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Potential role of post-transplant hypogammaglobulinemia in the risk of Clostridium difficile infection after kidney transplantation: a case-control study. [artículo]

Por: Origüen Sabater, Julia [Enfermedades Infecciosas] | Fernández Ruiz, Mario [Medicina Interna] | Lumbreras Bermejo, Carlos [Medicina Interna] | Orellana Miguel, María Ángeles [Microbiología y Parasitología] | López Medrano, Francisco [Enfermedades Infecciosas] | Ruiz Merlo, Tamara [Enfermedades Infecciosas] | San Juan Garrido, Rafael [Medicina Interna] | García Reyne, Ana [Medicina Interna] | Aguado García, José María [Enfermedades Infecciosas] | González Monte, Esther [Nefrología] | Polanco Fernández, Natalia [Nefrología] | Andrés Belmonte, Amado [Nefrología] | Paz Artal, Estela [Inmunología].
Colaborador(es): Servicio de Medicina Interna | Servicio de Microbiología y Parasitología | Servicio de Nefrología | Servicio de Inmunología | Instituto de Investigación imas12.
Tipo de material: materialTypeLabelArtículoEditor: Infection, 2015Descripción: 43(4):413-22.Recursos en línea: Solicitar documento Resumen: Purpose: To identify reversible risk factors for Clostridium difficile infection (CDI) after kidney transplantation (KT) that could lead to a reduction in its incidence and associated complications. Methods: We performed a single-center case-control study in which 41 patients undergoing KT between February 2009 and July 2013 who developed a first episode of post-transplant CDI were included as cases. Patients transplanted at the same calendar day (± 2 weeks) as each case with no evidence of CDI and comparable risk exposure period were chosen as controls (2:1 ratio). Serum immunoglobulin and complement levels were systematically measured at baseline and months 1 and 6 after transplantation. Results: Multivariate regression analysis identified age-adjusted Charlson comorbidity index (odds ratio [OR] per unitary increment 1.31; P value = 0.043), delayed graft function (OR 2.76; P value = 0.039), prior cytomegalovirus (CMV) disease (OR 6.85; P value = 0.011) and prior acute graft rejection (OR 5.92; P value = 0.008) as risk factors for post-transplant CDI. Cases with their first episode of CDI occurring beyond the first month were more likely to have IgG hypogammaglobulinemia (HGG) at month 1 (P value = 0.002), whereas cases with CDI beyond the sixth month were more likely to have HGG of any class at month 6 (P value = 0.003). Poor outcome (graft loss and/or all-cause mortality) was more common among cases (adjusted hazard ratio 5.69; P value = 0.001). Conclusion: The occurrence of CDI exerts a detrimental effect on graft and patient outcome. Post-transplant HGG was a potentially modifiable risk factor for CDI in KT recipients.
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Formato Vancouver:
Origüen J, Fernández Ruiz M, Lumbreras C, Orellana MÁ, López Medrano F, Ruiz Merlo T et al. Potential role of post-transplant hypogammaglobulinemia in the risk of Clostridium difficile infection after kidney transplantation: a case-control study. Infection. 2015 Aug;43(4):413-22.

PMID: 25676130

Contiene 41 referencias

Purpose: To identify reversible risk factors for Clostridium difficile infection (CDI) after kidney transplantation (KT) that could lead to a reduction in its incidence and associated complications.
Methods: We performed a single-center case-control study in which 41 patients undergoing KT between February 2009 and July 2013 who developed a first episode of post-transplant CDI were included as cases. Patients transplanted at the same calendar day (± 2 weeks) as each case with no evidence of CDI and comparable risk exposure period were chosen as controls (2:1 ratio). Serum immunoglobulin and complement levels were systematically measured at baseline and months 1 and 6 after transplantation.
Results: Multivariate regression analysis identified age-adjusted Charlson comorbidity index (odds ratio [OR] per unitary increment 1.31; P value = 0.043), delayed graft function (OR 2.76; P value = 0.039), prior cytomegalovirus (CMV) disease (OR 6.85; P value = 0.011) and prior acute graft rejection (OR 5.92; P value = 0.008) as risk factors for post-transplant CDI. Cases with their first episode of CDI occurring beyond the first month were more likely to have IgG hypogammaglobulinemia (HGG) at month 1 (P value = 0.002), whereas cases with CDI beyond the sixth month were more likely to have HGG of any class at month 6 (P value = 0.003). Poor outcome (graft loss and/or all-cause mortality) was more common among cases (adjusted hazard ratio 5.69; P value = 0.001).
Conclusion: The occurrence of CDI exerts a detrimental effect on graft and patient outcome. Post-transplant HGG was a potentially modifiable risk factor for CDI in KT recipients.

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