Download as pdf or txt
Download as pdf or txt
You are on page 1of 5

Cancer Epidemiology 51 (2017) 30–34

Contents lists available at ScienceDirect

Cancer Epidemiology
journal homepage: www.elsevier.com/locate/canep

Original Research Article

Self-rated health and associated factors in elderly patients with non-Hodgkin MARK
lymphoma

Lívia Maria Santiagoa,b, , Daniel Richard Mercanteb, Inês Echenique Mattosb
a
Federal University of Rio de Janeiro, Rua Rodolpho Paulo Rocco, 255/room 9E11, Cidade Universitária, Zip Code 21941- 913, Rio de Janeiro, RJ, Brazil
b
National School of Public Health/Oswaldo Cruz Foundation, Rua Leopoldo Bulhões, 1480/room 817b, Manguinhos, Zip Code 21041-210 Rio de Janeiro, RJ, Brazil

A R T I C L E I N F O A B S T R A C T

Keywords: Background: Self-rated health is a useful indicator for understanding health issues in elderly populations and
Self-rated health considered to be a predictor of adverse health outcomes in this group. This study aims to identify factors as-
Non-Hodgkin’s lymphoma sociated with self-rated health in elderly people with non-Hodgkin’s lymphoma.
Elderly patients Methods: Cross-sectional study performed at a cancer referral hospital in Rio de Janeiro, Brazil, included 162
patients, aged 60 or more years. All patients received a Multidimensional Geriatric Assessment, including seven
health dimensions, and socio-demographic, epidemiological and it were collected clinical data. Descriptive
analyses were performed and prevalence ratios were calculated to assess associations between self-rated health
and the independent variables. Multivariate analysis was performed using Poisson’s regression, to a ≤0.05 level
of statistical significance.
Results: The study population mean age was 68.8 (SD = 7.1) years; most were women, lived with a partner and
had little education. Prevalence of fair/poor self-rated health was 33.6%. Being female, not living with a partner,
functional dependence, depressive symptoms and nutritional risk/malnutrion showed associations with fair/
poor self-rated health. In the multiple model, dependence in instrumental activities of daily living (PR 2.96;
95%CI 1.66-5.30) and presence of depressive symptoms (PR 1.78; 95%CI 1.15-2.75) remained associated with
fair/poor health.
Conclusion: Variation in perceived health status supports the hypothesis that self-rated health is related to
multiple issues, regardless of disease status. The risk profile for poor self-rated health identified may be a useful
tool in care for older cancer patients, as it points to those at higher risk of adverse health outcomes.

1. Introduction an important predictor of treatment tolerance and mortality in elderly


women with breast cancer [14]. It was also associated with an in-
Self-rated (SRH) is a useful indicator for understanding health issues creasing number of comorbidities during treatment period among el-
in elderly populations and is considered an independent predictor of derly patients with solid tumours or haematological cancer [4,13].
adverse health outcomes in this group [1–4]. This measure represents a Non-Hodgkin’s lymphoma is a frequent haematological neoplasm in
perception by subjects themselves, based on their interpretations of the elderly. In 2012, mean age at diagnosis for non-Hodgkin’s lym-
physical and mental status and their expectations and benchmarks for phoma in the United States was 67 years [15]. In the United Kingdom,
comparison [5]. individuals 60 or more years old constituted two thirds of cases diag-
Studies have shown many factors associated with SRH among the nosed [16]. With advancing age, incidence of non-Hodgkin’s lymphoma
elderly, including socio-demographic variables, social support, lifestyle, has been observed to increase constantly, independently of sex and race
health and access to health services [6–9]. Self-reported health is also [17–19]. Although the literature demonstrates that world rates of in-
believed to associate with populations’ cultural values [10]. cidence and mortality for various types of cancer have declined in re-
Although most studies in the literature on self-rated health consider cent decades, non-Hodgkin’s lymphoma rates continues to show growth
overall health in community-dwelling elderly people, some studies do [17], for as yet unknown reasons [16].
report on specific chronic diseases, including cancer [4,11–13]. Poor This study aimed to identify factors associated with self-rated health
self-rated health was identified, over a seven-year follow-up period, as in elderly people with non-Hodgkin’s lymphoma in the city of Rio de


