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  1. Article ; Online: Estudio de los pacientes con elevación de enzima Creatinfosfokinasa en dos hospitales de tercer nivel de la ciudad de córdoba.

    Saad, Emanuel José / Rodríguez Ruiz, Andrés / Douthat Y Barrionuevo, Augusto / Milanesio, Martín / Flores Balverdi, Janet / Riscanevo, Nadia Claudine / Peñaranda, Gabriela Estefanía / Novatti, Elisa Beatriz / Saurit, Verónica / Alvarez, Ana Cecilia / Baenas, Diego Federico

    Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina)

    2022  Volume 79, Issue 4, Page(s) 327–333

    Abstract: Introduction: HyperCKemia is defined as the elevation of creatine phosphokinase (CK) levels greater than 1.5 times the upper limit (CK>285 U/L), being produced by multiple causes, which vary according different populations. The main objective of the ... ...

    Title translation Creatine phosphokinase enzyme elevation in two third-level hospitals of Córdoba.
    Abstract Introduction: HyperCKemia is defined as the elevation of creatine phosphokinase (CK) levels greater than 1.5 times the upper limit (CK>285 U/L), being produced by multiple causes, which vary according different populations. The main objective of the study was to know the frequency of hyperCKemia in two hospitals in Córdoba and its main causes.
    Methods: Retrospective analytical study in two hospitals in Córdoba, Argentina, where all patients over 18 years of age who presented CK values ​​greater than 285 U/L on at least 2 occasions in a period between 1 and 4 weeks were identified, between the years 2015 and 2017.
    Results: 254 patients with hyperCKemia were identified, the majority were male (n=181, 71.3%) and their median age was 65 years (interquartile range 25-75%=50-73 years). The main causes of hyperCKemia were ischemic myopathy in 99 (39%) patients and drug-induced myopathies in 45 (17.7%), with statins being the most frequently involved drugs in 31 cases. In only 3.1% of the cases the final diagnosis was not reached. Drug-induced hyperCKemias, when compared to other causes, occurred more frequently in patients with a history of chronic kidney disease (9/45 [20%] vs 18/209 [8.6%], p = 0.025) and in non-smokers (41/45 [91.1%] vs. 157/209 [75.1%], p=0.019).
    Main conclusion: 254 cases of hyperCKemia were observed, the main causes being of ischemic origin and secondary to drug use, especially statins.
    MeSH term(s) Humans ; Male ; Female ; Adolescent ; Adult ; Creatine Kinase ; Retrospective Studies ; Hydroxymethylglutaryl-CoA Reductase Inhibitors ; Hospitals ; Renal Insufficiency, Chronic
    Chemical Substances Creatine Kinase (EC 2.7.3.2) ; Hydroxymethylglutaryl-CoA Reductase Inhibitors
    Language Spanish
    Publishing date 2022-12-21
    Publishing country Argentina
    Document type English Abstract ; Journal Article
    ZDB-ID 390127-0
    ISSN 1853-0605 ; 0014-6722 ; 0301-7281
    ISSN (online) 1853-0605
    ISSN 0014-6722 ; 0301-7281
    DOI 10.31053/1853.0605.v79.n4.36031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Estudio de los pacientes con monoartritis aguda en un hospital de tercer nivel.

    Douthat, Augusto / Rodríguez Ruiz, Andrés / Milanesio, Martín / Novatti, Elisa / Flores Balverdi, Janet / Riscanevo, Nadia C / Saurit, Verónica / Álvarez, Ana C / Peñaranda, Gabriela E / Alvarellos, Alejandro / Caeiro, Francisco / Baenas, Diego F / Saad, Emanuel J

    Medicina

    2022  Volume 83, Issue 3, Page(s) 384–393

    Abstract: Introduction: Acute monoarthritis (AM) represents a relevant cause of morbidity that requires prompt medical care. The study of synovial fluid becomes relevant to allow a rapid diagnostic approach. The main objective of the study was to determine the ... ...

