I have a research plan and 5 references, and you can add one or two references. Academic writing is general.
T
The Effects of Kidney-Disease-Related Loss on Long-Term Dialysis Patients’ Depression and Quality of Life: Positive Affect as a Mediator
Ramony Chan,*† Robert Brooks,‡ Jonathan Erlich,§ Josephine Chow,† and Michael Suranyi† *Consultation Liaison Psychiatry, †Renal Unit, and ‡Centre for Population Mental Health Research, Liverpool Hospital,
and §Department of Nephrology, Prince of Wales Hospital, Sydney, New South Wales, Australia
Background and objectives: In kidney disease, the concept of loss is widely discussed but minimally researched. It appears
that dialysis patients who grieve a range of losses suffer increased depression and reduced quality of life (QoL). Limited
research is partly due to the lack of a relevant loss measure. The study presented here developed a measure and tested the
criterion validity of loss in relation to depression and QoL.
Design, setting, participants, & measurements: In a cross-sectional observational study, 151 long-term dialysis patients were
interviewed using standardized psychometric measures and the Kidney Disease Loss Scale (KDLS), developed for the study.
Factor, path and multigroup analyses were conducted.
Results: The factor structure and reliability of KDLS were supported. The path analyses supported the criterion validity of
loss. It was a stronger contributor to depression than other clinical variables. Its effect on QoL was fully mediated by depression
and positive affect (coping). The magnitude of the paths from loss to QoL through depression and positive affect was larger in
home-based dialysis patients than in hospital-based patients.
Conclusions: KDLS is a promising measure of loss. Patient-defined losses may contribute to the high level of depression and
in turn a reduction in patients’ coping and QoL. These findings suggest several points of intervention to improve long-term
dialysis patients’ QoL.
Clin J Am Soc Nephrol 4: 160 –167, 2009. doi: 10.2215/CJN.01520308
he concept of Kidney-Disease-Related Loss (KDRL) in
ESRD has been clinically and theoretically significant
for decades (1– 4). ESRD patients experience multiple
losses, both tangible and symbolic; for example, loss of physical
strengths, freedom, employment, and social life, resulting in
grief throughout the course of ESRD and dialysis (1,2,4). Re-
solving loss successfully is identified as one of the adaptational
factors in ESRD (3). Although widely discussed, there exists no
clear definition or measure of KDRL.
Loss, traditionally discussed in the context of death, has
recently been broadened to comprise loss of significant ele-
ments in a person’s life due to chronic illness (5,6). In chronic-
illness-caused losses, individual grief responses, rather than
actual losses, are of conceptual importance (6). These grief
responses, which can persist for many years and cause signif-
icant dysfunctions, are shown to be empirically and conceptu-
ally different from depression and anxiety in several studies (7–
10). The grief symptomatology is characterized by cognitive
preoccupation or rumination, yearning, disbelief, stunned re-
sponses, and nonacceptance of losses (7,9,11), which could be
summarized as cognitive and affective grief responses (6). Thus,
the study presented here defines KDRL as the cognitive and
affective grief responses after tangible and symbolic losses due
to kidney disease and its treatments. This definition will guide
the development of a measure for KDRL.
KDRL has traditionally been seen as one of the causes of
depression in ESRD patients. In the psychodynamic perspec-
tive, depression may be an extension of patients’ grief re-
sponses (1) or KDRL may increase patients’ vulnerability to
developing depression (4). In the cognitive-behavioral perspec-
tive, patients’ cognitive rumination over their losses may lead to
depression, as negative rumination has been found to be
associated with depression (12,13).
There exists a strong inverse relationship between depression
and quality of life (QoL) in ESRD patients (14,15). If KDRL is a
significant cause of depression, it may have a mediated effect on
QoL through depression or KDRL may also independently affect
both depression and QoL. Although the literature sug- gests a
direct relationship between depression and QoL, posi- tive affect
as a way of coping (16,17) may mediate the effect of depression
and loss (18). Positive affect may have adaptive
values in dealing with chronic stress (16,17) and thus moderate
Received March 31, 2008. Accepted July 23, 2008.
Published online ahead of print. Publication date available at www.cjasn.org.
Correspondence: Ramony Chan, Consultation Liaison Psychiatry, Liverpool Hos-
pital, Locked Bag 7103, Liverpool BC, New South Wales 1871, Australia. Phone: 61-
2-9616-4680; Fax: 61-2-9616-4691; E-mail: ramony.chan@sswahs.nsw.gov.au
the effect of depression and KDRL on QoL.
