Abstract
Purpose
Patients with a substance use disorder (SUD), admitted for detoxification, often suffer from a poor quality of life (QoL). We set out to monitor QoL, together with substance use, in a departure from the usual norm of measuring substance use alone as a treatment outcome. Literature searches revealed scant knowledge of how QoL is influenced. With this in mind, we aimed to investigate whether total abstinence, prior to follow-up, could influence QoL.
Methods
We studied a prospective cohort of 140 patients admitted for inpatient detoxification treatment at Sørlandet Hospital (Norway), from September 2008 to August 2010. QoL was measured by a generic five-item questionnaire, the QoL-5. The extremes of this scale ranged from the worst possible rating of 0.1 to 0.9, as the best. A norm for the general population was benchmarked at 0.69. Change in QoL was calculated by subtracting baseline QoL from that achieved at the 6-month follow-up interview; linear regression modeling was used to study the influence of individual QoL predictors.
Results
The mean QoL at baseline was 0.46, 39 % below that of the general reference population. By applying the clinical interpretation of the scale, we found a modest overall mean improvement in QoL at follow-up (0.11 points); the greatest increases were seen for patients with the lowest baseline QoL scores. Abstinence prior to follow-up correlated with improved QoL, while living alone and psychological distress were negative influences.
Conclusions
For patients with a SUD, clinicians should emphasize that abstinence may help to improve their QoL.
Keywords: Substance use disorders, Treatment outcome, Norway
Background
Substance use disorders (SUDs) cause a spectrum of health problems, one of which is to increase the number of years lived with a disability [1]. Research in this area indicates that a SUD can affect well-being and function across a number of areas in life, and may lead to a considerable deterioration of physical health [2, 3], and social functioning [4]. Psychiatric disorders and SUDs are also common comorbidities; thus, impaired psychological health and reduced well-being often co-exist [5]. Physical health and mental health are the two integral quality of life (QoL) components [6]. For SUD researchers, their evaluation represents a qualitative improvement in outcome measurement, beyond the established practice of focusing solely on substance use [7]. The addiction research field has, to some degree, responded to the need to investigate QoL more methodically, and the number of articles that derive correlates between QoL and substance use has increased in the last decade [3, 8, 9].
The goal of SUD treatment is to initiate rehabilitation, promote continued abstinence, or at least reduce substance use and to help patients to become engaged with their own long-term recovery [10, 11]. An overarching aim is therefore to improve QoL. If living without substance use is to be the goal for the SUD patient, then this outcome must be associated with improved well-being, for at least some facets of life. Otherwise, this aim will simply not be perceived as “worth” fighting for. Consequently, patients may lose motivation and interest in their rehabilitative process [12].
Detoxification (detox) treatment is considered to be one way to initiate the recovery process. Ideally, patients should transition post-detox, to more extensive and longer term SUD treatment. The reality though is that many patients will only experience detox [13]. As a stand-alone intervention, detox may fail to prevent the patient from reverting back to a state of continued substance use [13].
The QoL of patients admitted to detox has, to some degree, been assessed, but many studies only utilize cross-sectional designs, survey patients only at admission and discharge [14–16], or typically have short follow-up periods, e.g., up to 3 months [17]. Thus, there is still a lack of prospective studies that have examined QoL changes at lengthier time frames after detox. Encouraging exceptions exist though. Picci et al. [18] examined variations in QoL, up to 12 months following detox, to evaluate the predictive value of QoL for relapse and the severity of alcohol use. They found that baseline QoL was not predictive of either relapse or alcohol use severity at follow-up. A secondary finding was that a significant QoL improvement was seen among patients who had achieved abstinence, with QoL scores among relapsed patients unchanged.
This finding epitomizes a typical dispute in this field: whether abstinence is a necessary precondition for QoL improvement or whether any reduction in substance use will, as a byproduct, improve QoL [7, 19]. As previously mentioned, there is evidence to show that QoL improves with abstinence and deteriorates with relapse [18, 20], but the findings are mixed. For example, a recent Norwegian study found no association between abstinence and QoL among SUD patients at their six-month post-treatment follow-up [21]. In a second, US-based study, three months of outpatient SUD treatment also failed to reveal any correlates between QoL and changes in alcohol and drug consumption [22]. Similarly, in a series of shorter detox studies, Foster et al. [17, 23, 24] reported an improvement in QoL for only some alcohol-dependent individuals when they changed their pattern of alcohol usage. The question has also been raised as to the definition of the rather broad term “recovery”. Is abstinence a defining element, or is it just one of many strategies for achieving recovery [10, 25]. The present study is among the few studies focusing on QoL after detox treatment that have a longer follow-up than 3 months and have the relationship between QoL and abstinence as its main focus.