    Title translation Acute monoarthritis in a third level hospital.
    Abstract Introduction: Acute monoarthritis (AM) represents a relevant cause of morbidity that requires prompt medical care. The study of synovial fluid becomes relevant to allow a rapid diagnostic approach. The main objective of the study was to determine the frequency and clinical-analytical characteristics of episodes of AM and acute bursitis evaluated in a hospital during a period of 6 years.
    Methods: Cross-sectional retrospective analytical study in a hospital at Córdoba, Argentina. All episodes of acute monoarthritis and bursitis that occurred in patients aged 18 years or older between 2012 and 2017 were included. AM in pregnant women and chronic monoarthritis were excluded.
    Results: One hundred and eighty episodes of AM and 12 of acute bursitis were included. Among the AM, 120 (66.7%) occurred in male patients and the average age was 62.1±16.9 years. The main cause of AM was septic, identifying 70 (36%) cases, followed by microcrystalline AM identify 54 (28%) cases, which corresponded to gout and calcium pyrophosphate dihydrate (CPPD) with 27 (14%) cases each one. Monosodium urate crystals were identified in 26 (14.3%) patients, CPPD in 28 (15.6%) and cholesterol in 1 (0.6%).
    Discussion: The main cause of AM was septic arthritis, followed by microcrystalline AM (gout and secondary to CPPD). The main affected joint was the knee, followed by the shoulder. Synovial fluid analysis was a key element when making the differential diagnosis between the different causes of acute monoarthritis and bursitis.
    MeSH term(s) Pregnancy ; Humans ; Male ; Female ; Middle Aged ; Aged ; Retrospective Studies ; Cross-Sectional Studies ; Gout/diagnosis ; Calcium Pyrophosphate/analysis ; Bursitis ; Hospitals
    Chemical Substances Calcium Pyrophosphate (X69NU20D19)
    Language Spanish
    Publishing date 2022-01-28
    Publishing country Argentina
    Document type English Abstract ; Journal Article
    ZDB-ID 411586-7
    ISSN 1669-9106 ; 0025-7680 ; 0325-951X
    ISSN (online) 1669-9106
    ISSN 0025-7680 ; 0325-951X
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  3. Article ; Online: Inflammatory Involvement of Spermatic Vein in a Patient With Immunoglobulin 4-Related Disease.

    Baenas, Diego Federico / Orozco, Maira Johanna / Bernabeu, Francisco / Saad, Emanuel José / Balderramo, Domingo César / Alvarellos, Alejandro / Calafat, Patricia / Saurit, Verónica / Caeiro, Francisco

    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

    2020  Volume 26, Issue 2, Page(s) e28–e29

    MeSH term(s) Anti-Inflammatory Agents/administration & dosage ; Biopsy/methods ; Diagnosis, Differential ; Humans ; Immunoglobulin G4-Related Disease/diagnosis ; Immunoglobulin G4-Related Disease/drug therapy ; Immunoglobulin G4-Related Disease/immunology ; Immunoglobulin G4-Related Disease/physiopathology ; Male ; Middle Aged ; Mycophenolic Acid/administration & dosage ; Phlebitis/diagnosis ; Phlebitis/etiology ; Phlebitis/immunology ; Prednisone/administration & dosage ; Radiographic Image Enhancement/methods ; Radiography, Abdominal/methods ; Spermatic Cord/diagnostic imaging ; Spermatic Cord/pathology ; Splenic Vein/diagnostic imaging ; Splenic Vein/pathology ; Tomography, X-Ray Computed/methods ; Treatment Outcome
    Chemical Substances Anti-Inflammatory Agents ; Mycophenolic Acid (HU9DX48N0T) ; Prednisone (VB0R961HZT)
    Language English
    Publishing date 2020-02-19
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 1283266-2
    ISSN 1536-7355 ; 1076-1608
    ISSN (online) 1536-7355
    ISSN 1076-1608
    DOI 10.1097/RHU.0000000000000783
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Paravertebral Pseudotumour in Granulomatosis with Polyangiitis.

    Flores Balverdi, Janet / Federico Baenas, Diego / Riscanevo, Nadia Claudine / Chiple, Emilia / Orozco, Maira / Saurit, Verónica

    Reumatologia clinica

    2019  Volume 17, Issue 3, Page(s) 181–182

    Title translation Seudotumor paravertebral en granulomatosis con poliangeítis.
    Language Spanish
    Publishing date 2019-09-13
    Publishing country Spain
    Document type Letter
    ISSN 2173-5743
    ISSN (online) 2173-5743
    DOI 10.1016/j.reuma.2019.04.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Nefrocalcinosis y acidosis tubular renal proximal en síndrome de Sjögren.