Corresponding author at: National School of Public Health/Oswaldo Cruz Foundation, Rua Leopoldo Bulhões, 1480/room 817b, Manguinhos, Zip Code 21041-210 Rio de Janeiro, RJ,
Brazil.
E-mail addresses: liviamsantiago@gmail.com (L.M. Santiago), danielmercante@grupocoi.com.br (D.R. Mercante), imattos@ensp.fiocruz.br (I.E. Mattos).

http://dx.doi.org/10.1016/j.canep.2017.10.002
Received 23 June 2017; Received in revised form 26 September 2017; Accepted 1 October 2017
1877-7821/ © 2017 Elsevier Ltd. All rights reserved.
L.M. Santiago et al. Cancer Epidemiology 51 (2017) 30–34

Janeiro, Brazil. Table 1


Characterisation of elderly patients with non-Hodgkin lymphoma, Rio de Janeiro, Brazil,
2013 (N = 162).
2. Material and methods
Variables N %
This cross-sectional study was conducted at a cancer referral hos-
pital in Rio de Janeiro, Brazil. From February to July 2013, 176 con- Self-rated health Excellent 29 19.1
Very good 18 11.8
secutive patients with non-Hodgkin’s lymphoma, 60 or more years old
Good 54 35.6
and treated in the outpatient hematologic clinic were contacted, if able Fair 44 28.9
to answer a structured questionnaire. Of those, the 162 who agreed to Poor 7 4.6
participate in the study underwent a Multidimensional Geriatric Gender Male 75 46.3
Assessment (MGA), including functional capacity, comorbidity, nutri- Female 87 53.7
tion, emotional condition, social support and use of medication. Data
Marital Status Married 91 56.2
was also collected on socio-demographic and clinical variables. Living with partner 7 4.3
The study was approved by the Research Ethics Committees of the Divorced/separated 18 11.1
National School of Public Health/Oswaldo Cruz Foundation and Widowed 31 19.1
Single 15 9.3
National Cancer Institute and was conducted in accordance to the
principles of the declaration of Helsinki. Education level Upper Secondary/Higher 52 32.5
Lower Secondary 91 56.9
Did not attend school 17 10.6
2.1. Measuring instruments
Functional Capacity in ADL Independent 136 84.5
Dependent 25 15.5
The MGA used comprised a set of selected instruments commonly
used for health assessment in elderly populations. Functional capacity Functional Capacity in IADL Independent 85 52.5
Dependent 77 47.5
in Basic Activities of Daily Living (ADL), and in Instrumental Activities
of Daily Living (IADL), were assessed on the Katz [20] and Lawton [21] Severe Comorbidity No 125 77,2
Yes 37 22,8
scales, respectively. For both scales, individuals were “dependent” if
they needed help or were unable to perform any activity. The Cumu- Polypharmacy (4 or more regular No 108 66.7
lative Illness Scale-Geriatric (CIRS-G) was used to investigate co- medications) Yes 54 33.3

morbidity [22], and individuals were classified using an adapted ver- Depressive Symptoms No depressive symptoms 113 74.8
sion of the classification proposed by Rodriguez et al. [23]: no Mild depressive symptoms 29 19.2
Severe depressive 9 6.0
comorbidity (0 points), mild comorbidity (1–2 points), moderate co-
symptoms
morbidity (3–8 points) and severe comorbidity (> 8 points). Nutri-
Nutritional Risk No nutritional risk 83 53.9
tional status was evaluated by the short version of the Mini Nutritional
At nutritional risk 53 34.4
Assessment (MNA) [24] and patients were classified into no nutritional Malnourished 18 11.7
risk and nutritional risk/malnourished. The 15-item Geriatric Depres-

