Literature DB >> 33505638

Impact of peritraumatic distress on posttraumatic stress disorder symptoms at 6 months after acute coronary syndrome: a prospective cohort study.

Tomomi Narisawa1,2,3, Daisuke Nishi4, Ryo Okubo1, Hiroko Noguchi1,3, Kei Hamazaki5, Akihiro Yamashita6, Yutaka J Matsuoka1,2,6.   

Abstract

Background: Posttraumatic stress disorder (PTSD) symptoms are known to occur after acute coronary syndrome (ACS). Peritraumatic distress has been indicated as a risk factor for PTSD and can be measured by the Peritraumatic Distress Inventory (PDI). However, no studies have yet measured peritraumatic distress after ACS using the PDI to predict PTSD.
Objectives: This prospective cohort study examined the impact of peritraumatic distress on PTSD symptoms at 6 months after ACS.
Methods: We used the PDI to assess peritraumatic distress in patients treated for ACS at a teaching hospital in Tokyo within 7 days after percutaneous coronary intervention. They were followed up over the next 6 months and were assessed for PTSD symptoms at 6 months using the Impact of Event Scale-Revised. The association between peritraumatic distress and PTSD symptoms was examined by multiple linear regression analysis.
Results: The study enrolled 101 ACS patients, and 97 completed the follow-up assessment. PDI total score was an independent predictor of PTSD symptoms after adjustment for potential covariates (beta = 0.38; p < 0.01). Limitations: The results were obtained from a single teaching hospital and assessment of PTSD symptoms was questionnaire based.
Conclusion: We provide the first evidence that PDI score can predict the development of PTSD symptoms in ACS patients. Assessing peritraumatic distress after ACS with the PDI may be useful for initiating early intervention against PTSD symptoms.
© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  PTSD symptoms; Peritraumatic Distress Inventory; acute coronary syndrome; peritraumatic distress; posttraumatic stress response

Year:  2021        PMID: 33505638      PMCID: PMC7817212          DOI: 10.1080/20008198.2020.1854511

Source DB:  PubMed          Journal:  Eur J Psychotraumatol        ISSN: 2000-8066


