MO1004: Non-Antibiotic Prophylaxis with D-MANOSE for Uti in DE-NOVO Kidney Transplant Recipients: The Manotras Study
Abstract BACKGROUND AND AIMS Urinary tract infections (UTIs) are one of the most frequent complications in the first 6 months after kidney transplantation. (1) D-Mannose, a simple sugar, could play a very important role in the prevention of urinary infections, inhibiting the attachment of bacterial...
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description | Abstract
BACKGROUND AND AIMS
Urinary tract infections (UTIs) are one of the most frequent complications in the first 6 months after kidney transplantation. (1) D-Mannose, a simple sugar, could play a very important role in the prevention of urinary infections, inhibiting the attachment of bacterial type one fimbriae to the urothelium, reducing their ability to infect de host. Proanthocyanides (PAC) have also been shown in vitro activity to inhibit the adherence of Escherichia coli by a similar mechanism. Both have shown promising results in reducing the risk of UTI in healthy women, but its efficacy has not been evaluated in kidney transplant population yet. (2) In this single-cantre, double-blind, prospective, randomized clinical trial, we aimed to evaluate the impact and security of a 24-h prolonged release formulation of D-Mannose in de-novo kidney transplantation UTI's.
METHOD
Between April 2019 and September 2020, 60 patients were recruited and randomized in 1:1 ratio according to treatment arm. Control group was treated with PAC, while the study group received PAC plus Mannose. Treatments were given as a prophylaxis strategy immediate after renal transplantation and during the first 3 months. All patients were followed for 6 months.
RESULTS
No statistically differences were observed in the baseline characteristics among study groups (Table 1). During the follow up; 61% of patients had at least one UTI episode (asymptomatic bacteriuria 56%, cystitis 6% and acute graft pyelonephritis 17%). Escherichia coli accounted for 28% of all UTI episodes, followed by Enterococcus faecalis (15%), Enterobacter cloacae (13%) and Klebsiella pneumoniae (13%). The main renal outcomes (eGFR at 6 months, acute rejection and DGF) did not differ among study groups.
We found no statistically differences recording in the incidence of UTI between groups (Fig. 1). At univariate analysis the surgical complications, and female gender were independently associated with UTI. {OR 5.92, [95% confidence interval (95% CI) 1.021–34.36]; P = .041 and OR 3.59 95% CI 1.051–12.27; P = .047} with no effect of treatment with D-mannose.
CONCLUSION
In this study, a prophylaxis strategy based on Mannose + PAC did not show a significant impact compared with PAC alone on UTI in the de-novo kidney transplant population.
FIGURE 1:
% of UTI in each group
Table 1.
Baseline demographics and clinical characteristics depending on treatment group
Mannose + PAC
PAC
Characteristic
n = 27
n = 27
P
Sex (F/M) |
doi_str_mv | 10.1093/ndt/gfac088.006 |
format | Article |
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BACKGROUND AND AIMS
Urinary tract infections (UTIs) are one of the most frequent complications in the first 6 months after kidney transplantation. (1) D-Mannose, a simple sugar, could play a very important role in the prevention of urinary infections, inhibiting the attachment of bacterial type one fimbriae to the urothelium, reducing their ability to infect de host. Proanthocyanides (PAC) have also been shown in vitro activity to inhibit the adherence of Escherichia coli by a similar mechanism. Both have shown promising results in reducing the risk of UTI in healthy women, but its efficacy has not been evaluated in kidney transplant population yet. (2) In this single-cantre, double-blind, prospective, randomized clinical trial, we aimed to evaluate the impact and security of a 24-h prolonged release formulation of D-Mannose in de-novo kidney transplantation UTI's.
METHOD
Between April 2019 and September 2020, 60 patients were recruited and randomized in 1:1 ratio according to treatment arm. Control group was treated with PAC, while the study group received PAC plus Mannose. Treatments were given as a prophylaxis strategy immediate after renal transplantation and during the first 3 months. All patients were followed for 6 months.
RESULTS
No statistically differences were observed in the baseline characteristics among study groups (Table 1). During the follow up; 61% of patients had at least one UTI episode (asymptomatic bacteriuria 56%, cystitis 6% and acute graft pyelonephritis 17%). Escherichia coli accounted for 28% of all UTI episodes, followed by Enterococcus faecalis (15%), Enterobacter cloacae (13%) and Klebsiella pneumoniae (13%). The main renal outcomes (eGFR at 6 months, acute rejection and DGF) did not differ among study groups.