sion Scale was chosen to evaluate emotional condition [25]; a score of Differences between absolute numbers are due to missing values.
five or more was considered indicative of depressive symptoms. Poly-
pharmacy was considered to be regular use of 4 or more medications while 34.4% were at nutritional risk (Table 1).
[26]. Being female (PR 1.75; 95%CI 1.07-2.85), living without a partner,
The dependent variable was the answer to the question “Compared dependence in Activities of Daily Living (ADL) and in Instrumental
to other people your age, how is your health?”. Although this question Activities of Daily Living (IADL), presence of depressive symptoms and
had five possible answers (excellent, very good, good, fair and poor), being at nutritional risk/malnourished all showed associations with
these were aggregated into two categories (Excellent/Very good/Good fair/poor self-rated health (Table 2).
and Fair/Poor), following the tendency observed in the literature, In the multiple model, functional dependence in IADL and presence
which indicates predominance of responses in the intermediate cate- of depressive symptoms were independent risk factors for self-rated
gories [27–29]. fair/poor health (Table 3).

2.2. Data analysis 4. Discussion

Descriptive analysis of the distribution of individuals into self-rated Self-rated health proves to be an important marker of the diversity
health response groups, by study co-variable, was conducted using in aging and in the individual recognition of the concept of health at
measures of central tendency and dispersion for continuous variables, this stage in life. This is reflected in the results of this study, in which a
and frequency distributions for categorical variables. population of elderly people with a diagnosis of haematological cancer,
Prevalence ratios (PR) were calculated to assess associations be- fewer than 34% classified their health adversely. A similar value was
tween self-reported health and the independent variables, and multi- described in a study of 112 Canadians 65 years or more, with a diag-
variate analysis was performed using Poisson regression, to a ≤ 0.05 nosis of solid (breast, colorectal or lung) tumours or haematological
level of statistical significance. cancer (lymphoma or myeloma), in which only 38 patients (33.9%)
Statistical analyses were performed using the statistical software rated their own health as poor [4]. In a study of 181 Australians with a
STATA, version 10.0 (StataCorp LP). diagnosis of advanced-stage cancer, mean age 62 years (SD 12 years), it
was observed that 58% rated their own health as excellent, very good or
3. Results good, 28% as fair and only 14% as poor [30].
In the literature on health and aging, individuals who rated their
Study population mean age was 68.8 (SD = 7.1) years, most were own health as fair or poor are observed to display a greater likelihood of
women (53.7%), lived with a partner and had little formal education. illness and death, independently of their objective health status
Self-rated health prevalences were 33.6% fair/poor (N = 51) and [1,3,31,32]. The claim appears to hold even when individuals with
66.4% good/very good/excellent (N = 101). Prevalence of dependence cancer are rated. In a United States study, designed to assess self-rated
in Instrumental Activities of Daily Living (IADL) was high (47.5%), health as a variable indicative of health-adjusted life expectancy

