INTRODUCTIONPort-A catheter is the most common and preferable application device to be used because of ease of access, lower occurrence of complication rates, and significantly improved quality of life.1-2 However, it is not free from complications. Port-A catheter complications can be categorized into early-and late-related complications. Early-related complications usually detected between 24 h and 4 weeks after implantation; however, late complications can be observed after 4 weeks of implantation. Port-A catheter complications could also be followed up by the clinical pharmacist who might help in the assessment of the complications and provide further counselling and patient care services in collaboration with other healthcare professionals. Patient counselling by the clinical pharmacist is an essential part in the management of therapy-related problems as it involves provision of proper education to the patients regarding adverse effects, nutritional counselling and optimal lifestyle modification. It is principally aimed to minimize unnecessary hospital admissions, reducing and preventing therapy-related problems, achieving the desired therapeutic goals, and improving therapy outcomes.
4-5The objective of this study was to assess the incidence of early related -complications (ERCs) of port -A catheter insertion, and to evaluate the effective role of clinical pharmacist via the provision of appropriate counselling and patient care services on reducing those complications in cancer patients undergoing chemotherapy through port-A catheter application.
MATERIALS AND METHODSA prospective pilot study, single centre analysis conducted from February through May 2015. Approval of the study protocol was granted from the Ethical Committee of Dr. Lütfi Kırdar Kartal Teaching and Research Hospital at the Anatolian side of Istanbul -Turkey.
Patient recruitmentThe study was carried out on patients newly diagnosed with different types of cancers. Cancer patients attending for chemotherapy administration at the oncology centre of Dr. Lütfi Kırdar Kartal Teaching and Research Hospital were eligible for recruitment after meeting the inclusion criteria of the study. Several patients undergoing port-A catheter implementation and eligible for the inclusion criteria during the above period were used to estimate the sample size. Inclusion criteria included patients over the age of 18 years, patients with newly diagnosed cancer eligible for chemotherapy and have an indication for port A-catheter implantation. Patients who expressed willingness to take part in the study were provided with additional written information and were asked to sign the study consent form. Exclusion criteria included patients with pre-existing port A-catheter insertion and patients with skin disorders. Baseline data were collected from the medical records of the patients. The collected data were used to structure a detailed health report for the patients including socio-demographic and medical history data (age, gender, cancer family history, cigarette smok...