Clinical Trials Logo

Clinical Trial Summary

The objective of this study is to evaluate the outcomes of children who have sustained blunt renal injury and to evaluate our current bed rest protocol. The variables of concern are readmission, operation, subsequent hypertension and clearance of hematuria. The specific aim of the study is to prospectively collect the clinical data of these children to validate our hospital management and to define the natural history of these lesions.


Clinical Trial Description

The current management for blunt renal injury in children is based on level 5 evidence, which is the lowest score. Essentially, empiric decisions about therapy without physiologic rationale have been permeated through generations of teaching. Patients are therefore managed by historical opinion, borrowing some principles from spleen and liver injuries. Over the past few decades all authors have agreed that non-operative management should be followed in all these patients as almost all injuries will heal with preservation of renal function. However, as opposed to spleen and liver injuries, there are no published guidelines for a non-operative management scheme. The kidney possesses important anatomic and physiologic differences when compared to the intraperitoneal solid organs that may allow for a distinct method of management. Therefore, we conducted a retrospective review to examine the natural history of these injuries and identify potential recommendations for management (IRB 07 12-186X). In patients with isolated renal injury (n = 65), mean length of bedrest was 3.8 +/- 1.9 days resulting in a mean length of stay of 3.8 +/- 3.1 days. There were no transfusions in these patients. There were 3 patients readmitted after discharge, 2 for pain control, and one for new hematuria after discharge. There were 15 patients discharged with persistent hematuria, none of whom suffered long term sequelae. Children were released from bedrest in attending-specific manner which was a wide array of management schemes. Our data suggests the risk of significant hemorrhage from blunt renal trauma is low. Further, clearance of hematuria may not be a good marker for therapy. Therefore, a period of bedrest with serial blood and urine monitoring may not be justified, and there is clearly a role for prospective application of a single management protocol to validate at least one protocol for other institutions to follow. In the retrospective data, we found one patient developed intermittent hypertension. However, identifying this one patient requires that the hypertension is documented in our medical record, which means we may miss those patients managed by their pediatricians. More concerning is that we may be missing patients who have hypertension. These potential patients may get well into adulthood before the hypertension is detected which is why this study is imperative to define the natural history of renal healing, quantify the risk of hypertension, and potentially identify predictors of this complication. The management protocol currently being followed and proposed for this study will include one night of bedrest and then the patient may be ambulatory the next day. From this point, patients will be managed in the hospital until they meet general discharge criteria. Discharge criteria are adequate pain control with oral pain medications and tolerating regular diet. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00855036
Study type Observational
Source Children's Mercy Hospital Kansas City
Contact
Status Active, not recruiting
Phase
Start date August 2008
Completion date December 31, 2024

See also
  Status Clinical Trial Phase
Terminated NCT03940651 - Cardiac and Renal Biomarkers in Arthroplasty Surgery Phase 4
Completed NCT05092854 - The Effect of AMP Human Sodium Bicarbonate Lotion on Dehydrated Heat Stress N/A
Not yet recruiting NCT04078711 - Chinese Medicine Treat for Hypertensive Renal Injury Phase 2/Phase 3
Not yet recruiting NCT06109714 - Early Biomarker Kidney Injury Assessment After Acumen Directed Fluid Management in Cardiac Surgery N/A
Completed NCT03273751 - The Effect of Remote Ischemic Preconditioning on Kidney Function in Patients Undergoing Partial Nephrectomy N/A
Recruiting NCT04580329 - The Effect of Neuromuscular Electrical Stimulation (NMES) on the Renal Function and Renal Blood Flow N/A
Active, not recruiting NCT04070482 - Impact of in Utero and Breastfeeding Exposure to Tenofovir on Renal Function in HIV-exposed Uninfected Children
Completed NCT02660931 - Pediatric Acute Kidney Injury (AKI) Retrospective, Real-Time and Repository Research N/A
Not yet recruiting NCT06116383 - Evaluation of Renal Perfusion With NIRS in Laparoscopic Surgery
Recruiting NCT06056466 - Different Vascular and Renal Parameters in Living Kidney Donors
Completed NCT01925235 - Analysis of Remote-ischemic Preconditioning Effects on Kidney Function N/A
Completed NCT03877133 - Association of Intraoperative Renal Regional Oxygen Saturation and Acute Kidney Injury N/A
Recruiting NCT06021080 - Effects of Different Continuous Renal Replacement Therapy Patterns on Ionized Calcium in Patients With Citrate Anticoagulants Using Calcium-containing Replacement Solutions
Not yet recruiting NCT05276700 - Alpha -1- Microglobulin (α1M) as an Early Biomarker in Renal Extrahepatic Manifestations of HCV-infection
Recruiting NCT06203145 - A Clinical Study on the Whole-course Management (BCD-KPD-AutoHSCT) Scheme for Patients With RIMM N/A
Recruiting NCT04937868 - Developing a Decision Instrument to Guide Abdominal-pelvic CT Imaging of Blunt Trauma Patients
Completed NCT05358912 - Efficacy of Targeted Abdominal Perfusion Pressure in Septic Shock Phase 4
Completed NCT02221219 - Effects of Delayed Cord Clamp and/or Indomethacin on Preterm Infant Brain Injury Phase 1/Phase 2
Completed NCT04695951 - Efficacy and Safety of Renalof® in the Removal of Calculi Smaller Than 10 mm Located in the Reno-Ureteral Tract Phase 2
Recruiting NCT04265599 - Exploring Pathogenesis and Treatment of Hypercalcemia Caused by Intramuscular Injection of Paraffinoil