31
L.M. Santiago et al. Cancer Epidemiology 51 (2017) 30–34

Table 2 likelihood of rating their own health as poor (OR 4.11; 95%CI 3.06-
Prevalence ratios for self-rated health status among elderly patients with non-Hodgkin 5.54), as compared with cancer survivors who did not mention other
lymphoma, Rio de Janeiro, Brazil, 2013 (N = 162).
adverse health conditions [11]. This result draws attention to the im-
Variables Excellent/Very Fair/Poor Crude Prevalence portance of comorbidity in the individual experience of cancer in older
good/Good N (%) Ratios patients.
N (%) (95%CI) Similar to what was seen in this study, other research has found that
self-rated health displays an association with functional dependence
Gender
Male 54 (53.5) 17 (33.3) 1 [34,35]. In a study of 2135 elderly in the municipality of São Paulo,
Female 47 (46.5) 34 (66.7) 1.75 (1.07–2.85) Brazil, presence of functional incapacity in Instrumental Activities of
Marital Status
Daily Living (IADL) was found to associate with high risk (OR 2.50,
Married/Living with 67 (66.3) 24 (47.1) 1 p < 0.01) of poor self-rated health and, when incapacity in IADL was
partner assessed jointly with incapacity in ADL, the risk was even greater (OR
Divorced/Separated/ 34 (33.7) 27 (52.9) 1.68 (1.07–2.61) 2.66, p < 0.01) [34]. Among Canadians 55 or more years old, the
Widowed/Single
predictors of poor self-rated health observed were the presence of
Educational level limitations without functional dependence (OR 1.9; 95%CI 1.2-1.9) and
Upper Secondary/ 38 (38.4) 13 (25.5) 1
with functional dependence (OR 2.8; 95%CI 1.8-4.6), in addition to
University
Lower Secondary 52 (52.5) 33 (64.7) 1.52 (0.89–2.61) male sex, psychological stress and chronic diseases, low level of
Did not attend school 9 (9.1) 5 (9.8) 1.40 (0.60–3.26) schooling and income, in a model fitted for all these variables [35].
Functional Capacity in ADL
The relation between SRH and depressive symptoms observed in
Independent 94 (93.1) 40 (80.0) 1 this study has also been described in the scientific literature on aging.
Dependent 7 (6.9) 10 (20.0) 1.97 (1.22–3.17) SRH can be found in the long list of predictors of depressive sympto-
Functional Capacity in IADL matology, among other factors such as loneliness, sensory function
Independent 71 (70.3) 13 (25.5) 1 deficits, cardiac and other chronic diseases and functional dependence
Dependent 30 (29.7) 38 (74.5) 3.61 (2.10–6.21) [36]. Among 3187 Japanese aged 65 years or older in the city of Ta-
Comorbidity in severity categories 3 and 4 katsuki, absence of depressive symptoms, assessed by the Geriatric
No 79 (78.2) 40 (78.4) 1 Depression Scale (GDS), represented a higher likelihood of good self-
Yes 22 (21.8) 11 (21.6) 1.00 (0.57–1.71) rated health (OR 2.43; 95%CI 2.01-2.94) in a model adjusted for age,
Polypharmacy (4 or more regular medications) sex and variables related to health and disability [37]. In a study of 462
No 72 (71.3) 31 (60.8) 1 elderly living in long-stay institutions across four Brazilian munici-
Yes 29 (28.7) 20 (39.2) 1.35 (0.87–2.12)
palities, the variable showing the strongest association with depressive
Depressive Symptoms symptoms was poor self-rated health (PR 1.47; 95%CI 1.31-1.66), fol-
No depressive symptoms 85 (85.9) 27 (54.0) 1
lowed by comorbidities (PR 1.34; 95%CI 1.09-1.65), hospitalizations
Depressive symptoms 14 (14.1) 23 (46.0) 2.58 (1.70–3.90)
(PR 1.26; 95%CI 1.04-1.54) and lack of friends at the institution (PR
Nutritional Risk
1.24; 95%CI 1.03-1.49) [38]. In a study of 600 community-dwelling
No nutritional risk 61 (63.5) 21 (43.8) 1
At nutritional risk/ 35 (36.5) 27 (56.3) 1.70 (1.07–2.71)
