Journal List > Korean J Adult Nurs > v.30(2) > 1095608

Kim, Ku, and Choi: A Prospective Study of Extending the Implanted Port Heparin Flushing Cycle in Outpatients with Solid Tumors

Abstract

Purpose

This prospective study was done to determine if it is possible to extend the implanted port heparin flushing cycle.

Methods

Patients enrolled in the study had their port flushed once 8 weeks or more in a tertiary hospital between July 2015 and November 2016. They were observed until they had completed six scheduled flushes or developed any port-related complication. Functional outcomes at heparin flushing were evaluated by using port infection, normal saline injection, blood aspiration and patient's posture during heparin administration.

Results

A total of 24 patients were enrolled and total of 72 cases of heparin flush were observed. The median heparin flushing interval was 95 days. No infection of port or problem with saline injection occurred. But there were 6 cases of initial difficult and 1 case of difficult in blood aspiration. However, there was not any case to get rid of the heparin flush, nor were there any patients noted who were not able to use it.

Conclusion

It was confirmed that there was no problem in the status and function of the implanted port, even if the heparin flush cycle was extended to 8 weeks or more.

REFERENCES

1. Paleczny J, Banyś-Jafernik B, Gazurek K, Kierpieć K, Szczerba H, Zipser P. Longterm totally implantable venous access port systems-one center experience. Anaesthesiology Intensive Therapy. 2013; 45(4):215–22. https://doi.org/10.5603/AIT.2013.0042.
2. Dal Molin A, Rasero L, Guerretta L, Perfetti E, Clerico M. The late complications of totally implantable central venous access ports: the results from an Italian multicenter prospective observation study. European Journal of Oncology Nursing. 2011; 15(5):377–81. https://doi.org/10.1016/j.ejon.2010.11.007.
crossref
3. Bishop L, Dougherty L, Bodenham A, Mansi J, Crowe P, Kib-bler C, et al. Guidelines on the insertion and management of central venous access devices in adults. International Journal of Laboratory Hematology. 2007; 29(4):261–78. https://doi.org/10.1111/j.1751-553x.2007.00931.x.
crossref
4. Conley SB, Buckley P, Magarace L, Hsieh C, Pedulla LV. Stan-dardizing best nursing practice for implanted ports: applying evidence-based professional guidelines to prevent central line- associated bloodstream infections. Journal of Infusion Nursing. 2017; 40(3):165–74. https://doi.org/10.1097/nan.0000000000000217.
5. Schiffer CA, Mangu PB, Wade JC, Camp-Sorrell D, Cope DG, El-Rayes BF, et al. Central venous catheter care for the patient with cancer: American society of clinical oncology clinical practice guideline. Journal of Clinical Oncology. 2013; 31(10):1357–70. https://doi.org/10.1200/jco.2012.45.5733.
crossref
6. Baskin JL, Pui CH, Reiss U, Wilimas JA, Metzger ML, Ribeiro RC, et al. Management of occlusion and thrombosis associated with longterm indwelling central venous catheters. The Lancet. 2009; 374(9684):159–69. https://doi.org/10.1016/S0140-6736(09)60220-8. https://doi.org/10.1016/S0140-6736(09)60220-8.
crossref
7. Sousa B, Furlanetto J, Hutka M, Gouveia P, Wuerstlein R, Mariz JM, et al. Central venous access in oncology: ESMO clinical practice guidelines. Annals of Oncology. 2015; 26(Suppl 5):v152–68. https://doi.org/10.1093/annonc/mdv296.
crossref
8. Greater Glasgow and Clyde. Care and maintenance of central venous catheter devices [Internet]. Scotland: National Health Service;2011. [cited 2017 July 5]. Available from:. http://www.beatson.scot.nhs.uk/content/mediaassets/doc/cvad%20guidelines%20september%2008%20final.pdf. http://www.beatson.scot.nhs.uk/content/mediaassets/doc/cvad%20guidelines%20september%2008%20final.pdf.
9. Centers for Disease Control and Prevention. Basic infection control and prevention plan for outpatient oncology settings 2011 [Internet]. Atlanta: Centers for Disease Control and Prevention;2011. [cited 2017 July 5]. Available from:. https://www.cdc.gov/hai/pdfs/guidelines/basic-infection-control-prevention-plan-2011.pdf. https://www.cdc.gov/hai/pdfs/guidelines/basic-infection-control-prevention-plan-2011.pdf.
10. Camp-Sorrell D. Access device guidelines: recommendations for nursing practice and education. 3rd ed.Pittsburgh, PA: Oncology Nursing Society;2011. p. 40.
11. Korean Oncology Nursing Society. Oncology nursing practice guideline. Asian Oncology Nursing. 2009; 9(1):76–115.
