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Preventing Acute Kidney Injury (AKI) in Pediatric Patients (AKI)

Primary Purpose

Acute Kidney Injury

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Aminophylline
Placebo
Sponsored by
Le Bonheur Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Kidney Injury focused on measuring Aminophylline

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Cohort 1

  • All children undergoing open heart surgery for congenital heart defects with or without circulatory arrest
  • Neonates (<28 days old) and infants (<1 years of age)
  • Hypoplastic L heart syndrome or its variants.
  • Coarctation with aortic arch hypoplasia.
  • Interrupted aortic arch.
  • TAPVR (Total anomalous pulmonary venous return)
  • Patients with complex congenital heart defects

Cohort 2:

  • Orthotopic heart transplantation patients.
  • Patients ≤ 18 years of age
  • Congenital heart defects
  • Cardiomyopathy (Dilated/Hypertrophic/Restrictive/Left Ventricular Non-compaction)

Exclusion Criteria:

  • Children under the age of 12 months undergoing bypass for any condition that is not categorized as congenital heart defect
  • History of seizures
  • History of significant tachyarrhythmia.

Sites / Locations

  • LeBonheur Children's HospitalRecruiting
  • LeBonheur Children's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Aminophylline pre CPB & immediately post CPB

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Acute kidney injury state II/III by AKIN criteria
Acute kidney injury state II/III by AKIN criteria

Secondary Outcome Measures

Urine output during post op
Urine output during post op
Urine output during post op
Urine output during post op
Concentration of Delta serum cystatin C
Delta serum cystatin C
Acute kidney injury stage
Acute kidney injury stage Pediatric modified Acute Kidney Injury Network criteria (pAKIN) AKI Stage I-<0.5mL (milliliter)/kg/hour for 8 hours AKI Stage II-<0.5mL/kg/hour for 16 hours AKI Stage III-<0.3mL/kg/hour for 24 hours OR Anuria for 16 hours Using serum creatinine and AKIN criteria

Full Information

First Posted
February 20, 2019
Last Updated
April 11, 2022
Sponsor
Le Bonheur Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03897335
Brief Title
Preventing Acute Kidney Injury (AKI) in Pediatric Patients
Acronym
AKI
Official Title
The Effect of Aminophylline on Preventing Acute Kidney Injury in Pediatric Patients Undergoing Open Heart Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 7, 2019 (Actual)
Primary Completion Date
February 1, 2023 (Anticipated)
Study Completion Date
February 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Le Bonheur Children's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the effects of peri-operative administration of Aminophylline versus Saline placebo in the preservation of renal function and the attenuation of renal injury in pediatric patients undergoing open heart surgery.
Detailed Description
Cardiac palliative/ correction surgeries in pediatric patients involve significant morbidity and mortality risks. Kidney function is frequently affected from cardiac surgery in these children. Studies identify the incidence of acute kidney injury (AKI) to be approximately 54% when defined by serum biomarkers (e.g. serum creatinine) and urine output criteria. The need for renal replacement therapy (RRT) for newborns and infants after cardiac surgery is reported as 2% to 17% in the literature. There are several reported risk factors for the development of AKI in this population. These are the complexities of the underlying heart disease and the surgical procedure, duration of cardiopulmonary bypass, functional single ventricle heart disease, circulatory arrest and low cardiac output syndrome in the post-operative period. AKI can cause worsening fluid overload compromising ventilation and lung function, predisposition to overwhelming infections and cytokine-mediated inflammatory state. The presence of AKI significantly increases the mortality that is associated with cardiac surgery in these very young patients, reported as high as 79% in the literature. There have been several reports suggesting that early intervention with AKI using renal replacement therapy (RRT) may improve patient mortality. Successful prevention strategies for AKI have not been reported for this high-risk population. Adenosine has been demonstrated to regulate renal circulation and metabolism. It is a breakdown product of adenosine triphosphate/adenosine diphosphate (ATP/ADP) metabolism and accumulates in AKI. At baseline, the barely detectable renal parenchymal adenosine levels can increase to 10-100 times following an ischemic insult. These are typical seven trans-membrane spanning domains with a coupled G-protein at the intracellular end. Adenosine receptors are located ubiquitously in many tissues. Adenosine acts as a vasodilator in all other tissues but the renal parenchyma. The interaction of AT-II with adenosine converts adenosine to a vasoconstrictor in renal microvasculature. Adenosine acts on the A1 receptors (A1 R) in the afferent arterioles, causing reduced glomerular blood flow and glomerular filtration rate (GFR), as well as stimulating renin release from the kidney parenchyma. Adenosine plays an important role in generating the vasoconstrictive response in the renal vasculature to hypoxia and ischemia. Early interventions by blocking the actions of adenosine on A1 R may restore glomerular blood flow and recover GFR. The study rationale is that Aminophylline and Theophylline are competitive non-selective inhibitors of adenosine. Therefore, even though aminophylline infusion (iv) has no effect on renal blood flow rate at baseline, it can ameliorate the decrease in renal blood flow rate following adenosine infusion. This property can improve renal function when the main mechanism of insult induces vasoconstriction. Both early and late administration of aminophylline protects renal function after ischemia-reperfusion injury in rats. Aminophylline has also been reported to successfully reverse newborn renal failure, prevent renal failure in perinatal asphyxia, and reverse acute kidney injury secondary to calcineurin induced nephropathy. Both theophylline and aminophylline have been used for prophylaxis of renal impairment during aorto-coronary bypass surgery in adults and the results have not been consistent for either a positive or negative effect. There have been no trials reported on the effect of aminophylline or theophylline to prevent or ameliorate acute kidney injury in children with congenital heart defects going through cardiac surgery. Additionally, we are examining the components of serotonin biosynthesis to determine if these levels can act as markers of acute kidney injury in pediatric patients undergoing open heart surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Aminophylline