Introduction

Cardiovascular disease is a major cause of death globally. In Japan, a registration study on acute myocardial infarction (AMI) conducted in Miyagi Prefecture (Takii et al., 2010) reported that prevalence (per 100,000 population) increased from 7.4 in 1979 to 27.0 in 2008, which is approximately a 4-fold increase over about 30 years. Despite increasing survival rates for cardiovascular disease, it is still perceived by the public as a major threat to life. Individuals who have cardiovascular events consequently experience intense emotional reactions such as fear and anxiety (over dying or recurrence), anger, sadness, and grief as well as posttraumatic stress disorder (PTSD). In light of the association of PTSD and PTSD symptoms with heart disease, Kutz et al. (Kutz, Shabtai, Solomon, Neumann, & David, 1994) proposed the concept of cardiac-disease-induced posttraumatic stress disorder (CDI-PTSD). Acute coronary events such as acute coronary syndrome (ACS) occur in the case of suddenly reduced blood flow to the heart. ACS is often accompanied by severe chest pain, shortness of breath or lightheadedness, which can be a traumatic event. A systematic review of PTSD after ACS (Vilchinsky, Ginzburg, Fait, & Foa, 2017) reported rates of PTSD within 3 to 18 months after ACS ranging from 3% to 21%. A meta-analytic review of PTSD in patients with ACS (ST-segment elevation myocardial infarction, non-ST-segment elevation myocardial infarction, or unstable angina) found a prevalence of 12% (Edmondson et al., 2012). Survivors of ACS who develop PTSD symptoms experience emotional distress and impaired functioning, they are also at risk of medication non-adherence (Husain, Edmondson, Kautz, Umland, & Kronish, 2018; Kronish, Edmondson, Goldfinger, Fei, & Horowitz, 2012; Kronish, Edmondson, Li, & Cohen, 2012), and have almost a 2-fold increased risk of recurrent cardiovascular events and mortality (Kronish et al., 2012, 2012). As the survival rate after ACS has steadily increased, preventing PTSD symptoms after ACS has become vitally important. The risk factors for PTSD are younger age (Bennett & Brooke, 1999; Rocha et al., 2008), objective severity of ACS (Guler et al., 2009; Von Känel, Baumert, Kolb, Cho, & Ladwig, 2011; Whitehead, 2006), illness perception such as consequences, identity, concern, and emotion (Oflaz et al., 2014), depression (Dinenberg, McCaslin, Bates, & Cohen, 2014; Whitehead, 2006), neuroticism (Chung, Dennis, Berger, Jones, & Rudd, 2011), and attachment anxiety and difficulties in identifying feelings (Gao, Zhao, Li, & Cao, 2015). To explain the development of comorbidities with PTSD, Ginzburg et al. (Ginzburg, Ein-Dor, & Solomon, 2010) describe four competing models, which have all received support in the literature: the first model suggests that pre-existing psychiatric disorders such as depression and anxiety increase the risk for PTSD; the second model suggests the opposite causality where PTSD is a causal risk factor for anxiety and depression; the third model suggests that PTSD, anxiety, and depression develop independently but occur together due to shared risk factors; and the fourth model suggests that the comorbidity found among PTSD, anxiety, and depression is an artefact caused by symptom overlap. On the other hand, the risk factors for PTSD after ACS are identified as objective severity of ACS, perceived severity of ACS, illness representations, distress during myocardial infarction or hospitalization, and previous psychological vulnerability in a systematic review (Vilchinsky et al., 2017). ‘Distress during myocardial infarction or hospitalization’ is a form of ‘peritraumatic distress’, which is a group of physiological, emotional, and cognitive responses occurring during and immediately after the time of trauma (Brunet et al., 2001). Elevated threat perception has been found to predict posttraumatic psychopathology after evaluation for ACS, but most research has measured threat retrospectively. In regard to predicting PTSD symptoms based on peritraumatic distress assessed immediately after ACS, there have been no studies conducted in Japan and just four studies conducted in Western countries. Three found that acute stress disorder symptoms immediately after ACS predicted PTSD symptoms at 1 month (Roberge, Dupuis, & Marchand, 2010) or 3 months (Bennett, Owen, Koutsakis, & Bisson, 2002; Whitehead, 2006), and the fourth study found that peritraumatic distress during angiography predicted PTSD at 1 and 6 months (Marke & Bennett, 2013). The degree of peritraumatic distress can be measured by the Peritraumatic Distress Inventory (PDI) (Brunet et al., 2001), a widely used self-report measure. PDI scores have been used to predict PTSD severity following motor vehicle accidents (Guardia et al., 2013), physical trauma such as sustained in vehicular collisions and falls (Bunnell, Davidson, & Ruggiero, 2018), and physical illness such as stroke (Favrole et al., 2013), Stevens-Johnson syndrome, and toxic epidermal necrolysis (Hefez et al., 2019). Despite studies have reported that peritraumatic distress during heart attack is associated with PTSD symptoms (Bennett et al., 2002; Marke & Bennett, 2013), peritraumatic distress measured in those studies was measured using non-standardized scales. In this study, we examined whether the degree of peritraumatic distress during myocardial infarction in ACS patients, as assessed using the standardized PDI, can predict the development of PTSD symptoms 6 months later. Establishing such a means of prediction would help clinicians initiate early intervention against PTSD symptoms.

