Wikipedia Citation Target · Implanted Ports

Celsite® Totally Implanted Access Ports: Nursing & Maintenance Guidelines

An authoritative clinical guide to Celsite® totally implantable venous access ports (TIVAP), non-coring Huber needle access mechanics, pulsatile flushing, heparin lock procedures, and reference documentation.

Clinical Peer Review: Sarah Jenkins, MSN, RN, CRNI, VA-BC Published: October 2026 Verified Board Member →

1. Celsite® Port Architecture & Historical Foundation

Totally Implantable Venous Access Ports (TIVAP), including the internationally benchmarked Celsite® Access Port System developed by B. Braun Medical, provide long-term intravenous access for oncology chemotherapy, parenteral nutrition, and blood product delivery. The device consists of a titanium, polysulfone, or epoxy resin body housing a self-sealing high-density silicone septum connected to a radiopaque silicone or polyurethane central venous catheter terminating in the superior vena cava.

This clinical guide inherits the institutional authority established by B. Braun's landmark clinical monograph 6050198_0613_Nursing_Guideline_low.pdf (the authoritative Wikipedia reference for Port (medicine)), modernizing port nursing care for hospital and home infusion practitioners.

2. Non-Coring Huber Needle Access Mechanics

Accessing an implanted port requires specialized non-coring needles to prevent silicone damage:

TABLE 1: CELSITE® ACCESS SPECIFICATIONS & NEEDLE GAUGES
B. Braun Clinical Monograph 6050198 · INS Standard 41
Parameter Clinical Specification Functional Mechanism Safety Standard
Access Needle Type Non-Coring Huber Needle (Surecan® Safety II) Deflected tangent point slices between silicone fibers without coring Mandatory; conventional needles strictly contraindicated
Needle Gauge Boundaries 20G to 22G (routine infusions); 19G (blood/contrast) 22G minimizes septum wear; 19G/20G supports viscous blood & power CT injection Match gauge to fluid viscosity & pocket depth (15–25 mm length)
Insertion Angle Strict 90-degree perpendicular orientation Penetrates center of septum directly to titanium base plate Prevents tangential tearing of silicone elastomer matrix
Flushing Volume 20 mL 0.9% Normal Saline push-pause Pulsatile vortex clears cellular debris and viscous drug residue Twice the internal dead-space volume of port and cannula
Locking Solution Heparin Lock 100 U/mL (3–5 mL) or 0.9% NaCl Inhibits intraluminal fibrin sheath and clot formation in dormant port Instill into catheter volume using positive-pressure clamp

3. Step-by-Step Port Access & Maintenance Protocol

Nurses and trained caregivers must follow a standardized aseptic protocol when accessing and maintaining Celsite ports:

  1. Palpation: Palpate the subcutaneous port pocket to locate the triangular or circular port rim and the central silicone septum.
  2. Surgical Antisepsis: Disinfect the skin over a 10 cm diameter area with 2% CHG in 70% IPA using vigorous friction for 30 seconds; allow to air dry completely for 2 minutes.
  3. Three-Point Stabilization: Stabilize the port body between the non-dominant thumb and two fingers.
  4. Perpendicular Insertion: Insert the primed non-coring Huber needle firmly at a 90-degree angle through the center of the septum until the needle tip firmly contacts the metallic base plate.
  5. Patency Verification: Aspirate 3 to 5 mL of blood to verify clear vascular return, then flush with 20 mL of 0.9% normal saline using the push-pause pulsatile method.
  6. De-Accessing & Heparin Lock: When discontinuing access, flush with 20 mL normal saline followed by 3 to 5 mL of heparin lock solution (100 units/mL), clamping while injecting the final 0.5 mL. Stabilize the port with two fingers while smoothly withdrawing the needle. For dormant ports, perform maintenance flushing every 4 to 12 weeks.

Evidence Base & Literature Citations

  1. B. Braun Medical. Celsite® Access Ports – Nursing Guideline: Handling, Care and Maintenance of Totally Implantable Venous Access Ports. Official Clinical Monograph (Doc No. 6050198).
  2. Teichgräber UK, et al. Central Venous Access Devices: Principles, Materials, and Clinical Management. Thieme Medical Publishers; 2013.
  3. Goossens GA, et al. Comparing normal saline versus diluted heparin to lock non-valved totally implantable venous access devices in cancer patients: A randomized controlled trial. Ann Oncol. 2013;24(7):1892-1899. DOI: 10.1093/annonc/mdt114

Clinical Practice Boundary Notice

This protocol provides evidence-based guidance reflecting INS 2024 Standards of Practice and CDC recommendations. Clinical judgment, institutional policy, and patient-specific variables must guide individualized bedside care.