    Baenas, Diego Federico / Flores Balverdi, Janet / Retamozo, Soledad / Riscanevo, Nadia / Álvarez, Ana Cecilia / Saurit, Verónica / De la Fuente, Jorge / Caeiro, Francisco

    Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina)

    2018  Volume 75, Issue 2, Page(s) 139–142

    Title translation Nephrocalcinosis and proximal tubulopathy in Sjögren's Syndrome.
    MeSH term(s) Acidosis, Renal Tubular/complications ; Acidosis, Renal Tubular/diagnosis ; Creatinine/blood ; Electrolytes/blood ; Electrolytes/urine ; Female ; Humans ; Middle Aged ; Nephrocalcinosis/complications ; Nephrocalcinosis/diagnosis ; Proteinuria/urine ; Renal Colic/complications ; Sjogren's Syndrome/complications ; Sjogren's Syndrome/diagnosis ; Ultrasonography
    Chemical Substances Electrolytes ; Creatinine (AYI8EX34EU)
    Language Spanish
    Publishing date 2018-06-30
    Publishing country Argentina
    Document type Case Reports ; Journal Article
    ZDB-ID 390127-0
    ISSN 1853-0605 ; 0014-6722 ; 0301-7281
    ISSN (online) 1853-0605
    ISSN 0014-6722 ; 0301-7281
    DOI 10.31053/1853.0605.v75.n2.19161
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Primary Sjögren syndrome and development of another autoimmune rheumatic disease during the follow-up.

    Rodríguez, María Florencia / Asnal, Cecilia / Gobbi, Carla Andrea / Pellet, Antonio Carlos Catalán / Herscovich, Natalia / Amitrano, Cristina / Demarchi, Julia / Noé, Damián Duartes / Segura, Carolina / Caeiro, Francisco / Riscanevo, Nadia / Saurit, Verónica / Papasidero, Silvia / Alba, Paula B / Raiti, Laura / Cruzat, Vanesa / Santiago, María Lida / Vélez, Sofía / Salvatierra, Gabriela /
    Juárez, Vicente / Secco, Anastasia

    Advances in rheumatology (London, England)

    2022  Volume 62, Issue 1, Page(s) 19

    Abstract: Background: Primary Sjögren syndrome (pSS) is a chronic autoimmune disease with its main target being exocrine glands, and is the connective tissue disease more frequently associated with other autoimmune diseases. The aim of this study was to assess ... ...

    Abstract Background: Primary Sjögren syndrome (pSS) is a chronic autoimmune disease with its main target being exocrine glands, and is the connective tissue disease more frequently associated with other autoimmune diseases. The aim of this study was to assess the frequency of another autoimmune rheumatic disease (ARD) developed in primary Sjögren syndrome (pSS) patients and to describe it's clinical, serological and histologic characteristics.
    Materials and methods: This is a retrospective cohort study. Data of patients with pSS diagnosis (American-European criteria 2002), included in the GESSAR database (Grupo de Estudio Síndrome de Sjögren, Sociedad Argentina de Reumatología) were analyzed. The development of a second ARD was registered during the follow up.
    Results: 681 patients were included, 94.8% female. The mean age was 54 (SD 14) years and mean age at diagnosis of 50 (SD 13) years. The mean follow-up was 4.7 (SD 4.9) years; 30 patients (4.41%, CI 95%: 3.1-5.7) developed a second ARD during the follow up, incidence rate was 9.1/1000 patients-year (IR 95%: 5.8-12.4/1000 patients-year), the most frequent being rheumatoid arthritis (RA). 96% out of these 30 patients had xerophthalmia, 86.2% xerostomia, 92% positive Schirmer test, 88.24% positive Rosa Bengala test, lisamine green or Ocular Staining Score, 81.2% positive unstimulated salivary flow, 82.1% Ro(+) and 33.33% La(+). Minor salivary gland biopsy had been performed in 14 of the 30 patients, 12 with positive results. There were no statistically significant differences respect baseline characteristics when comparing the patients who developed another ARD to the ones that did not.
    Conclusions: Of all the patients analyzed, 4.4% presented another ARD during their follow-up. It is important to be aware of this, to make an early and proper diagnosis and treatment of our patients.
    MeSH term(s) Autoimmune Diseases/complications ; Autoimmune Diseases/epidemiology ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Sjogren's Syndrome/complications ; Sjogren's Syndrome/diagnosis ; Sjogren's Syndrome/epidemiology ; Xerostomia
    Language English
    Publishing date 2022-06-07
    Publishing country England
    Document type Journal Article
    ISSN 2523-3106
    ISSN (online) 2523-3106
    DOI 10.1186/s42358-022-00250-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Rheumatoid arthritis monotherapy in the Jak inhibitors Era. Current prevalence and associated factors in a multicenter study.

