Acute stress disorder medical therapy: Difference between revisions
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{{Family tree | | | | D01 | | | |D01= '''[[Benzodiazepines]], can be helpful in the initial stages, by there ability to limit hyperarousal and ability to foster sleep; however, continuous administration of benzodiazepines may interfere with readaptation and grieving. Longer-acting agents are beneficial when follow-up treatment is in short supply and medication is administered at the emergency site'''}} | {{Family tree | | | | D01 | | | |D01= '''[[Benzodiazepines]], can be helpful in the initial stages, by there ability to limit hyperarousal and ability to foster sleep; however, continuous administration of benzodiazepines may interfere with readaptation and grieving. Longer-acting agents are beneficial when follow-up treatment is in short supply and medication is administered at the emergency site'''}} | ||
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{{Family tree | | | | E01 | | | |E01= '''Comorbid conditions such as [[attention deficit hyperactivity disorder]] (ADHD) should be treated. Reduction in atleast one disabling symptom such as insomnia or hyperarousal may have a powerful positive impact on the individual’s ability to re-compensate. | {{Family tree | | | | E01 | | | |E01= '''Comorbid conditions such as [[attention deficit hyperactivity disorder]] (ADHD) should be treated. Reduction in atleast one disabling symptom such as [[insomnia]] or hyperarousal may have a powerful positive impact on the individual’s ability to re-compensate. | ||
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| rowspan="2" style="font-weight: bold;" | [[Alpha Adrenergic]] Receptors | | rowspan="2" style="font-weight: bold;" | [[Alpha Adrenergic]] Receptors | ||
| rowspan="2" | | | rowspan="2" | | ||
*The centrally acting | *The centrally acting alpha2 adrenergic agonists [[clonidine]] and [[guanfacine]] have been used to treat children with [[attention deficit hyperactivity disorder]] (ADHD) | ||
*Inhibition of [[norepinephrine]] in the brain may be its mechanism of action | *Inhibition of [[norepinephrine]] in the brain may be its mechanism of action | ||
| style="font-weight: bold;" | Clonidine | | style="font-weight: bold;" | Clonidine | ||
| Clonidine affects alpha1, alpha2, and | | Clonidine affects alpha1, alpha2, and alpha3-adrenergic receptors | ||
It is frequently given to children but is not approved by the US Food and Drug Administration (FDA) for any psychiatric uses in children | It is frequently given to children but is not approved by the US Food and Drug Administration (FDA) for any psychiatric uses in children | ||
It is available in tablets and in transdermal skin patches | It is available in tablets and in transdermal skin patches | ||
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==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Abnormal psychology]] | |||
[[Category:Psychological stress]] | |||
[[Category:Psychiatry]] | |||
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Latest revision as of 19:07, 16 February 2016
Acute stress disorder Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Acute stress disorder medical therapy On the Web |
American Roentgen Ray Society Images of Acute stress disorder medical therapy |
Risk calculators and risk factors for Acute stress disorder medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Simrat Sarai, M.D. [2]
Overview
Pharmacologic medical therapies for acute stress disorder include beta blockers, alpha adrenergic agents, benzodiazepines and/or SSRIs.
Medical Therapy
Basic principles of intervention after emotional trauma include the following: | |||||||||||||||||||
Reduce stress by all possible means | |||||||||||||||||||
Ensure that survivors have a safe environment | |||||||||||||||||||
Promote contact with loved ones and other sources of support | |||||||||||||||||||
Support self-esteem; help patients understand that their reaction to the trauma is a normal reaction to an abnormal situation, not a sign of weakness or psychopathology | |||||||||||||||||||
Help survivors focus on immediate needs, such as rest, food, shelter, social supports, or a sense of belonging to a community | |||||||||||||||||||
Promote coping mechanisms | |||||||||||||||||||
Help patients reframe any destructive cognitions | |||||||||||||||||||
Administer medication (eg, beta-blockers, alpha agonists, benzodiazepines, or nonactivating selective serotonin reuptake inhibitors [SSRIs]), if needed, to decrease arousal | |||||||||||||||||||
Avoid increasing stress - Avoid prompting discussion of issues that cannot be resolved; avoid abreaction in groups and the resulting contagion effect; respect defenses, and do not force reality on people who cannot handle it yet; keep in mind that debriefing may be harmful | |||||||||||||||||||