The clinical validity of KDRL can be understood not only by
measuring it, but also by examining its relations to clinical
variables, including medical comorbidity, length of time on
dialysis, and level of hemoglobin and its effects on hospital-
Copyright © 2009 by the American Society of Nephrology ISSN: 1555-9041/401–0160
Clin J Am Soc Nephrol 4: 160 –167, 2009 Role of Loss in Kidney Disease 161
and home-based dialysis patients. It is hypothesized that pa-
tients’ KDRL will covary with these clinical variables influenc-
ing QoL through depression and positive affect (15,19 –23).
Moreover, the clinical observation suggests that hospital-based
patients may experience more losses and become accustomed to
their effects, whereas home-based patients may regain or min-
imize some losses through the advantages of home treatments.
Thus, it is assumed that each additional loss for home-based
patients will have a greater effect on their well being and QoL, and
thus the clinical validity of the KDRL can be demonstrated.
The aim of this research is to show the criterion-related
validity of the KDRL construct by developing a measure for
KDRL, to examine its relationship with relevant psychologic
and clinical variables, and its effect on home-based dialysis
patients. It is hypothesized that (1) the proposed scale of KDRL
will consist of cognitive and affective grief responses and that
(2a) loss will lead to depression, (2b) covary with other clinical
variables to influence QoL through depression and positive
affect, and (2c) influence the home-based patients more.
Materials and Methods Participants
Participants were recruited from two major university teaching hos-
pitals in Sydney South West Area Health Service (SSWAHS) and South
Eastern Sydney & Illawarra Area Health Service (SESIAHS) Sydney,
Australia. The inclusion criteria were a diagnosis of ESRD, receiving
dialysis treatment for approximately 2 yr or more and aged 18 or above.
The main exclusion criterion was incapacity to complete questionnaires
and/or the semistructured interview with reasonable assistance. Of 209
eligible patients, 31 (14.8%) refused, 7 (3.4%) withdrew during the
interview as being too sick to continue, 16 (7.7%) did not return the
questionnaires, and 4 (1.9%) did not complete the data collection be-
cause of death, transplant, acute medical problems, or cognitive im-
pairment. Thus, 151 (72.2%) patients participated in the interview and
returned the questionnaires. The sample consisted of 90 (60%) men and
61 women (40%) with the mean age 58 ± 14.28 (SD) yr, the mean
duration of dialysis was 67.97 ± 42.84 (SD) mo (range 22 to 248 mo).
Approximately half (n 68, 45%) of the participants were doing home-
based dialysis, including home hemodialysis (n 26, 17%) and peritoneal
dialysis (n 42, 28%), and the others (n 83, 55%) were on hospital-based
dialysis including satellite (n 56, 37%) and in-center hemodialysis (n 27,
18%).
Procedures
This study was approved by the SSWAHS and SESIAHS Ethics
Committees. After being informed of the study details and having
signed a consent form, participants completed the semistructured in-
terview and returned completed questionnaires by mail. One reminder
letter and spare questionnaire were sent to those who did not return the
questionnaires. Two interviewers were trained in the application of
measures before the initiation of the study to ensure the quality of the
data collection.
Measures
Seven variables were examined in the study: QoL, depression, KDRL,
positive affect (a key component of coping), medical comorbidity, length
of time on dialysis, and hemoglobin. In addition to developing a scale
to measure KDRL, standardized measures were used in the study—the
Schedule for Evaluation of Individual Quality of Life—
Direct Weighting (SEIQoL-DW) (24), the Depression Scale of Depres-
sion Anxiety Stress Scale 21 (DASS21) (25), the Positive Affect Scale
(PAS) (18), and the Comorbidity Index (CMI) (26,27). Additional ques-
tions were included to collect participants’ demographic and dialysis
related information including length of time on dialysis (the total
number of months). Hemoglobin level was an average over 3 mo,
including the month of the research interview.
The Kidney Disease Loss Scale
The measurement context in which an individual considers their
losses will in part determine the validity of the measurement. The con-
text can be determined from individual-defined losses or from a stan-
dard set of losses. The type and importance of losses varies widely
between patients and thus a predefined set of losses may only be
partially relevant to any individual’s experience (6,24). The Kidney
Disease Loss Scale (KDLS) was constructed to first elicit the five most
important individual KDRL and second to obtain cognitive and affec-
tive grief responses. A second-order factor structure of KDLS was
hypothesized with four statements measuring cognitive rumination and
four measuring the affective response to loss.
The SEIQoL-DW
The SEIQoL-DW is a patient-centered semistructured interview to
measure individual QoL (24). It was chosen because of known limita-
tions in multidimensional measures of QoL (28) and its ability to
produce both qualitative and quantitative data. Of particular impor-
tance for renal patients are that preselected life domains may not be
relevant, and equal weighting of life domains is inconsistent with
patients’ own values (29,30).