12. Kefeli U, Dane F, Yumuk PF, Karamanoglu A, Iyikesici S, Ba-saran G, et al. Prolonged interval in prophylactic heparin flushing for maintenance of subcutaneous implanted port care in patients with cancer. European Journal of Cancer Care. 2009; 18(2):191–4. https://doi.org/10.1111/j.1365-2354.2008.00973.x.
crossref
13. Kuo YS, Schwartz B, Santiago J, Anderson PS, Fields AL, Goldberg GL. How often should a port-a-cath be flushed? Cancer Investigation. 2005; 23(7):582–5. https://doi.org/10.1080/07357900500276923.
crossref
14. Girda E, Phaeton R, Goldberg GL, Kuo D. Extending the interval for port-a-cath maintenance. Modern Chemotherapy. 2013; 2(2):15–8. https://doi.org/10.4236/mc.2013.22003.
crossref
15. Odabas H, Ozdemir NY, Ziraman I, Aksoy S, Abali H, Oksuzo-glu B, et al. Effect of port-care frequency on venous port catheter-related complications in cancer patients. International Journal of Clinical Oncology. 2014; 19(4):761–6. https://doi.org/10.1007/s10147-013-0609-7.
crossref
16. Ignatov A, Ignatov T, Taran A, Smith B, Costa SD, Bischoff J. Interval between port catheter flushing can be extended to four months. Gynecologic and Obstetric Investigation. 2010; 70(2):91–4. https://doi.org/10.1159/000294919.
crossref
17. Kim HK, Choi SE, Lee JH, We ES, Joh HJ, Kim KS. Current status of interval of heparin flushing for maintenance of an implanted port in solid tumor patients. Journal of Korean Biological Nursing Science. 2014; 16(3):251–7. https://doi.org/10.7586/jkbns.2014.16.3.251.
crossref
18. Palese A, Baldassar D, Rupil A, Bonanni G, Capellari Maria T, Contessi D, et al. Maintaining patency in totally implantable venous access devices (TIVAD): a time-to-event analysis of different lock irrigation intervals. European Journal of Oncology Nursing. 2014; 18(1):66–71. https://doi.org/10.1016/j.ejon.2013.09.002.
crossref
19. Bae JI. Insertion and management of central venous catheter. Hanyang Medical Reviews. 2011; 31(1):23–31. https://doi.org/10.7599/hmr.2011.31.1.23.
20. Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A. AJCC cancer staging manual. 7th ed.New York: Springer;2010.
21. Park KH. Diagnosis and management of central venous cathe-ter-related infections. The Korean Journal of Medicine. 2014; 86(3):282–94. https://doi.org/10.3904/kjm.2014.86.3.282.
crossref
22. Goossens GA, Stas M, Jérôme M, Moons P. Systematic review: malfunction of totally implantable venous access devices in cancer patients. Supportive Care in Cancer. 2011; 19(7):883–98. https://doi.org/10.1007/s00520-011-1171-3.
crossref
23. Tabatabaie O, Kasumova GG, Eskander MF, Critchlow JF, Tawa NE, Tseng JF. Totally implantable venous access devices: a review of complications and management strategies. American Journal of Clinical Oncology. 2017; 40(1):94–105. https://doi.org/10.1097/coc.0000000000000361.
24. Lebeaux D, Fernández-Hidalgo N, Chauhan A, Lee S, Ghi-go JM, Almirante B, et al. Management of infections related to totally implantable venous-access ports: challenges and perspectives. The Lancet Infectious Disease. 2014; 14(2):146–59. https://doi.org/10.1016/s1473-3099(13)70266-4.
crossref
25. Milani A, Mazzocco K, Gandini S, Pravettoni G, Libutti L, Zencovich C, et al. Incidence and determinants of port occlusions in cancer outpatients: a prospective cohort study. Cancer Nursing. 2017; 40(2):102–7. https://doi.org/10.1097/NCC.0000000000000357.
26. Rosenbluth G, Tsang L, Vittinghoff E, Wilson S, Wilson-Ganz J, Auerbach A. Impact of decreased heparin dose for flush-lock of implanted venous access ports in pediatric oncology patients. Pediatric Blood & Cancer. 2014; 61(5):855–8. https://doi.org/10.1002/pbc.24949.
crossref
27. Goossens GA, Jérôme M, Janssens C, Peetermans WE, Fieuws S, Moons P, et al. Comparing normal saline versus diluted heparin to lock non-valved totally implantable venous access devices in cancer patients: a randomised, non-inferiority, open trial. Annals of Oncology. 2013; 24(7):1892–9. https://doi.org/10.1093/annonc/mdt114.
crossref
28. Dal Molin A, Allara E, Montani D, Milani S, Frassati C, Cossu S, et al. Flushing the central venous catheter: is heparin neces-sary? The Journal of Vascular Access. 2014; 15(4):241–8. https://doi.org/10.5301/jva.5000225.
crossref
29. Solinas G, Platini F, Trivellato M, Rigo C, Alabiso O, Galetto AS. Port in oncology practice: 3-monthly locking with normal saline for catheter maintenance, a preliminary report. The Journal of Vascular Access. 2017; 18(4):325–7. https://doi.org/10.5301/jva.5000740.
crossref
30. Vescia S, Baumgärtner AK, Jacobs VR, Kiechle-Bahat M, Rody A, Loibl S, et al. Management of venous port systems in oncology: a review of current evidence. Annals of Oncology. 2008; 19(1):9–15. https://doi.org/10.1093/annonc/mdm272.
crossref