Purpose
The aim of this study was to (1) examine QoL changes from baseline to the six-month follow-up interview (post-discharge) and (2) determine whether abstinence in the month preceding the follow-up interview predicted outcome (QoL), while controlling for other potential variables. We hypothesized that being abstinent during the 30 days preceding the follow-up interview would positively predict improved QoL.
Methods
Study setting
This study reports pre- and post-treatment QoL status of a cohort of patients recruited to a controlled trial on a detoxification ward at the Addiction Unit, Sørlandet Hospital, in Kristiansand, Norway, between September 2008 and August 2010. Detoxification treatment in Norway typically engages three types of patient group; patients detoxed before their admittance into longer term, inpatient treatment; patients initiating opioid maintenance treatment (OMT); and patients who receive a detox and are subsequently discharged. The latter group, those discharged with no immediate plans for further inpatient or OMT treatment, was approached to enroll in this study. Their eligibility was based on the central tenet of this study, to test how patients, post-discharge, could be motivated to seek their own support in community-based, addiction-related, mutual-help groups (MHGs) [11]. Exclusion criteria for our study included severe psychiatric disorders or cognitive impairment. Of 156 eligible patients, 16 declined to participate, leaving a final cohort of 140 patients, representing 89 % of the original eligible respondents (Table 1). We have previously published a detailed description of our patient cohort, and their treatment setting, in the context of a separate study on motivational intervention [11]. The Regional Ethics Committee of the South-East Health Region, Norway, approved the study.
Table 1.
Characteristic | N (%) or mean (SD) |
---|---|
Age, years | 41 (14) |
Female | 45 (32) |
Proportion native Norwegians or European origin | 134 (96) |
Education, years | 11.2 (2.3) |
Relationship, proportion living in relationship | 74 (53) |
Main diagnosis (ICD-10) | |
(1) Alcohol dependence (N = 48) or harmful alcohol use (N = 6) | 54 (39) |
(2) Both alcohol and drug dependence | 26 (19) |
(3) Drug dependence | 60 (43) |
Severity variables | |
Earlier SUD treatment (prior to current detoxification) | 108 (77) |
Years of problematic usea of the major drugs of abuse | 11.4 (9.0) |
Alcohol composite score (EuropASI)b | 0.43 (0.36) |
Drug composite score (EuropASI)b | 0.25 (0.20) |
Self-rated substance use severityc | 4.2 (0.7) |
Injection use in the last 6 months | 40 (29) |
Psychological distressd | 2.4 (0.7) |
Quality of lifee | 0.46 (0.15) |
Days on the ward | 11 (5) |
aProblematic use, as defined in EuropASI, was the consumption of 5 or more standard drinks at least 3 times weekly, or binge drinking on 2 consecutive days to a level that affected daily functioning. For drug use, only frequency was needed; 3 times weekly or 2 consecutive days
bEuropASI composite score, scale 0–1
cSYRAAP, severity score of the substance use, scale 1–5
dSCL-10, global score index, scale 1–4
eQoL-5, scale 0.1–0.9
Measures and procedures
To avoid any influence of withdrawal symptoms on QoL baseline scores, patients were neither approached nor recruited to this study until they had passed the acute detoxification phase. Therefore, patients were first approached to participate in this study at a mean timepoint of 4.5 days after their admission. After providing informed consent, participants were assessed with a QoL measure (see below) and completed the semi-structured EuropASI interview to collect data on patient demographics, background, treatment history, and substance use [26]. The time frame for the EuropASI is the 30 days preceding the interview, and data on drug and alcohol use in the 30 days prior to admission yielded composite scores to indicate severity of substance abuse [27]. Scores ranged from 0 (no problem) to 1 (a severe problem). As the ward admitted patients with both alcohol and drug dependence, we also included an overall substance use severity measure; the Survey of Readiness for AA Participation (SYRAAP) severity subscale [28]. The five questions of the scale, e.g., “My substance use has hurt some other people” and “Using substances has interfered with my ability to deal with everyday problems,” were rated on a five-point Likert-type response format, from scale 1 (strongly disagree) to scale 5 (strongly agree). A mean score was computed; a higher score meant higher severity. A score ≥4 on the SYRAAP scale is considered to reflect a serious substance use problem [29]. The Mini International Neuropsychiatric Interview (MINI), version 5.0, was used to confirm the SUD diagnosis [27]. To assess mental health, we used Symptom Check List-10 (SCL-10), a measure of psychological distress (scale 1–4 [30]). A mean score (global score index) was computed; the higher the score, the greater the distress. A score of ≥1.85 using SCL-10 is considered to be a pathological score [29, 30].
