Thirty-day mortality after systemic anticancer treatment as a real-world, quality-of-care indicator: the Northland experience

被引:15
作者
Ang, Edmond [1 ]
Newton, Los Vincent [1 ]
机构
[1] Whangarei Base Hosp, Dept Med Oncol, Northland 0148, New Zealand
关键词
30-day mortality; systemic anticancer treatment; real world quality of care indicator; Whangarei Base Hospital; Northland; New Zealand; auditing medical oncology practice; CHEMOTHERAPY; ONCOLOGY; THERAPY; BREAST;
D O I
10.1111/imj.13618
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Systemic anticancer treatment (SACT) at the end of life is considered poor practice due to its futility and associated toxicities. Consequently, 30-day mortality after SACT is increasingly recognised as a potential real-world quality-of-care indicator in medical oncology. Aims: Whangarei Base Hospital (WBH) provides outpatient SACT treatment to all patients living in the Northland region of New Zealand. The goal of this study was to report our 30-day mortality after SACT and to contribute to the experience of its use in Australasia. Methods: In this retrospective study, the WBH electronic database was searched to identify all patients who had received SACT in WBH from 1 January 2012 to 31 December 2016. Patients who died within 30 days of their last treatment were short-listed. Records were reviewed identifying key demographic, disease, treatment and mortality data. Composite 30-day mortality index and that of each tumour stream were calculated. Key findings were described using descriptive statistics. Results: Over 5 years, 1103 patients received SACT in WBH, with 57 patients dying within 30 days of treatment, resulting in a composite 30-day mortality rate of 5.17%. One patient died receiving curative intent SACT. More deaths occurred in SACT-naive patients and during the first two cycles of therapy. Of the deaths, 28% was attributed to SACT, while 59.7% was attributed to cancer progression. Conclusion: Thirty-day mortality rates were comparable to studies from larger institutions. We demonstrated the feasibility of this index for auditing practice in smaller oncology units over a longer timeframe.
引用
收藏
页码:403 / +
页数:6
相关论文
共 17 条
[1]  
[Anonymous], 2017, CHEM BREAST LUNG CAN
[2]  
[Anonymous], 2017, FAST CANC TREATM PRO
[3]   Paradox of Prescribing Late Chemotherapy: Oncologists Explain [J].
Bluhm, Minnie ;
Connell, Cathleen M. ;
De Vries, Raymond G. ;
Janz, Nancy K. ;
Bickel, Kathleen E. ;
Silveira, Maria J. .
JOURNAL OF ONCOLOGY PRACTICE, 2016, 12 (12) :E1006-E1014
[4]   Reviewing deaths within 30 days of systemic anti-cancer therapy: Driving quality in a regional chemotherapy service. [J].
Forde, Caroline ;
Scullin, Paula ;
Edgar, Lynne ;
McAleer, James J. ;
Coyle, Victoria M. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (08)
[5]  
Giorgi F, 2004, J CLIN ONCOL, V22, p539S
[6]   Frequency and cost of chemotherapy-related serious adverse effects in a population sample of women with breast cancer [J].
Hassett, Michael J. ;
O'Malley, A. James ;
Pakes, Juliana R. ;
Newhouse, Joseph R. ;
Earle, Craig C. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (16) :1108-1117
[7]   30-day mortality of surgeries in disseminated cancer patients: An analysis using NSQIP, dividing surgeries into low, medium, and high risk [J].
John, Pesavento Anton ;
Silberstein, Peter T. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (34)
[8]   Chemotherapy use near end of life (EOL): Measuring real world benchmarks. [J].
Kraut, Joshua ;
Gippetti, James ;
Peterson, Dylan ;
Agarwala, Vineeta ;
Revol, Cindy ;
Fessele, Kristen Lee ;
Abernethy, Amy Pickar .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (08)
[9]   Palliative chemotherapy during the last month of life [J].
Nappa, U. ;
Lindqvist, O. ;
Rasmussen, B. H. ;
Axelsson, B. .
ANNALS OF ONCOLOGY, 2011, 22 (11) :2375-2380
[10]   Mortality within 30 days of chemotherapy: a clinical governance benchmarking issue for oncology patients [J].
O'Brien, M. E. R. ;
Borthwick, A. ;
Rigg, A. ;
Leary, A. ;
Assersohn, L. ;
Last, K. ;
Tan, S. ;
Milan, S. ;
Tait, D. ;
Smith, I. E. .
BRITISH JOURNAL OF CANCER, 2006, 95 (12) :1632-1636