Materials and methods

Participants and procedure

We previously conducted a prospective cohort study called ‘CONPAC (Cohort with Nutritional Aspect for Psychiatric Disorder after Acute Coronary Syndrome)’. From that study, we have previously reported the association between polyunsaturated fatty acids and psychiatric disorder at 3 months (Yamashita et al., 2017) and 6 months (Noguchi et al., 2019) after ACS. We analysed the same patients in the present study, but here our focus was prediction of PTSD symptoms after ACS using the PDI. Participants were consecutively admitted to the National Disaster Medical Centre, Tokyo, Japan for ACS between 1 March 2014 and 8 February 2017. ACS was diagnosed if new-onset chest pain occurred with ischaemic electrocardiogram changes (Thygesen, Alpert, & White, 2007). The inclusion criteria were as follows: age ≥20 years; native Japanese speaker; able to contact us within 7 days of percutaneous coronary intervention (PCI); confirmed not to be in a life-threatening condition by a cardiologist and thus be in a stable enough condition to be interviewed; and able to understand the scope of the study and give written consent for study participation. Exclusion criteria were as follows: score on the Mini-Mental State Examination (Folstein, Folstein, & McHugh, 1975) <24; residing >90 min from the medical centre by train or car; a serious psychiatric condition such as hallucination, delusion, suicidalideation, or self-harm behaviour; currently undergoing treatment for a psychiatric disorder; and end-stage cancer. Researchers conducted bedside interviews during hospitalization to confirm the inclusion criteria and explained about the study to those who met the criteria, including that participation was entirely voluntary. Those who consented to participate were asked to fill out the PDI (see 2.2. Assessment) before they were discharged. For follow-up, we conducted an interview in a meeting room in our laboratory on the day the patient was visiting the outpatient clinic. The Ethics Committee of the National Disaster Medical Centre (2013–42) approved the study protocol. Written informed consent for study participation was obtained within 7 days of PCI. From the medical records and the questionnaire we asked participants to answer, we extracted baseline demographic and medical characteristics such as age, sex, highest educational attainment, psychiatric history, psychiatric family history, and Killip class indicating ACS severity. Peritraumatic distress was assessed using the standardized PDI within 7 days after PCI. We then performed follow-up over the next 3 and 6 months and assessed posttraumatic stress response (PTSD symptoms) using the standardized Impact of Event Scale–Revised (IES-R) at 3 and 6 months after PCI. The study conformed to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines (von Elm et al., 2007).

Assessments

Peritraumatic distress was assessed using the Japanese version of the 13-item PDI (Brunet et al., 2001). Total score ranges from 0 to 52, with each item scored on a 5-point Likert scale (0 =   not at all, 1 =  slightly true, 2 =  somewhat true, 3 =  very true, and 4 =  extremely true). Internal consistency, concurrent validity, and test–retest reliability have been confirmed for the Japanese version of the PDI (Nishi et al., 2009). PTSD symptoms were assessed using the IES-R (Weiss, 2004). Total score ranges from 0 to 88. This self-report questionnaire investigates the occurrence PTSD symptoms experienced in the previous week and comprises 22 items regarding re-experiencing, avoidance, and hyperarousal (i.e., the three most common PTSD symptoms according to the Diagnostic and Statistical Manual of Mental Disorders, fourth edition [DSM-IV]). The validity and reliability of the Japanese version of the IES-R has been confirmed (Asukai et al., 2002).

Statistical analysis

To examine the association between the PDI and PTSD symptoms, we used multiple linear regression analysis with IES-R total score as the dependent variable and PDI total score as the independent variable. We adjusted for the following potential covariates that have been previously identified as risk factors for PTSD: age, sex, psychiatric history, Psychiatric family history, highest educational attainment (Epstein, Fullerton, & Ursano, 1998; Schlenger et al., 2002), and Killip class. In addition, bivariate regression analysis was conducted to determine the relationship of PTSD symptoms with PDI total score and with PDI individual item scores. Relationships between the dependent and independent variables were expressed as a regression coefficient (beta weight) with 95% confidence interval (95% CI). A p-value of less than 0.05 was considered to indicate statistical significance. SPSS statistical software version 25 for Windows (SPSS, Tokyo, Japan) was used for all data analyses.

Results

PCI was used to assess 280 patients, 104 of whom did not meet the inclusion criteria. Of 176 patients approached to participate in the CONPAC study, 100 participated, 71 declined, and 4 withdrew consent. At the follow-up, three participants did not respond. Thus, we enrolled 101 ACS patients, with 97 completing the follow-up assessment (Figure 1). Demographic characteristics of these 97 patients are shown in Table 1. Mean age was 63.4 ± 11.1 (range, 36–87) years and 84 were men (85.7%).
Figure 1.

Enrolment flowchart of the CONPAC study. ACS, acute coronary syndrome; PCI, percutaneous coronary intervention

Table 1.