In the SEIQoL-DW, the five most important areas of a respondent’s
life are elicited, then the level of satisfaction and relative importance of
each area is determined. Its global index score, ranging from 0 to 100, is
the sum of a product of the ratings and weightings of each nominated
area. Its reliability, validity, and utility in the medical and ESRD pop-
ulations are excellent (24,30 –33).
The DASS21
The DASS21 is a 21-item scale, comprising of three subscales: depres-
sion, anxiety, and stress (seven items each), a total score for each
subscale ranging from 0 to 21. Only scores on the depression subscale
were used in the analyses. The DASS21 focuses on the cognitive and
affective aspects of depression, limiting the methods bias of using a
measure that contains somatic elements common to depression and
kidney disease (2,34,35). Additionally, it was developed in the Austra-
lian population (the site of this study); it has strong psychometric
properties in both general and clinical populations (25,36,37); it is
relatively short, reducing administrative burden on patients; and dif-
ferentiates depression, anxiety, and stress.
PAS
The PAS is a four-item scale on a Likert scale ranging from 0 (not at
all) to 10 (very much), with a total score ranging from 0 to 40 to measure
individual positive feelings. Its reliability and discriminant and conver-
gent validities have been well established (18).
CMI
The CMI was compiled on the basis of Friedman’s Index (26) and
Charlson’s Index (27). It is in a checklist format, with scores ranging
from 0 to 15, higher scores indicating more comorbid conditions.
162 Clinical Journal of the American Society of Nephrology Clin J Am Soc Nephrol 4: 160 –167, 2009
Data Analyses Analyses were performed with SPSS 15 (38) and LISREL 8.72 (39).
Missing data were rare and nonsystematic and thus replaced using EM
(expectation-maximization) method (38,40). The first set of analyses
examined and validated the factor structure of the KDLS using confir-
matory factor analysis (CFA) and exploratory factor analysis (EFA).
Standard techniques of correlation, ANOVA, and t test were used with
a critical value of alpha set to 0.05. The final set of analyses used
structural equation modeling (SEM) to test, develop, and examine
alternative models. Multigroup analyses were used to compare hospital
and home dialysis.
The two-step approach was used with SEM (41). Composite scores of
the observed variables, using the unit-weighted addition method, were
calculated and error variances fixed in the measurement model (42,43)
before the structural model was tested. Because the distributions of the
observed variables were skewed, SEM was undertaken using “asymp-
tomatic distribution free covariance” matrices using the robust maxi-
mum likelihood and the Satorra-Bentler statistic for parameter estima-
tion (44 – 46). Several goodness-of-fit (GFI) indices were chosen to
evaluate the overall model fit (40): Satorra-Bentler x2 test (P > 0.05, in
SEM nonsignificant x2 indicates a good model fit), the GFI (>0.90),
adjusted GFI (AGFI) (>0.90), the root mean square residual (RMR; close
to 0), the root mean square error of approximation (RMSEA; <0.05, 90%
confidence interval <0.08), and the comparative fit index (CFI; >0.90).
Results Development of KDLS
The hypothesized factor structure of KDLS was not sup-
ported using CFA [x2 73.44, degrees of freedom (df) 19, P 0.00,
RMSEA 0.09, GFI 0.89, AGFI 0.80, CFI 0.99,
RMR 0.05; LISREL 8.72 39]. Re-examining the data, EFA using
SPSS (38) indicated two factors with 72.24% of the total variance
explained. There were two items loading onto both factors and
therefore excluded (42). The first factor consisted of four items
and resembled cognitive responses and the second factor
consisted of two items reflecting affective responses. The second
factor was retained for its theoretical importance and the items’
correlation was greater than 0.7 (47). The two factors were
strongly correlated (r 0.71, P < 0.01), suggesting the previously
hypothesized second-order factor. The new factor structure and
possible second-order factor model were exam- ined using CFA
(x2 12.63, df 8, P 0.128, RMSEA 0.00, GFI 0.97, AGFI 0.93,
CFI 1.00, RMR 0.03) (LISREL 8.72 39). The
first-order factors measure cognitive and affective responses
and a second-order factor reflects an overall sense of loss re-
garding self-defined KDRLs. Therefore, the KDLS comprises an
overall loss scale by summing the six items (48) and two sub-
scales (see Table 1). High scores are indicative of greater sense
of loss, with more rumination and stronger affect. The internal
consistence of KDLS was good (a 0.88 for both the cognitive and
affective subscales).