older individuals, depressive symptoms also showed the strongest as-
Malnourished sociation, after adjustment, with poor self-rated health (OR 6.57;
p < 0.001), followed by the need for caregiver support (OR 3.87;
p < 0.001) [39].
Table 3 Conspicuous among the socio-demographic variables related to self-
Poisson multiple regression model for self-rated health among elderly patients with non- rated health in the elderly are sex and marital status, which are com-
Hodgkin lymphoma, Rio de Janeiro, Brazil, 2013 (N = 162).
monly cited in the literature. In a study of 1505 individuals aged 60
Variables Adjusted Prevalence ratios* years or more, the women were more likely (OR 2.02; 95%CI 1.48-2.76)
(95%CI) than the men to rate their own health as poor/very poor [6], which is
similar to what was found in this study. On the other hand, in a Bra-
Functional Capacity in IADL (dependent) 2.96 (1.66–5.30)
zilian study based on the 2003 National Household Sample Survey, a
Depressive Symptoms (yes) 1.78 (1.15–2.75)
negative association was found between female sex and poor self-rated
* Adjusted for all variables in the model. health (OR 0.85; 95%CI 0.77-0.92), in a model including the variables
age group, education, number of chronic conditions, number of medical
(HALE), of 144 men, aged 50 years or more, with a recent diagnosis of appointments in the past year and hospital admission during the study
localised prostate cancer, life expectancy based on self-rated health was period [40]. In the study by Shooshtari et al. [35], with 3107 Canadians
observed to be on average two years greater than age-based life ex- aged 55 or more years, male sex was identified as a predictor of poor
pectancy, independently of race, family income and PSA level [30]. self-rated health (OR 1.9; 95%CI 1.3-2.8) in a model adjusted for other
Few studies in the literature were found to examine factors asso- socio-demographic and health variables. In the Japanese study by Sun
ciated with self-rated health in individuals with cancer. Accordingly, et al. [37], a response differential was observed among individuals aged
the results of this study were also compared with the literature on 65 to 74 years, with health self-rated positively more often by the
aging. women, which did not occur in the 75 or more year age group.
There are different instruments to evaluate comorbidity in cancer As regards marital status, Lima-Costa et al. [6] also found sepa-
patients [33] and the most used are the Charlson Comorbidity Index rated/divorced individuals as a group were more likely to self-rate their
and the Cumulative Illness Rating Scale – Geriatric (CIRS-G). We health adversely (OR 2.18; 95%CI 1.15-4.16). In a study of 2143 elderly
decided to use CIRS-G as it was designed to analyze comorbidity in Brazilians, those who were separated/divorced were more likely to rate
elders and it is a frequently used instrument in geriatric oncology stu- their health as poor (OR 1.08; p < 0.01) in a model that also con-
dies. Gallicchio et al. [11] studied 1261 cancer survivors to evaluate the templated sex, functional dependence, levels of schooling and income
relationship between adverse health conditions unrelated to cancer, [34]. In a study of 729 North American women, users of primary health
self-rated health and functional capacity. Cancer survivors who men- care services, 37.0% of whom were aged 65 years or more, it was in this
tioned two or more adverse health conditions displayed far greater age group that observed that health was self-rated positively least often
(78.6%) and that marital status was associated with self-rated health, in