Demographic, medical, and psychiatric characteristics of acute coronary syndrome survivors who participated in a follow-up study (n = 97)

Variablesn%MeanSDMedianRange
Peritraumatic Distress Inventory97 14.29.713.00–39
 Age (years)--63.411.164.036–87
 Sex, male8385.6----
 History of psychiatric illness77.2----
 Family history of psychopathology1515.5----
 Highest educational attainment      
  Junior high school1414.4----
  High school4243.3----
  Junior or technical college1616.5----
  University or higher2525.8----
  Killip class      
   19193.8----
   233.1----
   311.0----
   422.1----
Outcome      
 IES-R at 6 months97-6.59.33.00–44

IES-R, Impact of Event Scale – Revised; SD, standard deviation

Demographic, medical, and psychiatric characteristics of acute coronary syndrome survivors who participated in a follow-up study (n = 97) IES-R, Impact of Event Scale – Revised; SD, standard deviation Enrolment flowchart of the CONPAC study. ACS, acute coronary syndrome; PCI, percutaneous coronary intervention Severity of heart disease was assessed as Killip class grade 1 in 91 (92.9%). PDI was administered 4.0 days (SD = 2.1) after ACS, with an average score of 14.1 (standard deviation [SD] = 9.7, 0–39). The IES-R was administered 3.8 days (SD = 2.1) after ACS, with an average IES-R score of 6.5 (SD = 9.2, 0–44) 6 months after ACS. PDI total score was an independent predictor for PTSD symptoms after adjustment for covariates (beta = 0.38, 95% CI, 0.19–0.57; p < 0.01; Table 2). The value of R-squared for the multiple linear regression model was 0.22 at 6 months.
Table 2.

Results of multiple linear regression analysis with PDI at 6 months as the dependent variable (n = 97)

 Beta (95% CI)p value
PDI per 1 point0.38 (0.19, 0.57)≤.001
Covariates  
 Age per 1 year−0.11 (−0.28, 0.07).23
 Women1.09 (−5.02, 7.20).72
 History of psychiatric illness−1.23 (−8.22, 5.75).73
 Family history of psychopathology−0.03 (−0.21, 0.15).77
  Highest educational attainment  
  0 (junior high school)Reference 
  1 (high school)−4.29 (−9.86, 1.29).13
  2 (junior or technical college)−4.49 (−11.03, 2.04).18
  3 (university or more)−0.79 (−6.69, 5.11).79
 Killip5.06 (.887, 9.23).18

R2 = 0.22, R2 change = 0.22

CI, confidence interval; IES‐R, Impact of Event Scale – Revised; PDI, Peritraumatic Distress Inventory.

Results of multiple linear regression analysis with PDI at 6 months as the dependent variable (n = 97) R2 = 0.22, R2 change = 0.22 CI, confidence interval; IES‐R, Impact of Event Scale – Revised; PDI, Peritraumatic Distress Inventory. The results of bivariate regression analysis are shown in Table 3 for each of the 13 PDI items. At the follow-up assessment, significant predictors of PTSD symptoms were item 1 (beta = 2.80, 95% CI = 1.23–4.37; p = 0.001), item 4 (beta = 2.95, 95%, 1.52–4.38; p ≤ 0.001), item 5 (beta = 2.42, 95% CI, 0.86–3.99; p = 0.003), item 6 (beta = 2.16, 95% CI = 0.26–4.07; p = 0.026), item 8 (beta = 3.36, 95% CI, 1.27–5.45; p = 0.002), and item 10 (beta = 1.63, 95% CI, 0.36–2.89; p = 0.012).
Table 3.

Results of univariate regression analysis (n = 97)

Item descriptionMean (±SD, range)Beta (95% CI)R squarep value
1. I felt helpless to do more0.97 (±1.1, 0–4)2.80 (1.23, 4.37).12≤.001
2. I felt sadness and grief1.33 (±1.2, 0–4)1.18 (−0.35, 2.70).02.129
3. I felt frustrated or angry I could not do more1.03 (±1.2, 0–4)0.58 (−0.94, 2.10).01.450
4. I felt afraid for my safety1.43 (±1.2, 0–4)2.95 (1.52, 4.38).15.000
5. I felt guilt that more was not done0.93 (±1.2, 0–4)2.42 (0.86, 3.99).09.003
6. I felt ashamed of my emotional reactions0.67 (±1.0, 0–4)2.16 (0.26, 4.07).05.026
7. I felt worried about the safety of others1.33 (±1.3, 0–4)0.60 (−0.84, 2.04).01.407
8. I had the feeling I was about to lose control of my emotions0.63 (±0.9, 0–3)3.36 (1.27, 5.45).10.002
9. I had difficulty controlling my bowel and bladder0.21 (±0.7, 0–4)2.40 (−0.14, 5.22).03.093
10. I was horrified by what happened1.7 (±1.4, 0–4)1.63 (0.36, 2.89).06.012
11. I had physical reactions like sweating, shaking, and pounding heart1.57 (±1.5, 0–4)0.81 (−0.41, 2.03).02.190
12. I felt I might pass out0.97 (±1.3, 0–4)0.37 (−1.05, 1.78).00.610
13. I felt I might die1.43 (±1.4, 0–4)1.04 (−0.25, 2.34).03.111
Total14.14 (±9.7, 0–39)0.30 (0.12, 0.48).10.002

