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Post-traumatic Stress Disorder (PDQ®)
Patient Version   Health Professional Version   En español   Last Modified: 04/22/2009



Purpose of This PDQ Summary






Overview






Prevalence






Diagnostic Criteria and Characteristics






Risk Factors, Protective Factors, and Hypothesized Mechanism






Assessment of Post-traumatic Stress Disorder in the Cancer Setting






Treatment






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Changes to This Summary (04/22/2009)






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Risk Factors, Protective Factors, and Hypothesized Mechanism

Sociodemographic Variables
Disease-Related Variables
Psychosocial and Psychological Variables
Protective Factors
Hypothesized Mechanisms

A variety of sociodemographic, disease-related, psychosocial, and psychological variables have been investigated to determine their relationship to post-traumatic stress disorder (PTSD). At present, no clear picture emerges about who is at increased risk of developing PTSD following diagnosis or treatment of cancer.

Sociodemographic Variables

Few patient characteristics have been shown to predict the occurrence of PTSD. High levels of psychologic distress have been correlated with both stress symptoms [1-3] and full-syndrome PTSD diagnoses in adult survivors.[1] In addition, trait anxiety was found to predict post-traumatic symptoms in the parents of survivors of childhood cancer.[4] Women who are survivors of cancer and who have a diagnosis of lifetime PTSD tend to have a history of exposure to trauma.[1,5] Demographic characteristics such as age, sex, and education level at time of diagnosis have not been reliable predictors of stress symptoms.[1,6,7]

Demographic variables that have been associated with a higher incidence of PTSD include younger age,[8,9] fewer years of formal education, and lower income;[10,11] however, one study [1] failed to find any significant differences between the mean age of cancer patients with or without PTSD. In noncancer community samples, PTSD occurs almost twice as often in women; however, the gender differences in incidence of PTSD in cancer patients has been mixed.

Disease-Related Variables

Disease-related variables that have been associated with a higher incidence of PTSD in patients who underwent bone marrow transplant include more advanced disease and a longer hospital stay.[12] Other studies, however, have found no association between time since diagnosis and treatment, severity of disease, or type of cancer treatment received.[1,11,9] The relationship between disease stage and post-traumatic symptoms has not been adequately studied. Most studies have not found an association; however, they typically include a limited range of disease stages or are studying early-stage cancer.[13]

The time since diagnosis and treatment has been shown to correlate with and predict post-traumatic symptoms in survivors of osteogenic sarcoma [2] and Hodgkin lymphoma.[14,7] Specifically, persons who were farther from diagnosis and treatment tended to exhibit fewer symptoms. This effect, however, has not been found in studies of patients with recent recurrences,[15] survivors of breast cancer,[1] or survivors of childhood cancers.[16] Duration of treatment, rather than time since treatment, has been shown to predict stress symptoms in survivors of childhood cancer.[16] (Refer to the PDQ summary on Pediatric Supportive Care for more information.)

The presence of pain and other physical symptoms has been shown to correlate with levels of intrusive thoughts.[2] Cancer recurrence has also been shown to increase the likelihood of stress symptoms in patients.[15]

Psychosocial and Psychological Variables

The experience of past traumatic events appears to be an important psychosocial risk factor associated with post-traumatic symptoms,[17,18,5] as was found in both early-stage [19] and metastatic breast cancer.[20] Previous trauma in combination with recent stressful life events was significantly related to post-traumatic symptoms.[21]

Other psychosocial risk factors such as premorbid psychopathology,[22,23] high levels of general psychologic distress,[24] and dysfunctional coping and attributional styles [17,25,26] have been linked to a risk for PTSD in war veterans, Holocaust survivors, and other disaster victims. In addition, several investigators have linked predisposing genetic factors [27] and other biologic factors (e.g., overly reactive hormonal systems and reduced hippocampal volume) to risk for PTSD.[28-30] Among social factors, the quality of the recovery environment, often measured in terms of social support, has been shown to affect risk for PTSD following exposure to combat [22] and burn injury.[31] The effect of threat to life and body integrity has been documented in samples of adults and families [14,1,4] but not children.[16]

Psychological variables that have been related to a higher incidence of PTSD include a history (precancer diagnosis) of PTSD,[10,5] increased use of avoidance coping, and lower levels of social support.[32]

Protective Factors

Greater perceived availability of social support is associated with fewer stress response symptoms in early-stage breast cancer patients [19,21] and in bone marrow transplant patients.[32]

The availability and timeliness of accurate health-related information may also offer protection from stress response symptoms. Women who met the diagnostic criteria for Acute Stress Disorder (ASD) reported significantly less satisfaction with the communication of their cancer diagnosis;[33] similarly, women who were unaware of their cancer stage reported higher stress response symptoms than those who were more knowledgeable about the stage of their disease.[34] To the extent that adequacy of information reflects the quality of a patient's relationship with medical staff, another protective factor may be the quality of those relationships. Difficult patient-staff relationships have been reported to be predictors of stress response symptoms in women with cancer.[35]

Hypothesized Mechanisms

PTSD is precipitated by an intensely distressing event; however, this factor alone is not sufficient to explain the disorder. Not everyone exposed to a traumatic stressor develops the full-blown syndrome (or subsets of symptoms) or qualifies for the diagnosis. Attempts to explain these differences and to predict who is vulnerable have focused on psychologic (i.e., learning theory), biologic (especially hormonal), and social (i.e., social support) factors. Early studies of Vietnam War veterans suggested a two-factor learning theory to account for trauma-related pathology.[36,37] The same theory has also been applied to development of PTSD in patients with cancer.[38-40]

PTSD symptoms develop as a function of both classical conditioning and instrumental learning. Classical conditioning accounts for the fear responses elicited by various stimuli that are associated with the original traumatic event. Neutral stimuli (e.g., smells, sounds, and visual images) previously paired with the aversive stimuli (e.g., chemotherapy or painful procedures) eventually evoke anxiety, arousal, and fear when presented alone, even after the trauma has ended. Higher order conditioning and stimulus generalization account for the exacerbation and extension of symptoms to additional stimuli. Once established, PTSD symptoms are maintained through instrumental learning, i.e., avoidant responses are reinforced because avoidance of the stimuli prevents unpleasant feelings and thoughts.