At the six-month follow-up interview, 113 patients (81 %) were successfully contacted and re-assessed using Europ-ASI and the QoL survey described below. Those lost to follow-up were younger (35 vs. 43 years; t = 2.6, degrees of freedom = 138; p < 0.01), but otherwise had no defining characteristics. The mean QoL scores at baseline for those lost to follow-up were comparable to those who engaged with the study.
Outcome
Quality of life was measured at baseline and at follow-up using the QoL-5 test, a short, generic QoL instrument. This survey does not focus on any disease-related deficits, but instead assesses the patient’s satisfaction with life in general [31]. QoL-5 consists of five subjective statements: two questions are about health, physical, and mental; two questions address the quality of significant relationships (partner and friends); and one question addresses the existential self, i.e., the relationship with oneself. Responses were scored on a five-step ordinal scale from 1 to 5. A score of 1 is very good, and 5, very poor. The raw scores were then transposed, and inverted as a decimal scale ranging from 0.1 to 0.9; 0.9 was now the best score, and 0.1, the worst [32]. Mean scores for health, relationships, and the existential self, were calculated, and a total QoL score, derived. For patients without a partner, the relationship sub-score was based on one question only. Normative data from a previous survey of the general population showed a mean QoL score of 0.69 [31, personal communication]. This was used as our reference population QoL. The cutoff score for a markedly reduced QoL was suggested to be ~0.15 below that of the general population (≤0.55). Scores lower than 0.40 were considered to be severely reduced [21]. Changes in QoL were computed by subtracting the QoL determined at admission from the QoL obtained at follow-up, hereafter called the “QoL score change”. A QoL score increase from baseline to follow-up of 0.2 (a one-point increase on the raw score scale, e.g., from “good” to “very good”) or higher was denoted as substantial and indicated a clinically important improvement. Other QoL changes were considered moderate (≥0.1 score), small (≥0.05 score), or very small (<0.05) [31, 32]. The internal consistency of the scale was good; the Cronbach’s alpha coefficient was 0.75 and 0.81 for the QoL-5 at baseline and follow-up, respectively [33].
Factors associated with QoL
To examine determinants of QoL at follow-up, the socio-demographic variables of gender, age, and whether patients were in a relationship at baseline were included as potential predictors. Of the clinical variables collected at baseline, we included patients’ self-rated severity of substance use using the SYRAAP severity score and their perceived mental health status using the SCL-10 assessment. The reliability of the scales was good; the Cronbach’s alpha coefficient was 0.75 and 0.91 for the SYRAAP and SCL-10, respectively. We also took into account two additional predictors that could influence outcome: inpatient treatment (scored in days) and MHG support (scored as number of MHG meetings attended) during the six-month follow-up period. Substance use at follow-up was assessed with the EuropASI. Substance use status and whether patients were abstinent or not was determined according to self-reported alcohol and drug use for the 30 days preceding the follow-up interview, i.e., the abstinent group had no alcohol or drug use during this period.
Statistical analyses
Descriptive statistics were used to elaborate baseline characteristics. To descriptively show the 6-month change in relation to patients’ QoL status, QoL changes were grouped according to the baseline QoL status. These were either severely reduced (<0.40), markedly reduced (0.40–0.55), or close to normal QoL (>0.55). Two different t-tests were used; paired sample t-test was used to examine the 6-month change in substance use and QoL, and the Student’s t-test was used to explore between group differences on the QoL change score and QoL score at follow-up.
Linear regression with simultaneous entry of variables (the “enter” method) was used to examine predictors of QoL at follow-up. Baseline QoL was included in the analysis to control for a possible ceiling effect, i.e., those who already had a near-to-normal QoL at baseline were not expected to manifest any marked improvement. Results are presented as unstandardized beta coefficients with 95 % confidence interval (CI). The R-square (R2) value was used to assess the proportion of variability in the dataset. Analyses of variables were considered to be statistically significant at a p value of <0.05; all analyses were performed using IBM SPSS Statistics version 21.
