{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T01:46:22Z","timestamp":1782870382489,"version":"3.54.5"},"reference-count":20,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T00:00:00Z","timestamp":1777939200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"vor","delay-in-days":57,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"}],"funder":[{"DOI":"10.13039\/501100005743","name":"Universit\u00e0 Cattolica del Sacro Cuore","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100005743","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Tech Coloproctol"],"published-print":{"date-parts":[[2026,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>We assessed whether baseline endoscopic and clinical scores of diverticular disease (DD) may predict the severity of acute diverticulitis (AD), hospital admission and length of hospital stay (HS).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>We conducted a 3-year, multicentre, prospective cohort study involving 2215 patients. DD was scored according to the Diverticular Inflammation and Complication Assessment (DICA) classification and the Combined Overview on Diverticular Assessment (CODA) score.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Higher baseline DICA and CODA scores were associated with increased risk of complicated AD [relative risk ratio (RRR)\u2009=\u20095.57; 95% confidence interval (CI): 3.42\u20139.09 and RRR\u2009=\u20095.17; 95% CI: 3.01\u20138.88, respectively]. An average HS of 4.62\u00a0days (95% CI: 2.93\u20136.27) for DICA 1, 5.57\u00a0days (95% CI: 4.29\u20136.85) for DICA 2 and 6.73\u00a0days (95% CI: 5.81\u20137.64) for DICA 3 was recorded; an average HS of 4.14\u00a0days (95% CI: 2.32\u20135.96) for CODA A, 5.12\u00a0days (95% CI: 3.67\u20136.56) for CODA B and 6.32\u00a0days (95% CI: 5.35\u20137.30) for CODA C was recorded.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>DICA and CODA scores may predict the severity of AD and the length of the HS.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1007\/s10151-026-03324-6","type":"journal-article","created":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T15:34:21Z","timestamp":1777995261000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["The DICA endoscopic score and the CODA clinical 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Jaroslaw Regula served as a lecturer for AlfaSigma, Takeda, Ipsen and Servier;  Alfredo Papa served as a speaker for AlfaSigma and Janssen.  Silvio Danese served as speaker, consultant, and\/or advisory board member for Abbvie, Allergan, Alfa Wassermann, Biogen, Boehringer Ingelheim, Celgene, Celltrion, Ferring, Gilead, Hospira, Johnson & Johnson, Merck, MSD, Mundipharma, Pfizer Inc., Sandoz, Takeda, Tigenix, UCB Pharma and Vifor.  The remaining authors declare no competing interests.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interests"}},{"value":"The study has been conducted according to the World Medical Association Declaration of Helsinki of the 1975. It was approved by the Ethics Committee of the coordinating centre\u00a0and of all participating centres. The study was recorded at\n                      \n                      (NCT01534754).","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval"}},{"value":"All study participants provided informed written consent prior to endoscopic investigation and to take part in this study.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Patients consent statement"}}],"article-number":"85"}}