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1.
J Thorac Dis ; 16(2): 893-900, 2024 Feb 29.
Artigo em Inglês | MEDLINE | ID: mdl-38505053

RESUMO

Background: Currently, it is unknown whether polyglycolic acid (PGA) felt staplers can reduce the occurrence of intraoperative air leaks. We investigated whether staplers with bioabsorbable PGA felt reduced intraoperative air leakage compared to the conventional stapler in patients undergoing lung resection. Methods: From 2013 to 2021, 211 patients diagnosed with lung cancer or pulmonary metastasis underwent lung resection using only PGA felt (n=88) or conventional (n=123) staplers at Tokyo Rosai Hospital. One-to-one propensity score matching was used to compare intraoperative air leak rates, operation time, and intraoperative bleeding between the two groups. Results: The PGA felt group required more staples than the conventional stapler group. The forced expiratory volume in one second percentage of predicted in the PGA felt stapler group was lower than that in the conventional stapler group. In the PGA felt stapler group, 56.8% of patients had undergone anatomic lung resection, whereas 29.3% of patients in the conventional stapler group had undergone wedge resection. In a propensity-matched analysis of 67 pairs, the occurrence of intraoperative air leaks was significantly lower in the PGA felt stapler group than in the conventional stapler group (16.4% vs. 56.7%, P<0.001). The operation time was significantly shorter and intraoperative bleeding was significantly lower in the PGA felt stapler group than in the conventional stapler group (P=0.001 and P=0.016, respectively). Conclusions: Pulmonary resection using staplers with a PGA felt could reduce the occurrence of intraoperative air leaks among patients undergoing lung resection.

2.
Respir Med Case Rep ; 43: 101846, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37077237

RESUMO

An 87-year-old man presented with dyspnea. Computed tomography revealed progressive subpleural consolidation in the apex, reticular shadows in the lower lobes, and bilateral ground glass opacifications. He died of respiratory failure on day 3. The post-mortem examination showed exudative stage diffuse alveolar damage and pulmonary edema. Intraalveolar collagenous fibrosis and subpleural elastosis were observed in the upper lobes, accompanied by interlobular septal and pleural thickening and lung architecture remodeling in the lower lobes. He was diagnosed with acute exacerbation of pleuroparenchymal fibroelastosis with lower lobe usual interstitial pneumonia, which can be fatal.

3.
Gan To Kagaku Ryoho ; 45(Suppl 1): 107-109, 2018 Mar.
Artigo em Japonês | MEDLINE | ID: mdl-29650891

RESUMO

We conducted a clinical study involving cases of central venous(CV)port-related infection in Tokyo Rosai Hospital. Fourteen patients with suspected CV port-related infection at Tokyo Rosai Hospital between April 2015 and January 2017 were observed. Identical bacterial types were detected from 2 sets of blood cultures and cultures from the catheter tip, and a definitive diagnosis was made. Data on patient background, causative bacteria, quick sequentialorgan failure assessment (qSOFA)score, CV port placement period, presence or absence of local inflammatory findings, and prognosis were analysed. The causative bacteria were coagulase-negative Staphylococcus(CNS)in 7 cases(50%), Staphylococcus aureus in 3(21%), and Candida in 4(29%). Most CNS-infected cases(71%)exhibited a qSOFA score of 1 or less at the examination time, which indicated that even if bacteremia occurred in CNS cases, organopathy might not occur easily. Local inflammatory findings were found in only 3 CNS cases. Cases without local inflammatory findings showed methicillin-resistant Staphylococcus aureus(MRSA)(18%)or Candida(36%)at high proportions, indicating that treatments might be difficult.


Assuntos
Bacteriemia , Cateterismo Venoso Central , Infecção Hospitalar , Staphylococcus aureus Resistente à Meticilina , Infecções Estafilocócicas , Bacteriemia/etiologia , Cateterismo Venoso Central/efeitos adversos , Humanos , Infecções Estafilocócicas/etiologia , Tóquio
4.
Intern Med ; 53(16): 1825-7, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25130119

RESUMO

We herein describe the case of a 74-year-old man who experienced pulmonary consolidation and chest pain following administration of dabigatran, a novel oral anticoagulant. The consolidation settled spontaneously in another lung area, a condition sometimes referred to as "wandering pneumonia." Although we did not find specific pathological evidence of interstitial lung disease on transbronchial lung biopsy, a lung opacity spontaneously disappeared following discontinuance of dabigatran, and there was no recurrence. There are no other reports of dabigatran-induced lung injury, except alveolar hemorrhage and eosinophilic pneumonia. We should consider that any novel drug could cause various types of pulmonary injuries.


