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“The Reintegration of Veterans with PTSD Back into Their Communities Through the Use of Public Health Initiatives” Brief History of PTSD: There have been great advances over the course of the last 60 years in the documentation and acknowledgement of PTSD. It wasn’t until 1980 that PTSD was codified as a disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM). PTSD is an issue that will affect approximately between 1 in 5 or 1 in 6 Americans who will have undergone a traumatic event at least once in their lifetime. It is the most commonly studied and perhaps the most debilitating mental disorder that takes place after a disaster. (Galea, Nandi & Vlahov, 2004) Much of the knowledge that we have today comes from years of study of our nation’s veterans from where they have been placed in conflicts that have forever changed them. PTSD has been referred to in the past before it was classified as a mental disorder as “nervous shock, shell shock, traumatic neurosis, and rape related fear and anxiety.” (Galea, Nandi & Vlahov, 2004) PTSD can affect anyone that undergoes a traumatic event. Many of the studies conducted involve veterans because of the sample size of the population that is affected and the amount of research that has been done on this community. Relevant factors accounting for the variability of estimates in cohorts include the methodology and conceptual factors. This accounts for the differences in prevalence rates across nations, generations, cultures, conflicts/wars, and studies among other data. (Aust, 2010) The data can be “fuzzy” or difficult to interpret at times because symptoms can be underlying for as long as 30 years without surfacing. Many Vietnam era veterans reported having chronic PTSD symptoms 20-25 years after the experience. There are statistics for PTSD, TBI, depression, and suicide among this population of veterans and the fact that more soldiers die by their own hand than by combat operations now is a sobering thought of the reality that these men and women face. Statistics like 50% of those affected by PTSD do not seek help or treatment for it, and the belief that the real number of those affected by PTSD and or depression is actually much higher than the documented 1 in 5 people and that of these, only ½ of them get minimally adequate treatment. (Veterans & PTSD, 2013) PTSD as it Pertains to Epidemiology & Biostatistics: “Historically speaking, epidemiologic studies of wars have been conducted after the end of hostilities. This is not the case with the OEF/OIF conflicts. Studies on PTSD among OEF/OIF Veterans have brought about new observations and recommendations for future research. Because of the importance of specific study design and characteristics to inferential power, studies have been grouped by design type, and due to space limitations, do not always cover other important health or mental health outcomes.“ (Litz & Schlenger, 2009) The use of biostatistics to analyze and interpret data to better understand the underlying issues that affect one’s mental health is being done in numerous facilities by experts in multiple fields of mental & behavioral health as well as its affects to physical health. The relationships between these conditions and how they are interlinked is a subject that many people are unable to fully understand and it is one of the reasons that increases in research and funding have been a topic of concern in recent years in addition to the nation’s financial responsibility. Over 4 billion dollars per year is currently paid out in disability payments to veterans that suffer from PTSD. After 13 years of the country being at war, the estimates of 100,000 to 300,000 OIF/OEF veterans are considered to be at significant risk of developing chronic PTSD. The use of biostatistics will help guide the course of treatment that is provided to people who suffer from PTSD and possibly help alleviate some of the financial obligation required to address the growing population of veterans that are at risk for chronic PTSD. The Strong Star Research Consortium is one institute that is assigned to address this issue and more information can be found in regards to their research at www.strongstar.org for a list of the projects. (Thomas, 2012) Biostatistics in regards to PTSD comes from the statistical information of mental health studies and