32
L.M. Santiago et al. Cancer Epidemiology 51 (2017) 30–34

that single or divorced women (OR 0.38; 95%CI 0.20-0.74) and widows [7] V.H. Menec, S. Shooshtari, P. Lambert, Ethnic differences in self-rated health among
older adults: a cross-sectional and longitudinal analysis, J. Aging Health 19 (1)
(OR 0.61; 95%CI 0.32-1.16) were less likely than married women to (2007) 62–86.
rate their own health as good [41]. [8] M.B.A. Barros, L.M. Zanchetta, E.C. Moura, D.C. Malta, Auto-avaliação da saúde e
Given that there is a wide range of kinds of aging and that the fatores associados, Brasil, 2006, Rev. Saúde Pública 43 (Suppl. 2) (2009) 27–37.
[9] L.M. Santiago, C.O. Novaes, I.E. Mattos, Factors associated with self-rated health
impact of emotional factors brought on by the inability to manage among older men in a medium-sized city in Brazil, J. Men’s Health 7 (1) (2010)
oneself and perform everyday functions can overshadow objective 55–63.
health issues, considering only chronological age and disease char- [10] B. Roudijik, R. Donders, P. Stalmeier, Cultural values: can they explain self-reported
health? Qual. Life Res. 26 (2017) 1531–1539.
acteristics when choosing therapeutic conducts and regimes can lead to [11] L. Gallicchio, B. Kalesan, S.C. Hoffman, K.J. Helzlsouer, Non-cancer adverse health
non-individualise treatment and unfavourable prognoses [42,43]. Stu- conditions and perceived health and function among cancer survivors participating
dies to evaluate variables that can influence prognosis in elderly with a in a community-based cohort study in Washington County, Maryland, J. Cancer
Surviv. 2 (2008) 12.
diagnosis of cancer can contribute to establishing more singular and
[12] A.M. Nápoles, C. Ortíz, H. O’Brien, A.B. Sereno, C.P. Kaplan, Coping resources and
effective treatment protocols, thus fostering better prognoses [15]. self-rated health among latina breast cancer survivors, Oncol. Nurs. Forum. 38 (5)
There is a vast literature on the role of self-rated health in aging, (2011) 523–531.
while few studies address specifically elderly with cancer. This study is [13] Y. Rottenberg, H. Litwin, O. Manor, A. Paltiel, M. Barchana, O. Paltiel,
Prediagnostic self-assessed health and extent of social networks predict survival in
the first investigation of self-rated health in elderly patients with cancer older individuals with cancer: a population based cohort study, J. Geriatric. Oncol.
in Brazil, and is also pioneering in addressing the factors associated 5 (2014) 400–407.
with it in this population. [14] K.M. Clough-Gorr, A.E. Stuck, S.S. Thwin, R.A. Silliman, Older breast cancer sur-
vivors: geriatric assessment domains are associated with poor tolerance of treat-
ment adverse effects and predict mortality over 7 years of follow-up, J. Clin. Oncol.
5. Conclusion 28 (3) (2010) 380–386.
[15] M. Extermann, U. Wedding, Comorbidity and geriatric assessment for older patients
with hematologic malignancies: a review of the evidence, J. Geriatr. Oncol. 3
Our results support the hypothesis that the self-assessment of one’s (2012) 49–57.
health is related to multiple issues and does not depend on disease [16] K.R. Shankland, J.O. Armitage, B.W. Hancock, Non-Hodgkin lymphoma, Lancet 380
status. The risk profile identified in this study points to the older pa- (2012) 848–857.
[17] M.A.S. Müller, G. Ihorst, R. Mertelsmann, M. Engelhardt, Epidemiology of non-
tients at higher risk of adverse health outcomes. As self-rated health
Hodgkin’s lymphoma (NHL): trends geographic distribution, and etiology, Ann.
consists in an objective question, easily answered, we recommend its Hematol. 84 (2005) 1–12.
use in the oncologic care setting as part of the clinical evaluation of [18] C. Thieblemont, B. Coiffier, Lymphoma in older patients, J. Clin. Oncol. 25 (2007)
1916–1923.
older patients.
[19] A. Smith, D. Howell, R. Patmore, A. Jack, E. Roman, Incidence of haematological
malignancy by sub-type: a report from the haematological malignancy research
Authors’ contribution network, Br. J. Cancer 105 (2011) 1684–1692.
[20] S. Katz, T.D. Downs, H.R. Cash, R.C. Grotz, Progress in development of index of
ADL, Gerontologist 10 (1970) 20–30.
Lívia Maria Santiago: Guarantor of study integrity, study concept, [21] M.P. Lawton, M. Moss, M. Fulcomer, M.H. Kleban, A. Research, Service oriented
study design, literature research, data analysis and manuscript pre- multilevel assessment instrument, J. Gerontol. 37 (1982) 91–99.
paration. [22] M.D. Miller, C.F. Paradis, P.R. Houck, S. Mazumdar, J.A. Stack, A.H. Rifai,
B. Mulsant, C.H. Reynolds III, Rating chronic medical illness burden in ger-
Daniel Richard Mercante: Guarantor of study concept and literature opsychiatric practice and research: application of the cumulative illness rating
