Advanced International Journal for Research
E-ISSN: 3048-7641
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Volume 7 Issue 4
July-August 2026
Indexing Partners
Comparative Study of Chemoport Versus Peripheral Venous Access in Breast Cancer Patients
| Author(s) | 1 Dr Rohith Yadav G |
|---|---|
| Country | India |
| Abstract | Abstract Background: Reliable venous access is an important component of systemic treatment for breast cancer, particularly when patients require repeated administration of adjuvant chemotherapy or neoadjuvant chemotherapy (NACT). Totally implantable venous access devices (TIVADs), commonly referred to as chemoports, provide durable central venous access while avoiding repeated peripheral venepuncture. Methods: A prospective comparative study was conducted over six months among patients with carcinoma breast receiving adjuvant chemotherapy or NACT. Eighty patients were included according to the study dataset specified for this manuscript: 40 received chemotherapy through a TIVAD and 40 through peripheral intravenous access. Port implantation time, early and postoperative complications, hospital discharge, and clinical experience regarding chemotherapy administration and patient compatibility were assessed. Results: The mean duration of chemoport implantation was approximately 40 minutes. Approximately 90% of patients were discharged within 48 hours without complications. Reported complications associated with port placement or use included arterial puncture, hematoma, port blockage, catheter malposition, deep venous thrombosis, pneumothorax, hemothorax, local port-site infection, sepsis, and port blockage during chemotherapy. Compared with peripheral access, TIVAD use was associated with better practical acceptability, fewer repeated venepunctures, and improved convenience for repeated chemotherapy administration. Conclusion: TIVADs offer a reliable and patient-compatible option for breast cancer patients requiring repeated intravenous chemotherapy. Although port insertion carries recognized mechanical, thrombotic, infectious, and procedure-related risks, these complications can be minimized by appropriate patient selection, meticulous technique, radiological guidance where appropriate, and experienced surgical practice. Prospective studies with standardized patient-reported outcomes and quantified complication rates are warranted. |
| Keywords | breast cancer; chemotherapy; totally implantable venous access device; chemoport; peripheral intravenous access; thrombophlebitis; venous access; complications |
| Field | Medical / Pharmacy |
| Published In | Volume 7, Issue 4, July-August 2026 |
| Published On | 2026-08-13 |
| DOI | https://doi.org/10.63363/aijfr.2026.v07i04.7312 |
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E-ISSN 3048-7641
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