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
1 Patient randomization groups A) Group 1: Aminophylline pre CPB & immediately post cardiopulmonary bypass (CPB) B) Group 2: No aminophylline prophylaxis
Masking
ParticipantCare ProviderInvestigator
Masking Description
Cohort 1 will consist of all children undergoing open heart surgery for congenital heart defects with or without circulatory arrest, and Cohort 2 will consist of Orthotopic heart transplantation patients. All subjects will be randomized 1:1 to aminophylline or saline placebo. Cohort 1 will be randomized using block-stratification with stratification factors age (neonate vs infant) and circulatory arrest (yes vs no). Age will be categorized as neonates (0 to <28 days) and infants (28 days to <1 year). A total of 80 (60 in Cohort 1 and 20 in Cohort 2) participants are expected to be enrolled on this study.
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aminophylline pre CPB & immediately post CPB
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Aminophylline
Intervention Description
Aminophylline pre cardiopulmonary bypass and immediately post cardiopulmonary bypass. The dose will be Aminophylline 5 mg/kg/dose, max 350 mg slow infusion. The infusion rate duration will be standardized to 20 minutes. There will be no other aminophylline treatments for the first post-op five days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal Saline
Intervention Description
The placebo group will not receive any aminophylline treatments for the first post-op five days
Primary Outcome Measure Information:
Title
Acute kidney injury state II/III by AKIN criteria
Description
Acute kidney injury state II/III by AKIN criteria
Time Frame
At 48 hours post-operative
Secondary Outcome Measure Information:
Title
Urine output during post op
Description
Urine output during post op
Time Frame
first 12 hours post op
Title
Urine output during post op
Description
Urine output during post op
Time Frame
daily until 3 days post op
Title
Concentration of Delta serum cystatin C
Description
Delta serum cystatin C
Time Frame
24 hours post CPB
Title
Acute kidney injury stage
Description
Acute kidney injury stage Pediatric modified Acute Kidney Injury Network criteria (pAKIN) AKI Stage I-<0.5mL (milliliter)/kg/hour for 8 hours AKI Stage II-<0.5mL/kg/hour for 16 hours AKI Stage III-<0.3mL/kg/hour for 24 hours OR Anuria for 16 hours Using serum creatinine and AKIN criteria
Time Frame
max point within post CPB 72 hours
Other Pre-specified Outcome Measures:
Title
Concentration of Delta urinary neutrophil gelatinase-associated lipocalin (NGAL)
Description
1 Delta urinary NGAL at 6 hours post cardiopulmonary (CPB) and Delta plasma NGAL at 2 hours post CPB.
Time Frame
at 2 hours post CPB.
Title
Time to extubation (hours)
Description
Time to extubation (hours) number of hours post surgery
Time Frame
during hospitalization, up to 8 days
Title
Time to chest closure (hours)
Description
Time to chest closure (hours) from start time of incision to chest closure during procedure
Time Frame
during hospitalization, up to 3 days
Title
Time to discharge from cardiovascular intensive care unit (CVICU) (days)
Description
Time to discharge from CVICU (days)
Time Frame
during hospitalization, approximate 5 days
Title
Duration of hospital stay (Days).
Description
Duration of hospital stay (Days).
Time Frame
during hospitalization, approximate 8 days
Title
Dialysis requirement (yes/no)
Description
Dialysis requirement (yes/no)
Time Frame
during hospitalization, approximate 5 days
Title
Time to return to preoperative weight.
Description
Time to return to preoperative weight.
Time Frame
during hospitalization, approximate 8 days
Title
Inotropic score
Description
Inotropic score Calculation of Inotropic score (IS) and Vasoactive inotropic score (VIS). IS(a) = dopamine dose (lg/kg/min) ? dobutamine dose (lg/kg/min) ? 100 9 epinephrine dose (lg/kg/min) VIS(b) = IS ? 10 9 milrinone dose (lg/kg/ min) ? 10,000 9 vasopressin dose (U/kg/ min) ? 100 9 norepinephrine dose (lg/kg/min) IS inotrope score, VIS vasoactive-inotropic score
Time Frame
at 7 days post operative
Title
Peritoneal dialysis catheter output.
Description
Peritoneal dialysis catheter output through study completion
Time Frame
during hospitalization, up to 8 days
Title
Transfusion requirements intraoperatively and postoperatively
Description
Transfusion requirements intraoperatively and postoperatively through study completion
Time Frame
during hospitalization, up to 8 days
Title
Inotropic score
Description
Inotropic score Calculation of Inotropic score (IS) and Vasoactive inotropic score (VIS). IS(a) = dopamine dose (lg/kg/min) ? dobutamine dose (lg/kg/min) ? 100 9 epinephrine dose (lg/kg/min) VIS(b) = IS ? 10 9 milrinone dose (lg/kg/ min) ? 10,000 9 vasopressin dose (U/kg/ min) ? 100 9 norepinephrine dose (lg/kg/min) IS inotrope score, VIS vasoactive-inotropic score
Time Frame
at 5 days post operative