    Garcia-Salinas, Rodrigo / Sommerfleck, Fernando / Vargas-Caselles, Alfredo / Palomino-Romero, Luis / Rosa, Javier / Benegas, Mariana / Saturansky, Etel / Giorgis, Pamela / Martinez, Florencia / Abdala, Marcelo / Sanchez-Alcover, Jimene / Civit, Emma / Espasa, Vanesa / Bellomio, Veronica / Bande, Juan Manuel / Papasidero, Silvia / Saurit, Veronica / Ibañez-Zurlo, Leticia / Buschiazzo, Emilio

    ARP rheumatology

    2022  Volume 2, Issue 1, Page(s) 41–46

    Abstract: Background: Combined therapy constitutes the standard of care in RA. Jak inhibitors (Jaki) have shown efficacy in monotherapy, a modality used in cases where it is not possible to use Disease-Modifying Anti Rheumatic Drugs (csDMARDs).: Objectives: To ...

    Title translation Rheumatoid arthritis monotherapy in the Jak inhibitors Era. Current prevalence and associated factors in a multicenter study.
    Abstract Background: Combined therapy constitutes the standard of care in RA. Jak inhibitors (Jaki) have shown efficacy in monotherapy, a modality used in cases where it is not possible to use Disease-Modifying Anti Rheumatic Drugs (csDMARDs).
    Objectives: To estimate the prevalence (total and by drug), reason for using and the increase over the time of bDMARDs or tsDMARDs as monotherapy after the availability of the Jaki. To analyze the differential characteristics between patients with monotherapy vs combined therapy.
    Methods: Cross-sectional multicenter study. Consecutive patients with a diagnosis of RA (ACR/EULAR 2010) under treatment with bDMARDs or tsDMARDs started from 2013 were included. Socio-demographic, clinic, and therapeutic data were collected.
    Results: A total of 505 RA patients were included. Since 2013, the prevalence of monotherapy usage was (any) 49%. The drugs used as monotherapy were Jaki in 41% and TNF-blockers in 30%. The leading causes of monotherapy use were intolerance/adverse events (62%), medical decision or lack of adherence (37.7%). The highest socioeconomic level and a better functional status at diagnosis were predictors of monotherapy use. The use of the second line of treatments and less polypharmacy were independent factors associated with this therapeutic modality.
    Conclusions: The current prevalence of monotherapy in RA was 49%, the Jaki were the most used drug in this modality. Monotherapy increases from year to year. There are differential characteristics in patients using monotherapy.
    MeSH term(s) Humans ; Janus Kinase Inhibitors/therapeutic use ; Cross-Sectional Studies ; Prevalence ; Biological Products/therapeutic use ; Arthritis, Rheumatoid/drug therapy
    Chemical Substances Janus Kinase Inhibitors ; Biological Products
    Language English
    Publishing date 2022-12-28
    Publishing country Portugal
    Document type Multicenter Study ; Journal Article
    ISSN 2795-4552
    ISSN (online) 2795-4552
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Extensive calcinosis in adult dermatomyositis.

    Baenas, Diego Federico / Pirola, Juan Pablo / Benzaquén, Nadia Raquel / Caeiro, Francisco / Álvarez, Ana Cecilia / Saurit, Verónica / Retamozo, Soledad / Alvarellos, Alejandro

    Reumatologia clinica

    2017  Volume 15, Issue 2, Page(s) 121–123

    Title translation Calcinosis extensa en dermatomiositis del adulto.
    MeSH term(s) Calcinosis/etiology ; Dermatomyositis/complications ; Dermatomyositis/diagnosis ; Female ; Humans ; Middle Aged
    Language Spanish
    Publishing date 2017-04-07
    Publishing country Spain
    Document type Case Reports ; Journal Article
    ISSN 2173-5743
    ISSN (online) 2173-5743
    DOI 10.1016/j.reuma.2017.03.004
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  9. Article ; Online: Reactivation of Chagas Disease in Patients With Rheumatic Autoimmune Diseases Diagnosed by Molecular Quantification Techniques.

