Anales De Medicina Interna最新文献

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[Pneumonia above 80 years, admitted to the hospital]. [80岁以上肺炎入院]。
Anales De Medicina Interna Pub Date : 2008-03-01 DOI: 10.4321/s0212-71992008000300004
G Zubillaga Garmendia, E Sánchez Haya, J Benavente Claveras, E Ceciaga Elexpuru, I Zamarreño Gómez, E Zubillaga Azpíroz, C Sarasqueta Eizaguirre
{"title":"[Pneumonia above 80 years, admitted to the hospital].","authors":"G Zubillaga Garmendia,&nbsp;E Sánchez Haya,&nbsp;J Benavente Claveras,&nbsp;E Ceciaga Elexpuru,&nbsp;I Zamarreño Gómez,&nbsp;E Zubillaga Azpíroz,&nbsp;C Sarasqueta Eizaguirre","doi":"10.4321/s0212-71992008000300004","DOIUrl":"https://doi.org/10.4321/s0212-71992008000300004","url":null,"abstract":"<p><strong>Objective: </strong>To analyze and compare differences in patients older than 80 years with Community acquired Pneumonia admitted in Internal Medicine or Pneumology of a General Hospital from the Emergency Room.</p><p><strong>Material and methods: </strong>Retrospective study of all the 277 patients above 80 years admitted into the Hospital in 2005 with the main diagnosis of Pneumonia.</p><p><strong>Results: </strong>84% community-acquired, 16% from Institutions. Mean age: 85.8 y (48% men, 52% women). 19% FINE-3, 49% FINE-4, 32% FINE-5. Known etiology: 25% (Pneumococcal 19%, H. Influenzae and other Gram (-) 6%. 75% treated by Internists, 22% treated by Pneumologists. Standard Guidelines followed up by 30,5% a variant 60% (Equal by Internists or Pneumologists). Time door-1st antibiotic dose 6.6 hours. Global Mortality 16.7%. Women died at 87.4 y, men at 84.5 y (p = 0.035). Mortality FINE 3-4-5: 4.5, 12.4, 30% respectively. Mortality treated before 4 hours: 34.6%, after 4 hours: 11.5% (p = 0.01). Many more FINE 5 cases in Int. Medicine than Pneumology. Mortality by Internists 22%. Mortality by Pneumologists 3% (p = 0.001). Mortality similar following strict guidelines or variant.</p><p><strong>Conclusions: </strong>a) Internist receive patients sicker than Pneumologists; b) Important mortality in these very old patients of 16.7%, and progressive according the FINE severity index, in spite of correct therapy; c) Rapid initiation of Antibiotics did not decreased mortality; d) Mortality did not change following strict or variant Guidelines; and e) There are areas of quality improvement in our Hospitals.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 3","pages":"117-21"},"PeriodicalIF":0.0,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27504998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
[Adrenal failure caused by primary adrenal non-Hodgkin lymphoma: a case report and review of the literature]. 【原发性肾上腺非霍奇金淋巴瘤致肾上腺功能衰竭1例报告及文献复习】。
Anales De Medicina Interna Pub Date : 2008-03-01 DOI: 10.4321/s0212-71992008000300007
B Hernández Marín, V M Díaz Muñoz de la Espada, R Alvarez Alvarez, S Encinas García, P Khosravi Shahi, R Pérez Fernández, G Pérez Manga
{"title":"[Adrenal failure caused by primary adrenal non-Hodgkin lymphoma: a case report and review of the literature].","authors":"B Hernández Marín,&nbsp;V M Díaz Muñoz de la Espada,&nbsp;R Alvarez Alvarez,&nbsp;S Encinas García,&nbsp;P Khosravi Shahi,&nbsp;R Pérez Fernández,&nbsp;G Pérez Manga","doi":"10.4321/s0212-71992008000300007","DOIUrl":"https://doi.org/10.4321/s0212-71992008000300007","url":null,"abstract":"<p><p>We report a case of 78-year old man who presented with symptoms of adrenal insufficiency. The computed tomography (CT) scan showed the presence of bilateral adrenal masses. A CT-scan guided needle biopsy revealed diffuse large- B cell lymphoma. The absence of pathological findings in clinical, bone marrow and CT scan examinations supported the diagnosis of primary non-Hodgkin Lymphoma of the adrenal glands. The patient was treated with four cycles of R-CHOP chemotherapy with Rituximab, liposomal Doxorubicin, Cyclophosphamide, Vincristine and Prednisolone. At the end of fourth cycle there was radiological improvement but the chemotherapy was stopped because of IV grade toxicity. He completed treatment with radiotherapy of right adrenal mass. Few days after finishing radiation therapy the patient died due to a disseminated infection. No progressive disease was founded.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 3","pages":"131-3"},"PeriodicalIF":0.0,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27505001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