research, and manuscript edition/review. scale, Psychiatr. Res. 41 (1992) 237–248.
Inês Echenique Mattos: Guarantor of study concept, study design, [23] M.A.Z. Rodríguez, J.G. Pavón, P.S. Fernández, A.F. Salinas, L.M. Guzmán,
J.J. Baztán, Fiabilidad interobservador de los 4 índices de comorbilidad mós utili-
definition of intellectual content, data analysis, manuscript edition/ zados en pacientes ancianos, Rev. Esp. Geriatr. Gerontol. 47 (2) (2012) 67–70.
review. [24] L.Z. Rubenstein, J.O. Harker, A. Salva, Y. Guigoz, B. Vellas, Screening for under-
nutrition in geriatric practice: developing the short-form mini nutritional assess-
ment (MNA-SF), J. Gerontol. 56A (2001) M366–377.
Funding [25] J.A. Yesavage, T.L. Brink, T.L. Rose, O. Lum, V. Huang, M. Adey, V.O. Leirer,
Development and validation of a geriatric depression screening scale: a preliminary
This work was supported by the Carlos Chagas Filho Foundation for report, J. Psychiatr. Res. 17 (1982) 37–49.
[26] W. Denneboom, M.G. Dautzenberg, R. Grol, P.A. de Smet, Analysis of polypharmacy
Research Support of the State of Rio de Janeiro (FAPERJ). The FAPERJ
in older patients in primary care using a multidisciplinary expert panel, Br. J. Gen.
did not have any role in the preparation or decision to submit this Pract. 56 (2006) 504–510.
manuscript. [27] Y. Lee, S. Shinkai, A comparison of correlates of self-rated health and functional
disability of older persons in the far east: Japan and Korea, Arch. Gerontol. Geriatr.
37 (2003) 63–76.
Conflict of interest statement [28] M.F. Lima-Costa, J.O.A. Firmo, E. Uchoa, A. estrutura da auto-avaliação da saúde
entre idosos: projeto Bambuí, Rev. Saúde Publica 38 (6) (2004) 827–834.
The authors declare no conflicts of interests. [29] C.L. Szwarcwald, M.C. Leal, G.C. Gouveia, W.V. Souza, Desigualdades socio-
economicas em saúde no Brasil: resultados da Pesquisa Mundial de Saúde, 2003,
Rev. Bras. Matern. Infant. 5 (Suppl. 1) (2005) 511–522.
References [30] R. Mohan, H.A. Beydoun, M.A. Beydoun, M. Barnes-Eley, J. Davis, R. Lance,
P. Schellhammer, Self-rated health as a tool for estimating health-adjusted life ex-
pectancy among patients newly diagnosed with localized prostate cancer: a pre-
[1] K.B. DeSalvo, V.S. Fan, M.B. McDonell, S.D. Fihn, Predicting mortality and health
liminary study, Qual. Life Res. 20 (5) (2011) 713–721.
care utilization with a single question, Health Serv. Res. 40 (2005) 1234–1246.
[31] T. Ishizaki, I. Kai, Y. Imanaka, Self-rated health and social role as predictors for 6-
[2] C. Murata, T. Kondo, K. Tamakoshi, H. Yatsuya, H. Toyoshima, Determinants of
year total mortality among a non-disabled older Japanese population, Arch.
self-rated health: could health status explain the association between self-rated
Gerontol. Geriatr. 42 (2006) 91–99.
health and mortality? Arch. Gerontol. Geriatr. 43 (2006) 369–380.
[32] T.M. Lyyra, E. Heikkinen, A.L. Lyyra, M. Jylha, Self-rated health and mortality:
[3] L.M. Santiago, C.O. Novaes, I.E. Mattos, Self-rated health (SRH) as a predictor of
could clinical and performance-based measures of health and functioning explain
mortality in elderly men living in a medium size city in Brazil, Arch. Gerontol.
the association? Arch Gerontol. Geriatr. 42 (2006) 277–288.
Geriatr. 51 (2010) e88–e93.
[33] S. Marventano, G. Grosso, A. Mistretta, M. Bogusz-Czerniewicz, R. Ferranti,
[4] M. Puts, J. Monette, V. Girre, N. Sourial, C. Wolfson, M. Monette, G. Batist,
F. Nolfo, G. Giorgianni, S. Rametta, F. Drago, F. Basile, A. Bondi, Evaluation of four
H. Bergman, The relationship of self-rated health with functional status, toxicity
comorbidity indices and Charlson comorbidity index adjustment for colorectal
and mortality: results of a prospective pilot study of older patients with newly-
cancer patients, Int. J. Colorectal Dis. 29 (9) (2014) 1159–1169.
diagnosed cancer, J. Geriatr. Oncol. 4 (2013) 319–326.
[34] L.C. Alves, R.N. Rodrigues, Determinantes da autopercepção de saúde entre idosos
[5] N. Hoeymans, E.J.M. Feskens, G.A.M. van Den Bos, D. Kromhout, Non-response bias
do Município de São Paulo, Brasil, Pan Am. J. Public Health 17 (2005) 333–341.
in a study of cardiovascular diseases: functional status and self-rated health among
[35] S. Shooshtari, V. Menec, R. Tate, Comparing predictors of positive and negative self-
elderly men, Age Ageing 27 (1998) 35–40.
rated health between younger (25–54) and older (55+) canadian adults: a long-
[6] M.F. Lima-Costa, J.O.A. Firmo, E. Uchôa, Differences in self-rated health among
itudinal study of well-being, Res. Aging 29 (6) (2007) 512–554.
older adults according to socioeconomic circumstances: the Bambuí Health and
[36] R. Heikkinen, M. Kauppinen, Depressive symptoms in late life: a 10-year follow-up,
Aging Study, Cad. Saúde Pública. 21 (3) (2005) 830–839.