Results
The sample was a mixed population with either an alcohol and/or a drug use disorder. Patients had in excess of 11 years of problematic use of their major substance of abuse; 77 % had received prior specialized SUD treatment, and 29 % had used an injected drug in the 6 months prior to admission (Table 1). The mean QoL for our cohort at baseline was 0.46, which is 0.23 below that of the general population, representing a relative drop of 39 % when taking the lowest extreme of the scale into account. Thirty-seven percent of our patients had a markedly reduced QoL score (0.40–0.55), and a further 32 % had a severely reduced QoL (<0.40).
Although the patients were not intended to be directly transferred to further SUD treatment upon discharge, those who were reached at follow-up had received a mean of 18 days (median 0, range 0–180) of inpatient treatment during the 6-month follow-up period. They had also attended a mean of 12 MHG meetings (median 1, range 0–97). Patients reported a significant reduction in substance use; the alcohol composite score using the EuropASI test decreased from 0.45 to 0.21 (−0.24, 95 % CI for the difference = −0.18/−0.31, p < 0.001), and the drug composite score decreased from 0.25 to 0.10 (−0.14, 95 % CI for the difference = −0.11/−0.17, p < 0.001). Almost half of the sample, 52 patients (46 %), reported total abstinence from all substances for the 30 days preceding the follow-up interview.
In terms of QoL change, for the sample as a whole, there was only a modest improvement (0.11, 95 % CI 0.08–0.15, p < 0.001, paired sample t-test), contributed to in the main by more pronounced progress among those with the lowest baseline scores (Fig. 1 ). With reference to the main focus of this study, whether abstinence status was associated with differences in QoL, those who were abstinent before follow-up recorded substantial, and clinically relevant, improvements (0.19, 95 % CI 0.13–0.25). In comparison, those reporting continued substance use achieved small improvements in QoL (0.05, 95 % CI 0.01–0.08). Thus, the unadjusted mean difference between the groups was 0.14 and was found to be statistically significant (95 % CI 0.08–0.21, p < 0.001). Additionally, the two groups were assessed by a 6-month, post-treatment survey, for their mean scores for each individual QoL item. Collectively, abstinence prior to follow-up resulted in improved scores for psychological health, existential QoL, and overall QoL-5 (Fig. 2).
Considering abstinence as a predictor for QoL in a multiple linear model, and when controlling for demographic and clinical variables, abstinence was still found to be a significant predictor (β 0.12, 95 % CI 0.06–0.18, Table 2). The unadjusted significance of abstinence on QoL was slightly greater (0.14). Other significant predictors were living alone (β −0.08, 95 % CI −0.14/−0.02) and psychological distress (β −0.08, 95 % CI −0.13/−0.02); these both influenced QoL negatively. Our analysis was adjusted for the QoL-5 score at baseline, which in itself was not significant. Neither inpatient treatment, nor MHG attendance during follow-up, contributed to any variance for our dependent variable. In terms of data fit, our model explained 33 % (R2) of the variance found for QoL.
Table 2.
Predictor | β (95 % CI)a | p value |
---|---|---|
Socio-demographic variables | ||
Gender (female) | 0.00 (−0.07/0.05) | 0.844 |
Age, years | 0.00 (−0.00/0.00) | 0.921 |
Living alone | −0.08 (−0.14/−0.02) | 0.007 |
Psychological distressc | −0.08 (−0.13/−0.02) | 0.007 |
Self-rated substance use severityb | 0.00 (−0.04/0.06) | 0.796 |
QoL-5 at baseline | 0.19 (−0.05/0.43) | 0.114 |
Follow-up variables | ||
Mutual-help group participationd | 0.00 (−0.00/0.00) | 0.759 |
Inpatient SUD treatment during follow-up (days) | 0.00 (−0.00/0.00) | 0.779 |
Abstinence in the 30 days before follow-up | 0.12 (0.06/0.18) | <0.001 |
aMultiple linear regression with simultaneous entry of variables (the “enter” method); unstandardized beta coefficient with 95 % confidence interval (CI)
bPerceived severity of the substance use, a subscale of the Survey of Readiness for AA Participation; SYRAAP
cSymptom Check List-10, global score index
dNumber of meetings in addiction-related mutual-help groups during follow-up
Discussion
The majority of patients with SUDs undergoing detoxification had markedly impaired QoL at treatment inclusion. At the six-month follow-up, those who were abstinent had a substantial improvement in their QoL, while those still using substances manifested a modest improvement in QoL. Multivariate analysis corroborated these findings, with abstinence identified as a positive predictor of QoL, while living alone and psychological distress were negative influences.