the treatment of these patients. One of the influences that a recent study attributes to the increase in PTSD is the fact that many people are now commonly exposed to multiple deployments due to the high troop levels in both Iraq & Afghanistan. This phenomenon has created a higher number of (PTSS) posttraumatic stress symptoms or homefront stressors such as occupational problems and relationship or family problems. This is an increasingly common occurrence among National Guard soldiers. Nearly ½ of the soldiers in the military have experienced multiple deployments and the soldiers chances of being affected by PTSD significantly increases with each consecutive deployment. Homefront stressors pertaining to marriage, family, or work, are among the factors associated with this increased PTSD risk from soldiers serving on multiple tours. This causes the soldier to manage repeat cycles of deployment separations and readjustments to the homefront. Previous research has found that these readjustment stressors are related to PTSD. (Interian, Kline & Janal, 2014) This study on PTSS had one major aim, to better understand the role of homefront stressors as a pre-deployment risk factor for PTSS among service members with multiple deployments. The study examined these stressors at two time points. Post-deployment and pre-deployment. By examining homefront stressors at these two time-points, the study assesses the impact of different longitudinal patterns that these stressors have on PTSS. This is done by assessing the effects of having homefront stressors at both time points versus one time point or another, or neither. The study focuses on 196 respondents out of a possible 922 because the 196 had previously been deployed at least once to either OIF/OEF in the past and 27.6% had tours before OEF/OIF. Information collected from the study included age, gender, marital status, education level, rank, employment status, ethnicity, parental status, pre-disposition to stressors or existing PTSD, combat exposure and other variables. Please see the attached tables for more info. (Interian, Kline & Janal, 2014) The below tables will give you a perspective of the demographics of those involved in this study and the information that is used to derive the biostatistics for this study. A summary of what the study revealed is included. Table 1. Sample Characteristics Variable n or M % or SD Note 1. N = 196. Age, marital status, education, employment status, rank, and military occupational specialty were reported during Wave 1. OEF/OIF = Operation Enduring Freedom/Operation Iraqi Freedom; PTSS = posttraumatic stress symptoms; MOS = military occupational specialty. Gender Male 169 86.2 Female 27 13.8 17–25 23 11.8 26–39 112 57.4 40+ 60 30.8 Married or living as 93 47.4 Never married 75 38.3 Widow/separated/divorced 26 13.3 Age (years) Marital status Parental status No children 104 53.1 One or more children 92 46.9 White 83 42.3 Latino 47 24.0 Black 51 26.0 Other 15 7.7 High school or less 55 28.1 Some college 102 52.0 College graduate or more 39 19.9 Fulltime 167 85.2 Part-time 12 6.1 Unemployed 17 8.7 1 177 90.3 >1 19 9.7 Enlisted 176 91.2 Officer 17 8.8 Combat arms 60 32.3 Combat support 73 39.2 Race/ethnicity Education Employment Previous OEF/OIF deployments Rank MOS Combat service support 53 28.5 0 143 73.0 ≥1 53 27.0 0 124 63.3 ≥1 72 36.7 Wave 1 PTSS 26.9 11.8 Wave 2 PTSS 31.1 15.5 Combat exposure 5.2 7.2 Homefront stressors (Wave 1) Homefront stressors (Wave 2) PTSS was assessed using a well-established measure the 17-item PTSD Checklist-Civilian Version or (PCL-C). For descriptive analyses the utilization of the 50-point cutoff for identifying PTSD cases was used, which is commonly used in other research. The PCL-C was administered at Waves 1 and 2. Internal consistency with the current sample was .95 at Wave 1 and .97 at Wave 2. Home front stressors were measured in waves 1 & 2 with a series of yes & no questions as it pertained to various amounts of time in regards to wave 1 because the variable of time since the soldier’s last deployment was different to each candidate. Wave 2 pertained to a 15 month window of 3 months prior to deployment and the 12 months for the duration of the deployment. For all control measures, please see the actual study at this link. http://onlinelibrary.wiley.com/doi/10.1002/jts.21885/full Table 2. Multivariate Analysis of the Risk of Homefront Stressors on PTSS at Post deployment Step 1 Variable B SE B Step 2 B SE B Step 3 B SE B Note 1. N = 193. Model 1: R2 =.36; Adj R2 = .33; Model 2: R2 =.38; Adj R2 = .35 R-squared change p = .015; Model 3: R2 = .41; Adj R2 = .38 R-squared change p = .002. Model 2: Pre deployment home front stressors, β = .154. Model 3: Post deployment home front stressors, β = .214. PTSS measured with PTSD Checklist. Marital status was dichotomized to meet linear regression assumptions (never married vs. other categories). PTSS = posttraumatic stress symptoms; SE = standard error. 