[Evaluation of the management of inhalers by the nursing personnel in a reference hospital]. [某参考医院护理人员吸入器管理评价]。
Anales De Medicina Interna Pub Date : 2008-03-01 DOI: 10.4321/s0212-71992008000300003
J Díaz-López, M J Cremades-Romero, F Carrión-Valero, M Maya-Martínez, I Fontana-Sanchís, E Cuevas-Cebrián
{"title":"[Evaluation of the management of inhalers by the nursing personnel in a reference hospital].","authors":"J Díaz-López,&nbsp;M J Cremades-Romero,&nbsp;F Carrión-Valero,&nbsp;M Maya-Martínez,&nbsp;I Fontana-Sanchís,&nbsp;E Cuevas-Cebrián","doi":"10.4321/s0212-71992008000300003","DOIUrl":"https://doi.org/10.4321/s0212-71992008000300003","url":null,"abstract":"<p><strong>Objectives: </strong>To evaluate the knowledge and skills of nurses on the management of inhaled therapy in different hospitalization wards.</p><p><strong>Material and methods: </strong>We carried out a cross-sectional study, in which nurses were asked to perform a practical demonstration of the management of a pressurized canister with an inhalation chamber, without previous theoretical instruction about the technique. The inhalation technique was evaluated step by step following the recommendations of the Spanish Society of Pneumologists and Chest Surgeons (SEPAR).</p><p><strong>Results: </strong>We could obtain the participation of 144 of the 177 nurses working in different wards (29 males, 115 females, mean age 42.5 + 7 years). Previous knowledge of the management of inhalers was declared by 85.4%. We found that 70.8% of the nurses did not correctly perform all the steps: 24.5% made only one mistake, while the rest had mistakes in two or more steps. The most common mistakes were: not to perform a slow and deep exhalation before using the inhaler (27.3%), not to hold the breath after the inhalation (24.4%), and not to wait 30 seconds between inhalation manoeuvres (21.5%). When evaluating different wards, we found that 44.4% of the nurses in the Short Stay Unit performed the technique correctly in contrast to 31.3% of the nurses in the Pneumology Ward.</p><p><strong>Conclusions: </strong>The percentage of mistakes in the inhalation technique by the nursing personnel was high. The health personnel must have an adequate level of training in order to correctly instruct the patient, because the efficacy of inhaled treatment greatly depends on the adequacy of the technique.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 3","pages":"113-6"},"PeriodicalIF":0.0,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27504997","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
[Systemic mastocytosis: systematic review]. 系统性肥大细胞增多症:系统综述。
Anales De Medicina Interna Pub Date : 2008-03-01 DOI: 10.4321/s0212-71992008000300008
M J Molina-Garrido, A Mora, C Guillén-Ponce, M Guirado-Risueño, M J Molina, M A Molina, A Carrato
{"title":"[Systemic mastocytosis: systematic review].","authors":"M J Molina-Garrido,&nbsp;A Mora,&nbsp;C Guillén-Ponce,&nbsp;M Guirado-Risueño,&nbsp;M J Molina,&nbsp;M A Molina,&nbsp;A Carrato","doi":"10.4321/s0212-71992008000300008","DOIUrl":"https://doi.org/10.4321/s0212-71992008000300008","url":null,"abstract":"<p><p>Mastocytosis is a hematologic malignance characterized by an abnormal proliferation of mastocytes. In a consensus classification in 2001, it was distinguished between matters limited to skin and systemic matters (70% of osseous involvement and 50% of hepatomegaly). The most typical symptoms are skin lesions and systemic manifestations due to mediators secreted by tumoral cells. They are useful chemotherapy to reduce the tumoral burden and antihistaminic to control systemic manifestations. Interferon is useful in most of systemic and local manifestations, and it is recommended to use prednisona before the use of this medication.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 3","pages":"134-40"},"PeriodicalIF":0.0,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27505002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 27
[The autoimmune hepatitis-primary biliary cirrhosis overlap syndrome: a case report]. 自身免疫性肝炎-原发性胆汁性肝硬化重叠综合征1例
Anales De Medicina Interna Pub Date : 2008-03-01 DOI: 10.4321/s0212-71992008000300005
N Mallo-González, R López-Rodríguez, J Campos-Franco, I Abdulkader, E Otero-Antón, M R Alende-Sixto
