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31.
Priporočila Onkološkega inštituta za zdravljenje bolnikov z adenokarcinomom želodca
2021, druge monografije in druga zaključena dela

Povzetek: V Sloveniji vsako leto zboli zaradi raka želodca okrog 450 bolnikov, od tega ima tri četrtine bolnikov ob postavitvi diagnoze razširjeno ali razsejano bolezen. Zato je pomembno, da imamo razvito sodobno multidisciplinarno zdravljenje. Onkološki inštitut je na poti pridobitve evropske onkološke akreditacije, ki jo podeljuje priznana Evropska organizacija onkoloških inštitutov (OECI), katere član je tudi Onkološki inštitut Ljubljana. Namen tega projekta je razvoj kliničnih poti, ki bodo omogočile celostno obravnavo bolnikov z rakom. Slovenskih priporočil za zdravljenje adenokarcinoma želodca trenutno nimamo, zato smo bili primorani sprejeti te, ki jim bomo sledili na Onkološkem inštitutu. V teh priporočilih, zaradi drugačne narave bolezni, ni zajeto zdravljenje raka ezofagogastričnega stika.
Ključne besede: rak želodca, adenokarcinom, onkološko zdravljenje, priporočila
Objavljeno v DiRROS: 14.09.2021; Ogledov: 1359; Prenosov: 361
.pdf Celotno besedilo (983,68 KB)

32.
Novosti v sistemskem zdravljenju raka jajčnikov
Erik Škof, 2021, objavljeni povzetek znanstvenega prispevka na konferenci

Ključne besede: rak jajčnikov, sistemsko zdravljenje, kemoterapija
Objavljeno v DiRROS: 16.06.2021; Ogledov: 840; Prenosov: 437
.pdf Celotno besedilo (7,80 MB)
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33.
Temporal changes in the epidemiology, management, and outcome from acute respiratory distress syndrome in European intensive care units : a comparison of two large cohorts
Yasser Sakr, Bruno François, Jordi Solé-Violan, Katarzyna Kotfis, Ulrich Jaschinski, Angel Estella, Marc Leone, Stephan M. Jakob, Xavier Wittebole, Luis E. Fontes, Viktorija Tomič, 2021, izvirni znanstveni članek

Povzetek: Background. Mortality rates for patients with ARDS remain high. We assessed temporal changes in the epidemiology and management of ARDS patients requiring invasive mechanical ventilation in European ICUs. We also investigated the association between ventilatory settings and outcome in these patients. Methods. This was a post hoc analysis of two cohorts of adult ICU patients admitted between May 1–15, 2002 (SOAP study, n = 3147), and May 8–18, 2012 (ICON audit, n = 4601 admitted to ICUs in the same 24 countries as the SOAP study). ARDS was defined retrospectively using the Berlin definitions. Values of tidal volume, PEEP, plateau pressure, and FiO2 corresponding to the most abnormal value of arterial PO2 were recorded prospectively every 24 h. In both studies, patients were followed for outcome until death, hospital discharge or for 60 days. Results. The frequency of ARDS requiring mechanical ventilation during the ICU stay was similar in SOAP and ICON (327[10.4%] vs. 494[10.7%], p = 0.793). The diagnosis of ARDS was established at a median of 3 (IQ: 1–7) days after admission in SOAP and 2 (1–6) days in ICON. Within 24 h of diagnosis, ARDS was mild in 244 (29.7%), moderate in 388 (47.3%), and severe in 189 (23.0%) patients. In patients with ARDS, tidal volumes were lower in the later (ICON) than in the earlier (SOAP) cohort. Plateau and driving pressures were also lower in ICON than in SOAP. ICU (134[41.1%] vs 179[36.9%]) and hospital (151[46.2%] vs 212[44.4%]) mortality rates in patients with ARDS were similar in SOAP and ICON. High plateau pressure (> 29 cmH2O) and driving pressure (> 14 cmH2O) on the first day of mechanical ventilation but not tidal volume (> 8 ml/kg predicted body weight [PBW]) were independently associated with a higher risk of in-hospital death. Conclusion. The frequency of and outcome from ARDS remained relatively stable between 2002 and 2012. Plateau pressure > 29 cmH2O and driving pressure > 14 cmH2O on the first day of mechanical ventilation but not tidal volume > 8 ml/kg PBW were independently associated with a higher risk of death. These data highlight the continued burden of ARDS and provide hypothesis-generating data for the design of future studies.
Ključne besede: respiratory insufficiency, artificial respiration, tidal volume, airway pressures, driving pressure
Objavljeno v DiRROS: 16.06.2021; Ogledov: 1140; Prenosov: 533
URL Povezava na datoteko
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Izkušnje z zdravilom olaparib pri zdravljenju recidivnega epitelijskega raka jajčnikov z mutacijami v genih BRCA 1 in BRCA 2
Erik Škof, 2021, izvirni znanstveni članek

