A prospective exploration of symptom burden clusters in women with breast cancer during chemotherapy treatment
Purpose The aim was to prospectively map symptom clusters in patients with stage I–IIIa breast cancer during standard chemotherapy treatment in a randomised study. Methods Participants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 7...
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Published in: | Supportive care in cancer Vol. 25; no. 5; pp. 1423 - 1429 |
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01-05-2017
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Abstract | Purpose
The aim was to prospectively map symptom clusters in patients with stage I–IIIa breast cancer during standard chemotherapy treatment in a randomised study.
Methods
Participants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 75 or FEC 100, and day 12 after the last cycle of Taxotere. Cut-off values for symptom scores, a mean value based on each individual reporting a symptom including occurrence, frequency, severity and distress for inclusion in analysis, were determined.
Results
The symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48–79%), difficulty sleeping (54–78%), difficulty concentrating (53–74%), worrying (54–74%) and pain (29–67%).
Conclusion
In summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. |
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AbstractList | The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study.
Participants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 75 or FEC 100, and day 12 after the last cycle of Taxotere. Cut-off values for symptom scores, a mean value based on each individual reporting a symptom including occurrence, frequency, severity and distress for inclusion in analysis, were determined.
The symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48-79%), difficulty sleeping (54-78%), difficulty concentrating (53-74%), worrying (54-74%) and pain (29-67%).
In summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. Purpose The aim was to prospectively map symptom clusters in patients with stage I–IIIa breast cancer during standard chemotherapy treatment in a randomised study. Methods Participants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 75 or FEC 100, and day 12 after the last cycle of Taxotere. Cut-off values for symptom scores, a mean value based on each individual reporting a symptom including occurrence, frequency, severity and distress for inclusion in analysis, were determined. Results The symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48–79%), difficulty sleeping (54–78%), difficulty concentrating (53–74%), worrying (54–74%) and pain (29–67%). Conclusion In summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. Purpose The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study. Methods Participants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 75 or FEC 100, and day 12 after the last cycle of Taxotere. Cut-off values for symptom scores, a mean value based on each individual reporting a symptom including occurrence, frequency, severity and distress for inclusion in analysis, were determined. Results The symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48-79%), difficulty sleeping (54-78%), difficulty concentrating (53-74%), worrying (54-74%) and pain (29-67%). Conclusion In summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study. The symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48-79%), difficulty sleeping (54-78%), difficulty concentrating (53-74%), worrying (54-74%) and pain (29-67%). In summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. PURPOSEThe aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study.METHODSParticipants completed the Memorial Symptom Assessment Scale (MSAS) at baseline, day 12 after the first and third cycle of FEC 75 or FEC 100, and day 12 after the last cycle of Taxotere. Cut-off values for symptom scores, a mean value based on each individual reporting a symptom including occurrence, frequency, severity and distress for inclusion in analysis, were determined.RESULTSThe symptom burden cluster analysis was conducted in two steps and included