7 research outputs found
SpecifiÄnosti biometrijskih Äimbenika oka u glaukomskih bolesnika s pseudoeksfolijativnim sindromom mjerenih optiÄkom niskokoherentnom reflektometrijom
The aim of the study was to assess biometric factor aberrations and differences among groups of eyes with cataract and pseudoexfoliative syndrome, cataract and pseudoexfoliative glaucoma, and cataract and primary open-angle glaucoma (POAG), and to determine biometric factors of the eye specific for the group of glaucomatous patients with pseudoexfoliative syndrome by use of optical low-coherence reflectometry. This retrospective study included 72 patients, and the study sample of 102 eyes was divided into the following three groups according to diagnosis: 29 eyes with pseudoexfoliative syndrome and cataract; 36 eyes with POAG and cataract; and 37 eyes with pseudoexfoliative glaucoma and cataract. Data on biometric measurements (central corneal thickness, pupillary diameter, anterior chamber depth, lens thickness, axial length, retinal thickness, astigmatism and white-to-white) obtained by use of optical low-coherence reflectometry on a Lenstar LS 900Ā® (Haag-Streit International) were collected and analyzed by thorough survey of medical documentation of patients scheduled for cataract surgery at Department of Ophthalmology, Sveti Duh University Hospital
in Zagreb, Croatia. Comparative analysis of the groups yielded statistically significant differences in central corneal thickness (F2/99=7.066; p=0.001) and lens thickness (F2/96=5.133; p=0.008).
The group of eyes diagnosed with pseudoexfoliative glaucoma and cataract had a significantly thinner cornea as compared with the other two groups and a significantly thicker lens as compared with the group of eyes with POAG and cataract. In conclusion, optical low-coherence reflectometry revealed differences in biometric factors among the three groups of eyes, with a statistically significantly thinner cornea and thicker lens in the group of glaucomatous patients with pseudoexfoliative syndrome.Cilj je bio optiÄkom niskokoherentnom reflektometrijom utvrditi odstupanja i razlike biometrijskih Äimbenika izmeÄu skupina ispitivanih uzoraka oÄiju s kataraktom i pseudoeksfolijativnim sindromom, kataraktom i pseudoeksfolijativnim glaukomom i kataraktom i primarnim glaukomom otvorenog kuta te odrediti biometrijske Äimbenike oka specifiÄne za skupinu glaukomskih bolesnika s pseudoeksfolijativnim sindromom. U retrospektivnu studiju bilo je ukljuÄeno 72 ispitanika, a uzorak su Äinila 102 oka podijeljena u tri skupine prema dijagnozi: 29 oÄiju s pseudoeksfolijativnim sindromom i kataraktom, 36 oÄiju s primarnim glaukomom otvorenog kuta i kataraktom, 37 oÄiju s pseudoeksfolijativnim glaukomom i kataraktom.
Detaljnom analizom medicinske dokumentacije ispitanika predviÄenih za operaciju katarakte u Klinici za oÄne bolesti KliniÄke bolnice Sveti Duh u Zagrebu prikupljeni su i analizirani podaci biometrijskih mjerenja (centralna debljina rožnice, promjer zjenice, dubina prednje sobice, debljina leÄe, aksijalna duljina, debljina rožnice, astigmatizam i horizontalni promjer rožnice izmjereni primjenom optiÄke niskokoherentne reflektometrije na ureÄaju Lenstar LS 900Ā®, Haag Streit International). Usporednom analizom skupina zabilježene su statistiÄki znaÄajne razlike za centralnu debljinu rožnice (F2/99=7,066;
p=0,001) i debljinu leÄe (F2/96=5,133; p=0,008). Skupina oÄiju s dijagnozom pseudoeksfolijativnog glaukoma i katarakte imala je znaÄajno tanju rožnicu u odnosu na ostale dvije skupine oÄiju i znaÄajno deblju leÄu od skupine s primarnim glaukomom otvorenog kuta i kataraktom. U zakljuÄku, primjenom optiÄke niskokoherentne reflektometrije utvrÄene su razlike u biometrijskim Äimbenicima promatranih skupina i statistiÄki znaÄajno tanja rožnica te zadebljana leÄa u skupini glaukomskih bolesnika s pseudoeksfolijativnim sindromom
Analysis and the results of serological testing of Croatian organ donors from 2006 to 2012
Uvod: UspjeÅ”nost transplantacije i preživljavanja presatka usko su povezani s odsustvom infekcije u primatelja. Infekcija primatelja je posljedica infekcije presatkom, reaktivacije latentnih infekcija primatelja, nozokomijalnih infekcija i kasnije, zbog doživotne imunosupresije infekcija iz okoline. Hrvatski zavod za transfuzijsku medicinu (HZTM) od 2006. provodi obvezna testiranja donora organa (DO) na uzroÄnike krvlju prenosivih bolesti (24h/7 dana) za potrebe cijele Hrvatske.
