Comparison of the clinical course of Clostridium difficile infection in glutamate dehydrogenase-positive toxin-negative patients diagnosed by PCR to those with a positive toxin test. (April 2018)

• Record Type: Journal Article
• Authors: Origüen, J.; Corbella, L.; Orellana, M.Á.; Fernández-Ruiz, M.; López-Medrano, F.; San Juan, R.; Lizasoain, M.; Ruiz-Merlo, T.; Morales-Cartagena, A.; Maestro, G.; Parra, P.; Villa, J.; Delgado, R.; Aguado, J.M.
• Is Part Of: Clinical microbiology and infection. Volume 24:Number 4(2018)
• Page Start: 414
• Page End: 421
• Publication Date: 2018-04
• Subjects: Clostridium difficile -- Enzyme-immunoassay -- Outcome -- Overdiagnosis -- Polymerase chain reaction -- Recurrence -- Retrospective study; Medical microbiology -- Periodicals; Diagnostic microbiology -- Periodicals; Communicable diseases -- Periodicals; Infection -- Periodicals; 616.01
• DOI: 10.1016/j.cmi.2017.07.033
• Languages: English
• ISSNs: 1198-743X

Abstract

Abstract: Objectives: To evaluate the potential role of PCR-based assays in the over-diagnosis of Clostridium difficile infection (CDI) by using a validated diagnostic algorithm in daily clinical practice. Methods: We performed a retrospective cohort study evaluating all C. difficile -positive stool samples identified at our institution during a 12-month period, to compare outcomes and recurrence rates between patients with a positive enzyme immunoassay (EIA) for both glutamate dehydrogenase (GDH) and toxin A/B ('toxin-positive group'), with those with GDH-positive, toxin-negative samples in whom the diagnosis was made by a positive PCR-based assay ('toxin – /PCR + group'). Medical records were reviewed by two independent investigators blinded to the mode of diagnosis. Results: We analysed 231 first CDI episodes (106 (45.8 %) in the 'toxin-positive group' and 125 (54.1%) in the 'toxin – /PCR + group'). Both groups had similar baseline characteristics. Patients in the 'toxin-positive group' presented more frequently with a severe/severe complicated form than those in the 'toxin – /PCR + group' (36 (33.9%) versus 24 (19.2%); p 0.011) and had more recurrences (27 (25.5%) versus 9 (7.2%); p 0.001). Diagnosis of CDI based on a GDH/toxin-positive EIA independently predicted severe/severe-complicated course (adjusted OR 2.11; 95% CI 1.06–4.22; p 0.033) and recurrence (adjusted OR 3.79; 95% CI 1.65–8.69; p 0.002). There were no differences in all-cause mortality (12.3% versus 12.0%; p 0.95) or CDI-attributable mortality (4.7% versus 4.8%; p 0.93). Conclusions: Toxin-positive patients were more likely to have severe-complicated forms of CDI and recurrences. Nevertheless, CDI-related complications may still occasionally occur among toxin-negative patients diagnosed by PCR, which stresses the need for individualized clinical evaluation.