Povzetek: Izhodišče: Zdravilo olaparib uporabljamo za vzdrževalno peroralno zdravljenje recidivnega epitelijskega raka jajčnikov z mutacijami v genih BRCA 1 in BRCA 2 pri bolnicah, ki se odzovejo na kemoterapijo s preparati platine. Namen: Prikazati varnost in učinkovitost zdravljenja s poli-ADP riboza polimeraznim (PARP) inhibitorjem olaparibom v redni klinični praksi v sklopu vzdrževalnega zdravljenja recidivnega epitelijskega raka jajčnikov z mutacijami v genih BRCA 1 in BRCA 2. Metode: V retrospektivno analizo smo vključili bolnice z recidivnim epitelijskim rakom jajčnikov z mutacijami v genih BRCA 1 in BRCA 2, ki so se začele zdraviti z olaparibom na Onkološkem inštitutu Ljubljana v obdobju od 1. novembra 2015 do 31. decembra 2020. Cilja raziskave sta bila oceniti varnost in učinkovitost zdravila olaparib (preživetje brez ponovitve bolezni, celokupno preživetje). Raziskavo je odobrila etična komisija na Onkološkem inštitutu Ljubljana. Rezultati: V opazovanem obdobju je bilo z olaparibom zdravljenih 88 bolnic z recidivnim epitelijskim rakom jajčnikov z mutacijami v genih BRCA 1 in BRCA 2. Mediana starost bolnic je bila 60 let. Večina (61 %) je imela prvi recidiv bolezni, prav tako večina (74 %) je imela tudi zarodno mutacijo v genu BRCA 1. Večina bolnic (85 %) je nadalje imela vsaj en neželeni učinek zdravljenja z olaparibom. Najpogostejši (vse stopnje) so bili: slabost (59 %), utrujenost (59 %), anemija (25 %), dispepsija (14 %), tekoče blato (11 %), spremembe okusa (10 %), nevtropenija (6 %) in aritmija (1 %). Resne neželene učinke (stopnje 3/4) je imelo 10 % bolnic: pojavljali sta se anemija (9 %) in slabost (1 %). Mediani čas sledenja je bil 40 mesecev. Mediano preživetje brez ponovitve bolezni je bil 14,3 meseca, mediano celokupno preživetje pa 20,4 meseca. Preživetje brez napredovanja bolezni je bilo odvisno od vrste mutacije v genih BRCA: pri somatski mutaciji v genih BRCA 1/2 je bilo 80 % bolnic brez progresa bolezni, pri zarodni mutaciji BRCA 2 je bilo teh 55 % bolnic, pri zarodni mutaciji BRCA 1 pa 32 % (p = 0,021). Vrsta mutacije v genih BRCA 1/2 ni imela vpliva na celokupno preživetje bolnic.
Ključne besede: epitelijski rak jajčnikov, olaparib, BRCA 1/2, genska mutacija
Objavljeno v DiRROS: 10.06.2021; Ogledov: 1085; Prenosov: 319
.pdf Celotno besedilo (121,58 KB)