The markedly reduced QoL of SUD patients at admission confirms findings in previous studies that patients with SUDs experience low levels of QoL compared with the general population and compared to those with other chronic health conditions [34]. This has also been seen in previous samples of patients admitted for detox [15, 35]. For example, compared to the normative score for the general population, a ~22 % reduction in score was found using the SF-36 survey, for patients on their admission to detoxification in a French study [15]. The mean QoL score in the present study was even lower, 39 % lower than that of the reference population. We should, however, note one caveat for this comparison that different measures were used to assess QoL. Therefore, the French study [15] and the current study are not directly comparable.
Considering QoL change, there appeared to be a ceiling effect in that those patients with a near-normal QoL at baseline had unchanged QoL at follow-up; any substantial improvement was confined to those who were initially worse off. This has previously been shown in a study that measured QoL during a short residential stay of 3 weeks [15]. Our study, with its 6-month follow-up interview, showed that a higher QoL at baseline was not predictive of a superior QoL at the 6-month after discharge. This is somewhat contrary to findings in the large New European Alcoholism Treatment study (NEAT), in which the patients with an initially poor QoL had a worse prognosis [35] However, although those with markedly reduced and severely reduced QoL at baseline achieved the most pronounced progress in the current study, they still failed to attain the QoL scores of those who had a near-normal QoL score at baseline.
As hypothesized, abstinence was associated with a better QoL at follow-up, similar to the findings of Picci et al. [18]. Unlike that study, however, our non-abstinent participants also reported some improvement in their QoL, but this was considered to be a minor influence when evaluated clinically. Thus, our study indicates that achieving abstinence is an important factor in improving QoL. Both abstinent and non-abstinent patients rated the quality of their relationships to friends and partners at a similar level, but the groups differed significantly in their psychological health, and relationship to self, assessments. Broadly put, the improved QoL of those who were abstinent seemed to be brought about by improved psychological health and a positive change in their relationship to self. This indicates that individual components of QoL change differently with time in relation to recovery status and that abstinence predominantly influenced these two QoL components. Thus, with abstinence, there are parallel gains in emotional and ontological health.
Living alone, i.e., living without support from a close partner resulted in a deterioration in QoL. Patients with a SUD often suffer from broken relationships or the family and/or social network may be worn out by trying to help or mitigate the consequences of the condition [36, 37]. Hence, in the case of a patient with a SUD, living alone may not necessarily be a choice. The upshot is that positive familial restraining influences may no longer be present. There may also be a lack of motivational support to promote self-help and agency in the patient. Our data agree with an earlier study among alcoholics undergoing rehabilitation [38]. In that case, the authors found that the perception of being lonely and feelings of loneliness were robust predictors of poor QoL and prognosis.
A previous meta-analysis found that the most powerful predictor of lower levels of QoL at admission to SUD treatment was the perceived severity of substance abuse [34]. Concerning variables predictive of QoL at study end, the large longitudinal NEAT study found that substance use severity at baseline did not negatively influence QoL at follow-up [35]. We reached a similar conclusion, finding that substance use severity at treatment admission did not lead to a worse prognosis in terms of perceived QoL at a later stage. On the other hand, distress in the mental health domain was a potent negative predictor of QoL at follow-up, as previously found in a study of outpatient participants, in which better mental health at baseline predicted better QoL at a 3-month follow-up [22]. These findings imply that patients with a greater psychiatric deficit are inherently disadvantaged when it comes to improving their QoL.
Unexpectedly, neither inpatient SUD treatment nor MHG support positively influenced QoL at follow-up. However, our mean values for these data may have been skewed by the fact that the majority of our patients had no inpatient treatment and attended less than two MHG meeting during the six months, as evidenced by the median values for these variables.
Methodological considerations
The strength of the study is its use of a prospective design that allows the examination of QoL change with time. Our findings must, however, be interpreted in the context of certain study limitations such as a moderate sample size. Substance use outcomes were only taken into account for the 30 days preceding the follow-up interview, with no data for the first 5 months after discharge. Thus, we were not able to evaluate whether the duration of abstinence influenced outcome, which has been mentioned as an important factor for any increase in QoL following treatment [7, 35].