Discuss the experience with patients who want to talk about it, and avoid pressuring those who do not wish to discuss it | |||||||||||||||||||
Identify persons at high risk - Screen for physical causes of psychiatric problems (eg, dehydration, head trauma, infection, metabolic abnormality, or toxins) | |||||||||||||||||||
Have faith in the normal healing processes | |||||||||||||||||||
- The use of medications to decrease arousal and insomnia may have a long-term impact in the treatment of acute stress disorder (ASD). Pharmacologic agents that may be helpful in acute stress disorder include beta-adrenergic blocking agents, selective serotonin reuptake inhibitors (SSRIs), benzodiazepines, alpha adrenergic agonists, and sedating antihistamines.[1][2]
Medications to decrease arousal and insomnia have a long-term impact on acute stress disorder | |||||||||||||||||||
Alpha adrenergic agents and beta blockers limit hyperarousal. An atypical neuroleptic or mood stabilizer may be needed for an extreme aggression, agitation, dissociation, or psychosis | |||||||||||||||||||
SSRIs may be helpful in dealing with the symptoms such as depression, anxiety, withdrawal, and avoidance and can be effective in longer-term treatment | |||||||||||||||||||
Benzodiazepines, can be helpful in the initial stages, by there ability to limit hyperarousal and ability to foster sleep; however, continuous administration of benzodiazepines may interfere with readaptation and grieving. Longer-acting agents are beneficial when follow-up treatment is in short supply and medication is administered at the emergency site | |||||||||||||||||||
Comorbid conditions such as attention deficit hyperactivity disorder (ADHD) should be treated. Reduction in atleast one disabling symptom such as insomnia or hyperarousal may have a powerful positive impact on the individual’s ability to re-compensate. | |||||||||||||||||||
The mechanism of action and common features of various pharmacological agents that may be helpful in acute stress disorder is shown below in a tabular form:
Drug class | Drug Action | Examples | Features |
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Beta-Adrenergic blocking agents | Beta blockers inhibit inotropic, chronotropic, and vasodilatory responses to beta adrenergic stimulation | Propranolol | Propranolol may be useful for the treatment of hyperarousal |
Selective Serotonin Reuptake Inhibtors |
|
Escitalopram | Escitalopram i sthe S-enantiomer of citalopram
Escitalopram has a faster onset of depression relief, usually 1-2 weeks in comparison with other antidepressants |
Sertraline | Sertraline selectively inhibits presynaptic serotonin reuptake with minimal or no effect on the reuptake of norepinephrine or dopamine | ||
Citalopram | Citalopram enhances serotonin activity through selective reuptake inhibition at the neuronal membrane
Citalopram is the least activating of the SSRIs and is particularly useful in acute stress disorder The incidence of adverse effects especially sexual is less with citalopram than with other SSRIs | ||
Benzodiazepines |
|
Clonazepam | Clonazepam is a long-acting benzodiazepine that increases presynaptic GABA inhibtion and reduces the monosynaptic and polysynaptic reflexes |
Diazepam | Diazepam depresses all levels of the CNS such as limbic and reticular formations, by increasing activity of GABA | ||
Lorazepam | Lorazepam is a sedative-hypnotic with short onset of effect and a relatively long half-life
By increasing the action of GABA, lorazepam may depress all levels of the CNS, including limbic and reticular formations It is important to monitor the patient's blood pressure after administering a dose and to adjust the dose as necessary | ||
Alpha Adrenergic Receptors |
|
Clonidine | Clonidine affects alpha1, alpha2, and alpha3-adrenergic receptors
It is frequently given to children but is not approved by the US Food and Drug Administration (FDA) for any psychiatric uses in children It is available in tablets and in transdermal skin patches |
Guanfacine | Guanfacine has an action similar to that of clonidine but has a longer half-life and is less sedating
It is more selective alpha agonist, affecting only alpha2-adrenergic receptors Guanfacine is not recommended for children younger than 12 years | ||
Antihistamines | Older, sedating antihistamines such as diphenhydramine are often prescribed as sedatives because of their CNS- depressing properties | Diphenhydramine | Diphenhydramine is available as nonprescription preparations containing 25 mg of diphenhydramine in liquid, chewable, and capsule forms |
References
- ↑ Famularo R, Kinscherff R, Fenton T (1988). "Propranolol treatment for childhood posttraumatic stress disorder, acute type. A pilot study". Am J Dis Child. 142 (11): 1244–7. PMID 3177336.
- ↑ Gelpin E, Bonne O, Peri T, Brandes D, Shalev AY (1996). "Treatment of recent trauma survivors with benzodiazepines: a prospective study". J Clin Psychiatry. 57 (9): 390–4. PMID 9746445.