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cohort 1 All children undergoing open heart surgery for congenital heart defects with or without circulatory arrest Neonates (<28 days old) and infants (<1 years of age) Hypoplastic L heart syndrome or its variants. Coarctation with aortic arch hypoplasia. Interrupted aortic arch. TAPVR (Total anomalous pulmonary venous return) Patients with complex congenital heart defects Cohort 2: Orthotopic heart transplantation patients. Patients ≤ 18 years of age Congenital heart defects Cardiomyopathy (Dilated/Hypertrophic/Restrictive/Left Ventricular Non-compaction) Exclusion Criteria: Children under the age of 12 months undergoing bypass for any condition that is not categorized as congenital heart defect History of seizures History of significant tachyarrhythmia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren Davis
Phone
901-287-4594
Email
lauren.davis2@lebonheur.org
First Name & Middle Initial & Last Name or Official Title & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org
Facility Information:
Facility Name
LeBonheur Children's Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lauren Davis
Phone
901-287-4594
Email
lauren.davis2@lebonheur.org
First Name & Middle Initial & Last Name & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org
Facility Name
LeBonheur Children's Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Umar S Boston, MD
Phone
901-287-5958
Email
uboston@uthsc.edu
First Name & Middle Initial & Last Name & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
1.KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int. Suppl 2 ; 2012:1-138
Results Reference
background
PubMed Identifier
22622499
Citation
Bojan M, Gioanni S, Vouhe PR, Journois D, Pouard P. Early initiation of peritoneal dialysis in neonates and infants with acute kidney injury following cardiac surgery is associated with a significant decrease in mortality. Kidney Int. 2012 Aug;82(4):474-81. doi: 10.1038/ki.2012.172.
Results Reference
background
Citation
11.Gouyon JB, Guignard JP. Glomerular filtration rates in neonates. In Oh w, Guignard JP, Baumgart S (Eds.): Nephrology and Fluid / Electrolyte Physiology, First edn (pp 79-96). Philadelphia: Saunders Elsevier 2008
Results Reference
background
Citation
Linden J and Jacobson KA. Molecular biology and pharmacology of adenosine receptors. Cardiovascular Biology of Purines, 1-20 (Eds Burnstock G et al.) Dordrecht: Kluwer Academic Publishers.
Results Reference
background
PubMed Identifier
7092306
Citation
Rigden SP, Barratt TM, Dillon MJ, De Leval M, Stark J. Acute renal failure complicating cardiopulmonary bypass surgery. Arch Dis Child. 1982 Jun;57(6):425-30. doi: 10.1136/adc.57.6.425.
Results Reference
result
PubMed Identifier
10502118
Citation
Sorof JM, Stromberg D, Brewer ED, Feltes TF, Fraser CD Jr. Early initiation of peritoneal dialysis after surgical repair of congenital heart disease. Pediatr Nephrol. 1999 Oct;13(8):641-5. doi: 10.1007/s004670050672.
Results Reference
result
PubMed Identifier
14602265
Citation
Chan KL, Ip P, Chiu CS, Cheung YF. Peritoneal dialysis after surgery for congenital heart disease in infants and young children. Ann Thorac Surg. 2003 Nov;76(5):1443-9. doi: 10.1016/s0003-4975(03)01026-9.
