valganciclovir and Heart-Diseases

valganciclovir has been researched along with Heart-Diseases* in 2 studies

Other Studies

2 other study(ies) available for valganciclovir and Heart-Diseases

ArticleYear
Impact of donor and recipient cytomegalovirus serology on long-term survival of heart transplant recipients.
    Transplant infectious disease : an official journal of the Transplantation Society, 2019, Volume: 21, Issue:1

    Some studies have shown that pre-transplant cytomegalovirus (CMV) serostatus is associated with heart transplant patient survival while others have not. We analyzed the relationship between pre-transplant donor/recipient CMV serostatus and long-term mortality in a retrospective cohort of heart transplant recipients at our center.. Adult (Age >17 years) heart recipients transplanted between July 1985-December 2015 were analyzed. Variables included age, sex, pre-transplant donor (D)/recipient (R) serostatus [D-/R-, D-/R+, D+/R+, D+/R-], CMV infection within 2 years of transplant and transplant eras divided by changes in CMV prevention strategies: Era 1 (Pre-ganciclovir, July 1985-April 1998), Era 2 (Oral ganciclovir, May 1998-December 2004), Era 3 (Valganciclovir, January 2005-December 2015). Survival analysis and Cox regression were performed at 10 years.. A total of 620 heart transplants were included in our analysis; 20% were CMV mismatched pre-transplant. Thirty-eight percent of patients were infected with CMV within the first two post-transplant years. Survival analysis showed D/R CMV serostatus did not significantly impact survival of heart recipients at 10 years (P = 0.11). Survival was significantly different across eras for D-/R+, D+/R+, and D+/R+ (P = 0.043) but not D-/R- patients (P = 0.8). Cox regression revealed that patients transplanted in the valganciclovir era have an estimated 29% reduced risk of death (P = 0.047) compared to patients transplanted in the pre-ganciclovir era after controlling for age at transplantation, D/R CMV serostatus and CMV infection.. Our review of the impact of CMV managed differently across eras suggests in heart transplantation there is no influence of D/R CMV serostatus on 10 year survival.

    Topics: Adult; Aged; Antiviral Agents; Cytomegalovirus; Cytomegalovirus Infections; Female; Follow-Up Studies; Ganciclovir; Graft Survival; Heart Diseases; Heart Transplantation; Humans; Male; Middle Aged; Prospective Studies; Retrospective Studies; Risk Assessment; Serologic Tests; Survival Analysis; Tissue Donors; Transplant Recipients; Valganciclovir; Young Adult

2019
Correlation between body mass index and leucopenia after administration of valganciclovir for cytomegalovirus infection in chinese cardiac recipients.
    Circulation journal : official journal of the Japanese Circulation Society, 2007, Volume: 71, Issue:6

    Valganciclovir (VGC) has recently been proved efficacious for the prophylaxis and treatment of cytomegalovirus (CMV) infection in transplant recipients. Leucopenia is a troublesome complication of VGC but the possible risk factors are unknown.. Once a cardiac recipient's quantitative real-time CMV-polymerase chain reaction result showed positive, VGC was administered for 3 months. The 61 cardiac recipients enrolled in this study were divided into 2 groups: non-leucopenia group (n=29) and leucopenia group (n=32). The white blood cell (WBC) counts in the leucopenia group dropped approximately 55.6% in the first month after VGC therapy (pre-VGC WBC count: 5,544 cells/mm(3) vs post-VGC WBC count: 2,460 cells/mm(3), p<0.0001). The most significant difference between the 2 groups was body mass index (BMI, 23.04 vs 25.84, p=0.008), which was the impact factor of VGC-induced leucopenia.. Severe leucopenia may develop after VGC therapy in Chinese cardiac recipients, especially those with lower BMI.

    Topics: Adult; Aged; Antiviral Agents; Asian People; Body Mass Index; China; Cytomegalovirus Infections; DNA, Viral; Female; Ganciclovir; Heart Diseases; Humans; Leukocyte Count; Leukopenia; Male; Middle Aged; Polymerase Chain Reaction; Retrospective Studies; Risk Factors; Valganciclovir

2007