36.
Priporočila za obravnavo bolnikov z rakom debelega črevesa in danke
Erik Brecelj, 2020, ni določena

Ključne besede: rak (medicina), debelo črevo, danka, diagnostika, zdravljenje
Objavljeno v DiRROS: 08.04.2021; Ogledov: 1175; Prenosov: 361
.pdf Celotno besedilo (597,15 KB)

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Immunohistochemistry of pulmonary biomarkers : a perspective from members of the pulmonary pathology society
Erik Thunnissen, Timothy Craig Allen, Julien Adam, Dara L. Aisner, Mary Beth Beasley, Alain C. Borczuk, Philip T. Cagle, Vera Luiza Capelozzi, Wendy Cooper, Izidor Kern, 2018, izvirni znanstveni članek

Povzetek: The use of immunohistochemistry for the determination of pulmonary carcinoma biomarkers is a well-established and powerful technique. Immunohistochemisty is readily available in pathology laboratories, is relatively easy to perform and assess, can provide clinically meaningful results very quickly, and is relatively inexpensive. Pulmonary predictive biomarkers provide results essential for timely and accurate therapeutic decision making; for patients with metastatic non-small cell lung cancer, predictive immunohistochemistry includes ALK, (ROS1, EGFR in Europe), and programmed death ligand-1 (PD-L1) testing. Handling along proper methodologic lines is needed to ensure patients receive the most accurate and representative test outcomes.
Ključne besede: pulmonary biomarkers, immunohistochemistry, pathology
Objavljeno v DiRROS: 17.12.2020; Ogledov: 1089; Prenosov: 402
URL Povezava na datoteko

40.
Comparison of European ICU patients in 2012 (ICON) versus 2002 (SOAP)
Jean Louis Vincent, Jean-Yves Lefrant, Katarzyna Kotfis, Rahul Nanchal, Ignacio Martin-Loeches, Samir G. Sakka, Xavier Wittebole, Peter Pickkers, Rui P. Moreno, Yasser Sakr, 2018, izvirni znanstveni članek

Povzetek: Purpose: To evaluate differences in the characteristics and outcomes of intensive care unit (ICU) patients over time. Methods: We reviewed all epidemiological data, including comorbidities, types and severity of organ failure, interventions, lengths of stay and outcome, for patients from the Sepsis Occurrence in Acutely ill Patients (SOAP) study, an observational study conducted in European intensive care units in 2002, and the Intensive Care Over Nations (ICON) audit, a survey of intensive care unit patients conducted in 2012. Results: We compared the 3147 patients from the SOAP study with the 4852 patients from the ICON audit admitted to intensive care units in the same countries as those in the SOAP study. The ICON patients were older (62.5 +/- 17.0 vs. 60.6 +/- 17.4 years) and had higher severity scores than the SOAP patients. The proportion of patients with sepsis at any time during the intensive care unit stay was slightly higher in the ICON study (31.9 vs. 29.6%, p = 0.03). In multilevel analysis, the adjusted odds of ICU mortality were significantly lower for ICON patients than for SOAP patients, particularly in patients with sepsis [OR 0.45 (0.35-0.59), p < 0.001]. Conclusions: Over the 10-year period between 2002 and 2012, the proportion of patients with sepsis admitted to European ICUs remained relatively stable, but the severity of disease increased. In multilevel analysis, the odds of ICU mortality were lower in our 2012 cohort compared to our 2002 cohort, particularly in patients with sepsis.
Ključne besede: intensive care units -- analysis -- epidemiology -- mortality, sepsis, severity of disease
Objavljeno v DiRROS: 30.11.2020; Ogledov: 1575; Prenosov: 1094
.pdf Celotno besedilo (867,51 KB)
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