 0.92-1.35, respectively, all P>0.05); SLIT group resulted in lower overall incidence of adverse reactions than that of SCIT group (RR=1.79, 95%CI: 1.42-2.26, P<0.05). Conclusion: Both SCIT and SLIT have similar eppecacy and compliance for treatment of AR, while adverse reactions are more frequently observed in SCIT.


Asunto(s)
Cooperación del Paciente , Rinitis Alérgica , Inmunoterapia Sublingual , Administración Sublingual , Alérgenos , Desensibilización Inmunológica , Humanos , Inyecciones Subcutáneas , Proyectos de Investigación , Rinitis Alérgica/inmunología , Rinitis Alérgica/terapia , Inmunoterapia Sublingual/efectos adversos , Inmunoterapia Sublingual/métodos
5.
Int J Artif Organs ; 31(10): 882-90, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19009506

RESUMEN

BACKGROUND: Continuous renal replacement therapy (CRRT) showed promising results in the management of critically ill patients with systemic inflammatory response syndrome (SIRS)/sepsis. However, the underlying mechanism is still not very clear. A change of immune homeostasis in critically ill patients during CRRT was observed only to a smaller degree. OBJECTIVE: The purpose of this study was to test the hypothesis that high-volume continuous venovenous hemofiltration (HV-CVVH) treatment could improve monocyte function and restore immune homeostasis in patients with severe acute pancreatitis (SAP). METHODS: This was a prospective clinical trial in the surgical intensive care unit of a teaching hospital. Subjects were 16 patients with severe acute pancreatitis: sepsis group (n=7): positive culture result and in the late phase of disease (from onset of SAP to receiving CVVH therapy: more than 3 days); and nonseptic group (n=9): negative culture result and early phase of disease (less than 3 days). Patients received 72 hours of HV-CVVH. We measured the change in mean arterial pressure, APACHE II score, monocyte functions (including antigen-presenting and cytokine production ability), and plasma cytokines. RESULTS: Mean arterial pressure were stable accompanied with APACHE II score improvements. HLA-DR expression on monocytes (antigen-presenting ability) were markedly decreased (p<0.0001) in all patients. Lipopolysaccharide (LPS)-induced TNF-alpha, interleukin-6 (IL-6), and IL-10 production from patients' monocytes markedly decreased in septic patients, but significantly increased in nonseptic patients. During HV-CVVH treatment, HLA-DR expression was markedly increased in nonseptic patients in 24 hours (p<0.05), and in septic patients in 72 hours (p<0.05). LPS-induced cytokine production was decreased in nonseptic patients, but not significantly changed in septic patients. The change of plasma cytokines showed the same trend. CONCLUSIONS: In patients with SAP, HV-CVVH was associated with improved hemodynamics. HV-CVVH restores monocytes functions, especially in patients in the early phase of the disease and without sepsis. These findings suggest a potential role for HV-CVVH in the treatment of SAP.


Asunto(s)
Hemofiltración/métodos , Monocitos/fisiología , Pancreatitis/terapia , Terapia de Reemplazo Renal , Enfermedad Aguda , Adulto , Anciano de 80 o más Años , Femenino , Antígenos HLA-DR/sangre , Homeostasis , Humanos , Sistema Inmunológico/fisiología , Interleucina-10/sangre , Interleucina-6/sangre , Masculino , Persona de Mediana Edad , Pancreatitis/sangre , Pancreatitis/inmunología , Estudios Prospectivos , Factor de Necrosis Tumoral alfa/sangre
6.
Nat Commun ; 9(1): 2965, 2018 07 27.
Artículo en Inglés | MEDLINE | ID: mdl-30054461

RESUMEN

Creating oxide interfaces with precise chemical specificity at the atomic layer level is desired for the engineering of quantum phases and electronic applications, but highly challenging, owing partially to the lack of in situ tools to monitor the chemical composition and completeness of the surface layer during growth. Here we report the in situ observation of atomic layer-by-layer inner potential variations by analysing the Kikuchi lines during epitaxial growth of strontium titanate, providing a powerful real-time technique to monitor and control the chemical composition during growth. A model combining the effects of mean inner potential and step edge density (roughness) reveals the underlying mechanism of the complex and previously not well-understood reflection high-energy electron diffraction oscillations observed in the shuttered growth of oxide films. General rules are proposed to guide the synthesis of atomically and chemically sharp oxide interfaces, opening up vast opportunities for the exploration of intriguing quantum phenomena at oxide interfaces.

