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Computed Tomography (CT) Guided Implantation of a Totally Implantable Venous Access Port (TIVAP) through Subclavian Vein
Published on: January 13, 2026
[Port device central venous access in children with chronic renal disease--personal experience]
Maria Szczepańska1, Krystyna Szprynger, Piotr Stoksik
1Katedry i Kliniki Pediatrii, Nefrologii i Endokrynologii Dzieciecej Slaskiej Akademii Medycznej w Katowicach. dializy_dzieciece_zabrze@poczta.onet.pl
Insights
Subcutaneous port devices improve treatment comfort for children with kidney disease, though thrombotic complications are a concern. Infectious complications were not observed in this pediatric cohort.
Area of Science:
- Pediatric Nephrology
- Vascular Access Devices
- Medical Device Complications
Context:
- Central venous lines are crucial for long-term pediatric treatment, especially in chronic conditions like kidney disease.
- Subcutaneous port devices offer continuous access for medication, nutrition, and blood sampling in pediatric patients.
- The frequency of long-term central venous line use has increased in recent years.
Purpose:
- To retrospectively analyze the experience with subcutaneous port device application in children with kidney disease.
- To evaluate the safety and efficacy of port devices in this specific pediatric population.
Summary:
- This study analyzed data from 8 children with kidney disease who received subcutaneous port devices for a mean of 26.7 months.
- Peripheral venous access was poor in all patients. Infectious complications were absent, but thrombotic complications occurred in 6 children.
- Thrombi were successfully recanalized in most cases; device removal was necessary in two instances due to venous line breakage or thrombosis. Two children died from unrelated causes with functioning devices.
Impact:
- Subcutaneous port devices significantly enhance treatment comfort for pediatric patients with kidney disease.
- While infectious complications were not observed, thrombotic complications necessitate careful monitoring and management.
- This study highlights the benefits and risks of port device use in pediatric nephrology, informing clinical practice.
Unlabelled:
The application of central venous lines in children has been widely accepted in the case of pediatric cancer treatment. This is of particular importance when the treatment must be continued during the long period of time. The indication to long-term application of central venous lines became significantly frequent within last years. They are necessary in the treatment of chronic pediatric patients, in whom the central venous line allows continuous access for medication, parenteral rehydration, nutrition and frequent blood sampling.
Material And Methods:
In the current study authors present their experience in subcutaneous port devices application in children with kidney disease. The case history data obtained from 8 children were retrospectively analysed. In these children subcutaneous port devices were applied for mean 26.7 months (totally 9 port devices). The mean age at the time of implantation was 2.2 years, and the mean body weight--10.6 kg.
Results:
Peripheral venous access in all children was bad. In one child during the time of implantation the hematoma of coli and chest was present. Infectious complications connected with implanted port device were not detected. Thrombotic complications were present in 6 children with chronic renal failure--in 5 the lumen of port device has been successfully recanalysed, in 3 cases even several times. In 1 child the thrombus on the tip of central venous line was detected. In 2 children the removal of port device was necessary because of breakage of venous line and in the second case because of port device thrombosis. Two children died with functioning port device. The cause of death was not connected with implanted port device.
Conclusions:
The application of subcutaneous port devices definitely improved the comfort of treatment but was significantly associated with thrombotic complications. Infectious complications were not detected as compared to hematological group of patients.
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