Estimates from epidemiologic studies suggest that on average, 25% to 33% of individuals who are exposed to traumatic events, including cancer, develop PTSD.[28,41] Although the disorder appears to be a result of learning processes, many factors have been suggested to explain why one person develops PTSD and another does not.

References

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  2. Kornblith AB, Herr HW, Ofman US, et al.: Quality of life of patients with prostate cancer and their spouses. The value of a data base in clinical care. Cancer 73 (11): 2791-802, 1994.  [PUBMED Abstract]

  3. Kornblith AB, Anderson J, Cella DF, et al.: Quality of life assessment of Hodgkin's disease survivors: a model for cooperative clinical trials. Oncology (Huntingt) 4 (5): 93-101; discussion 104, 1990.  [PUBMED Abstract]

  4. Stuber ML, Gonzalez S, Meeske K, et al.: Post-traumatic stress after childhood cancer II: a family model. Psychooncology 3: 313-319, 1994. 

  5. Shelby RA, Golden-Kreutz DM, Andersen BL: PTSD diagnoses, subsyndromal symptoms, and comorbidities contribute to impairments for breast cancer survivors. J Trauma Stress 21 (2): 165-72, 2008.  [PUBMED Abstract]

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  7. Kornblith AB, Anderson J, Cella DF, et al.: Hodgkin disease survivors at increased risk for problems in psychosocial adaptation. The Cancer and Leukemia Group B. Cancer 70 (8): 2214-24, 1992.  [PUBMED Abstract]

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  21. Green BL, Krupnick JL, Rowland JH, et al.: Trauma history as a predictor of psychologic symptoms in women with breast cancer. J Clin Oncol 18 (5): 1084-93, 2000.  [PUBMED Abstract]

  22. Green BL, Grace MC, Lindy JD, et al.: Risk factors for PTSD and other diagnoses in a general sample of Vietnam veterans. Am J Psychiatry 147 (6): 729-33, 1990.  [PUBMED Abstract]

  23. Smith EM, North CS, McCool RE, et al.: Acute postdisaster psychiatric disorders: identification of persons at risk. Am J Psychiatry 147 (2): 202-6, 1990.  [PUBMED Abstract]

  24. Jacobsen PB, Sadler IJ, Booth-Jones M, et al.: Predictors of posttraumatic stress disorder symptomatology following bone marrow transplantation for cancer. J Consult Clin Psychol 70 (1): 235-40, 2002.  [PUBMED Abstract]

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  30. Bremner JD, Randall P, Scott TM, et al.: MRI-based measurement of hippocampal volume in patients with combat-related posttraumatic stress disorder. Am J Psychiatry 152 (7): 973-81, 1995.  [PUBMED Abstract]

  31. Perry S, Difede J, Musngi G, et al.: Predictors of posttraumatic stress disorder after burn injury. Am J Psychiatry 149 (7): 931-5, 1992.  [PUBMED Abstract]

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  33. McGarvey EL, Canterbury RJ, Koopman C, et al.: Acute stress disorder following diagnosis of cancer. International Journal of Rehabilitation and Health 4 (1): 1-15, 1998. 

  34. Naidich JB, Motta RW: PTSD-related symptoms in women with breast cancer. Journal of Psychotherapy in Independent Practice 1 (1): 35-54, 2000. 

  35. Carlier IV, Gersons BP: Partial posttraumatic stress disorder (PTSD): the issue of psychological scars and the occurrence of PTSD symptoms. J Nerv Ment Dis 183 (2): 107-9, 1995.  [PUBMED Abstract]

  36. Keane TM, Zimering RT, Caddell JM, et al.: A behavioral formulation of posttraumatic stress disorder in Vietnam veterans. Behavior Therapist 8(1): 9-12, 1985. 

  37. Charney DS, Deutch AY, Krystal JH, et al.: Psychobiologic mechanisms of posttraumatic stress disorder. Arch Gen Psychiatry 50(4): 294-305, 1993. 

  38. Cella DF, Pratt A, Holland JC: Persistent anticipatory nausea, vomiting, and anxiety in cured Hodgkin's disease patients after completion of chemotherapy. Am J Psychiatry 143 (5): 641-3, 1986.  [PUBMED Abstract]

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  40. Jacobsen PB, Bovbjerg DH, Redd WH: Anticipatory anxiety in women receiving chemotherapy for breast cancer. Health Psychol 12 (6): 469-75, 1993.  [PUBMED Abstract]

  41. Greenberg DB, Goorin A, Gebhardt MC, et al.: Quality of life in osteosarcoma survivors. Oncology (Huntingt) 8 (11): 19-25; discussion 25-6, 32, 35, 1994.  [PUBMED Abstract]

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