The convergent and discriminant validity of KDLS were
supported by its significant positive correlation with depres-
sion (r 0.60, P < 0.01), and negative correlation with QoL (r
-0.20, P < 0.05) and positive affect (r -0.36, P < 0.01). It was
unrelated to clinical variables (hemoglobin r 0.07, comorbid-
ity r 0.04, length of time since dialysis r -0.15). Construct
validity was examined by conducting a two-factor EFA of the
six KDLS and the seven DASS21 depression items. The depres-
sion items loaded onto one factor and KDRL items loaded onto
another without cross-loading items.
Patients’ nominated losses on KDLS were codified by two
independent coders by iteratively examining the data. The
intercoder agreement was 95% and the differences in the re-
maining 5% were resolved by consensus. In total, 109 of 151
respondents nominated 431 losses. Of the 23 types of losses
identified, the seven most common were travel (18.56% of the
total nominated losses), leisure activities (12.06%), physical
functioning (10.90%), employment/work (9.74%), family/per-
sonal relationships (6.50%), freedom (perception of being free
from constraints; 4.87%) and social life (4.87%). The mean score
difference on KDLS between those who did not nominate losses
(x- 5.41) and those who did (x- 5.84) was nonsignificant (t 0.49,
df 149, P > 0.05).
Univariate Analyses
There was no gender differences in the variables used in the
study. An examination of differences between the two hospitals
identified a significant difference in hemoglobin levels (SS-
WSAH x- 123.84 (13.88), SESIAHS x- 117.13 (14.05), P <
0.01); there were no differences on other variables. There were
no treatment modality (in-center hemodialysis, home hemodi-
alysis, peritoneal dialysis, satellite hemodialysis) differences on
any variable.
Path Analyses
Model Testing and Modification. The structural relation-
ships between length of time on dialysis, hemoglobin, comor-
bidity, loss, depression, positive affect, and individual QoL
were examined using SEM. The hypothesized path model was
not supported (x2 16.57, df 8, P 0.04, RMSEA 0.09; for all
fit statistics see Table 2). Therefore, the model modification
process was conducted to improve the model fit by examining
the t-values of path coefficients, standardized residual values,
and modification indexes. The path from hemoglobin to de-
pression was insignificant and thus deleted, and an additional
path from comorbidity to positive affect added (x2 7.91, df 13,
P 0.85, RMSEA 0.00; see Table 2 and Figure 1), indi- cating a
plausible model for the observed data.
As shown in Table 3, each variable explained a small pro-
portion of variance in QoL with positive affect (9.6%) and
hemoglobin (4.8%) having the highest direct effect. The effects
on positive affect from comorbidity and length of time since
dialysis were moderate whereas depression explained the larg-
est proportion (29.2%) of variance in positive affect. Loss ex-
plained 38.4% of variances in depression, larger than comor-
bidity (2.3%) and length of time since dialysis (5.3%), and only
had a small effect on QoL fully mediated by depression and
positive affect.
Alternative Models
In covariance structure modeling, several equivalent mod- els
may exist (40). Two theoretically based alternative mod-
Clin J Am Soc Nephrol 4: 160 –167, 2009 Role of Loss in Kidney Disease 163
Table 1. The final version of the Kidney Disease Loss Scale (KDLS)a
When you consider life as it is now with kidney disease and dialysis treatments, it is clearly different from what your life used to be or would have been. You might find yourself having lost many things. Please consider LOSSES: things that you used to do before kidney disease/dialysis and now you cannot do anymore or things that you would have been doing if you did not have kidney disease/dialysis. Please list below the five most important things you have lost because of the kidney disease/dialysis.
1: 2: 3: 4: 5: In regard to the five losses described above, please read each of the following statements carefully and circle a
number 0, 1, 2 or 3 that indicates how much the statement applied to you The rating scale is as follows: 0 Did not apply to me at all 1 Applied to me to some degree, or some of the time 2 Applied to me to a considerable degree, or a good part of time 3 Applied to me very much, or most of the time
1. I think about these losses so much that it is hard for me to do the everyday things I normally do 0 1 2 3
2. Memories of the losses upset me 0 1 2 3
3. I am preoccupied with thoughts of the losses 0 1 2 3
4. I feel myself longing for regaining what I have lost 0 1 2 3
5. I feel disbelief over what happened 0 1 2 3
6. I feel stunned or dazed over what happened 0 1 2 3
aThe first part of the KDLS that requires respondents to nominate the five most important losses must be retained when the KDLS is used, because it sets the context for rating the six items.
els were also tested. Alternative model 1 was to examine if
depression has a direct effect on QoL, and alternative model 2
was to investigate the ordinal relations between KDRL and
depression. The x2 difference statistics showed that alterna-
tive model 1 was not a better model (x2D 1.85, dfD 1,
nonsignificant, P < 0.05; also see Table 2). Alternative model 2
was rejected by the fit statistics (Table 2); depression does not
precede KDRL.