Materijal i metode: U razdoblju od 5.11.2006. ā 31.12.2012. ispitano je u HZTM 642 uzoraka plazme DO pri Äemu su koriÅ”teni testovi Abbott ā Architect i bioMerieux ā Vidas. U ovom radu analizirani su kvaliteta uzorka, brzina i rezultati testiranja na biljege infekcije virusima humane imunodeficijencije 1 i 2 (HIV), virusima hepatitisa B (HBV) i C (HCV), citomegalovirusom (CMV), Epstein-Barr virusom (EBV), T. pallidum i T. gondii.
Rezultati: Seroprevalencija EBV, CMV i T. gondii oÄekivano je visoka i iznosi 96,8%, 92% i 71%. HIV pozitivnih meÄu DO nije bilo, a biljege HBV infekcije, HBsAg i antitijela na HBcAg (anti-HBc) imalo je 0,5% odnosno 8,9% DO. U 1,3% ispitanih dokazan je HCV antigen, a antitijela na virus hepatitisa C (anti-HCV) bila su pozitivna u njih 1,6%. UÄestalost treponemskih antitijela bila je 0,8%. 2,5% uzoraka bilo je razrijeÄeno viÅ”e od 50%, a prosjeÄno vrijeme testiranja DO bilo je 2,04 sata.
ZakljuÄak: Rezultati testiranja DO upuÄuju na primjerenost odabranih testova i algoritama testiranja kao i metoda selekcije DO u donorskim bolnicama, a prevalencije patogena sukladne su epidemioloÅ”kim karakteristikama opÄe populacije.Introduction: The success of transplantation and graft survival are closely related to the absence of infection in transplant recipients through infected graft, reactivated recipient\u27s latent infections, nosocomial infections and community acquired infections. Since 2006, the Croatian Institute of Transfusion Medicine has been providing mandatory testing of organ donors (OD) for bloodborne pathogens (24/7) for the entire country.
Materials and methods: In the period from 5.11.2006. to 31.12.2012. a total of 642 organ donor plasma samples were tested by means of Abbott ā Architect and bioMerieux ā Vidas tests. In this paper, the quality of samples measured against rate of dilution, turnaround time and prevalence of human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), T. pallidum and T. gondii markers were analyzed.
Results: Seroprevalence of EBV, CMV and Toxoplasma gondii was as high as expected (96.8%, 92% and 71%, respectively). There were no HIV positive OD, while in 0.5% HBsAg, in 8.9% anti-HBc, in 1.6% anti-HCV, in 1.3% HCVAg and in 0.8% T. pallidum Ab were found positive. 2.5% of the samples were diluted by more than 50% and the average testing time per OD was 2.04 hours.
Conclusion: The results indicate the adequacy of organ donor selection methods in donor hospitals, appropriate tests and testing algorithms used. The prevalence of pathogens is in accordance with epidemiological characteristics of the general population
Heat isolation of chilling chumber for food storage
Izvedena je toplinska bilanca za hlaÄenje 1850 kg treÅ”anja i 2420 kg bresaka, u rashladnoj komori, sa poÄetne temperature 20Ā°C na konaÄnih 0Ā°C odnosno 2Ā°C. Uzorci hlaÄenog voÄa imaju razliÄitu održivost u rashladnim komorama. Na temperaturama od 0Ā°C do 2Ā°C uz prosjeÄnu vlažnost od 90%, održivost treÅ”anja je oko 14 dana, a bresaka od 14 do 42 dana. U toplinskom proraÄunu uzeti su u obzir svi procesni parametri i kvaliteta izolacije komore, koji utjeÄu na ukupno toplinsko optereÄenje.The heat balance for chilling of 1850 kg cherrys and 2420 kg of peaches, from starting temperature of 20Ā°C to finally 0Ā°C or 2Ā°C, in chilling chamber, was established. The samples of chilled fruits have different preservation capabilites in chilling chambers. At temperatures from 0Ā°C to 2Ā°C, with average relative humidity of 90%, duration of cherrys is about 2 weeks, and for peaches 2 to 4 weeks. In the heat balance calculation, all process parameters and quality of isolation, have been taken in to consideration
Heat isolation of chilling chumber for food storage
