Abstract:Although basiliximab and rabbit anti-thymocyte globulin (ATG) are effective in delaying and reducing the incidence of acute rejection (AR) thus improving short-term graft survival, their impact on long-term graft survival has not been well established in renal transplant recipients. To evaluate the long-term efficacy after induction therapy with ATG/basiliximab in renal transplant recipients, we studied retrospectively 86 renal transplant recipients of living donor renal transplantation from 2003 to 2006; of t… Show more
“…This includes the effects of CMV infection and Valganciclovir used for prophylaxis. This is more than previously done retrospective study in India by Kesiraju et al 4 The rate of bacterial, fungal and viral infections was comparable in both the groups. Similar to Liborio et al 11 The rate of Lower respiratory tract infection was higher in ATG group 15.2% vs. 10.5% in basiliximab group similar to Wang et al 13 The incidence of UTI was similar between the two groups (13.3% vs. 12.5%) in contrast to Huang et al 20 where there was higher incidence of UTI in ATG group.…”
Section: Image 1 Discussionsupporting
confidence: 57%
“…In contrast to these studies Brennan et al 7 found higher incidence in basiliximab group. The incidence of CMV infection is more in both groups when compared to previous studies Kesiraju et al 4 who used lesser doses of ATG and used CMV prophylaxis in both groups but less than the incidence in Ulrich et al and Kim et al 12,14 There were two previous studies from India Kesiraju et al 4 and Patel et al The death censored graft loss was 3.8% in ATG group and 4.1% in the basiliximab group. Total graft loss was 8.9% in the ATG group and 7.58% in the basiliximab group less than previous studies done in India.…”
Section: Image 1 Discussionmentioning
confidence: 71%
“…There was one previous retrospective study in India comparing induction strategies with ATG and basiliximab. 4 Many randomised controlled trials 3,5,6,7,8 and retrospective trials 4,9-17 were done to compare the induction agents.…”
BACKGROUND Renal transplantation is the best available form of renal replacement therapy. Induction therapy pre-transplant reduces the incidence of graft rejections. We present a retrospective study comparing different induction methods in living donor kidney transplantation in our institute. MATERIALS AND METHODS We analysed 423 live kidney transplant recipients of our center from Dec 2010 to Nov 2015, 344 of whom received basiliximab as induction and 79 r-ATG as induction. Primary outcomes like patient survival and graft survival, secondary outcomes like graft rejections, infections, PTDM, recurrence of disease were compared. RESULTS 5yr patient survival rates were observed to be 91% and 88% respectively whereas graft survival rates were 93% and 86% respectively for ATG and basiliximab. Incidence of rejections was similar (p=0.867). Cellular rejections were more common with basiliximab (7.9% vs. 3.8%) but statistically not significant (P=0.498). Infections in the post-operative period were more common in r-ATG arm especially LRTI (P=0.011) and diarrhoeal episodes (P=0.005). Incidence of cytopenias was more in r-ATG arm during hospital stay (10.1 vs. 2.6% P=0.002) and also the later followup period (25 vs. 12.4% P<0.001). Incidence of PTDM was more in basiliximab (33.8% vs. 22.8%) arm but not significant (P=0.061). CONCLUSION ATG and basiliximab are non-inferior to one another as induction therapy. ATG is effective in high immunological risk groups with equivalent graft and patient survival with increased risk of Lower respiratory tract infections and diarrhoea in immediate post-transplant periods and increased risk for cytopenias compared to basiliximab. Basiliximab has slightly increased risk of post-transplant diabetes mellitus. Careful selection of the agent in an individual based on risk rather than a question of efficacy of agents is the key to successful transplantation.
“…This includes the effects of CMV infection and Valganciclovir used for prophylaxis. This is more than previously done retrospective study in India by Kesiraju et al 4 The rate of bacterial, fungal and viral infections was comparable in both the groups. Similar to Liborio et al 11 The rate of Lower respiratory tract infection was higher in ATG group 15.2% vs. 10.5% in basiliximab group similar to Wang et al 13 The incidence of UTI was similar between the two groups (13.3% vs. 12.5%) in contrast to Huang et al 20 where there was higher incidence of UTI in ATG group.…”
Section: Image 1 Discussionsupporting
confidence: 57%
“…In contrast to these studies Brennan et al 7 found higher incidence in basiliximab group. The incidence of CMV infection is more in both groups when compared to previous studies Kesiraju et al 4 who used lesser doses of ATG and used CMV prophylaxis in both groups but less than the incidence in Ulrich et al and Kim et al 12,14 There were two previous studies from India Kesiraju et al 4 and Patel et al The death censored graft loss was 3.8% in ATG group and 4.1% in the basiliximab group. Total graft loss was 8.9% in the ATG group and 7.58% in the basiliximab group less than previous studies done in India.…”
Section: Image 1 Discussionmentioning
confidence: 71%
“…There was one previous retrospective study in India comparing induction strategies with ATG and basiliximab. 4 Many randomised controlled trials 3,5,6,7,8 and retrospective trials 4,9-17 were done to compare the induction agents.…”
BACKGROUND Renal transplantation is the best available form of renal replacement therapy. Induction therapy pre-transplant reduces the incidence of graft rejections. We present a retrospective study comparing different induction methods in living donor kidney transplantation in our institute. MATERIALS AND METHODS We analysed 423 live kidney transplant recipients of our center from Dec 2010 to Nov 2015, 344 of whom received basiliximab as induction and 79 r-ATG as induction. Primary outcomes like patient survival and graft survival, secondary outcomes like graft rejections, infections, PTDM, recurrence of disease were compared. RESULTS 5yr patient survival rates were observed to be 91% and 88% respectively whereas graft survival rates were 93% and 86% respectively for ATG and basiliximab. Incidence of rejections was similar (p=0.867). Cellular rejections were more common with basiliximab (7.9% vs. 3.8%) but statistically not significant (P=0.498). Infections in the post-operative period were more common in r-ATG arm especially LRTI (P=0.011) and diarrhoeal episodes (P=0.005). Incidence of cytopenias was more in r-ATG arm during hospital stay (10.1 vs. 2.6% P=0.002) and also the later followup period (25 vs. 12.4% P<0.001). Incidence of PTDM was more in basiliximab (33.8% vs. 22.8%) arm but not significant (P=0.061). CONCLUSION ATG and basiliximab are non-inferior to one another as induction therapy. ATG is effective in high immunological risk groups with equivalent graft and patient survival with increased risk of Lower respiratory tract infections and diarrhoea in immediate post-transplant periods and increased risk for cytopenias compared to basiliximab. Basiliximab has slightly increased risk of post-transplant diabetes mellitus. Careful selection of the agent in an individual based on risk rather than a question of efficacy of agents is the key to successful transplantation.