We found no statistically differences recording in the incidence of UTI between groups (Fig. 1). At univariate analysis the surgical complications, and female gender were independently associated with UTI. {OR 5.92, [95% confidence interval (95% CI) 1.021–34.36]; P = .041 and OR 3.59 95% CI 1.051–12.27; P = .047} with no effect of treatment with D-mannose.
CONCLUSION
In this study, a prophylaxis strategy based on Mannose + PAC did not show a significant impact compared with PAC alone on UTI in the de-novo kidney transplant population.
FIGURE 1:
% of UTI in each group
Table 1.
Baseline demographics and clinical characteristics depending on treatment group
Mannose + PAC
PAC
Characteristic
n = 27
n = 27
P
Sex (F/M), n (%)
13/14 (48/52%)
12/15 (44/55%)
0.78
Age (years), median (IQR)
62
57
0.68
Waiting time on dialysis (months), median (IQR)
31
27
0.35
Cause of ESKD
0.83
Undetermined, n (%)
5 (18%)
6 (22%)
Diabetes, n (%)
3 (11,1%)
3 (11,1%)
Vascular nephropathy, n (%)
2 (7.4%)
2(7,4%)
Tubulo-interstitial nephritis, n (%)
3 (11.1%)
0 (0 %)
ADPKD, n (%)
2 (7,4%)
7 (25,9%)
Glomerulonephritis, n (%)
8 (29,96%)
7 (25,9%)
Others, n (%)
4 (14,1%)
2 (7,4%)
Type of donor, n (%)
0.58
Living
13 (48%)
12 (40%)
Deceased
14 (52%)
16 (60%)
Induction Therapy, n (%)
0.26
Basiliximab
18 (66%)
13 (52%)
Thymoglobulin
9 (33%)
12 (48%)
ESKD, end stage kidney decease; ADPKD, autosomic dominant kidney decease; CMV, citomegalovirius.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfac088.006</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>Nephrology, dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the ERA. 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Melissa Rau Lertora, Ana</creatorcontrib><creatorcontrib>Santelli, Adrián</creatorcontrib><creatorcontrib>Fiol, Maria</creatorcontrib><creatorcontrib>Riera, Luis</creatorcontrib><creatorcontrib>Etcheverry, Begoña</creatorcontrib><creatorcontrib>Ardanuy Tisaire, Carmen</creatorcontrib><creatorcontrib>Marti, Sara</creatorcontrib><creatorcontrib>Cruzado, Josep</creatorcontrib><creatorcontrib>Melilli, Edoardo</creatorcontrib><title>MO1004: Non-Antibiotic Prophylaxis with D-MANOSE for Uti in DE-NOVO Kidney Transplant Recipients: The Manotras Study</title><title>Nephrology, dialysis, transplantation</title><description>Abstract
BACKGROUND AND AIMS
Urinary tract infections (UTIs) are one of the most frequent complications in the first 6 months after kidney transplantation. (1) D-Mannose, a simple sugar, could play a very important role in the prevention of urinary infections, inhibiting the attachment of bacterial type one fimbriae to the urothelium, reducing their ability to infect de host. Proanthocyanides (PAC) have also been shown in vitro activity to inhibit the adherence of Escherichia coli by a similar mechanism. Both have shown promising results in reducing the risk of UTI in healthy women, but its efficacy has not been evaluated in kidney transplant population yet. (2) In this single-cantre, double-blind, prospective, randomized clinical trial, we aimed to evaluate the impact and security of a 24-h prolonged release formulation of D-Mannose in de-novo kidney transplantation UTI's.
METHOD
Between April 2019 and September 2020, 60 patients were recruited and randomized in 1:1 ratio according to treatment arm. Control group was treated with PAC, while the study group received PAC plus Mannose. Treatments were given as a prophylaxis strategy immediate after renal transplantation and during the first 3 months. All patients were followed for 6 months.
RESULTS
No statistically differences were observed in the baseline characteristics among study groups (Table 1). During the follow up; 61% of patients had at least one UTI episode (asymptomatic bacteriuria 56%, cystitis 6% and acute graft pyelonephritis 17%). Escherichia coli accounted for 28% of all UTI episodes, followed by Enterococcus faecalis (15%), Enterobacter cloacae (13%) and Klebsiella pneumoniae (13%). The main renal outcomes (eGFR at 6 months, acute rejection and DGF) did not differ among study groups.
