14.2.R2 Recommendation

Counseling for depression

Published August 25, 2022

Strength of recommendation:
Strong for intervention
Level of evidence:
Very low
How the strength and level of evidence are graded

What the strength of a recommendation means

The strength of a recommendation reflects the extent to which a guideline panel is confident that desirable effects of an intervention outweigh undesirable effects, or vice versa, across the range of patients for whom the recommendation is intended.

Strong for (↑↑) or against (↓↓) intervention
For patients: Most individuals in this situation would want the recommended course of action and only a small proportion would not.
For clinicians: Most individuals should receive the recommended course of action.

Conditional for (↑) or against (↓) intervention
For patients: The majority of individuals in this situation would want the suggested course of action, but many would not.
For clinicians: Recognize that different choices will be appropriate for different patients, and that you must help each patient arrive at a management decision consistent with her or his values and preferences.

Neither intervention nor comparison (—)
The panel did not recommend for or against the intervention.

Source: GRADE Handbook, section 6.1, Table 6.1 (GRADE uses “weak” and “conditional” interchangeably).

For the rating of the strength of the recommendation, in addition to evidence from studies in FRDA, evidence from like conditions, clinical experience and expert consensus are taken into account when published evidence is not available.

The level of evidence is based on published evidence from studies in FRDA. If there is no published evidence in FRDA, evidence from other like conditions or clinical expertise may have been used to make the recommendation – this is graded as ‘very low’ or in some cases ‘low’ level evidence. See the table below for an explanation of the symbols used to grade recommendations.

Strength of recommendation Symbol Level of evidence Symbol
Strong for intervention ↑↑ High ⨁⨁⨁⨁
Conditional for intervention ↑ Moderate ⨁⨁⨁◯
Neither intervention nor comparison — Low ⨁⨁◯◯
Conditional against intervention ↓ Very low ⨁◯◯◯
Strong against intervention ↓↓
Chapter PDF

We recommend counseling or therapy over no counseling in individuals with Friedreich ataxia who present with symptoms of depression.

Question

Should counseling or therapy versus none or antidepressant prescription be used for depressed individuals with Friedreich ataxia?

Justification

Cohort studies indicate that the presence of depressive symptoms may be greater in individuals with Friedreich ataxia than those without Friedreich ataxia. Whilst there is no published evidence in Friedreich ataxia, if counseling is efficacious then the desirable effect on individuals who are depressed would be large. Given individuals with Friedreich ataxia may be reluctant to recognize symptoms of depression, the first line of clinical management may be counseling. It is important that clinicians explore what will work best for individuals with Friedreich ataxia, particularly in the context of the other aspects of their lives (accessibility requirements of face to face counseling, time constraints for work/study/family, etc.). The clinician may need to consider treating depressive symptoms with both counseling and medication. In addition, it is important for the clinician to be aware of the role of fatigue in depression (and perhaps presenting as depression).

Subgroup consideration

This recommendation is for individuals with Friedreich ataxia and depression. It may be difficult for a person with severe dysarthria to engage in counseling. Counseling may be very helpful at major life stages such as going to college, leaving home etc. Counseling may also be appropriate for parents/carers of individuals with Friedreich ataxia.

Evidence to recommendation table (PDF)

Part of 14.2 Management of depression in Friedreich ataxia

References (19)

1. Flood MK, Perlman SL. The mental status of patients with Friedreich's ataxia. J Neurosci Nurs. 1987;19(5):251-5.

2. Giordani B, Boivan M, Berent S, Gilman S, Junck L, Lehtinen S, et al. Cognitive and emotional function in Friedreich's ataxia (Abstract). J Clin Exp Neuropsychol. 1989;11(1):53-4.

3. Mantovan MC, Martinuzzi A, Squarzanti F, Bolla A, Silvestri I, Liessi G, et al. Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioural and neuroimaging study. Eur J Neurol. 2006;13:827-35.

4. White M, Lalonde R, Botez-Marquard T. Neuropsychologic and neuropsychiatric characteristics of patients with Friedreich's ataxia. Acta Neurol Scand. 2000;102(4):222-6.

5. Ciancarelli I, Cofini V, Carolei A. Evaluation of neuropsychological functions in patients with Friedreich ataxia before and after cognitive therapy. Funct Neurol. 2010;25(2):81-5.

6. Sayah S, Rotge JY, Francisque H, Gargiulo M, Czernecki V, Justo D, et al. Personality and neuropsychological profiles in Friedreich ataxia. Cerebellum. 2018;17(2):204-12.

7. Corben LA, Delatycki MB, Bradshaw JL, Horne MK, Fahey MC, Churchyard AC, et al. Impairment in motor reprogramming in Friedreich ataxia reflecting possible cerebellar dysfunction. J Neurol. 2010;257(5):782-91.

