@article{JuddHofBeladdaleetal.2022, author = {Judd, L. and Hof, L. and Beladdale, L. and Friederich, P. and Thoma, J. and Wittmann, M. and Zacharowski, K. and Meybohm, P. and Choorapoikayil, S.}, title = {Prevalence of pre-operative anaemia in surgical patients: a retrospective, observational, multicentre study in Germany}, series = {Anaesthesia}, volume = {77}, journal = {Anaesthesia}, number = {11}, doi = {10.1111/anae.15847}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-318199}, pages = {1209 -- 1218}, year = {2022}, abstract = {Anaemia is a risk factor for several adverse postoperative outcomes. Detailed data about the prevalence of anaemia are not available over a long time-period in Germany. In this retrospective, observational, multicentre study, patients undergoing surgery in March in 2007, 2012, 2015, 2017 and 2019 were studied. The primary objective was the prevalence of anaemia at hospital admission. The secondary objectives were the association between anaemia and the number of units of red blood cells transfused, length of hospital stay and in-hospital mortality. A total of 23,836 patients were included from eight centres. The prevalence of pre-operative anaemia in patients aged ≥ 18 years decreased slightly from 37\% in 2007 to 32.5\% in 2019 (p = 0.01) and increased in patients aged ≤ 18 years from 18.8\% in 2007 to 26.4\% in 2019 (p > 0.001). The total amount of blood administered per 1000 patients decreased from 671.2 units in 2007 to 289.0 units in 2019. Transfusion rates in anaemic patients declined from 33.8\% in 2007 to 19.1\% in 2019 (p < 0.001) and in non-anaemic patients from 8.4\% in 2007 to 3.4\% in 2019 (p < 0.001). Overall, the mortality rate remained constant over the years: 2.9\% in 2007, 2.1\% in 2012, 2.5\% in 2015, 1.9\% in 2017 and 2.5\% in 2019. In the presence of anaemia, mortality was significantly increased compared with patients without anaemia (OR 5.27 (95\%CI 4.13-6.77); p < 0.001). Red blood cell transfusion was associated with an increased risk of mortality (OR 14.98 (95\%CI 11.83-19.03); p < 0.001). Using multivariable linear regression analysis with fixed effects, we found that pre-operative anaemia (OR 2.08 (95\%CI 1.42-3.05); p < 0.001) and red blood cell transfusion (OR 4.29 (95\%CI 3.09-5.94); p < 0.001) were predictors of mortality but not length of stay (0.99 (95\%CI 0.98-1.00) days; p = 0.12) and analysed years (2007 vs. 2019: OR 1.49 (95\%CI 0.86-2.69); p = 0.07). Pre-operative anaemia affects more than 30\% of surgical patients in Germany and multidisciplinary action is urgently required to reduce adverse outcomes.}, language = {en} } @article{HackerHofEmoedyetal.1986, author = {Hacker, J{\"o}rg and Hof, H. and Em{\"o}dy, L. and Goebel, W.}, title = {Influence of cloned Escherichia coli hemolysin genes, S fimbriae and serum resistance on pathogenicity in different animal models}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-59423}, year = {1986}, abstract = {The virulence of the uropathogenic E. coli strain 536 (06: K 1 5: H31) which produces the S-fimbrial adhesin (Sfa•), is serum-resistant (Sre+) and hemolytic (Hiy+) and its derivatives were assessed in five different animal models. Cloned hemolysin (h/y) determinants from the Chromosomes of 06,018 and 075 E. colistrains and from the plasmid pHiy152 were introduced into the spontaneaus Sfa-, Sre-, Hly- mutant 536-21 and its Sfa+, Sre+, Hly- variant 536-31. As already demonstrated for the 536-21 strains {lnfect. Immun. 42: 57-63) the 018-hly determinant but not the plasmid-encoded hly determinant of pHiy 1 52 transformed into 536-31 contribute to lethality in a mouse peritonitis modal. Similar results were obtained with both Hlyhost strains and their Hly+ transformants in a chicken embryo test and in a mouse nephropathogenicity assay in which the renal bacterial counts were measured 1 5 min to 8 hours after i.v. infection. S-fimbriae and serum resistance had only a marginal influence in these three in vivo systems. ln centrast all three factors, S-fimbriae, serum resistance and hemolysin, were necessary for full virulence in a respiratory mouse infection assay. ln a subcutaneously-induced sepsis model in the mouse restoration of S-fimbriae and serum resistance and separately chromosomally-encoded hemolysis increased virulence to a Ievel comparable to that of the parental 536 strain.}, subject = {Infektionsbiologie}, language = {en} }