Piccolo Francesco, Tai Anna Sze, Ee Hooi, Mulrennan Siobhain, Bell Scott, Ryan Gerard
Department of Respiratory Medicine Sir Charles Gairdner Hospital Perth Australia; Department of Respiratory and Sleep Medicine St John of God Healthcare Perth Australia.
Department of Respiratory Medicine Sir Charles Gairdner Hospital Perth Australia; Department of Thoracic Medicine The Prince Charles Hospital Brisbane Queensland.
Respirol Case Rep. 2016 Dec 7;5(1):e00204. doi: 10.1002/rcr2.204. eCollection 2017 Jan.
Adults with cystic fibrosis (CF) have significant rates of asymptomatic Clostridium difficile carriage and are frequently exposed to risk factors for C. difficile infection (CDI). Despite this, the rate of reported CDI in CF is low. We describe three cases of near fatal CDI in adults with CF and review the literature regarding presentation, management, and recurrence prevention. Early recognition is important as the clinical presentation may be atypical and the illness can be severe and even life-threatening. Management can be complicated by respiratory and nutritional failure. CF-related gastrointestinal dysfunction may alter the typical host-pathogen interaction between patient and C. difficile, potentially explaining the low rates of CDI and atypical presentation.
患有囊性纤维化(CF)的成年人无症状艰难梭菌携带率很高,且经常接触艰难梭菌感染(CDI)的危险因素。尽管如此,CF患者中报告的CDI发生率较低。我们描述了3例成年CF患者发生的近乎致命的CDI病例,并回顾了有关其临床表现、治疗及预防复发的文献。早期识别很重要,因为临床表现可能不典型,病情可能严重甚至危及生命。呼吸和营养衰竭可能使治疗变得复杂。CF相关的胃肠功能障碍可能改变患者与艰难梭菌之间典型的宿主-病原体相互作用,这可能解释了CDI发生率低和临床表现不典型的原因。