Table 2. The goodness-of-fit statistics of the hypothesized, modified, and alternative modelsa
Path Models Goodness-of-Fit Statistics
Hypothesized path model x2 df P GFI AGFI RMR RMSEA 90%CI CFI 16.57 8 0.04 0.97 0.89 16.25 0.09 0.02 to 0.14 0.95
Modified path model x2 df P GFI AGFI RMR RMSEA 90%CI CFI 7.91 13 0.85 0.99 0.97 15.81 0.00 0.00 to 0.05 1.00
Alternative model 1b x2 df P GFI AGFI RMR RMSEA 90%CI CFI 6.06 12 0.91 0.99 0.98 17.42 0.00 0.00 to 0.03 1.00
Alternative model 2c x2 df P GFI AGFI RMR RMSEA 90%CI CFI
41.20 13 0.00 0.93 0.84 13.33 0.12 0.08 to 0.16 0.84
ax2, Satorra-Bentler scaled chi-square; df, degrees of freedom; GFI, goodness-of-fit index; AGFI, adjusted GFI; RMR, root mean square residual; RMSEA, root mean square error of approximation; NNFI, non-normed fit index; CFI, comparative fit index.
bAdditional path from depression to quality of life was added in the model. cKidney-disease-related loss precedes depression, given all other parameters being constant.
164 Clinical Journal of the American Society of Nephrology Clin J Am Soc Nephrol 4: 160 –167, 2009
Figure 1. Path diagram of the final modified model of KDRL. QoL, quality of life; PA, positive affect; KDRL, kidney-disease-related loss; CM, comorbidity; LT, length of time since dialysis (months); Hb, hemoglobin level. Figures in gray are standardized coefficients. Figures in brackets are estimates.
KDRL in Relation to the Treatment Location Effect To further demonstrate the criterion validity of KDRL, a
multigroup analysis on the hospital- and home-based dialy- sis
patients was conducted. The poor global fit statistics (x2
135.66, df 38, P 0.00, RMESA 0.19) suggested
differences between the two groups. A reasonable fit (x2 43.87,
df 34, P 0.12, RMSEA 0.06) of the re-specified model
suggested that the main difference was a greater strength of
the relations between KDRL, depression, positive affect, and
QoL in home-based dialysis patients, although
Table 3. Standardized direct, indirect, total effects of the variablesa
CMI Loss Hemoglobin Length of Time Since Dialysis Positive Affect Depression
Direct effects QoLb - Positive affect -0.23 Depression 0.16
Indirect effects QoL
-0.10
-0.11
-
-0.04
-
-0.17 Positive affect -0.08 -0.34 - -0.12 - -
Depression - - - - - -
Total effects QoL
-0.10
-0.11
0.22
-0.04
0.31
-0.17
Positive affect -0.31 -0.34 - -0.12 - -0.54
Depression 0.16 0.62 - 0.23 - -
aStandardized total effect is the sum of direct and indirect effects of one variable on another variable. Its value ranges from 0 to 1 with either negative or positive direction. The larger the value is, the stronger the effect is.
bQoL, quality of life.
- -
0.22 -
- -
0.31 -
- -0.54
0.62 - 0.23 - -
Clin J Am Soc Nephrol 4: 160 –167, 2009 Role of Loss in Kidney Disease 165
mean score differences on these variables between the
groups were nonsignificant.
Discussion The study presented here provides empirical support for
KDLS and the hypotheses that loss leads to depression, cova-
ries with length of time since dialysis to influence QoL through
depression and positive affect, and has greater effect on home-
based patients. Moreover, the moderate direct effect that he-
moglobin has on QoL is consistent with previous clinical trials
showing erythropoietin treatment enhances ESRD patients’
QoL (49).
The concept of KDRL is operationalized by KDLS, which has
encouraging psychometric properties. Consistent with previ-
ous research, depressive and loss symptoms loaded onto sep-
arate factors, and the path analyses demonstrated that KDRL
precedes depression (7–10). Thus the KDRL is empirically dis-
tinct from depression. The cognitive rumination, yearning, dis-
belief, and stunned responses remain the key symptomatology
that contributes to depression.