Assuntos
Antitrombinas/efeitos adversos , Benzimidazóis/efeitos adversos , Pneumonia/induzido quimicamente , Pneumonia/diagnóstico por imagem , beta-Alanina/análogos & derivados , Idoso , Antitrombinas/administração & dosagem , Benzimidazóis/administração & dosagem , Dabigatrana , Humanos , Pulmão/diagnóstico por imagem , Masculino , Radiografia , Remissão Espontânea , beta-Alanina/administração & dosagem , beta-Alanina/efeitos adversos
5.
Antiviral Res ; 77(2): 150-2, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18055026

RESUMO

The antiviral effects of chloroquine (CQ) on human coronavirus 229E (HCoV-229E) infection of human fetal lung cell line, L132 are reported. CQ significantly decreased the viral replication at concentrations lower than in clinical usage. We demonstrated that CQ affects the activation of p38 mitogen-activated protein kinase (MAPK) and extracellular signal-regulated kinase (ERK). Furthermore, p38 MAPK inhibitor, SB203580, inhibits CPE induced by HCoV-229E infection and viral replication. Our findings suggest that CQ affects the activation of MAPKs, involved in the replication of HCoV-229E.


Assuntos
Antivirais/farmacologia , Cloroquina/farmacologia , Coronavirus Humano 229E/efeitos dos fármacos , Células Epiteliais/virologia , MAP Quinases Reguladas por Sinal Extracelular/antagonistas & inibidores , Pulmão/virologia , Proteínas Quinases p38 Ativadas por Mitógeno/antagonistas & inibidores , Linhagem Celular , Efeito Citopatogênico Viral/efeitos dos fármacos , Humanos , Imidazóis/farmacologia , Pulmão/citologia , Piridinas/farmacologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Replicação Viral/efeitos dos fármacos
7.
Chest ; 131(5): 1387-92, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17494788

RESUMO

BACKGROUND: Obesity, hypertension, dyslipidemia, and hyperglycemia are prevalent in obstructive sleep apnea syndrome (OSAS). Metabolic syndrome, however, is defined by visceral fat obesity plus at least two of these factors. However, whether OSAS contributes to the development of metabolic syndrome has not been defined. We investigated whether the components of metabolic syndrome were associated with OSAS in nonobese patients. METHODS: We investigated the occurrence of hypertension, dyslipidemia, and hyperglycemia in 42 men with OSAS and 52 men without OSAS matched for age, body mass index (BMI), and visceral fat accumulation. RESULTS: Although serum levels of triglycerides, high-density lipoprotein cholesterol, and diastolic BP did not differ significantly between the two groups, fasting blood glucose (111 +/- 6 mg/dL vs 93 +/- 3 mg/dL) [mean +/- SE] and the percentage of hypertensive patients (45% vs 15%) were significantly higher in the group with OSAS. In addition, a significantly higher percentage of patients with OSAS (19% vs 4%) had at least two of the following: hypertension, hyperglycemia, and dyslipidemia. Logistic regression analysis showed that the apnea-hypopnea index value was the predictor of number of metabolic syndrome parameters such as hypertension, hyperglycemia, and dyslipidemia, while BMI and lowest arterial oxygen saturation during sleep did not. CONCLUSION: Independent of visceral fat obesity, OSAS was associated with hypertension, dyslipidemia, and hyperglycemia. It is possible that OSAS may predispose even nonobese patients to the development of metabolic syndrome.


Assuntos
Síndrome Metabólica/complicações , Síndrome Metabólica/fisiopatologia , Apneia Obstrutiva do Sono/complicações , Apneia Obstrutiva do Sono/fisiopatologia , Pressão Sanguínea/fisiologia , HDL-Colesterol/sangue , Dislipidemias/complicações , Dislipidemias/fisiopatologia , Humanos , Hiperglicemia/complicações , Hiperglicemia/fisiopatologia , Hipertensão/complicações , Hipertensão/fisiopatologia , Modelos Logísticos , Masculino , Análise por Pareamento , Pessoa de Meia-Idade , Obesidade/complicações , Obesidade/fisiopatologia , Fatores de Risco , Triglicerídeos/sangue
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