{"title":"[The autoimmune hepatitis-primary biliary cirrhosis overlap syndrome: a case report].","authors":"N Mallo-González,&nbsp;R López-Rodríguez,&nbsp;J Campos-Franco,&nbsp;I Abdulkader,&nbsp;E Otero-Antón,&nbsp;M R Alende-Sixto","doi":"10.4321/s0212-71992008000300005","DOIUrl":"https://doi.org/10.4321/s0212-71992008000300005","url":null,"abstract":"<p><p>The autoimmune hepatitis-primary biliary cirrhosis overlap syndrome is an entity characterized by clinical, analytical, immunological and histological manifestations of both entities. We present the case of a 26-year-old woman with a serious acute hepatitis that fulfills the diagnostic criteria of the overlap syndrome and that showed a satisfactory response to oral corticoid therapy.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 3","pages":"122-4"},"PeriodicalIF":0.0,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27504999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
[Periodic familial fever]. [周期性家族性热]。
Anales De Medicina Interna Pub Date : 2008-02-01 DOI: 10.4321/s0212-71992008000200010
M Estébanez Muñoz, J Gómez Cerezo, M López Rodríguez, B Pagán Muñoz, F J Barbado Hernández
{"title":"[Periodic familial fever].","authors":"M Estébanez Muñoz,&nbsp;J Gómez Cerezo,&nbsp;M López Rodríguez,&nbsp;B Pagán Muñoz,&nbsp;F J Barbado Hernández","doi":"10.4321/s0212-71992008000200010","DOIUrl":"https://doi.org/10.4321/s0212-71992008000200010","url":null,"abstract":"<p><p>The familial periodic fevers are Known as autoinflammatory syndromes. It is important in clinical practice to recognize these uncommon illnesses characterized by recurrent bouts of unspecific systemic symptoms associated to elevation of acute phase reactants without autoantibodies or underlying infection. The clinical suspicion supported on the molecular diagnosis represents a new perspective in relation to treatment and prognosis of these patients.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 2","pages":"93-7"},"PeriodicalIF":0.0,"publicationDate":"2008-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27399953","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
[Hemoperitoenum as presentation of hepatocellular carcinoma: experience in three cases with spontaneous tumoral rupture and review of the literature]. [腹膜积血作为肝细胞癌的表现:3例自发性肿瘤破裂的经验及文献复习]。
Anales De Medicina Interna Pub Date : 2008-02-01 DOI: 10.4321/s0212-71992008000200007
M Fernández-Ruiz, J M Guerra-Vales, J Llenas-García, J M Delgado-García, C Gómez-Pellico, A González-Barber
{"title":"[Hemoperitoenum as presentation of hepatocellular carcinoma: experience in three cases with spontaneous tumoral rupture and review of the literature].","authors":"M Fernández-Ruiz,&nbsp;J M Guerra-Vales,&nbsp;J Llenas-García,&nbsp;J M Delgado-García,&nbsp;C Gómez-Pellico,&nbsp;A González-Barber","doi":"10.4321/s0212-71992008000200007","DOIUrl":"https://doi.org/10.4321/s0212-71992008000200007","url":null,"abstract":"<p><p>Hemoperitoneum due to spontaneous rupture of hepatocellular carcinoma (HCC) constitutes a life-threatening situation if no appropriate therapy is provided. This complication is a well-known form of HCC presentation in countries with high incidence of liver tumours, but is an unusual event in Western countries, where it has been described in 5% or less of cases with HCC. We report three patients admitted to our centre with acute hemoperitoneum secondary to non-traumatic rupture as a first manifestation of not previously diagnosed HCC. A review of the related literature is also performed.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 2","pages":"81-4"},"PeriodicalIF":0.0,"publicationDate":"2008-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27399950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
[Hemoglobinopathies diagnosed at the University Hospital Ntra. Sra. de Candelaria and its area of reference in Santa Cruz de Tenerife during one year]. 在Ntra大学医院诊断的血红蛋白病。Sra。de Candelaria及其在圣克鲁斯de Tenerife的参考区域[一年]。
Anales De Medicina Interna Pub Date : 2008-02-01
S de las Heras Flórez, L M Pérez Hernández