7.
Int J Artif Organs ; 30(5): 393-400, 2007 May.
Artículo en Inglés | MEDLINE | ID: mdl-17551902

RESUMEN

OBJECTIVES: Endothelium dysfunction is one of the critical pathophysiologic disorders in patients with severe acute pancreatitis (SAP). To investigate the effect of continuous blood purification (CBP) on endothelial function, we conducted a prospective study of 20 patients with SAP, 9 of whom had evidence of sepsis. METHODS: All patients underwent CVVH for 72 h. Soluble E-selectin (sE-selectin), soluble thrombomodulin, permeability of the endothelial monolayer, and endothelial intracellular calcium ([Ca2+]i ) levels were used as the markers for the assessment of endothelial function and the effect of CBP therapy in patients with SAP. Blood samples were taken from the patients at 0, 2, 12, 24, 48, and 72 h during CVVH therapy. sE-selectin and thrombomoduiln were measured by ELISA. The endothelial permeability and activation were evaluated using cultured endothelial monolayer and intracellular Ca2+ concentration. RESULTS: The results showed that during CVVH treatment, the hemodynamics and mean arterial pressure (MAP) were stable. The Acute Physiology and Chronic Health Evaluation (APACHE) II score was improved significantly after CVVH. Endothelial dysfunction was evident in patients with SAP as compared to normal controls. Patients with SAP had increased levels of sE-selectin, endothelial permeability and intracellular [Ca2+]i , which was higher in patients with sepsis than in those without sepsis. The level of thrombomodulin showed a tendency to increase; however, these changes were not significant between SAP patients and controls. After CBP treatment, sE-selectin levels substantially decreased in all patients. CBP treatment also significantly diminished the endothelial permeability and decreased the intracellular [Ca2+] concentration. CONCLUSIONS: These data demonstrate that endothelial dysfunction is present in patients with SAP and the degree of endothelial damage may be correlated with the disease severity. CBP therapy can not only improve the general conditions, as measured by the APACHE II score, but also effectively improve endothelial dysfunction.


Asunto(s)
Endotelio Vascular/fisiopatología , Hemofiltración , Pancreatitis/fisiopatología , Enfermedad Aguda , Adulto , Anciano , Anciano de 80 o más Años , Calcio/metabolismo , Células Cultivadas , Selectina E/sangre , Endotelio Vascular/metabolismo , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pancreatitis/terapia , Permeabilidad , Trombomodulina/sangre
8.
Int J Artif Organs ; 30(2): 176-80, 2007 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-17377913

RESUMEN

OBJECTIVES: To evaluate the treatment effect of continuous veno-venous hemofiltration (CVVH) in patients with acute severe hyponatremia. METHODS: Eleven patients with severe acute hyponatremia, including 6 males and 5 females, aged 25-61 years (mean age 48.36), were treated with CVVH. Hyponatremia occurred 38-48 hours prior to the initiation of CVVH. RESULTS: All patients tolerated CVVH well, with an average treatment duration of 57.19 (45.6-86) hours. During CVVH, the serum sodium concentration increased significantly from 100.9+/-3.99 mmol/L at initiation of CVVH to 140.3+/-1.6 mmol/L after 48 hours of treatment (P<0.01). The serum osmolarity increased concurrently, from 216.7+/-7.4 mOsm/kgH2O to 295.0+/-4.2 mOsm/kgH2O (P<0.01). The Glasgow scores and APACHE II scores in these patients improved significantly during treatment. CONCLUSIONS: CVVH is a safe and effective option for the treatment of patients with severe acute hyponatremia due to its slow and continuous nature.