Results Reference
result
PubMed Identifier
14726035
Citation
Boigner H, Brannath W, Hermon M, Stoll E, Burda G, Trittenwein G, Golej J. Predictors of mortality at initiation of peritoneal dialysis in children after cardiac surgery. Ann Thorac Surg. 2004 Jan;77(1):61-5. doi: 10.1016/s0003-4975(03)01490-5.
Results Reference
result
PubMed Identifier
17944638
Citation
Pedersen KR, Povlsen JV, Christensen S, Pedersen J, Hjortholm K, Larsen SH, Hjortdal VE. Risk factors for acute renal failure requiring dialysis after surgery for congenital heart disease in children. Acta Anaesthesiol Scand. 2007 Nov;51(10):1344-9. doi: 10.1111/j.1399-6576.2007.01379.x.
Results Reference
result
PubMed Identifier
18379554
Citation
Pedersen KR, Hjortdal VE, Christensen S, Pedersen J, Hjortholm K, Larsen SH, Povlsen JV. Clinical outcome in children with acute renal failure treated with peritoneal dialysis after surgery for congenital heart disease. Kidney Int Suppl. 2008 Apr;(108):S81-6. doi: 10.1038/sj.ki.5002607.
Results Reference
result
PubMed Identifier
19007588
Citation
Ronco C, Haapio M, House AA, Anavekar N, Bellomo R. Cardiorenal syndrome. J Am Coll Cardiol. 2008 Nov 4;52(19):1527-39. doi: 10.1016/j.jacc.2008.07.051.
Results Reference
result
PubMed Identifier
21798562
Citation
Blinder JJ, Goldstein SL, Lee VV, Baycroft A, Fraser CD, Nelson D, Jefferies JL. Congenital heart surgery in infants: effects of acute kidney injury on outcomes. J Thorac Cardiovasc Surg. 2012 Feb;143(2):368-74. doi: 10.1016/j.jtcvs.2011.06.021. Epub 2011 Jul 27.
Results Reference
result
PubMed Identifier
3046670
Citation
Gouyon JB, Guignard JP. Functional renal insufficiency: role of adenosine. Biol Neonate. 1988;53(4):237-42. doi: 10.1159/000242796.
Results Reference
result
PubMed Identifier
3883810
Citation
Hall JE, Granger JP, Hester RL. Interactions between adenosine and angiotensin II in controlling glomerular filtration. Am J Physiol. 1985 Mar;248(3 Pt 2):F340-6. doi: 10.1152/ajprenal.1985.248.3.F340.
Results Reference
result
PubMed Identifier
12954591
Citation
Hansen PB, Schnermann J. Vasoconstrictor and vasodilator effects of adenosine in the kidney. Am J Physiol Renal Physiol. 2003 Oct;285(4):F590-9. doi: 10.1152/ajprenal.00051.2003.
Results Reference
result
PubMed Identifier
23093787
Citation
Rabb H. The promise of immune cell therapy for acute kidney injury. J Clin Invest. 2012 Nov;122(11):3852-4. doi: 10.1172/JCI66455. Epub 2012 Oct 24.
Results Reference
result
PubMed Identifier
11734617
Citation
Fredholm BB, IJzerman AP, Jacobson KA, Klotz KN, Linden J. International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors. Pharmacol Rev. 2001 Dec;53(4):527-52.
Results Reference
result
PubMed Identifier
16049319
Citation
Pawelczyk T, Grden M, Rzepko R, Sakowicz M, Szutowicz A. Region-specific alterations of adenosine receptors expression level in kidney of diabetic rat. Am J Pathol. 2005 Aug;167(2):315-25. doi: 10.1016/S0002-9440(10)62977-X.
Results Reference
result
PubMed Identifier
8618962
Citation