Izvedena je toplinska bilanca za hlaÄenje 1850 kg treÅ”anja i 2420 kg bresaka, u rashladnoj komori, sa poÄetne temperature 20Ā°C na konaÄnih 0Ā°C odnosno 2Ā°C. Uzorci hlaÄenog voÄa imaju razliÄitu održivost u rashladnim komorama. Na temperaturama od 0Ā°C do 2Ā°C uz prosjeÄnu vlažnost od 90%, održivost treÅ”anja je oko 14 dana, a bresaka od 14 do 42 dana. U toplinskom proraÄunu uzeti su u obzir svi procesni parametri i kvaliteta izolacije komore, koji utjeÄu na ukupno toplinsko optereÄenje.The heat balance for chilling of 1850 kg cherrys and 2420 kg of peaches, from starting temperature of 20Ā°C to finally 0Ā°C or 2Ā°C, in chilling chamber, was established. The samples of chilled fruits have different preservation capabilites in chilling chambers. At temperatures from 0Ā°C to 2Ā°C, with average relative humidity of 90%, duration of cherrys is about 2 weeks, and for peaches 2 to 4 weeks. In the heat balance calculation, all process parameters and quality of isolation, have been taken in to consideration
Analysis and the results of serological testing of Croatian organ donors from 2006 to 2012
Uvod: UspjeÅ”nost transplantacije i preživljavanja presatka usko su povezani s odsustvom infekcije u primatelja. Infekcija primatelja je posljedica infekcije presatkom, reaktivacije latentnih infekcija primatelja, nozokomijalnih infekcija i kasnije, zbog doživotne imunosupresije infekcija iz okoline. Hrvatski zavod za transfuzijsku medicinu (HZTM) od 2006. provodi obvezna testiranja donora organa (DO) na uzroÄnike krvlju prenosivih bolesti (24h/7 dana) za potrebe cijele Hrvatske.
Materijal i metode: U razdoblju od 5.11.2006. ā 31.12.2012. ispitano je u HZTM 642 uzoraka plazme DO pri Äemu su koriÅ”teni testovi Abbott ā Architect i bioMerieux ā Vidas. U ovom radu analizirani su kvaliteta uzorka, brzina i rezultati testiranja na biljege infekcije virusima humane imunodeficijencije 1 i 2 (HIV), virusima hepatitisa B (HBV) i C (HCV), citomegalovirusom (CMV), Epstein-Barr virusom (EBV), T. pallidum i T. gondii.
Rezultati: Seroprevalencija EBV, CMV i T. gondii oÄekivano je visoka i iznosi 96,8%, 92% i 71%. HIV pozitivnih meÄu DO nije bilo, a biljege HBV infekcije, HBsAg i antitijela na HBcAg (anti-HBc) imalo je 0,5% odnosno 8,9% DO. U 1,3% ispitanih dokazan je HCV antigen, a antitijela na virus hepatitisa C (anti-HCV) bila su pozitivna u njih 1,6%. UÄestalost treponemskih antitijela bila je 0,8%. 2,5% uzoraka bilo je razrijeÄeno viÅ”e od 50%, a prosjeÄno vrijeme testiranja DO bilo je 2,04 sata.
ZakljuÄak: Rezultati testiranja DO upuÄuju na primjerenost odabranih testova i algoritama testiranja kao i metoda selekcije DO u donorskim bolnicama, a prevalencije patogena sukladne su epidemioloÅ”kim karakteristikama opÄe populacije.Introduction: The success of transplantation and graft survival are closely related to the absence of infection in transplant recipients through infected graft, reactivated recipient\u27s latent infections, nosocomial infections and community acquired infections. Since 2006, the Croatian Institute of Transfusion Medicine has been providing mandatory testing of organ donors (OD) for bloodborne pathogens (24/7) for the entire country.
Materials and methods: In the period from 5.11.2006. to 31.12.2012. a total of 642 organ donor plasma samples were tested by means of Abbott ā Architect and bioMerieux ā Vidas tests. In this paper, the quality of samples measured against rate of dilution, turnaround time and prevalence of human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), cytomegalovirus (CMV), Epstein-Barr virus (EBV), T. pallidum and T. gondii markers were analyzed.
Results: Seroprevalence of EBV, CMV and Toxoplasma gondii was as high as expected (96.8%, 92% and 71%, respectively). There were no HIV positive OD, while in 0.5% HBsAg, in 8.9% anti-HBc, in 1.6% anti-HCV, in 1.3% HCVAg and in 0.8% T. pallidum Ab were found positive. 2.5% of the samples were diluted by more than 50% and the average testing time per OD was 2.04 hours.
Conclusion: The results indicate the adequacy of organ donor selection methods in donor hospitals, appropriate tests and testing algorithms used. The prevalence of pathogens is in accordance with epidemiological characteristics of the general population