Implications
Measuring outcome following SUD treatment should not only be based on a traditional assessment of SUD symptoms and SUD-related problems, but instead should incorporate measurements of global health. This innovation would allow us to examine whether a reduction in SUD symptoms occurs contemporaneously with improved physical, emotional, relational, and ontological health [10]. Thus, measurements of QoL should be used to complement traditional outcome assessments. This would help to emphasize and personalize the patient’s own experience and perception of their illness and promote a greater awareness of the value of QoL outcomes following therapy. It would also help the clinical field to shift to a more solution-focused recovery paradigm. Although our findings indicate that abstinence from substance usage is important, rehabilitation should be seen as a more complex process than simply an altered pattern of substance use [10].
Conclusions
SUD populations admitted for inpatient detox treatment suffer from poor QoL at admission. Improvements in QoL were hampered by psychological distress and by living without close support, but were enhanced by total abstinence. Patients should be encouraged to obtain abstinence-oriented support, e.g., from formal treatment and/or addiction-related mutual aid groups, in order to maximize QoL improvements. Treatment providers need to address the patient’s psychological status, implement strategies to improve social function, and thereby promote the patient’s interest and inclination to seek further help and support.
Acknowledgments
This study was supported by the Norwegian Research Council (185511/V50).
Compliance with ethical standards
Conflict of interest
The authors declare that they have no competing interest.
Ethical approval
All procedures performed were in accordance with the ethical standards of the national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Informed consent
Informed consent was obtained from all individual participants included in the study.
Contributor Information
John-Kåre Vederhus, Phone: +47 381 32 600, Email: john-kare.vederhus@sshf.no.
Bente Birkeland, Email: bente.b@sshf.no.
Thomas Clausen, Email: thomas.clausen@medisin.uio.no.
References
- 1.Global Burden of Disease Study 2013 Collaborators Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: A systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015;386(9995):743–800. doi: 10.1016/S0140-6736(15)60692-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Dalen E, Holmen J, Nordahl HM. Somatic health of patients at an outpatient clinic for substance abuse. Tidsskrift for den Norske Laegeforening. 2015;135(2):127–131. doi: 10.4045/tidsskr.13.0801. [DOI] [PubMed] [Google Scholar]
- 3.Fischer JA, Conrad S, Clavarino AM, Kemp R, Najman JM. Quality of life of people who inject drugs: characteristics and comparisons with other population samples. Quality of Life Research. 2013;22(8):2113–2121. doi: 10.1007/s11136-013-0350-8. [DOI] [PubMed] [Google Scholar]
- 4.Longabaugh R, Mattson ME, Connors GJ, Cooney NL. Quality of life as an outcome variable in alcoholism treatment research. Journal of Studies on Alcohol. Supplement. 1994;12:119–129. doi: 10.15288/jsas.1994.s12.119. [DOI] [PubMed] [Google Scholar]
- 5.Hasin DS, Stinson FS, Ogburn E, Grant BF. Prevalence, correlates, disability, and comorbidity of DSM-IV alcohol abuse and dependence in the United States: Results from the National Epidemiologic Survey on Alcohol and Related Conditions. Archives of General Psychiatry. 2007;64(7):830–842. doi: 10.1001/archpsyc.64.7.830. [DOI] [PubMed] [Google Scholar]
- 6.Smith KW, Larson MJ. Quality of life assessments by adult substance abusers receiving publicly funded treatment in Massachusetts. American Journal of Drug and Alcohol Abuse. 2003;29(2):323–335. doi: 10.1081/ADA-120020517. [DOI] [PubMed] [Google Scholar]
- 7.Laudet AB. The case for considering quality of life in addiction research and clinical practice. Addiction Science and Clinical Practice. 2011;6(1):44–55. [PMC free article] [PubMed] [Google Scholar]