Navar LG, Inscho EW, Majid SA, Imig JD, Harrison-Bernard LM, Mitchell KD. Paracrine regulation of the renal microcirculation. Physiol Rev. 1996 Apr;76(2):425-536. doi: 10.1152/physrev.1996.76.2.425.
Results Reference
result
PubMed Identifier
15086457
Citation
Vitzthum H, Weiss B, Bachleitner W, Kramer BK, Kurtz A. Gene expression of adenosine receptors along the nephron. Kidney Int. 2004 Apr;65(4):1180-90. doi: 10.1111/j.1523-1755.2004.00490.x.
Results Reference
result
PubMed Identifier
11171666
Citation
Silldorff EP, Pallone TL. Adenosine signaling in outer medullary descending vasa recta. Am J Physiol Regul Integr Comp Physiol. 2001 Mar;280(3):R854-61. doi: 10.1152/ajpregu.2001.280.3.R854.
Results Reference
result
PubMed Identifier
11181402
Citation
Nishiyama A, Inscho EW, Navar LG. Interactions of adenosine A1 and A2a receptors on renal microvascular reactivity. Am J Physiol Renal Physiol. 2001 Mar;280(3):F406-14. doi: 10.1152/ajprenal.2001.280.3.F406.
Results Reference
result
PubMed Identifier
10484524
Citation
Okusa MD, Linden J, Macdonald T, Huang L. Selective A2A adenosine receptor activation reduces ischemia-reperfusion injury in rat kidney. Am J Physiol. 1999 Sep;277(3):F404-12. doi: 10.1152/ajprenal.1999.277.3.F404.
Results Reference
result
PubMed Identifier
11532695
Citation
Lee HT, Emala CW. Systemic adenosine given after ischemia protects renal function via A(2a) adenosine receptor activation. Am J Kidney Dis. 2001 Sep;38(3):610-8. doi: 10.1053/ajkd.2001.26888.
Results Reference
result
PubMed Identifier
11380813
Citation
Okusa MD, Linden J, Huang L, Rosin DL, Smith DF, Sullivan G. Enhanced protection from renal ischemia-reperfusion [correction of ischemia:reperfusion] injury with A(2A)-adenosine receptor activation and PDE 4 inhibition. Kidney Int. 2001 Jun;59(6):2114-25. doi: 10.1046/j.1523-1755.2001.00726.x. Erratum In: Kidney Int 2001 Aug;60(2):820.
Results Reference
result
PubMed Identifier
15313386
Citation
Reece TB, Davis JD, Okonkwo DO, Maxey TS, Ellman PI, Li X, Linden J, Tribble CG, Kron IL, Kern JA. Adenosine A2A analogue reduces long-term neurologic injury after blunt spinal trauma. J Surg Res. 2004 Sep;121(1):130-4. doi: 10.1016/j.jss.2004.04.006.
Results Reference
result
PubMed Identifier
10561110
Citation
Ross SD, Tribble CG, Linden J, Gangemi JJ, Lanpher BC, Wang AY, Kron IL. Selective adenosine-A2A activation reduces lung reperfusion injury following transplantation. J Heart Lung Transplant. 1999 Oct;18(10):994-1002. doi: 10.1016/s1053-2498(99)00066-2.
Results Reference
result
PubMed Identifier
16012931
Citation
Odashima M, Bamias G, Rivera-Nieves J, Linden J, Nast CC, Moskaluk CA, Marini M, Sugawara K, Kozaiwa K, Otaka M, Watanabe S, Cominelli F. Activation of A2A adenosine receptor attenuates intestinal inflammation in animal models of inflammatory bowel disease. Gastroenterology. 2005 Jul;129(1):26-33. doi: 10.1053/j.gastro.2005.05.032.
Results Reference
result
PubMed Identifier
15591104
Citation
Glover DK, Riou LM, Ruiz M, Sullivan GW, Linden J, Rieger JM, Macdonald TL, Watson DD, Beller GA. Reduction of infarct size and postischemic inflammation from ATL-146e, a highly selective adenosine A2A receptor agonist, in reperfused canine myocardium. Am J Physiol Heart Circ Physiol. 2005 Apr;288(4):H1851-8. doi: 10.1152/ajpheart.00362.2004. Epub 2004 Dec 9.