“…Anti-thymocyte globulin (ATG) induction before transplantation, followed by a triple immunosuppressive regimen (MMF, prednisone, and tacrolimus) post-transplantation is common practice at KAMC. Studies have shown the effectiveness of immunosuppressive therapy, encompassing triple therapy and IL-2 receptor antibody basiliximab in reducing the rates of DGF among kidney recipients, and though the induction used differs from that of KAMC, both ATG and basiliximab are safe and effective options [28]. Triple immunosuppressive therapy and ATG induction were given to all patients in the present study.…”
BackgroundDelayed graft function (DGF) is the most common early postoperative complication of renal transplantation. The occurrence of DGF can lead to both early and late devastating consequences on the allograft's survival. The risk of developing this complication can increase with certain factors that are related to both the donor and the recipient. In the present study, we aimed to detect the incidence rate of DGF among patients attending a tertiary care hospital in Riyadh, Saudi Arabia, and to investigate potential predictors of DGF.
Materials and methodsThis retrospective chart review was conducted at King Abdulaziz Medical City (KAMC), a tertiary care hospital in Riyadh, Saudi Arabia. The inclusion criteria were all patients, 18 years or older, who had renal transplantation from January 1, 2016, to March 31, 2020. Patients who had a second renal transplant, or renal transplantation in a different hospital and were followed up at KAMC were excluded. Patients' medical records were accessed using the BESTCare electronic system to obtain the patients' demographic data. A Chisquare test was used to test for the association between a predictor and a delay in graft function.
ResultsA total of 344 patients were enrolled in the present study, approximately half of whom were males (56.6%, n=189). Around one-half (49.4%) were aged between 40 and 64 years. The most common cause of renal failure was hypertension, which was found in 117 (35%) patients, followed by diabetes mellitus (DM) in 94 (28.1%) patients. Most organ donors 258 (77.2%) were alive. A total of 23 (6.9%) participants developed DGF. Mycophenolate mofetil (MMF) was found to be significantly associated with DGF (P < 0.001). Those who took MMF (5.9%) had a significantly lower rate of DGF compared to those who did not (36.4%). A significantly higher rate of DGF was seen in patients whose transplants were taken from deceased donors (15.5%) compared to living donor transplants (3.9%). Gender, age, body mass index (BMI), recipient blood type, donor blood type, and cause of renal failure were not associated with DGF.
ConclusionsOnly 6.9% of the study's participants exhibited DGF. The observed rate was lower than the ones detected in the literature. Those who took MMF had a significantly lower rate of DGF compared to those who did not. Transplants of deceased donors (15.5%) showed a significantly higher rate of DGF. Larger multicenter studies are required to further investigate DGF in a region with a high prevalence of organ failure and a higher need for transplantations, such as Saudi Arabia.
“…Incidence of leucopenia and thrombocytopenia in basiliximab-treated renal transplant patients are approximately 10%–15% and 5%, respectively [ 76 ]. Many comparative studies have demonstrated that leucopenia and thrombocytopenia occurred less in basiliximab [ 64 , 76 , 141 , 147 , 148 ] when compared to other agents used in induction. In the 3 C trial, leucopenia was 3.6 times higher in KTR receiving alemtuzumab as compared to basiliximab [ 147 ].…”
Section: Insight Into Etiology Of Hematological Cytopenia and Subsmentioning
Drug-induced hematological cytopenia is common in kidney transplantation. Various cytopenia including leucopenia (neutropenia), thrombocytopenia, and anemia can occur in kidney transplant recipients. Persistent severe leucopenia or neutropenia can lead to opportunistic infections of various etiologies. On the contrary, reducing or stopping immunosuppressive medications in these events can provoke a rejection. Transplant clinicians are often faced with the delicate dilemma of balancing cytopenia and rejection from adjustments of immunosuppressive regimen. Differentials of drug-induced cytopenia are wide. Identification of culprit medication and subsequent modification is also challenging. In this review, we will discuss individual drug implicated in causing cytopenia and correlate it with corresponding literature evidence.
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