We found no statistically differences recording in the incidence of UTI between groups (Fig. 1). At univariate analysis the surgical complications, and female gender were independently associated with UTI. {OR 5.92, [95% confidence interval (95% CI) 1.021–34.36]; P = .041 and OR 3.59 95% CI 1.051–12.27; P = .047} with no effect of treatment with D-mannose.
CONCLUSION
In this study, a prophylaxis strategy based on Mannose + PAC did not show a significant impact compared with PAC alone on UTI in the de-novo kidney transplant population.
FIGURE 1:
% of UTI in each group
Table 1.
Baseline demographics and clinical characteristics depending on treatment group
Mannose + PAC
PAC
Characteristic
n = 27
n = 27
P
Sex (F/M), n (%)
13/14 (48/52%)
12/15 (44/55%)
0.78
Age (years), median (IQR)
62
57
0.68
Waiting time on dialysis (months), median (IQR)
31
27
0.35
Cause of ESKD
0.83
Undetermined, n (%)
5 (18%)
6 (22%)
Diabetes, n (%)
3 (11,1%)
3 (11,1%)
Vascular nephropathy, n (%)
2 (7.4%)
2(7,4%)
Tubulo-interstitial nephritis, n (%)
3 (11.1%)
0 (0 %)
ADPKD, n (%)
2 (7,4%)
7 (25,9%)
Glomerulonephritis, n (%)
8 (29,96%)
7 (25,9%)
Others, n (%)
4 (14,1%)
2 (7,4%)
Type of donor, n (%)
0.58
Living
13 (48%)
12 (40%)
Deceased
14 (52%)
16 (60%)
Induction Therapy, n (%)
0.26
Basiliximab
18 (66%)
13 (52%)
Thymoglobulin
9 (33%)
12 (48%)
ESKD, end stage kidney decease; ADPKD, autosomic dominant kidney decease; CMV, citomegalovirius.</description><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PwjAchhujiYievfZsUvh1W7eVGwH8iMCMTK9L165Sg93Sluj-ezFw9_Renuc9PAjdUhhR4PHYqjD-0EJCno8A0jM0oEkKJIpzdo4GB4ISYMAv0ZX3nwDAoywboLAqKEAywevWkqkNpjZtMBK_uLbb9jvxYzz-NmGL52Q1XRebBdatw2_BYGPxfEHWxXuBn42yTY9LJ6zvdsIG_NpI05nGBj_B5bbBK2Hb4ITHm7BX_TW60GLnm5vTDlF5vyhnj2RZPDzNpksiM5aShvKUQ5LUMQNWC6VUFkOaQ6R0LiXLdEZroXMec6Y0RAnjUa0Vr0XGqKwbGg_R-HgrXeu9a3TVOfMlXF9RqP6aVYdm1alZdWh2MO6ORrvv_oV_AZqLbhQ</recordid><startdate>20220503</startdate><enddate>20220503</enddate><creator>Melissa Rau Lertora, Ana</creator><creator>Santelli, Adrián</creator><creator>Fiol, Maria</creator><creator>Riera, Luis</creator><creator>Etcheverry, Begoña</creator><creator>Ardanuy Tisaire, Carmen</creator><creator>Marti, Sara</creator><creator>Cruzado, Josep</creator><creator>Melilli, Edoardo</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20220503</creationdate><title>MO1004: Non-Antibiotic Prophylaxis with D-MANOSE for Uti in DE-NOVO Kidney Transplant Recipients: The Manotras Study</title><author>Melissa Rau Lertora, Ana ; Santelli, Adrián ; Fiol, Maria ; Riera, Luis ; Etcheverry, Begoña ; Ardanuy Tisaire, Carmen ; Marti, Sara ; Cruzado, Josep ; Melilli, Edoardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c756-e1969044b3505baddd7306802df8cc57f71baf89395df024592bfd9ba751cbe13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Melissa Rau Lertora, Ana</creatorcontrib><creatorcontrib>Santelli, Adrián</creatorcontrib><creatorcontrib>Fiol, Maria</creatorcontrib><creatorcontrib>Riera, Luis</creatorcontrib><creatorcontrib>Etcheverry, Begoña</creatorcontrib><creatorcontrib>Ardanuy Tisaire, Carmen</creatorcontrib><creatorcontrib>Marti, Sara</creatorcontrib><creatorcontrib>Cruzado, Josep</creatorcontrib><creatorcontrib>Melilli, Edoardo</creatorcontrib><collection>CrossRef</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Melissa Rau Lertora, Ana</au><au>Santelli, Adrián</au><au>Fiol, Maria</au><au>Riera, Luis</au><au>Etcheverry, Begoña</au><au>Ardanuy Tisaire, Carmen</au><au>Marti, Sara</au><au>Cruzado, Josep</au><au>Melilli, Edoardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MO1004: Non-Antibiotic Prophylaxis with D-MANOSE for Uti in DE-NOVO Kidney Transplant Recipients: The Manotras Study</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><date>2022-05-03</date><risdate>2022</risdate><volume>37</volume><issue>Supplement_3</issue><issn>0931-0509</issn><eissn>1460-2385</eissn><abstract>Abstract