8. Corben LA, Delatycki MB, Bradshaw JL, Churchyard AJ, Georgiou-Karistianis N. Utilisation of advance motor information is impaired in Friedreich ataxia. Cerebellum. 2011;10(4):793-803.

9. Corben LA, Akhlaghi H, Georgiou-Karistianis N, Bradshaw JL, Egan GF, Storey E, et al. Impaired inhibition of prepotent motor tendencies in Friedreich ataxia demonstrated by the Simon interference task. Brain Cogn. 2011;76(1):140-5.

10. Corben LA, Georgiou-Karistianis N, Bradshaw JL, Hocking DR, Churchyard AJ, Delatycki MB. The Fitts task reveals impairments in planning and online control of movement in Friedreich ataxia: reduced cerebellar-cortico connectivity? Neuroscience 2011;192(382-390).

11. White BV, Leib JR, Farmer JM, Biesecker BB. Exploration of transitional life events in individuals with Friedreich ataxia: implications for genetic counseling. Behav Brain Funct. 2010;6(65).

12. da Silva CB, Yasuda CL, D'Abreu A, Cendes F, Lopes-Cendes I, Franca MC, Jr. Neuroanatomical correlates of depression in Friedreich's ataxia: a voxel-based morphometry study. Cerebellum. 2013;12(3):429-36.

13. Nieto A, Hernandez-Torres A, Perez-Flores J, Monton F. Depressive symptoms in Friedreich ataxia. Int J Clin Health Psychol. 2018;18(1):18-26.

14. Perez-Flores J, Hernandez-Torres A, Monton F, Nieto A. Health-related quality of life and depressive symptoms in Friedreich ataxia. Qual Life Res. 2020;29(2):413-20.

15. Reetz K, Dogan I, Hohenfeld C, Didszun C, Giunti P, Mariotti C, et al. Nonataxia symptoms in Friedreich Ataxia: Report from the Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS). Neurology. 2018;91(10):e917-e30.

16. Chan YC. Aripiprazole treatment for psychosis associated with Friedreich's ataxia. Gen Hosp Psychiatry. 2005;27(5):372.

17. Ganos C, Schottle D, Zuhlke C, Munchau A. Psychosis complicating Friedreich ataxia. Mov Disord Clin Pract. 2015;2(1):84-5.

18. Salbenblatt MJ, Buzan RD, Dubovsky SL. Risperidone treatment for psychosis in end-stage Friedreich's ataxia. Am J Psychiatry. 2000;157(2):303.

19. Oruç S, Gulseren G, Kusbeci OY, Yaman M, Geçici O. Quetiapine treatment for psychosis in Friedreich's ataxia. Klinik Psikofarmakoloji Bulteni - Bulletin of Clinical Psychopharmacology. 2012;22:357-8.

Disclaimer, intended use and funding

Disclaimer
The Clinical Management Guidelines for Friedreich ataxia (‘Guidelines’) are protected by copyright owned by the authors who contributed to their development or said authors’ assignees.

These Guidelines are systematically developed evidence statements incorporating data from a comprehensive literature review of the most recent studies available (up to the Guidelines submission date) and reviewed according to the Grading of Recommendations, Assessment Development and Evaluations (GRADE) framework © The Grade Working Group.

Guidelines users must seek out the most recent information that might supersede the diagnostic and treatment recommendations contained within these Guidelines and consider local variations in clinical settings, funding and resources that may impact on the implementation of the recommendations set out in these Guidelines.

The authors of these Guidelines disclaim all liability for the accuracy or completeness of the Guidelines, and disclaim all warranties, express or implied to their incorrect use.

Intended Use
These Guidelines are made available as general information only and do not constitute medical advice. These Guidelines are intended to assist qualified healthcare professionals make informed treatment decisions about the care of individuals with Friedreich ataxia. They are not intended as a sole source of guidance in managing issues related to Friedreich ataxia. Rather, they are designed to assist clinicians by providing an evidence-based framework for decision-making.

These Guidelines are not intended to replace clinical judgment and other approaches to diagnosing and managing problems associated with Friedreich ataxia which may be appropriate in specific circumstances. Ultimately, healthcare professionals must make their own treatment decisions on a case-by-case basis, after consultation with their patients, using their clinical judgment, knowledge and expertise.
Guidelines users must not edit or modify the Guidelines in any way – including removing any branding, acknowledgement, authorship or copyright notice.

Funding
The authors of this document gratefully acknowledge the support of the Friedreich Ataxia Research Alliance (FARA). The views and opinions expressed in the Guidelines are solely those of the authors and do not necessarily reflect the official policy or position of FARA.