symptoms with high frequency and high levels of distress. The factor analysis revealed three symptom clusters; physical, gastro (phys/gastro) and emotional, with core symptoms that remained stable over time. The most prevalent symptoms for the total sample during all cycles were as follows: lack of energy (range between 48 and 90%), feeling sad (48-79%), difficulty sleeping (54-78%), difficulty concentrating (53-74%), worrying (54-74%) and pain (29-67%).CONCLUSIONIn summary, we have prospectively established that symptom clusters remain stable over time with a basis of core symptoms. This knowledge will aid in the development of effective core symptom-focused interventions to minimise symptom burden for patients treated with chemotherapy for breast cancer. |
Audience | Academic |
Author | Brandberg, Yvonne Xie, Hanjing Nasic, Salmir Bergh, Jonas Eriksson, Irene Wengström, Yvonne Rydberg, Per Rydén, Andreas Browall, Maria |
Author_xml | – sequence: 1 givenname: Maria orcidid: 0000-0003-0976-531X surname: Browall fullname: Browall, Maria email: maria.brovall@his.se organization: Department of Neurobiology, Care Science and Society, Division of Nursing, Karolinska Institutet, School of Health and Education, University of Skövde – sequence: 2 givenname: Yvonne surname: Brandberg fullname: Brandberg, Yvonne organization: Department of Oncology-Pathology, Karolinska Institutet – sequence: 3 givenname: Salmir surname: Nasic fullname: Nasic, Salmir organization: Research and Development Centre, Skaraborg Hospital – sequence: 4 givenname: Per surname: Rydberg fullname: Rydberg, Per organization: Department of Oncology-Pathology, Karolinska Institutet – sequence: 5 givenname: Jonas surname: Bergh fullname: Bergh, Jonas organization: Radiumhemmet and Cancer Centre Karolinska, Karolinska University Hospital – sequence: 6 givenname: Andreas surname: Rydén fullname: Rydén, Andreas organization: Department of Oncology-Pathology, Karolinska Institutet – sequence: 7 givenname: Hanjing surname: Xie fullname: Xie, Hanjing organization: Radiumhemmet and Cancer Centre Karolinska, Karolinska University Hospital – sequence: 8 givenname: Irene surname: Eriksson fullname: Eriksson, Irene organization: School of Health and Education, University of Skövde – sequence: 9 givenname: Yvonne surname: Wengström fullname: Wengström, Yvonne organization: Department of Neurobiology, Care Science and Society, Division of Nursing, Karolinska Institutet, Radiumhemmet and Cancer Centre Karolinska, Karolinska University Hospital |
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References | Kirkova, Rybicki, Walsh, Aktas, Davis, Karafa (CR19) 2011; 28 Yeon, Jung, Choi, Kim, Youn, Park, Huh (CR32) 2011; 25 Miaskowski, Cooper, Paul, Dodd, Lee, Aouizerat (CR20) 2006; 33 Bender, Ergyn, Rosenzweig, Cohen, Sereika (CR4) 2005; 28 Schover, Rhodes, Baum, Adams, Jenkins, Lewis, Jackson (CR27) 2011; 117 Davis, Kirkova (CR7) 2008; 16 Barsevick (CR3) 2007; 34 Kenne Sarenmalm, Öhlén, Jonsson, Gaston-Johansson (CR10) 2007; 34 Portenoy, Thaler, Kornblith, Lepore, Friedlander-Klar, Kiyasu (CR24) 1994; 30A Sanford, Beaumont, Butt, Sweet, Cella, Wagner (CR26) 2014; 47 Walsh, Rybicki (CR30) 2006; 14 Denieffe, Cowman, Gooney (CR8) 2013; 23 Kenne Sarenmalm, Browall, Gaston-Johansson (CR12) 2014; 47 Kim (CR13) 2009; 39 Ochsenkühn, Hermelink, Clayton, von Schönfeldt, Gallwas, Ditsch, Kahlert (CR23) 2011; 8 Wikman, Johar, Lagergren (CR31) 2014; 120 Browall, Sarenmalm, Nasic, Wengström, Gaston-Johansson (CR5) 2013; 46 Kim, Abraham (CR14) 2008; 31 Kenne Sarenmalm, Browall, Gaston-Johansson (CR11) 2014; 47 Tishelman, Lovgren, Broberger, Hamberg, Sprangers (CR28) 2010; 28 CR29 Kim, Barsevick, Tulman, McDermott (CR15) 2008; 36 Charalambous, Giannakopoulou, Bozas, Marcou, Kitsios, Paikousis (CR6) 2016; 11 CR21 Kirkova, Walsh, Rybicki, Davis, Aktas, Tao (CR17) 2010; 24 Deshields, Potter, Olsen, Liu (CR9) 2014; 22 Roscoea, Kaufmana, Matteson-Rusbyb, Palesha, Ryana, Kohlia (CR25) 2007; 12 Aktas, Walsh, Rybicki (CR1) 2010; 24 Aktas, Walsh, Rybicki (CR2) 2012; 20 Molassiotis, Wengström, Kearney (CR22) 2010; 39 Kirkova, Walsh, Aktas, Davis (CR16) 2010; 27 Kirkova, Aktas, Walsh, Rybicki, Davis (CR18) 2010; 27 18256858 - Support Care Cancer. 