Catatanoia Mk2
Catatonia
Catatonia is a complex disorder covering a range of abnormalities of posture, movement, speech and behaviour associated with over- as well as under-activity (Rogers, 1992; Bush et al, 1996; Lishman, 1998).
There is increasing research and clinical evidence that some individuals with autism spectrum disorders, including Asperger syndrome, develop a complication characterised by catatonic and Parkinsonian features (Wing and Shah, 2000; Shah and Wing, 2001; Realmuto and August, 1991).
In individuals with autistic spectrum disorders, catatonia is shown by the onset of any of the following features:
1. increased slowness affecting movements and/or verbal responses;
2. difficulty in initiating completing and inhibiting actions;
3. increased reliance on physical or verbal prompting by others;
4. increased passivity and apparent lack of motivation.
Other manifestations and associated behaviours include Parkinsonian features including freezing, excitement and agitation, and a marked increase in repetitive and ritualistic behaviour.
Behavioural and functional deterioration in adolescence is common among individuals with autistic spectrum disorders (Gillberg and Steffenburg, 1987). When there is deterioration or an onset of new behaviours, it is important to consider the possibility of catatonia as an underlying cause. Early recognition of problems and accurate diagnosis are important as it is easiest to manage and reverse the condition in the early stages. The condition of catatonia is distressing for the individual concerned and likely to exacerbate the difficulties with voluntary movement and cause additional behavioural disturbances.
There is little information on the cause or effective treatment of catatonia. In a study of referrals to Elliot House who had autistic spectrum disorders, it was found that 17% of all those aged 15 and over, when seen, had catatonic and Parkinsonian features of sufficient degree to severely limit their mobility, use of speech and carrying out daily activities. It was more common in those with mild or severe learning disabilities (mental retardation), but did occur in some who were high functioning. The development of catatonia, in some cases, seemed to relate to stresses arising from inappropriate environments and methods of care and management. The majority of the cases had also been on various psychotropic drugs.
There is very little evidence about effective treatment and management of catatonia. No medical treatment was found to help those seen at Elliot House (Wing and Shah, 2000). There are isolated reports of individuals treated with anti-depressive medication and electro-convulsive therapy (ECT) (Realmuto and August, 1991; Zaw et al, 1999).
Given the scarcity of information in the literature and possible adverse side effects of medical treatments, it is important to recognise and diagnose catatonia as early as possible and apply environmental, cognitive and behavioural methods of the management of symptoms and underlying causes. Detailed psychological assessment of the individuals, their environment, lifestyle, circumstances, pattern of deterioration and catatonia are needed to design an individual programme of management. General management methods on which to base an individual treatment programme are discussed in Shah and Wing (2001).
There are times where I experience something like catatonia. I would freeze and not move for a period of time. I wouldn't respond to anything. A long time ago I even had according to the doctors, "catatonic walking." It was where I walked in extremely slow motion. I don't have that as often anymore. There was a time where I froze 50 times or more a day. Most of those freezes were just a few minutes though. But sometimes in the car I would freeze the whole trip which could be an hour. Now it is just a couple of times a day and I am thankful for that. I think it is because of my autism.
When people think of catatonia they think of stereotypical concepts of it such as statue postures. I believe it can be far more subtle however and influencing thought as well as postural.
I have noticed in unfamiliar company that my mind shuts down in conversation and i am able to respond but not to instigate changes in conversation. Also, i may adopt fairly rigid and uncomfortable positions sometimes without noticing.
It would seem that inertia may also be a big problem in catatonia. Its not surprising that it is fairly prominent in autism as it and other neurological conditions such as tourettes and add/adhd seem to be connected to damage (physical genetic or chemical) to the amygdala and hippocampus as is autism and add.