{"title":"[Hemoglobinopathies diagnosed at the University Hospital Ntra. Sra. de Candelaria and its area of reference in Santa Cruz de Tenerife during one year].","authors":"S de las Heras Flórez,&nbsp;L M Pérez Hernández","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Objective: </strong>To describe number and type of hemoglobinopathies diagnosed in our area of reference during one year as well as the origin of these patients, to have a first contact with this pathology not characterized in our province until now.</p><p><strong>Material and method: </strong>All hemoglobinopathies diagnosed in one year were reviewed, either for suspected patients, after analyzing chromatogram to quantify hemoglobin (Hb) A1c or hemogram suspicious of beta-thalassemia. The screening method was high pressure liquid chromatography (HPLC), to identify and quantify HbA2, HbS and HbC. The other variants were diagnosed at reference laboratory.</p><p><strong>Results: </strong>198 hemoglobinopathies were diagnosed, 105 after measure HbA1c. The more frequent diagnoses were beta-thalassemia trait and heterozygote HbS. 61.1% of patients are from Canary Islands, mainly from Tenerife.</p><p><strong>Conclusions: </strong>The high number of carriers found from Canary Islands, should be the start to design prospective studies on population groups, in order to know the hemoglobinopathies prevalence and to perform control and prevention official programs in the province of Santa Cruz de Tenerife.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 2","pages":"61-6"},"PeriodicalIF":0.0,"publicationDate":"2008-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27400010","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Coxsackie virus infection associated with myositis and polyarthritis]. [柯萨奇病毒感染与肌炎和多发性关节炎相关]。
Anales De Medicina Interna Pub Date : 2008-02-01 DOI: 10.4321/s0212-71992008000200009
N Gómez Rodríguez, J Ibáñez Ruán, M González Rodríguez
{"title":"[Coxsackie virus infection associated with myositis and polyarthritis].","authors":"N Gómez Rodríguez,&nbsp;J Ibáñez Ruán,&nbsp;M González Rodríguez","doi":"10.4321/s0212-71992008000200009","DOIUrl":"https://doi.org/10.4321/s0212-71992008000200009","url":null,"abstract":"A wide spectrum of muscle disorders caused by Coxsackie B virus, ranging from acute nonspecific myalgia to rhabdomyolisis have been described. Arthritis in not widely recognised as an either manifestation of Coxsackie virus infection, and only ten patients has been reported previously. A case of polymyositis and polyarthritis associated with primary Coxsackie B infection in a 6-year-old girl is reported. Seroconversion of IgM and IgG antibodies for Coxsackie virus B was observed coinciding with the clinical features: fever, herpangine, polyarthritis, erythematous macular rash, myalgia and muscle weakness with high levels of aldolase and creatine kinase. Electromyographic changes of myositis were found. However, histopathologically biopsied muscle demonstrated a slight inflammatory mononuclear cell infiltrate without necrosis or regeneration of muscle fibres. Polyarthritis and full muscle strength was recovered 8 and 32 weeks after the onset, respectively.","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 2","pages":"90-2"},"PeriodicalIF":0.0,"publicationDate":"2008-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27399952","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
[Myelomatous ascites]. [骨髓瘤样腹水]。
Anales De Medicina Interna Pub Date : 2008-02-01 DOI: 10.4321/s0212-71992008000200008
P Young, B B Finn, D Pellegrini, J E Bruetman, C M Shanley, C Tolosa Vilell, H Trimarchi
{"title":"[Myelomatous ascites].","authors":"P Young,&nbsp;B B Finn,&nbsp;D Pellegrini,&nbsp;J E Bruetman,&nbsp;C M Shanley,&nbsp;C Tolosa Vilell,&nbsp;H Trimarchi","doi":"10.4321/s0212-71992008000200008","DOIUrl":"https://doi.org/10.4321/s0212-71992008000200008","url":null,"abstract":"<p><p>Ascites is rare in patients with multiple myeloma (MM). It may be due to diverse mechanisms, most frequently because of an increased permeability of the peritoneum or because of portal hypertension due to liver infiltration. Myelomatous ascites occurs more frequently in patients having Ig-G or Ig-A paraprotein and their prognosis is poor. It is submitted the case of a female patient aged 50 years with IgA-kappa MM, who evolved with cardiac failure (CF), plasma cells leukemia and ascites of mixed cause, because of peritoneal infiltrate of myelomatous cells, hepatic compromise and CF. A review of the different causes of ascites in patients with MM is performed. There are also summarized all myelomatous ascites cases published in the literature. Our report presents the first case of myelomatous ascites in a patient with plasma cells leukemia.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":"25 2","pages":"85-9"},"PeriodicalIF":0.0,"publicationDate":"2008-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27399951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
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