- 8.Essex HN, White IR, Khadjesari Z, Linke S, McCambridge J, Murray E, et al. Quality of life among hazardous and harmful drinkers: EQ-5D over a 1-year follow-up period. Quality of Life Research. 2014;23(2):733–743. doi: 10.1007/s11136-013-0521-7. [DOI] [PubMed] [Google Scholar]
- 9.Levola J, Aalto M, Holopainen A, Cieza A, Pitkanen T. Health-related quality of life in alcohol dependence: A systematic literature review with a specific focus on the role of depression and other psychopathology. Nordic Journal of Psychiatry. 2014;68(6):369–384. doi: 10.3109/08039488.2013.852242. [DOI] [PubMed] [Google Scholar]
- 10.White WL. Addiction recovery: Its definition and conceptual boundaries. Journal of Substance Abuse Treatment. 2007;33(3):229–241. doi: 10.1016/j.jsat.2007.04.015. [DOI] [PubMed] [Google Scholar]
- 11.Vederhus JK, Timko C, Kristensen O, Hjemdahl B, Clausen T. Motivational intervention to enhance post-detoxification 12-Step group affiliation: A randomized controlled trial. Addiction. 2014;109(5):766–773. doi: 10.1111/add.12471. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Laudet AB, Becker JB, White WL. Don’t wanna go through that madness no more: Quality of life satisfaction as predictor of sustained remission from illicit drug misuse. Substance Use and Misuse. 2009;44(2):227–252. doi: 10.1080/10826080802714462. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Timko C, Below M, Schultz NR, Brief D, Cucciare MA. Patient and program factors that bridge the detoxification-treatment gap: A structured evidence review. Journal of Substance Abuse Treatment. 2015;52:31–39. doi: 10.1016/j.jsat.2014.11.009. [DOI] [PubMed] [Google Scholar]
- 14.Ginieri-Coccossis M, Liappas IA, Tzavellas E, Triantafillou E, Soldatos C. Detecting changes in quality of life and psychiatric symptomatology following an in-patient detoxification programme for alcohol-dependent individuals: The use of WHOQOL-100. In Vivo. 2007;21(1):99–106. [PubMed] [Google Scholar]
- 15.Lahmek P, Berlin I, Michel L, Berghout C, Meunier N, Aubin HJ. Determinants of improvement in quality of life of alcohol-dependent patients during an inpatient withdrawal programme. International Journal of Medical Science. 2009;6(4):160–167. doi: 10.7150/ijms.6.160. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Lugoboni F, Mirijello A, Faccini M, Casari R, Cossari A, Musi G, et al. Quality of life in a cohort of high-dose benzodiazepine dependent patients. Drug and Alcohol Dependence. 2014;142:105–109. doi: 10.1016/j.drugalcdep.2014.06.020. [DOI] [PubMed] [Google Scholar]
- 17.Foster JH, Marshall EJ, Peters TJ. Application of a quality of life measure, the life situation survey (LSS), to alcohol-dependent subjects in relapse and remission. Alcoholism, Clinical and Experimental Research. 2000;24(11):1687–1692. doi: 10.1111/j.1530-0277.2000.tb01970.x. [DOI] [PubMed] [Google Scholar]
- 18.Picci RL, Oliva F, Zuffranieri M, Vizzuso P, Ostacoli L, Sodano AJ, et al. Quality of life, alcohol detoxification and relapse: Is quality of life a predictor of relapse or only a secondary outcome measure? Quality of Life Research. 2014;23(10):2757–2767. doi: 10.1007/s11136-014-0735-3. [DOI] [PubMed] [Google Scholar]
- 19.Owen P, Marlatt GA. Should abstinence be the goal for alcohol treatment? Affirmative viewpoint. American Journal on Addictions. 2001;10(4):289–295. doi: 10.1111/j.1521-0391.2001.tb00518.x. [DOI] [PubMed] [Google Scholar]
- 20.Kraemer KL, Maisto SA, Conigliaro J, McNeil M, Gordon AJ, Kelley ME. Decreased alcohol consumption in outpatient drinkers is associated with improved quality of life and fewer alcohol-related consequences. Journal of General Internal Medicine. 2002;17(5):382–386. doi: 10.1007/s11606-002-0045-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Pasareanu AR, Opsal A, Vederhus JK, Kristensen O, Clausen T. Quality of life improved following in-patient substance use disorder treatment. Health Qual Life Outcomes. 2015;13:35. doi: 10.1186/s12955-015-0231-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Morgan TJ, Morgenstern J, Blanchard KA, Labouvie E, Bux DA. Health-related quality of life for adults participating in outpatient substance abuse treatment. American Journal on Addictions. 2003;12(3):198–210. doi: 10.1080/10550490390201803. [DOI] [PubMed] [Google Scholar]