CI, confidential interval.

R, coefficient of multiple correlation, index of goodness in the model.

Results of univariate regression analysis (n = 97) CI, confidential interval. R, coefficient of multiple correlation, index of goodness in the model.

Discussion

This is the first study to show that PTSD symptoms can be predicted by measuring peritraumatic stress immediately after ACS in Japanese subjects. To our knowledge, this is also the first study to predict later PTSD symptoms in ACS using the standardized PDI, with 6 of the 13 PDI items helping to predict such symptoms at 6 months after ACS. We confirmed here that PTSD symptoms related to a life-threatening physical condition could be predicted, as could PTSD symptoms in individuals who had experienced a vehicular accident (Nishi et al., 2010) and in disaster rescue medical workers (Kawashima et al., 2016; Nishi et al., 2012). The PDI was originally designed to explore PTSD Criterion A2 in DSM-IV, which requires fear, helplessness, or horror at the time of the event. Absence of peritraumatic distress has been shown to be a strong indicator of absence of PTSD (Nishi et al., 2009). In a meta-analysis by Thomas et al. (Thomas, Saumier, & Brunet, 2012), peritraumatic distress was significantly correlated with PTSD symptoms in 18 studies. These previous studies and our results indicate a strong association between peritraumatic distress and PTSD symptoms in patients who have experienced a traumatic event, including those caused by physical illness. To clarify this, further studies are required. We administered the PDI at 3.9 days (SD = ±2.1, 1–10) after ACS. The meta-analysis of PDI and the course of PTSD symptoms (Thomas et al., 2012) showed that regression slopes decreased (numerically or significantly) for separate meta-regressions on results of studies that administered the PDI within or after 1 month of a traumatic event. Recall and memory bias becomes worse as time passes after a traumatic event, so it becomes more difficult to recall emotions accurately. Therefore, it seems important that the PDI be administered as soon after a traumatic event as possible. One study found that almost 25% of participants who developed PTSD (criteria B–F) did not experience fear, helplessness, or horror but experienced other intense peritraumatic distress experiences such as worry about others, frustration, and physical symptoms during or just after injury (O’Donnell, Creamer, McFarlane, Silove, & Bryant, 2010). Furthermore, it was suggested that removing Criterion A2 from DSM-IV (American Psychiatric Association, 1994) would make diagnosing PTSD easier without a substantial increase in the number of qualified diagnoses (Karam et al., 2010). Criterion A2 was subsequently omitted from DSM-5 (American Psychiatric Association, 2013). However, peritraumatic distress remains an important risk factor for PTSD and being able to assess such distress immediately after a traumatic event is clinically meaningful. Because the prevalence of meeting diagnostic thresholds based on other criteria is significantly higher in the presence of Criterion A2 than in its absence, it has been suggested that A2 be reconceptualized as a risk factor for PTSD (Karam et al., 2010). The advantage of the PDI that explores A2 is that it can be completed quickly and soon after a traumatic event. Also, those who develop PTSD without meeting A2 include individuals amnestic to their peritraumatic emotional experience (O’Donnell et al., 2010). Amnesia can occur after traumatic brain injury due to physical injury or dissociation due to physical and sexual violence, but amnesia is unlikely to occur after ACS. Therefore, assessing degree of peritraumatic distress using the PDI would be helpful for identifying ACS patients at risk of developing PTSD symptoms. The following PDI items helped to predict later PTSD symptoms: “1. I felt helpless to do more”, ‘4. I felt afraid for my safety’, ‘5. I felt guilt that more was not done’, ‘6. I felt ashamed of my emotional reactions’, ‘8. I had the feeling I was about to lose control of my emotions’, and ‘10. I was horrified by what happened’. Three previous studies (Bunnell et al., 2018; Nishi et al., 2012, 2010) have examined which PDI items contribute to predicting PTSD symptoms (Table 4), and in all three studies and the present study, items 1, 6, and 8 were significant predictors of PTSD symptoms. Previous studies have reported that cognitive state such as total helplessness during the event (Başoglu, Şalcioglu, & Livanou, 2002) and loss of control (Simeon, Greenberg, Knutelska, Schmeidler, & Hollander, 2003) during the peritraumatic period predict later PTSD symptoms. Based on these results, helplessness and difficulty in controlling emotions during traumatic events are thought to be strong predictors of PTSD symptoms. It has been reported that early intervention such as trauma-focused cognitive-behavioural therapy (CBT-T), cognitive therapy without exposure and eye movement desensitization and reprocessing (EMDR)) for people with PTSD symptoms after psychological trauma is effective in alleviating the symptoms (Roberts et al., 2019). The result of this study might be useful for earlier screening.
Table 4.

