Psychological Distress in Physical Long-Term Conditions


Study

Long-term condition

Design (location)

Psychological distress assessment method

Number of participants (n) or studies (k)

Prevalence (95 % confidence intervals)

Depression

Moussavi et al. [29]

Coronary Heart Disease

Observational (worldwide, 60 countries)

Diagnostic clinical interview conforming to the International Classification of Disease (ICD-10) criteria

n = 245,404

Angina: 15.0 % (12.9–17.2 %)

Gunn et al. [30]

Coronary Heart Disease

Observational (Australia)

Self-report measure: Centre for Epidemiologic Studies Depression Scale (CES-D)

n = 6,864

Hypertension: 24.0 % (Not reported)

Heart disease: 29.0 % (Not reported)

Rutledge et al. [25]

Coronary Heart Disease

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of depression

k = 27

Heart Failure: 22 % (18–26 %)

Gunn et al. [30]

Cerebrovascular disease

Observational (Australia)

Self-report measure: Centre for Epidemiologic Studies Depression Scale (CES-D)

n = 6,864

Stroke: 37.7 % (Not reported)

Hackett et al. [26]

Cerebrovascular disease

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of depression

k = 51

Stroke: 33 % (29–36 %)

Palmer et al. [22]

End stage renal disease

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of depression

n = 198 (independent sample populations on dialysis)

On-dialysis, Clinical Interview: 22.8 %, (18.6–27.6 %)

On-dialysis, Self-report: 39.3 % (36.8–42.0 %)

Anderson et al. [23]

Diabetes mellitus (Type 1 and 2)

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of depression

k = 42

Type 1 and 2: 25.3 % (Not reported)

Anxiety

Tully et al. [27]

Coronary Heart Disease

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of GAD

k = 12

10.9 % (7.8–14.0 %)

Campbell Burton et al. [28]

Cerebrovascular disease

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of all anxiety disorders and symptoms

k = 44

Clinical Interview: 18.3 % (8.1–28.5 %)

Self-report: 24.3 % (20.5–28.1 %)

Cukor et al. [31]

End stage renal disease

Observational (US)

Diagnostic clinical interview (SCID). All anxiety disorders

n = 70

Haemodialysis: 27 % (Not reported)

Preljevic et al. [32]

End stage renal disease

Observational (Norway)

Diagnostic clinical interview (SCID). All anxiety disorders

n = 109

Haemodialysis and peritoneal dialysis: 16.5 % (Not reported)

Grigsby et al. [24]

Diabetes mellitus (Type 1 and 2)

Systematic review with meta-analysis (NA)

Both diagnostic clinical interviews and self-report measures of all anxiety disorders and symptoms

k = 18

Type 1 and 2: Meta-analysed prevalence estimates ranged from 1.3 to 39.6 % depending anxiety disorder studied and symptoms measured


CES-D Center for epidemiologic studies depression scale, GAD Generalised anxiety disorder, NA Not applicable, SCID Structured Clinical Interview



Detecting the presence of mood disorders in people with physical LTCs is complicated further by somatic symptoms associated with the mood disorder (i.e. reduced energy and weight loss) overlapping with the symptoms that occur because of the physical LTC [34]. Unique diagnostic criteria and/or adjusted diagnostic thresholds are recommended to determine the presence of a mood disorder in the context of a physical LTC. Sultan et al. [35] suggest excluding somatic symptoms from self-report measures of distress to prevent wrongly diagnosing mood disorders, a position supported by others [36]. The measurement of psychological distress in physical LTCs remains contentious. A more consistent approach to measurement is needed. This will allow greater comparisons across studies, to explore the impact of disease specific stressors (i.e. treatment regimens and underlying disease physiology) and socio-demographic factors on physical and emotional health outcomes.



Aetiology of Psychological Distress and Its Mechanisms of Action


Understanding the factors that contribute to the aetiology and exacerbation of psychological distress in people with LTCs will help to identify treatment targets for clinical intervention. Furthermore, a detailed examination of the mechanisms through which psychological distress leads to poorer physical health outcomes and vice versa will pinpoint intervention targets that have potential for simultaneous improvements in a person’s physical and mental health.


Do LTCs Cause the Onset of Psychological Distress or Vice Versa?


Evidence from observational studies show that among people with physical LTCs the odds of psychological distress occurring is two to three times greater compared with people in which, LTCs are absent [37, 30, 23]. Thus the presence of a physical LTC appears to be a key driver for the development of distress. Conversely, studies exploring the reverse direction of effect show that among people with a diagnosed mood disorder, there is a 34–81 % increased risk of developing a physical LTC [38, 1, 39], relative to people without a mood disorder. In sum, the relationship between psychological distress and LTCs appears to be bi-directional.