- 23.Foster JH, Peters TJ, Kind P. Quality of life, sleep, mood and alcohol consumption: A complex interaction. Addiction Biology. 2002;7(1):55–65. doi: 10.1080/135562101200100616. [DOI] [PubMed] [Google Scholar]
- 24.Foster JH, Powell JE, Marshall EJ, Peters TJ. Quality of life in alcohol-dependent subjects—A review. Quality of Life Research. 1999;8(3):255–261. doi: 10.1023/A:1008802711478. [DOI] [PubMed] [Google Scholar]
- 25.Betty Ford Institute Consensus, P What is recovery? A working definition from the Betty Ford Institute. Journal of Substance Abuse Treatment. 2007;33(3):221–228. doi: 10.1016/j.jsat.2007.06.001. [DOI] [PubMed] [Google Scholar]
- 26.Kokkevi A, Hartgers C. EuropASI: European adaptation of a multidimensional assessment instrument for drug and alcohol dependence. European Addiction Research. 1995;1(4):208–210. doi: 10.1159/000259089. [DOI] [Google Scholar]
- 27.McGahan PL, Griffith JA, McLellan AT. Composite scores from the addiction severity index: Manual and computer software. Philadelphia: Veteran Administration Press; 1986. [Google Scholar]
- 28.Kingree JB, Simpson A, Thompson M, McCrady B, Tonigan JS. The predictive validity of the survey of readiness for alcoholics anonymous participation. Journal of Studies on Alcohol. 2007;68(1):141–148. doi: 10.15288/jsad.2007.68.141. [DOI] [PubMed] [Google Scholar]
- 29.Vederhus JK. Addiction professionals’ and substance abuse patients’ attitudes towards and usage of 12-step-based self-help groups. Oslo: University of Oslo; 2012. [Google Scholar]
- 30.Strand BH, Dalgard OS, Tambs K, Rognerud M. Measuring the mental health status of the Norwegian population: A comparison of the instruments SCL-25, SCL-10, SCL-5 and MHI-5 (SF-36) Nordic Journal of Psychiatry. 2003;57(2):113–118. doi: 10.1080/08039480310000932. [DOI] [PubMed] [Google Scholar]
- 31.Lindholt JS, Ventegodt S, Henneberg EW. Development and validation of QoL5 for clinical databases. A short, global and generic questionnaire based on an integrated theory of the quality of life. European Journal of Surgery. 2002;168(2):107–113. doi: 10.1080/11024150252884331. [DOI] [PubMed] [Google Scholar]
- 32.Ventegodt S, Merrick J, Andersen NJ. Measurement of quality of life II. From the philosophy of life to science. ScientificWorldJournal. 2003;3:962–971. doi: 10.1100/tsw.2003.76. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.DeVellis, R. F. (2012). Scale development: Theory and applications (3rd ed., Applied social research methods series, Vol. 26). Thousand Oaks, CA: Sage.
- 34.Donovan D, Mattson ME, Cisler RA, Longabaugh R, Zweben A. Quality of life as an outcome measure in alcoholism treatment research. Journal of Studies on Alcohol. Supplement. 2005;15:119–139. doi: 10.15288/jsas.2005.s15.119. [DOI] [PubMed] [Google Scholar]
- 35.Morgan MY, Landron F, Lehert P, New European Alcoholism Treatment Study, G Improvement in quality of life after treatment for alcohol dependence with acamprosate and psychosocial support. Alcoholism, Clinical and Experimental Research. 2004;28(1):64–77. doi: 10.1097/01.ALC.0000108652.73143.4B. [DOI] [PubMed] [Google Scholar]
- 36.Levola J, Kaskela T, Holopainen A, Sabariego C, Tourunen J, Cieza A, et al. Psychosocial difficulties in alcohol dependence: A systematic review of activity limitations and participation restrictions. Disability and Rehabilitation. 2014;36(15):1227–1239. doi: 10.3109/09638288.2013.837104. [DOI] [PubMed] [Google Scholar]
- 37.Beattie M. Codependent no more: How to stop controlling others and start caring for yourself. 2. Center City, MN: Hazelden; 1992. [Google Scholar]
- 38.Akerlind I, Hornquist JO, Hansson B. Loneliness correlates in advanced alcohol abusers. I. Social factors and needs. Scandinavian Journal of Social Medicine. 1987;15(3):175–183. doi: 10.1177/140349488701500309. [DOI] [PubMed] [Google Scholar]