Impact of a laparoscopic resection on the quality of life in rectal cancer patients: Results of 135 patients

Surgery Today ◽  
2010 ◽  
Vol 40 (10) ◽  
pp. 917-922 ◽  
Author(s):  
Jun Li ◽  
Rong Chen ◽  
Yong-Qiang Xu ◽  
Xiao-Chen Wang ◽  
Shu Zheng ◽  
...  
2016 ◽  
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A.M. Couwenberg ◽  
J.P.M. Burbach ◽  
M. Van Vulpen ◽  
M.P.W. Intven ◽  
O. Reerink ◽  
...  

2013 ◽  
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Javier Suárez ◽  
Fernando Arias-de-la-Vega ◽  
Ruth Vera ◽  
Berta Ibáñez ◽  
...  

2017 ◽  
Vol 123 ◽  
pp. S171-S172
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F.S.A. De Beer ◽  
M.P.W. Intven ◽  
M.E. Hamaker ◽  
W.M.U. Van Grevenstein ◽  
...  

2003 ◽  
Vol 12 (3) ◽  
pp. 215-223 ◽  
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J. ENGEL ◽  
J. KERR ◽  
A. SCHLESINGER-RAAB ◽  
R. ECKEL ◽  
H. SAUER ◽  
...  

2009 ◽  
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Ilknur B. Gorken ◽  
Ilhan Oztop ◽  
Selman Sokmen ◽  
...  

2011 ◽  
Vol 29 (4_suppl) ◽  
pp. 468-468
Author(s):  
J. Boucher ◽  
B. Piperdi ◽  
D. Lundquist

468 Background: In 2010, the American Cancer Society has estimated rectal cancer affects over 39,670 adult patients in the United States. Five-year disease-free survival for rectal cancer patients with stage II/III disease ranges from 60-70%. Current gaps exist regarding long-term effects after treatment including altered bowel function and health-related quality of life (HR-QOL) concerns from rectal cancer patient and partners' perspectives both individually and together during rehabilitation and as cancer survivors. The purpose of this study was to: (1) describe the experiences of adult rectal cancer patients and their partners during rehabilitation from cancer treatment, including long- term effects; (2) examine health-related quality of life (HR-QOL) issues for rectal cancer patients and their partners including well-being and coping during their rehabilitation and as survivors. Methods: A qualitative descriptive study for a planned sample of 20 adult rectal cancer patients, stage II/III, and their partners from an academic health science hospital and cancer center has been conducted. Twelve patients and their partners have currently completed face to face semi-structured interviews. Patient participants were at least 6 months to 5 years post treatment. Qualitative descriptive design used purposive sampling to obtain broad information on rectal cancer patients' and partners' perspectives for content analysis. Results: Preliminary findings have revealed unexpected difficulties; chronic bowel function alterations; symptom unpredictability; nutrition intolerances; patient/partner adjustments; social concerns in going places, reactions by friends, work and financial strains; and, acceptance in living with it or chronic life changes as survivors. Partners acknowledged their own needs for information and support to assist their spouse or significant other. Further rich, thick descriptions will be presented in presentation of findings for 20 patient and partner responses. Conclusions: Survivorship follow-up regarding these concerns should be emphasized for rectal cancer patients and their partners to formalize interventions for study to enhance HR-QOL well-being. No significant financial relationships to disclose.


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