However, the above studies have largely focussed exclusively on depression and overlooked anxiety and more general symptoms of distress. In addition, definitive causal conclusions cannot be made because of potential confounders that may better explain the relationship between LTC onset and the development of depression and vice versa, for example, personality traits or genetic factors. Nevertheless, quantitative findings complement those observed in the qualitative literature. Adults with diabetes and co-morbid depression described their causal beliefs about the aetiology of their conditions [40]. Some perceived their depression to be a causal consequence of their diabetes, others felt that their depressive disorder triggered the onset of their diabetes, and a third group felt that there was no connection between their physical and mental health. An understanding of both actual and patient perceived causes of their psychological distress will help to refine treatments further by offering individuals treatments that are consistent with their perceived causal triggers of their distressing symptoms.


How Do LTCs Impact on Psychological Distress Outcomes?



Biological Pathways


Inflammatory responses which often occur in the context of physical LTCs can stimulate a series of hormone responses in the body to promote the secretion of pro-inflammatory cytokines. Studies have shown increased cytokine secretion to be linked to a response known as “sickness behaviour”. Sickness behaviour presents with symptoms akin to depression and includes loss of motivation, energy, and appetite. This response is adaptive for acute episodes of illness as it encourages the preservation of energy, but in the context of LTCs it can exacerbate physical symptoms further [41]. The person specific genetic factors that determine this response is currently being explored in the literature. In a study of people with ESRD, Holtzman et al. [42] identified greater depressive symptoms among people with a genetic pre-disposition for heightened inflammatory responses. To elaborate, people who were low producers of a genotype for anti-inflammatory responses (A/A genotype for IL-10 1082 polymorphism) had greater depressive symptoms compared with intermediate (G/A) and high (G/G) genotype producers. Thus there are likely specific subgroups of individuals more susceptible to the development of distress in the context of LTCs because of their pre-disposing genetic factors. But this area of research is in its infancy.


Cognitive Pathways


A person’s unhelpful (cognitive) appraisal of their LTC (i.e. perceiving they have little control over their illness) and its perceived or actual limiting effects on their day to day functioning (i.e. self-care behaviours needed for the management of their condition and its effects on other roles including work and family) can engender feelings of helplessness, hopelessness, and worry about future health consequences [43, 44]. These thinking styles are core features that trigger and sustain depression and anxiety [45].


How Does Psychological Distress Impact on LTC Outcomes?



Biological Pathways


The experience of psychological distress can activate the hypothalamic-pituitary-adrenal (HPA) axis, sympathetic nervous system (SNS), and increase cytokine secretion. Their activation can promote insulin resistance in diabetes [46] and atherosclerosis and platelet activation in vascular conditions [47]. These pathophysiological mechanisms are correlates of both objective health outcome measures (i.e. glycosylated haemoglobin) [46] and the onset of physical health complications (i.e. increased risk of myocardial infarction) [46]. These pathways have yet to be explored extensively among people with ESRD. Nevertheless studies are emerging identifying important relationships between depression and cytokine secretion in people with ESRD (see Chilcot et al. [48] for a review).


Behavioural Pathways


The somatic features of distress (i.e. loss of energy) and its affective elements (i.e. feelings of hopelessness, fear of confronting the illness) disrupt a person’s ability to adhere to necessary self-care behaviours by (i) lowering their motivation to engage in treatment behaviours AND/OR (ii) promoting avoidance of threatening illness related environments (i.e. dialysis). Indeed, studies show that psychological distress in the context of LTCs is associated with lower adherence to: lifestyle behaviours (diet, exercise, and smoking), [4951], medications [52, 53, 49], and appointment attendance [54, 55].


Interventions to Manage Psychological Distress in LTCs


Because we have an awareness of the likely causal pathways that trigger and sustain psychological distress in the context of LTCs we can apply existing evidence-based treatments used to manage psychological distress [56] to target these pathways specifically. Figure 22.1 summarises the pathways that maintain psychological distress and perpetuate poorer LTC outcomes described above. Mapped onto these pathways are treatment interventions that can target the antecedents of psychological distress. These interventions are described below, although a degree of caution is required. Effective mental health treatments may be antagonistic to effective LTC management [43]. Figure 22.1 therefore, also highlights potential antagonistic relationships (see Detweiller-Bedell et al. [43] for a full review).

A317150_1_En_22_Fig1_HTML.gif


Fig. 22.1
Pathways linking the vicious cycle between long term conditions and psychological distress and potential treatment interventions. Curved arrows with text show the hypothesised mechanisms of action for the onset and exacerbation of both psychological distress and long-term conditions, boxes outside the vicious cycle linked with straight arrows show potential intervention techniques for targeting specific mechanisms, arrow through the centre of the vicious cycle shows the potential for psychological distress treatments to conflict with LTC management. HPA hypothalamic-pituitary-adrenal axis, LTC Long-term condition, SNS sympathetic nervous system


Targeting Cognitive and Behavioural Pathways


Cognitive behavioural therapy (CBT) is a psychological talking therapy used to manage depression and anxiety [56]. Two meta-analyses exploring the effectiveness of psychological talking therapies (including CBT) for the management of depression in people with coronary heart disease [57] and diabetes [58] showed that these types of interventions improve depressive symptoms. However the size of improvements in depressive symptoms was small. This likely reflects the need to refine psychological treatments further to manage illness specific beliefs and challenging treatment demands and health consequences that present uniquely for each LTC. However, components of CBT can address the more generic mechanisms of action that perpetuate distressing symptoms and physical health outcomes in LTCs (See Fig. 22.1).