Results Reference
result
PubMed Identifier
16493070
Citation
Day YJ, Huang L, Ye H, Li L, Linden J, Okusa MD. Renal ischemia-reperfusion injury and adenosine 2A receptor-mediated tissue protection: the role of CD4+ T cells and IFN-gamma. J Immunol. 2006 Mar 1;176(5):3108-14. doi: 10.4049/jimmunol.176.5.3108.
Results Reference
result
PubMed Identifier
16816141
Citation
Vallon V, Muhlbauer B, Osswald H. Adenosine and kidney function. Physiol Rev. 2006 Jul;86(3):901-40. doi: 10.1152/physrev.00031.2005.
Results Reference
result
PubMed Identifier
3404810
Citation
Gouyon JB, Guignard JP. Theophylline prevents the hypoxemia-induced renal hemodynamic changes in rabbits. Kidney Int. 1988 Jun;33(6):1078-83. doi: 10.1038/ki.1988.114.
Results Reference
result
PubMed Identifier
15947981
Citation
Bakr AF. Prophylactic theophylline to prevent renal dysfunction in newborns exposed to perinatal asphyxia--a study in a developing country. Pediatr Nephrol. 2005 Sep;20(9):1249-52. doi: 10.1007/s00467-005-1980-z. Epub 2005 Jun 10.
Results Reference
result
PubMed Identifier
15583947
Citation
Ng GY, Baker EH, Farrer KF. Aminophylline as an adjunct diuretic for neonates--a case series. Pediatr Nephrol. 2005 Feb;20(2):220-2. doi: 10.1007/s00467-004-1692-9. Epub 2004 Dec 4.
Results Reference
result
PubMed Identifier
10742366
Citation
Jenik AG, Ceriani Cernadas JM, Gorenstein A, Ramirez JA, Vain N, Armadans M, Ferraris JR. A randomized, double-blind, placebo-controlled trial of the effects of prophylactic theophylline on renal function in term neonates with perinatal asphyxia. Pediatrics. 2000 Apr;105(4):E45. doi: 10.1542/peds.105.4.e45.
Results Reference
result
PubMed Identifier
16887430
Citation
Bhat MA, Shah ZA, Makhdoomi MS, Mufti MH. Theophylline for renal function in term neonates with perinatal asphyxia: a randomized, placebo-controlled trial. J Pediatr. 2006 Aug;149(2):180-4. doi: 10.1016/j.jpeds.2006.03.053.
Results Reference
result
PubMed Identifier
15840666
Citation
McLaughlin GE, Abitbol CL. Reversal of oliguric tacrolimus nephrotoxicity in children. Nephrol Dial Transplant. 2005 Jul;20(7):1471-5. doi: 10.1093/ndt/gfh785. Epub 2005 Apr 19.
Results Reference
result
PubMed Identifier
11981083
Citation
Kramer BK, Preuner J, Ebenburger A, Kaiser M, Bergner U, Eilles C, Kammerl MC, Riegger GA, Birnbaum DE. Lack of renoprotective effect of theophylline during aortocoronary bypass surgery. Nephrol Dial Transplant. 2002 May;17(5):910-5. doi: 10.1093/ndt/17.5.910.
Results Reference
result
PubMed Identifier
23087551
Citation
Mahaldar AR, Sampathkumar K, Raghuram AR, Kumar S, Ramakrishnan M, Mahaldar DA. Risk prediction of acute kidney injury in cardiac surgery and prevention using aminophylline. Indian J Nephrol. 2012 May;22(3):179-83. doi: 10.4103/0971-4065.98752.
Results Reference
result
PubMed Identifier
9396079
Citation
Aki Y, Tomohiro A, Nishiyama A, Kiyomoto K, Kimura S, Abe Y. Effects of KW-3902, a selective and potent adenosine A1 receptor antagonist, on renal hemodynamics and urine formation in anesthetized dogs. Pharmacology. 1997 Oct;55(4):193-201. doi: 10.1159/000139528.