BACKGROUND AND AIMS
Urinary tract infections (UTIs) are one of the most frequent complications in the first 6 months after kidney transplantation. (1) D-Mannose, a simple sugar, could play a very important role in the prevention of urinary infections, inhibiting the attachment of bacterial type one fimbriae to the urothelium, reducing their ability to infect de host. Proanthocyanides (PAC) have also been shown in vitro activity to inhibit the adherence of Escherichia coli by a similar mechanism. Both have shown promising results in reducing the risk of UTI in healthy women, but its efficacy has not been evaluated in kidney transplant population yet. (2) In this single-cantre, double-blind, prospective, randomized clinical trial, we aimed to evaluate the impact and security of a 24-h prolonged release formulation of D-Mannose in de-novo kidney transplantation UTI's.
METHOD
Between April 2019 and September 2020, 60 patients were recruited and randomized in 1:1 ratio according to treatment arm. Control group was treated with PAC, while the study group received PAC plus Mannose. Treatments were given as a prophylaxis strategy immediate after renal transplantation and during the first 3 months. All patients were followed for 6 months.
RESULTS
No statistically differences were observed in the baseline characteristics among study groups (Table 1). During the follow up; 61% of patients had at least one UTI episode (asymptomatic bacteriuria 56%, cystitis 6% and acute graft pyelonephritis 17%). Escherichia coli accounted for 28% of all UTI episodes, followed by Enterococcus faecalis (15%), Enterobacter cloacae (13%) and Klebsiella pneumoniae (13%). The main renal outcomes (eGFR at 6 months, acute rejection and DGF) did not differ among study groups.
We found no statistically differences recording in the incidence of UTI between groups (Fig. 1). At univariate analysis the surgical complications, and female gender were independently associated with UTI. {OR 5.92, [95% confidence interval (95% CI) 1.021–34.36]; P = .041 and OR 3.59 95% CI 1.051–12.27; P = .047} with no effect of treatment with D-mannose.
CONCLUSION
In this study, a prophylaxis strategy based on Mannose + PAC did not show a significant impact compared with PAC alone on UTI in the de-novo kidney transplant population.
FIGURE 1:
% of UTI in each group
Table 1.
Baseline demographics and clinical characteristics depending on treatment group
Mannose + PAC
PAC
Characteristic
n = 27
n = 27
P
Sex (F/M), n (%)
13/14 (48/52%)
12/15 (44/55%)
0.78
Age (years), median (IQR)
62
57
0.68
Waiting time on dialysis (months), median (IQR)
31
27
0.35
Cause of ESKD
0.83
Undetermined, n (%)
5 (18%)
6 (22%)
Diabetes, n (%)
3 (11,1%)
3 (11,1%)
Vascular nephropathy, n (%)
2 (7.4%)
2(7,4%)
Tubulo-interstitial nephritis, n (%)
3 (11.1%)
0 (0 %)
ADPKD, n (%)
2 (7,4%)
7 (25,9%)
Glomerulonephritis, n (%)
8 (29,96%)
7 (25,9%)
Others, n (%)
4 (14,1%)
2 (7,4%)
Type of donor, n (%)
0.58
Living
13 (48%)
12 (40%)
Deceased
14 (52%)
16 (60%)
Induction Therapy, n (%)
0.26
Basiliximab
18 (66%)
13 (52%)
Thymoglobulin
9 (33%)
12 (48%)
ESKD, end stage kidney decease; ADPKD, autosomic dominant kidney decease; CMV, citomegalovirius.</abstract><pub>Oxford University Press</pub><doi>10.1093/ndt/gfac088.006</doi></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); Alma/SFX Local Collection |
title | MO1004: Non-Antibiotic Prophylaxis with D-MANOSE for Uti in DE-NOVO Kidney Transplant Recipients: The Manotras Study |
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