Activity scheduling can address sickness behaviour and its consequential effects on motivation. It encourages the planning of pleasurable activities into a person’s day to day routine to allow them to experience positive mood states. For example, a patient receiving dialysis may plan to go to the theatre with a friend. But also, activity scheduling encourages the explicit planning of necessary tasks (i.e. attending for dialysis treatments). It allows a person to gain a sense of achievement when necessary tasks are completed. By thoroughly planning pleasurable and necessary activities, a person can better incorporate LTC management challenges into their lives, whilst sustaining opportunities to experience pleasurable events. But caution is required to ensure that people’s pleasurable activities do not conflict with LTC management strategies. To elaborate, eating out with friends may generate challenges for people who are on restricted diets because of their condition; indeed it may trigger further distress because it reinforces the impact of the LTC on their day to day living.

Thought challenge techniques is another approach used in CBT. It encourages people to question the validity of their pessimistic thoughts. For example, a person may feel distressed because they perceive they have little control over their condition. Thought challenge techniques help people to identify situations where they have successfully managed their condition and encourage them to re-evaluate their initial pessimistic thoughts that are sustaining their distress. Skill building may also be used to encourage greater confidence in LTC management [59]. But not all pessimistic and distressing cognitions are amenable to thought challenge techniques. They are accurate perceptions about the seriousness of a LTC such as ESRD. Use of acceptance based approaches may be more appropriate for these types of beliefs [60] because it encourages people to distance themselves from their thoughts. But the efficacy of these approaches in people with LTCs has received little research attention to date. The interested reader should refer to Westbrook et al. [61] for a more thorough introduction to the principles of CBT and to McCracken [62] for examples of the application of acceptance based approaches in people with LTCs.


Targeting Biological Pathways


Pharmacotherapy can be used to treat clinically significant distress in LTCs [56]. According to the National Institute of Health and Care Excellence (NICE) depression [63] and generalised anxiety disorder guidelines [64], pharmacotherapy should only be used to treat patients who meet diagnostic criteria [14] for moderate to severe symptoms of distress. Currently, however there are no evidence-based guidelines with detailed pharmacotherapy algorithms for managing distress in the context of specific LTCs. Generating such algorithms is perhaps unfeasible given the heterogeneity of the patient population and high prevalence of multi-morbidity. Indeed, in England alone it is estimated that by 2018, 2.9 million people will have two or more LTCs [65].

When prescribing drug treatments to manage distress in people with physical LTCs the following factors need to be considered: (i) the potential for drug-drug interactions, (ii) the likely side effects of the medication, (iii) the patient’s previous history of pharmacotherapy treatments, (iv) patient preference, and (v) the toxicity of the drug and the risk of overdose among patients with suicidal ideation. NICE recommend selective serotonin reuptake inhibitors (SSRIs) as a first line treatment for depression and generalised anxiety disorders. However, SSRIs should be prescribed with particular caution among older patients because of increased risk of bleeding.

The US TEAMcare trial [66, 67] in primary care generated a medication treatment algorithm to manage depression in people with diabetes and/or coronary heart disease as part of a complex intervention (see website [68] for detailed treatment manual and medication algorithm). Consistent with NICE guidelines, patients were offered the SSRI citalopram. An initial dose of 10 mg per day was used, with doses gradually titrated upwards until a clinically meaningful improvement in depressive symptoms was observed. Citalopram was used as a first line treatment because of a decreased likelihood of drug-drug interactions with diabetes and/or coronary heart disease medications. If patients had tried SSRIs on two or more previous occasions and observed no improvements in their depressive status then they were offered the dopamine-noradrenaline reuptake inhibitor (DNRI) bupropion SR at a starting dose of 100 mg per day. Likewise to citalopram their dose was titrated upwards where necessary until a clinically meaningful response in their depressive symptoms was observed. Buproprion SR was chosen as an alternative first line drug treatment to citalopram because of: (i) its decreased potential for hepatic enzyme inhibition, (ii) fewer sexual functioning side effects, and (iii) evidence of weight loss when used in people with diabetes, which may indeed promote synergistic gains in physical and mental health.
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Jul 10, 2016 | Posted by in CARDIOLOGY | Comments Off on Psychological Distress in Physical Long-Term Conditions

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