    Sánchez, Ariel German / Baenas, Diego Federico / Bonisconti, Florencia / Salinas, María Jezabel Haye / Alvarellos, Alejandro / Saurit, Verónica / Caeiro, Francisco / Salomone, Oscar / Caeiro, Juan Pablo / Carballo, Viviana / Medeot, Marcela / Albertini, Ricardo / Alvarellos, Teresita

    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

    2019  Volume 27, Issue 8S, Page(s) S533–S536

    MeSH term(s) Autoimmune Diseases/diagnosis ; Chagas Disease/complications ; Chagas Disease/diagnosis ; Humans ; Rheumatic Diseases/diagnosis
    Language English
    Publishing date 2019-07-11
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1283266-2
    ISSN 1536-7355 ; 1076-1608
    ISSN (online) 1536-7355
    ISSN 1076-1608
    DOI 10.1097/RHU.0000000000001108
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  10. Article ; Online: Time to diagnosis in systemic lupus erythematosus: Associated factors and its impact on damage accrual and mortality. Data from a multi-ethnic, multinational Latin American lupus cohort.

    Nieto, Romina / Quintana, Rosana / Zavala-Flores, Ernesto / Serrano, Rosa / Roberts, Karen / Catoggio, Luis J / García, Mercedes A / Berbotto, Guillermo A / Saurit, Verónica / Bonfa, Eloisa / Borba, Eduardo F / Lavras Costallat, Lilian T / Da Silva, Nilzio A / Sato, Emilia I / Tavares Brenol, Joao C / Massardo, Loreto / Neira, Oscar J / Vázquez, Gloria / Guibert Toledano, Marlene /
    Pascual-Ramos, Virginia / Sauza Del Pozo, María J / Barile-Fabris, Leonor A / Amigo, Mary-Carmen / García De La Torre, Ignacio / Acevedo-Vásquez, Eduardo M / Segami, María I / Chacón-Díaz, Rosa / Esteva-Spinetti, María H / Alarcón, Graciela S / Pons-Estel, Bernardo A / Pons-Estel, Guillermo J

    Lupus

    2024  Volume 33, Issue 4, Page(s) 340–346

    Abstract: Background: Systemic lupus erythematosus (SLE) often mimics symptoms of other diseases, and the interval between symptom onset and diagnosis may be long in some of these patients. Aims: To describe the characteristics associated with the time to SLE ... ...

    Abstract Background: Systemic lupus erythematosus (SLE) often mimics symptoms of other diseases, and the interval between symptom onset and diagnosis may be long in some of these patients. Aims: To describe the characteristics associated with the time to SLE diagnosis and its impact on damage accrual and mortality in patients with SLE from a Latin American inception cohort.
    Methods: Patients were from a multi-ethnic, multi-national Latin-American SLE inception cohort. All participating centers had specialized lupus clinics. Socio-demographic, clinical/laboratory, disease activity, damage, and mortality between those with a longer and a shorter time to diagnosis were compared using descriptive statistical tests. Multivariable Cox regression models with damage accrual and mortality as the end points were performed, adjusting for age at SLE diagnosis, gender, ethnicity, level of education, and highest dose of prednisone for damage accrual, plus highest dose of prednisone, baseline SLEDAI, and baseline SDI for mortality.
    Results: Of the 1437 included in these analyses, the median time to diagnosis was 6.0 months (Q1-Q3 2.4-16.2); in 721 (50.2%) the time to diagnosis was longer than 6 months. Patients whose diagnosis took longer than 6 months were more frequently female, older at diagnosis, of Mestizo ethnicity, not having medical insurance, and having "non-classic" SLE symptoms. Longer time to diagnosis had no impact on either damage accrual (HR 1.09, 95% CI 0.93-1.28,
    Conclusions: In this inception cohort, a maximum time of 24 months with a median of 6 months to SLE diagnosis had no apparent negative impact on disease outcomes (damage accrual and mortality).
    MeSH term(s) Humans ; Female ; Lupus Erythematosus, Systemic/diagnosis ; Lupus Erythematosus, Systemic/drug therapy ; Lupus Erythematosus, Systemic/complications ; Prednisone/therapeutic use ; Latin America/epidemiology ; Disease Progression ; Hispanic or Latino ; Severity of Illness Index
    Chemical Substances Prednisone (VB0R961HZT)
    Language English
    Publishing date 2024-02-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 1154407-7
    ISSN 1477-0962 ; 0961-2033
    ISSN (online) 1477-0962
    ISSN 0961-2033
    DOI 10.1177/09612033241232821
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