KDRL as a strong contributor to depression is consistent with
the previous theories that loss is a significant cause of depres-
sion. Although the findings presented here may not support
depression as being an extension of KDRL, whether depression
is due to increased vulnerability or cognitive rumination over
negative contents of loss remains equivocal. Perhaps, more
cognitive rumination items contributing to the total score of
KDLS may suggest that cognitive rumination is the underlying
mechanism between KDRL and depression. Nevertheless, the
findings that travel, leisure activities, and physical functioning
are the most nominated types of losses may not be surprising
clinically, because many dialysis patients commonly describe
their dialysis experiences as being restrictive. Therefore, these
results may suggest that to improve patients’ depression and
QoL, psychosocial interventions could target loss; for example,
helping patients to regain losses by helping them to travel or
perform activities more, or to process their related thoughts and
feelings by reducing their cognitive ruminations. Encour-
agingly, these findings have already changed the educational
practice of one of the renal units where the study was con-
ducted.
Another interesting finding of the study is that the effect of
both KDRL and clinical variables on QoL is mediated by de-
pression and positive affect. This shows that disease-specific
variables may influence QoL indirectly through psychologic
states (50). However, the type of psychologic states has not been
explicitly specified, but rather implicitly assumed to be
depression in the ESRD literature. The findings presented here
suggest that both positive and negative psychologic states could
act as mediators. Positive affect may be a distinct factor and has
adaptive values buffering the effect of loss and depres- sion on
QoL (17,18).
The criterion validity of the KDRL construct is also illustrated
by the multigroup analyses showing that a stronger magnitude
of the relations between KDRL and other psychologic variables
exists for home-dialysis patients. For a small increase in their
sense of loss, home-based patients experience more depression
and greater decline in positive affect and QoL than do the
hospital-based. This may mean that psychosocial interventions
for home-based dialysis patients, especially on the KDLS and
depression, could result in greater improvement in their QoL
and potentially delay the need for hospital-based treatment.
The study presented here has several limitations. The KDLS is
a newly developed scale and awaits further research to
crossvalidate its validity and reliability. Future research may
also focus on item generation for the affective subscale of KDLS
to improve its construct validity. Because the main purpose of
the path analyses results was to examine the construct validity
of the KDLS, the substantive meaning of the model requires
replication in different samples. The sample size for the multi-
group analyses is considered small in SEM, and although con-
sistent with preliminary expectations, the interpretation of these
results should be cautious.
Overall, the study presented here demonstrated the construct
and criterion validity of KDRL and the promising psychometric
properties of KDLS. KDRL may lead to depression and through
it reduces QoL. The effect of depression is mediated by the
coping mechanism of positive affect. The development of any
new scale requires multiple studies to fully understand its
properties. Studies in different populations (e.g., pre- and early-
dialysis patients) will also add to the construct validity.
Acknowledgments
The results of this paper were presented at the American Society of
Nephrology 40th Annual Scientific Conference, San Francisco, Califor-
nia, 2007 and the 43rd Annual Scientific Meeting of the Australian and
New Zealand Society of Nephrology, Gold Coast, Australia, 2007. The
abstract of this paper has been published in Nephrology (Chan, R, Brooks,
R, Erlich, J, Chow, J, Suranyi, M: The role of kidney disease related loss
in dialysis patients’ quality of life: depression and positive affect as
mediating factors [Abstract], Nephrology 12[Suppl 2]: A6, 2007). The
authors thank all staff and patients at both participating hospitals for
their support and Ms. Ruth Orchison for reviewing this paper.
Disclosures None.