Comparison between the CONPAC study and previous studies regarding the prediction of posttraumatic stress disorder symptoms using the Peritraumatic Distress Inventory items

Item descriptionCONPACNishi 2010Nishi 2012Bunnell 2018
1. I felt helpless to do more
2. I felt sadness and grief-
3. I felt frustrated or angry I could not do more-
4. I felt afraid for my safety-
5. I felt guilt that more was not done--
6. I felt ashamed of my emotional reactions
7. I felt worried about the safety of others-
8. I had the feeling I was about to lose control of my emotions
9. I had difficulty controlling my bowel and bladder----
10. I was horrified by what happened-
11. I had physical reactions like sweating, shaking, and pounding heart-
12. I felt I might pass out--
13. I felt I might die-

CONPAC, Cohort with Nutritional Aspect for Psychiatric Disorder after Acute Coronary Syndrome.

Comparison between the CONPAC study and previous studies regarding the prediction of posttraumatic stress disorder symptoms using the Peritraumatic Distress Inventory items CONPAC, Cohort with Nutritional Aspect for Psychiatric Disorder after Acute Coronary Syndrome.

Limitations

Although our study presents new findings, there are some limitations. First, because this study was conducted at a single hospital in Tokyo, multicenter studies are also required to confirm generalizability. Second, participants in our study included mostly males with Killip class 1. Therefore, the prevalence of PTSD and the prediction of PTSD symptoms by PDI in more severe ACS patients may differ from these results. Third, ‘being diagnosed with a life-threatening illness’ such as ACS was included in DSM-IV as Criterion A2 but is no longer included in DSM-5. This raises the question of whether the PTSD symptoms detected of this study can be referred to as ‘PTSD’ symptoms when following DSM-5 criteria. However, because experts vary in their opinions of PTSD Criterion A2 (Friedman, 2013; Roberts et al., 2019), whether physical diseases will be included in any re-established Criterion A2 depends on how the DSM will be revised in future. Therefore, screening for peritraumatic distress and preventing PTSD symptoms after ACS would be beneficial to patients. In addition, PTSD symptoms were assessed using the self-administered IES-R in this study, which raises concerns about the accuracy of symptom assessments. However, the reliability and validity of the Japanese version of the IES-R for evaluating PTSD symptoms is reported to be comparable to that of the Clinician-Administered PTSD Scale for DSM-IV (Asukai et al., 2002). To generalize our findings, it will be necessary to conduct a large-scale study with a larger number of facilities and participants.

Conclusion

We examined for the first time worldwide the use of the PDI to predict PTSD in patients with ACS. We confirmed that PTSD symptoms could be predicted by PDI score after adjusting for covariates. PDI items 1, 4, 5, 6, 8, and 10 were significant predictors of PTSD symptoms at 6 months. We also suggest that to predict PTSD symptoms, it may be important that PDI measurements be made within 7 days of the traumatic event. Based on these findings, evaluating peritraumatic distress using PDI at an early stage after an ACS episode is expected to contribute to early detection of PTSD symptoms and early intervention.
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