Table 1.
Patients' General and Implanted Heparin Port related Characteristics at Baseline (N=24)
Characteristics Categories n (%)
Age (year) 50 6 (25.0)
50~59 6 (25.0)
60~69 9 (37.5)
≥70 3 (12.5)
Gender Male 7 (29.2)
Female 17 (70.8)
Location Seoul, Incheon, Gyeonggido 17 (70.8)
Other Province 7 (29.2)
Past history No 11 (45.8)
Hypertension 8 (33.3)
Diabetes 3 (12.5)
Asthma 1 (4.2)
Hepatitis 1 (4.2)
Hyperlipidemia 1 (4.2)
Type of cancer Colon cancer 11 (45.8)
Gynecologic cancer 9 (37.5)
Breast cancer 2 (8.3)
Stomach cancer 1 (4.2)
Sarcoma 1 (4.2)
Stage of cancer I 1 (4.2)
II 2 (8.3)
III 10 (41.7)
IV 11 (45.8)
Number of chemotherapy 1~10 12 (50.0)
11~20 12 (50.0)
Use of anticoagulant agent No 22 (91.7)
Yes 2 (8.3)
Catheter diameter 8 Fr. 3 (13.6)
9.6 Fr. 19 (86.4)
Implanted port inserted place Operating room 6 (26.1)
Angiography room 17 (73.9)
Implanted port inserted location Right 21 (87.5)
Left 3 (12.5)
Last infusion medication by implanted port Chemotherapy 15 (62.5)
Fluid 9 (37.5)

Check multiple domain availability;

AJCC TNM stage.

Table 2.
Patients' Heparin Flushing Status (N=24)
Characteristics Categories n (%) Median (IQR)
Number of heparin flushing 1 4 (16.7)
2 8 (33.3)
3 4 (16.7)
4 3 (12.5)
5 2 (8.3)
6 3 (12.5)
Heparin flushing interval (day) 61 2 (8.3) 94.83
61~90 10 (41.7) (72.00~117.00)
91~120 7 (29.2)
≥121 5 (20.8)

IQR=inter-quartile range.

Table 3.
Evaluation of Functional Outcomes at Heparin Flushing (N=24)
Variables Categories 1st 2nd 3rd 4th 5th 6th Total
n (%) n (%) n (%) n (%) n (%) n (%) n (%)
Infection Erythema/Swelling/Heat/ 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Tenderness/Purulent discharge/Fever (38℃)/
Increased WBC/
Increased CRP/Blood culture
Normal saline injection Easy injection 24 (100.0) 20 (100.0) 12 (100.0) 8 (100.0) 5 (100.0) 3 (100.0) 72 (100.0)
Difficult injection 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Impossible injection 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Blood aspiration Easy aspiration 20 (83.3) 18 (90.0) 11 (91.6) 8 (100.0) 5 (100.0) 3 (100.0) 65 (90.3)
Initial difficult aspiration 3 (12.5) 2 (10.0) 1 (8.4) 0 (0.0) 0 (0.0) 0 (0.0) 6 (8.3)
Difficult aspiration 1 (4.2) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 1 (1.4)
Impossible aspiration 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Patient's posture during heparin administration Lying position 21 (87.5) 17 (85.0) 12 (100.0) 8 (100.0) 4 (80.0) 3 (100.0) 65 (90.3)
Sitting position 3 (12.5) 3 (15.0) 0 (0.0) 0 (0.0) 1 (20.0) 0 (0.0) 7 (9.7)

WBC=white blood cell; CRP=C-reactive protein.

Table 4.
Median Heparin Flushing Intervals according to Reason for Prolonged Heparin Flushing Cycles (N=24)
Reasons n (%) Median (IQR)
On the instruction of doctor 9 (37.5) 83.00 (65.00~100.17)
Depending on the outpatient schedule 7 (29.2) 74.00 (69.50~103.00)
Lack of explanation about heparin flushing 4 (16.7) 108.25 (99.92~114.25)
Too busy to visit hospitals 3 (12.5) 164.25 (140.00~243.00)
No response 1 (4.1) 75.00 (75.00~75.00)

IQR=inter-quartile range.

Table 5.
The Cost of Management for Implanted Heparin Port (N=24)
Characteristics Categories n (%) Median (IQR)
With caregivers No 15 (62.5)
Yes 9 (37.5)
Transportation to hospitals Public 14 (58.3)
Car 9 (37.5)
Airplane 1 (4.2)
Transportation fee (won) 10,000 10 (41.8) 11,500
10,000~19,999 7 (29.1) (4,500~21,500)
≥20,000 7 (29.1)
Meal cost (won) 10,000 13 (54.2) 5,500
10,000~19,999 5 (20.8) (0~17,500)
≥20,000 6 (25.0)
Time for coming a hospital (min) 60 4 (16.7) 120
61~120 9 (37.5) (85~240)
121~180 4 (16.7)
≥181 7 (29.1)

IQR=inter-quartile range.

TOOLS
Similar articles