References 1. Kimmel PL, Weihs K, Peterson RA: Survival in hemodial-
ysis patients: The role of depression. J Am Soc Nephrol 4: 12– 27, 1993
2. Kimmel PL: Psychosocial factors in adult end-stage renal disease patients treated with hemodialysis: Correlates and outcomes. Am J Kidney Dis 35: S132–S140, 2000
3. Wright S, Kirby A: Deconstructing conceptualizations of ‘Adjustment’ to chronic illness: A proposed integrative framework. J Health Psych 4: 259 –272, 1999
4. Israel M: Depression in dialysis patients: A review of psy- chological factors. Can J Psychiatry 31: 445– 451, 1986
5. Harvey JH, Miller ED: Toward a psychology of loss. Psy- chol Sci 9: 429 – 434, 1998
6. Niemeier JP, Kennedy RE, McKinley WO, Cifu DX: The Loss Inventory: Preliminary reliability and validity data
166 Clinical Journal of the American Society of Nephrology Clin J Am Soc Nephrol 4: 160 –167, 2009
for a new measure of emotional and cognitive responses to disability. Disabil Rehabil 26: 614 – 623, 2004
7. Prigerson HG, Bierhals AJ, Kasl SV, Reynolds CF III, Shear MK, Newsom JT, Jacobs S: Complicated grief as a disorder distinct from bereavement-related depression and anxiety: A replication study. Am J Psychiatry 153: 1484 –1486, 1996
8. Boelen PA, van den Bout J: Complicated grief, depression, and anxiety as distinct postloss syndromes: A confirmatory factor analysis study. Am J Psychiatry 162: 2175–2177, 2005
9. Prigerson HG, Frank E, Kasl SV, Reynolds CF III, Ander- son B, Zubenko GS, Houck PR, George CJ, Kupfer DJ: Complicated grief and bereavement-related depression as distinct disorders: Preliminary empirical validation in el- derly bereaved spouses. Am J Psychiatry 152: 22–30, 1995
10. Ogrodniczuk JS, Piper WE, Joyce AS, Weideman R, Mc- Callum M, Azim HR, Rosie JS: Differentiating symptoms of complicated grief and depression among psychiatric out- patients. Can J Psychiatry 48: 87–93, 2003
11. Prigerson HG, Maciejewski PK, Reynolds CF III, Bierhals AJ, Newsom JT, Fasiczka A, Frank E, Doman J, Miller M: Inventory of Complicated Grief: A scale to measure mal- adaptive symptoms of loss. Psychiatry Res 59: 65–79, 1995
12. Thomsen DK: The association between rumination and negative affect: A review. Cogn Emot 20: 1216 –1235, 2006
13. Ito T, Takenaka K, Tomita T, Agari I: Comparison of ru- minative responses with negative rumination as a vulner- ability factor for depression. Psychol Rep 99: 763–772, 2006
14. Berlim MT, Mattevi BS, Duarte APG, Thome FS, Barros EJG, Fleck MP: Quality of life and depressive symptoms in patients with major depression and end-stage renal dis- ease: A matched-pair study. J Psychosom Res 61: 731–734, 2006
15. Vazquez I, Valderrabano F, Fort J, Jofre R, Lopez-Gomez JM,, Moreno F, Sanz-Guajardo D, Spanish Cooperative Renal Patients Quality of Life Study Group: Psychosocial factors and health-related quality of life in hemodialysis patients. QualLife Res 14: 179 –190, 2005
16. Folkman S, Moskowitz JT: Positive affect and the other side of coping. Am Psychol 55: 647– 654, 2000
17. Folkman S, Moskowitz JT: Coping: Pitfalls and promise. Ann Rev Psychol 55: 745–774, 2004
18. Brooks R: Health related quality of life of intensive care patients: Development of the Sydney quality of life ques- tionnaire. School of Community Medicine. Sydney, Uni- versity of New South Wales, 1999
19. Martin CR, Thompson DR: Prediction of quality of life in patients with end-stage renal disease. Brit J Health Psychol 5: 41–55, 2000
20. Steele TE, Baltimore D, Finkelstein SH, Juergensen PPA, Kliger AS, Finkelstein FO: Quality of life in peritoneal dialysis patients. J Nerv Ment Dis 184: 368 –374, 1996
21. Bommer J, Muller-Buhl E, Ritz E, Eifert J: Recombinant human erythropoietin in anaemic patients on haemodialy- sis. Lancet 1: 392, 1987
22. Evans RW, Rader B, Manninen DL: The quality of life of hemodialysis recipients treated with recombinant human erythropoietin. J Am Med Assoc 263: 825– 830, 1990
23. Winearls CG, Oliver DO, Pippard MJ, Reid C, Downing MR, Cotes PM: Effect of human erythropoietin derived from recombinant DNA on the anaemia of patients main- tained by chronic haemodialysis. Lancet 2: 1175–1178, 1986
24. O’Boyle CA, McGee HM, Hickey A, Joyce CRB, Browne J,
O’Malley K, Hiltbrunner B: The Schedule for the Evalua- tion of Individual Quality of Life (SEIQoL): a direct weight- ing procedure for quality of life domains (SEIQoL-DW) administration manual. Dublin, Department of Psychol- ogy, Royal College of Surgeons in Ireland, 1993