2008 Jul;16(7):757-61 21366876 - J Sex Med. 2011 May;8(5):1486-94 16482450 - Support Care Cancer. 2006 Aug;14(8):831-6 16955115 - Oncol Nurs Forum. 2006 Sep 01;33(5):E79-89 24555183 - Cancer. 2014 Jan 15;120(2):286-93 21148160 - Am J Hosp Palliat Care. 2011 Aug;28(5):350-5 19571640 - J Korean Acad Nurs. 2009 Jun;39(3):433-45 7999421 - Eur J Cancer. 1994;30A(9):1326-36 18718735 - J Pain Symptom Manage. 2008 Nov;36(5):468-79 17544244 - J Pain Symptom Manage. 2007 Jul;34(1):24-39 20015920 - Palliat Med. 2010 Apr;24(3):330-9 17878126 - Oncol Nurs Forum. 2007 Sep;34(5):971-80 20351131 - Am J Hosp Palliat Care. 2010 Jun;27(4):282-8 22361827 - Support Care Cancer. 2012 Nov;20(11):2837-43 20507866 - Palliat Med. 2010 Jun;24(4):373-85 17573454 - Oncologist. 2007;12 Suppl 1:35-42 25296389 - Eur J Cancer Care (Engl). 2015 Sep;24(5):605-17 18772651 - Cancer Nurs. 2008 Sep-Oct;31(5):E1-10 15915067 - Cancer Nurs. 2005 May-Jun;28(3):219-25 23195392 - J Pain Symptom Manage. 2013 Jul;46(1):131-41 20212257 - J Clin Oncol. 2010 Apr 10;28(11):1942-9 20226621 - J Pain Symptom Manage. 2010 May;39(5):847-58 20466939 - Am J Hosp Palliat Care. 2010 Aug;27(5):342-6 27341675 - PLoS One. 2016 Jun 24;11(6):e0156911 20569283 - J Eur Acad Dermatol Venereol. 2011 Feb;25(2):211-4 23880589 - J Pain Symptom Manage. 2014 Apr;47(4):721-30 17951230 - J Natl Cancer Inst Monogr. 2007;(37):39-46 21495025 - Cancer. 2011 Nov 1;117(21):4983-92 24292095 - Support Care Cancer. 2014 Apr;22(4):1089-96 24329603 - J Clin Nurs. 2014 Sep;23(17-18):2491-502 23916827 - J Pain Symptom Manage. 2014 Apr;47(4):731-41 M Browall (3527_CR5) 2013; 46 RK Portenoy (3527_CR24) 1994; 30A D Walsh (3527_CR30) 2006; 14 CM Bender (3527_CR4) 2005; 28 E Kenne Sarenmalm (3527_CR10) 2007; 34 S Denieffe (3527_CR8) 2013; 23 MP Davis (3527_CR7) 2008; 16 E Kenne Sarenmalm (3527_CR12) 2014; 47 J Kirkova (3527_CR17) 2010; 24 HJ Kim (3527_CR14) 2008; 31 A Aktas (3527_CR1) 2010; 24 A Aktas (3527_CR2) 2012; 20 3527_CR29 HJ Kim (3527_CR15) 2008; 36 AM Barsevick (3527_CR3) 2007; 34 MY Kim (3527_CR13) 2009; 39 3527_CR21 A Wikman (3527_CR31) 2014; 120 A Molassiotis (3527_CR22) 2010; 39 C Tishelman (3527_CR28) 2010; 28 JA Roscoea (3527_CR25) 2007; 12 R Ochsenkühn (3527_CR23) 2011; 8 J Kirkova (3527_CR16) 2010; 27 C Miaskowski (3527_CR20) 2006; 33 SD Sanford (3527_CR26) 2014; 47 J Kirkova (3527_CR18) 2010; 27 J Kirkova (3527_CR19) 2011; 28 LR Schover (3527_CR27) 2011; 117 A Charalambous (3527_CR6) 2016; 11 JH Yeon (3527_CR32) 2011; 25 E Kenne Sarenmalm (3527_CR11) 2014; 47 TL Deshields (3527_CR9) 2014; 22 |
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The aim was to prospectively map symptom clusters in patients with stage I–IIIa breast cancer during standard chemotherapy treatment in a randomised... The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study.... Purpose The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised... The aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised study. The... PURPOSEThe aim was to prospectively map symptom clusters in patients with stage I-IIIa breast cancer during standard chemotherapy treatment in a randomised... |
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SubjectTerms | Adult Age and Ageing Aged Analysis Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - therapeutic use Breast cancer Breast Neoplasms - diagnosis Breast Neoplasms - drug therapy Breast Neoplasms - pathology Breast Neoplasms - psychology Chemotherapy Clinical outcomes Cluster Analysis Cyclophosphamide - administration & dosage Drug therapy Epirubicin - administration & dosage Female Fluorouracil - administration & dosage Humans Medicin och hälsovetenskap Medicine Medicine & Public Health Middle Aged Neoplasm Staging Nursing Nursing Research Oncology Original Original Article Pain - etiology Pain Medicine Patient reported outcome measures Prevalence Prospective Studies Rehabilitation Medicine Symptom Symptom cluster Syndrome Women Äldre och åldrande |
Title | A prospective exploration of symptom burden clusters in women with breast cancer during chemotherapy treatment |
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