Results Reference
result
PubMed Identifier
11138732
Citation
Yao K, Ina Y, Nagashima K, Ohno T, Karasawa A. Effect of the selective adenosine A1-receptor antagonist KW-3902 on lipopolysaccharide-induced reductions in urine volume and renal blood flow in anesthetized dogs. Jpn J Pharmacol. 2000 Nov;84(3):310-5. doi: 10.1254/jjp.84.310.
Results Reference
result
PubMed Identifier
17936154
Citation
Givertz MM, Massie BM, Fields TK, Pearson LL, Dittrich HC; CKI-201 and CKI-202 Investigators. The effects of KW-3902, an adenosine A1-receptor antagonist,on diuresis and renal function in patients with acute decompensated heart failure and renal impairment or diuretic resistance. J Am Coll Cardiol. 2007 Oct 16;50(16):1551-60. doi: 10.1016/j.jacc.2007.07.019. Epub 2007 Oct 1.
Results Reference
result
PubMed Identifier
18926433
Citation
Cotter G, Dittrich HC, Weatherley BD, Bloomfield DM, O'Connor CM, Metra M, Massie BM; Protect Steering Committee, Investigators, and Coordinators. The PROTECT pilot study: a randomized, placebo-controlled, dose-finding study of the adenosine A1 receptor antagonist rolofylline in patients with acute heart failure and renal impairment. J Card Fail. 2008 Oct;14(8):631-40. doi: 10.1016/j.cardfail.2008.08.010. Epub 2008 Sep 14.
Results Reference
result
PubMed Identifier
20925544
Citation
Massie BM, O'Connor CM, Metra M, Ponikowski P, Teerlink JR, Cotter G, Weatherley BD, Cleland JG, Givertz MM, Voors A, DeLucca P, Mansoor GA, Salerno CM, Bloomfield DM, Dittrich HC; PROTECT Investigators and Committees. Rolofylline, an adenosine A1-receptor antagonist, in acute heart failure. N Engl J Med. 2010 Oct 7;363(15):1419-28. doi: 10.1056/NEJMoa0912613.
Results Reference
result
PubMed Identifier
21545947
Citation
Voors AA, Dittrich HC, Massie BM, DeLucca P, Mansoor GA, Metra M, Cotter G, Weatherley BD, Ponikowski P, Teerlink JR, Cleland JG, O'Connor CM, Givertz MM. Effects of the adenosine A1 receptor antagonist rolofylline on renal function in patients with acute heart failure and renal dysfunction: results from PROTECT (Placebo-Controlled Randomized Study of the Selective Adenosine A1 Receptor Antagonist Rolofylline for Patients Hospitalized with Acute Decompensated Heart Failure and Volume Overload to Assess Treatment Effect on Congestion and Renal Function). J Am Coll Cardiol. 2011 May 10;57(19):1899-907. doi: 10.1016/j.jacc.2010.11.057.
Results Reference
result
PubMed Identifier
17130306
Citation
Morecroft I, Dempsie Y, Bader M, Walther DJ, Kotnik K, Loughlin L, Nilsen M, MacLean MR. Effect of tryptophan hydroxylase 1 deficiency on the development of hypoxia-induced pulmonary hypertension. Hypertension. 2007 Jan;49(1):232-6. doi: 10.1161/01.HYP.0000252210.58849.78. Epub 2006 Nov 27.
Results Reference
result
PubMed Identifier
3702223
Citation
Sole MJ, Madapallimattam A, Baines AD. An active pathway for serotonin synthesis by renal proximal tubules. Kidney Int. 1986 Mar;29(3):689-94. doi: 10.1038/ki.1986.53.
Results Reference
result

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Preventing Acute Kidney Injury (AKI) in Pediatric Patients

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