33
L.M. Santiago et al. Cancer Epidemiology 51 (2017) 30–34

Arch. Gerontol.Geriatr. 38 (3) (2004) 239–250. Minas Gerais, Brasil. Cad. Saúde Pública 23 (8) (2007) 1893–1902.
[37] W. Sun, M. Watanabe, Y. Tanimoto, T. Shibutani, R. Kono, M. Saito, K. Usuda, [41] J.E. Rohrer, M.E. Bernard, Y. Zhang, N.H. Rasmussen, H. Woroncow, Marital status,
K. Kono, Factors associated with good self-rated health of non-disabled elderly feeling depressed and self-rated health in rural female primary care patients, J.
living alone in Japan: a cross-sectional study, BMC Public Health 7 (2007) 297. Eval. Clin. Pract. 14 (2008) 214–217.
[38] L.M. Santiago, I.E. Mattos, Depressive symptoms in institutionalized older adults, [42] N. Winkelmann, I. Petersen, M. Kiehntopf, H.J. Fricke, A. Hochhaus, U. Wedding,
Rev. Saúde Pública 48 (2) (2014) 216–224. Results of comprehensive geriatric assessment effect survival in patients with ma-
[39] J.C. Millán-Calenti, A. Sánchez, T. Lorenzo, A. Maseda, Depressive symptoms and lignant lymphoma, J. Cancer Res. Clin. Oncol. 137 (2011) 733–738.
other factors associated with poor self-rated health in the elderly: gender differ- [43] C. Nabhan, S.M. Smith, I. Helenowski, E. Ramsdale, B. Parsons, R.J. Karmali,
ences, Geriatr. Gerontol. Int. 12 (2012) 198–206. Feliciano, B. Hanson, S. Smith, J. McKoy, A. Larsen, A. Hantel, S. Gregory,
[40] M.F. Lima-Costa, S.V. Peixoto, D.L. Matos, J.O.A. Firmo, E. Uchoa, A influência de A.M. Evens, Analysis of very elderly (≥80 years) non-Hodgkin lymphoma: impact
respondente substituto na percepção da saúde idosos: um estudo baseado na of functional status and co-morbidities on outcome, Br. J. Aematol. 156 (2) (2011)
Pesquisa Nacional por Amostra de Domicílios (1998–2003) e na coorte de Bambuí, 196–204.

34

You might also like