Asunto(s)
Hemofiltración , Hiponatremia/terapia , Enfermedad Aguda , Adulto , Femenino , Humanos , Hiponatremia/sangre , Hiponatremia/etiología , Masculino , Persona de Mediana Edad , Concentración Osmolar , Sodio/sangre
9.
Transplant Proc ; 38(10): 3459-63, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17175303

RESUMEN

The aim of this study was to investigate the efficacy of immunoadsorption (IA) in combination with tacrolimus (TAC; 0.14 to 0.16 mg/kg/d) and mycophenolate mofetil (MMF; 1.5 to 2.0 g/d) rescue therapy for C4d-positive acute humoral rejection in nine cadaveric renal allograft recipients. Initial Panel reactive antibody (PRA-I and PRA-II levels were as high as 28.8% +/- 16.2% and 15.3% +/- 8.9%, IA therapy significantly decreased PRA-I and PRA-II levels to 5.9% +/- 2.9% and 2.2% +/- 0.6%, respectively. Total serum immunoglobulin levels were markedly decreased. Repeated allograft renal biopsy in nine patients revealed remission of acute humoral rejection (AHR), and the deposition of C4d disappeared and reduced. With a mean follow-up of 29.4 +/- 5.4 months, patient and allograft survivals were 100%, and renal function remained stable with a mean serum creatinine of 1.1 +/- 0.3 mg/dL. Our findings suggested that a therapeutic approach combining IA and TAC and MMF rescue improved the outcomes of AHR.


Asunto(s)
Formación de Anticuerpos , Complemento C4b/análisis , Rechazo de Injerto/terapia , Técnicas de Inmunoadsorción , Trasplante de Riñón/inmunología , Ácido Micofenólico/análogos & derivados , Fragmentos de Péptidos/análisis , Tacrolimus/uso terapéutico , Enfermedad Aguda , Adulto , Femenino , Rechazo de Injerto/tratamiento farmacológico , Rechazo de Injerto/inmunología , Antígenos HLA/análisis , Humanos , Trasplante de Riñón/patología , Masculino , Persona de Mediana Edad , Ácido Micofenólico/uso terapéutico , Reoperación/estadística & datos numéricos , Trasplante Homólogo
10.
Transplant Proc ; 36(7): 2101-3, 2004 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-15518760

RESUMEN

OBJECTIVE: We investigated the efficacy of immunoadsorption (IA) in combination with tacrolimus (FK506) and mycophenolate mofetil (MMF) rescue therapy for C4d-positive acute humoral rejection (AHR) of renal transplants. METHODS: Six of 185 cadaveric renal allograft recipients developed AHR at a mean of 4.8 +/- 0.8 days after the operation. C4d deposits were observed in peritubular capillaries (PTC) with accumulation of granulocytes. IA with staphylococcal protein A and FK506-MMF combination therapy were administered. RESULTS: After treatment with IA for 6.3 +/- 1.03 sessions combined with FK506 (0.14 to 0.16 mg.kg(-1).d(-1)) and MMF (1.5 g/d) therapy, renal function recovered in all the patients. The mean duration of treatment to a serum creatinine decrease was 14 +/- 2.9 days. The pre-IA panel reactive antibody reactivity (PRA) peaked at 50.2% +/- 6.1%, and was significantly reduced to 8.3% +/- 2.9% after IA. In four of six patients repeat allograft biopsy revealed a remission of AHR. With a mean follow-up of 18.8 +/- 5.46 months, patient and allograft survival are 100% and renal function remains stable with a mean serum creatinine of 1.2 +/- 0.22 mg/dL. CONCLUSION: The optimal treatment for alloantibody-mediated AHR remains uncertain. Our findings suggest that a therapeutic approach combining IA and FK506-MMF rescue improves the outcome of AHR.


Asunto(s)
Antígenos CD/sangre , Antígenos CD4/sangre , Rechazo de Injerto/inmunología , Técnicas de Inmunoadsorción , Trasplante de Riñón/inmunología , Ácido Micofenólico/análogos & derivados , Ácido Micofenólico/uso terapéutico , Tacrolimus/uso terapéutico , Enfermedad Aguda , Adulto , Formación de Anticuerpos , Antígenos CD/inmunología , Antígenos CD4/inmunología , Femenino , Rechazo de Injerto/tratamiento farmacológico , Rechazo de Injerto/terapia , Humanos , Terapia de Inmunosupresión/métodos , Inmunosupresores/uso terapéutico , Isoanticuerpos/sangre , Isoanticuerpos/inmunología , Trasplante de Riñón/patología , Masculino , Persona de Mediana Edad
11.
Chin Med J (Engl) ; 102(3): 159-64, 1989 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-2503301