25. Lovibond PF, Lovibond SH: The structure of negative emo- tional states: comparison of the Depression Anxiety Stress Scales (DASS) with the Beck Depression and Anxiety In- ventories. Behav Res Ther 33: 335–343, 1995
26. Friedman EA: Diabetic nephropathy. In: Therapy of Renal Diseases and Related Disorders, 2nd Ed., edited by Suki WN, Massry SG. Boston, Kluwer Academic Publishers, 1991, pp 533–542
27. Charlson ME, Pompei P, Ales KL, MacKenzie CR: A new method of classifying prognostic comorbidity in longitudi- nal studies: Development and validation. J Chronic Dis 40: 373–383, 1987
28. Kalantar-Zadeh K, Unruh M: Health related quality of life in patients with chronic kidney disease. Int Urol Nephrol 37: 367–378, 2005
29. Addington-Hall J, Kalra L: Who should measure quality of life? BMJ 322: 1417–1420, 2001
30. Tovbin D, Gidron Y, Jean T, Granovsky R, Schnieder A: Relative importance and interrelations between psychoso- cial factors and individualized quality of life of hemodial- ysis patients. Qual Life Res 12: 709 –717, 2003
31. O’Boyle CA: Assessment of quality of life in surgery. Br J Surg 79: 395–398, 1992
32. Joyce CRB, Hickey A, McGee HM, O’Boyle CA: A theory- based method for the evaluation of individual quality of life: The SEIQoL. Qual Life Res 12: 275–280, 2003
33. Hickey AM, Bury G, O’Boyle CA, Bradley F, O’Kelly FD, Shannon W: A new short form individual quality of life measure (SEIQoL-DW): Application in a cohort of individ- uals with HIV/AIDS. BMJ 313: 29 –33, 1996
34. Kimmel PL, Peterson RA: Depression in end-stage renal disease patients treated with hemodialysis: Tools, corre- lates, outcomes, and needs. Semin Dial 18: 91–97, 2005
35. O’Donnell K, Chung JY: The diagnosis of major depression in end-stage renal disease. Psychother Psychosom 66: 38 – 43, 1997
36. Clara IP, Cox BJ, Enns MW: Confirmatory factor analysis of the depression-anxiety-stress scales in depressed and anx- ious patients. J Psychopathol Behav Assess 23: 61– 67, 2001
37. Antony MM, Bieling PJ, Cox BJ, Enns MW, Swinson RP: Psychometric properties of the 42-item and 21-item ver- sions of the Depression Anxiety Stress Scales in clinical groups and a community sample. Psychol Assess 10: 176 – 181, 1998
38. SPSS for Windows: SPSS for Windows, 15th Ed., Chicago, SPSS Inc., 2006
39. Joreskog K, Sorbom D: LISREL 8.72: User’s Reference Guide. Chicago, Scientific Software International, 2004
40. Kline RB: Principles and Practice of Structural Equation Mod- eling. New York, The Guilford Press, 2005
41. Anderson JC, Gerbing DW: Structural equation modeling in practice: A review and recommended two-step ap- proach. Psychol Bull 103: 411– 423, 1988
42. Comrey AL: Factor-analytic methods of scale development in personality and clinical psychology. J Consult Clin Psy- chol 56: 754 –761, 1988
43. Munck IME: Model building in comparative education:
Clin J Am Soc Nephrol 4: 160 –167, 2009 Role of Loss in Kidney Disease 167
Applications of the LISREL method to cross-national sur- vey data.: International Association for the Evaluation of Education Achievement Monograph Series No 10. Stock- holm, Almqvist & Wiksell, 1979
44. Satorra A, Bentler PM: Corrections to test statistics and standard errors in covariance structure analysis. In: Latent Variable Analysis: Applications for Developmental Research, edited by von Eye A, Clogg CC, Thousand Oaks CA, Sage, 1994, pp 399 – 419
45. Chou C-P, Bentler PM: Estimates and tests in structural equation modeling. In: Structural Equation Modeling: Concepts, Issues, and Applications, edited by Hoyle RH, Thousand Oaks CA, Sage Publications, Inc., 1995, pp 37– 55
46. Chou CP, Bentler PM, Satorra A: Scaled test statistics and robust standard errors for non-normal data in covariance
structure analysis: A Monte Carlo study. Br J Math StatPsy- chol 44: 347–357, 1991
47. Worthington RL, Whittaker TA: Scale development re- search: A content analysis and recommendations for best practices. Couns Psychol 34: 806 – 838, 2006
48. Gerbing DW, Ahadi SA, Patton JH: Toward a conceptual- ization of impulsivity: Components across the behavioral and self-report domains. Multivariate Behav Res 22: 357–379, 1987
49. Beusterien KM, Nissenson AR, Port FK, Kelly M, Steinwald B, Ware JE Jr: The effects of recombinant human erythro- poietin on functional health and well-being in chronic di- alysis patients. J Am Soc Nephrol 7: 763–773, 1996
50. Brenner MH, Curbow B, Legro MW: The proximal-distal continuum of multiple health outcome measures: The case of cataract surgery. Med Care 33: AS236-AS244, 1995