RESUMEN

The morphologic classification and clinical spectrum of 1,001 cases of primary glomerulonephritis (GN) in Jinling Hospital during 1980-1988 were analysed. It was found that the incidence of mesangial type lesion including mesangial proliferative GN, IgA nephropathy and IgM nephropathy ranks first (21.5%, 32.1% and 10.1% respectively), which is not only the commonest cause of patients clinically manifesting nephrotic syndrome and gross hematuria but also the predominant type of nephritis causing uremia and hypertension.


Asunto(s)
Glomerulonefritis/patología , Adolescente , Adulto , Biopsia , Niño , Femenino , Glomerulonefritis/clasificación , Glomerulonefritis por IGA/patología , Glomerulonefritis Membranoproliferativa/patología , Glomerulonefritis Membranosa/patología , Antígenos de Superficie de la Hepatitis B/análisis , Humanos , Masculino , Persona de Mediana Edad
12.
Zhonghua Nei Ke Za Zhi ; 32(2): 100-2, 1993 Feb.
Artículo en Zh | MEDLINE | ID: mdl-8404323

RESUMEN

Recombinant human erythropoietin (r-HuEPO) was administered in 68 dialyzed patients (32 on acetate hemodialysis, 24 bicarbonate hemodialysis and 12 on hemo-filtration). The mean initial Hb 52.7 +/- 8.0g/L, Ht 19.4 +/- 2.2%, serum ferritin > 100ng/L. Each patients received r-HuEPO intravenously, at the dose of 300U/Kg/w for 6.2 +/- 4.3 months. Target range: Hb 100-120g/L, Ht 30-35%. After r-HuEPO treatment, blood transfusion was not needed for any of the patients, anemia was ameliorated with increase of Hb and Ht levels. It was found that the minimum effective dose of the r-HrEPO was 150-300U/Kg/w. We conclude that r-HuEPO is effective as treatment for the anemia of dialyzed patients. However, hypertension, clotted dialyzers and dialysis access thromboses were been developed in some patients after correction of anemia. There is now a general consensus that these side effects may be minimized if r-HuEPO is initially given in small doses with increments to avoid a too rapid correction of the anemia.


Asunto(s)
Anemia/terapia , Eritropoyetina/uso terapéutico , Diálisis Renal/efectos adversos , Adulto , Anemia/sangre , Anemia/etiología , Eritropoyetina/efectos adversos , Femenino , Hematócrito , Hemoglobinas/metabolismo , Humanos , Hipertensión/inducido químicamente , Masculino , Persona de Mediana Edad , Insuficiencia Renal/terapia
13.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 13(2): 71-3, 67, 1993 Feb.
Artículo en Zh | MEDLINE | ID: mdl-8334339

RESUMEN

A clinical trial, to evaluate the effects of Baoshen Pill (Rheum palmatum extract, RPE) on hemodialytic patients was conducted. 42 cases with terminal stage of renal failure (Scr < 10 ml/min) on HD were divided at random into RPE treated group and control group. The results showed there were no statistically significant differences between two groups for Scr or BUN. Serum levels of TC, LDL-c, apo B and apo B/apo A1 dropped down and HDL-c, apo A1, albumin, pro-albumin and fibrinectin increased during the follow-up period (P < 0.05) in the treated patients. It is considered that the mechanisms of RPE in preventing chronic renal failure were not the action of whole body. Improving serum levels of albumin, lipoprotein, apolipoproteins might play important role in treatment.


Asunto(s)
Medicamentos Herbarios Chinos/uso terapéutico , Fallo Renal Crónico/terapia , Plantas Medicinales , Rheum , Adulto , Apolipoproteínas/metabolismo , Femenino , Humanos , Fallo Renal Crónico/sangre , Fallo Renal Crónico/etiología , Lipoproteínas/sangre , Masculino , Persona de Mediana Edad , Nefritis/complicaciones , Diálisis Renal , Albúmina Sérica/metabolismo
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