2. *p < .05. **p < .01. ***p < .001. Intercept 2.73 9.02 4.58 8.93 3.99 8.73 0.57*** 0.08 0.54*** 0.08 0.52*** 0.08 Previous trauma 0.10 0.54 −0.05 0.54 −0.20 0.53 Age 0.31** 0.12 0.28* 0.12 0.30** 0.11 Gender 5.20 2.78 4.62 2.76 4.50 2.69 Marital status 2.46 2.71 1.82 2.68 0.62 2.65 Parental status −0.22 2.42 −0.72 2.39 −0.77 2.34 Military preparedness −0.03 0.53 0.04 0.53 0.00 0.51 Combat exposure 0.42** 0.14 0.40** 0.14 0.25 0.15 Unit cohesion −0.18* 0.08 −0.19* 0.08 −0.16* 0.08 home front Stressors – – 1.97* 0.80 1.25 0.81 Post deployment home front – – – – 2.88** 0.92 Pre deployment PTSS stressors “First, 7.1% of the respondents had probable PTSD (i.e., PCL-C ≥ 50) at Wave 1; 14.3% met this criterion at Wave 2. Next, Wave 2 PTSS, as well as Wave 1 and Wave 2 home front stressors, were compared according to the sample characteristics listed in Table 1. Wave 2 PTSS were significantly higher among female respondents, F(1, 194) = 4.88, p = .028. Home front stressors significantly differed according to age category (17–25, 26–39, and ≥ 40 years) at both waves: Wave 1, F(1, 192) = 3.61, p = .029; Wave 2, F(1, 194) = 3.47, p = .033. Home front stressors at both waves also significantly differed according to marital status: Wave 1, F(1, 191) = 10.48, p < .001; Wave 2, F(1, 191) = 7.35, p < .001. Pairwise comparisons (not shown) showed that the youngest age group and those who were single reported significantly fewer home front stressors at both waves. Finally, soldiers with children reported significantly more home front stressors at Wave 1, F (1, 194) = 8.4, p = .004, and Wave 2, F(1, 194) = 6.40, p = .012).” (Interian, Kline & Janal, 2014) Table 3. Patterns of Homefront Stressors Occurring Before and After a New Deployment and the Risk of PTSS at Post deployment Variable B SE B Note 1. PTSS measured with PTSD Checklist-Civilian Version. R2 = .43; Adj R2 = .39. No stressors: n = 102; new stressors: n = 41; reduced stressors: n = 22; chronic stressors: n = 31. Chronic homefront stress, β = .22. Marital status was dichotomized to meet linear regression assumptions (never married vs. other categories). PTSS = posttraumatic stress symptoms. 2. *p < .05. **p < .01. ***p < .001. Intercept 7.56 8.73 No stress vs. new stress −2.44 2.43 Relieved stress vs. new stress −4.33 3.28 Chronic stress vs. new stress 9.39** 2.98 PTSS 0.50*** 0.08 Homefront stressor group Previous trauma −0.14 0.52 Age 0.34** 0.11 Gender 5.58* 2.66 Marital status 1.30 2.69 Parental status −1.48 2.32 Military preparedness −0.15 0.51 Combat exposure 0.35* 0.14 −0.20** 0.08 Unit cohesion “Analyses examined the effects of four subgroups with different patterns of home front stressors: (a) no home front stressors before or after the new deployment (no stressors); (b) home front stressors after but not before the new deployment (new stressors); (c) home front stressors before but not after the new deployment (relieved stressors); and (d) home front stressors both before and after the new deployment (chronic stressors). First, means for Wave 2 PTSS were generated for each of these groups and were found to be significantly different, F(3, 192) = 13.78, p < .001: (a) no stressors (M = 26.37, SD = 13.26), (b) new stressors (M = 32.24, SD = 15.41), (c) relieved stressors (M = 31.09, SD = 12.44), and (d) chronic stressors (M = 44.94, SD = 16.22). The pattern of home front stressors was examined via multivariate analysis in (Table 3). The group with new stressors was compared to each of the other three groups showing a significant difference with the chronic stressors group. Compared to soldiers who reported home front stressors occurring only after the new deployment (new stressors), soldiers who had home front stressors both before and after the deployment (chronic stressors) produced Wave 2 PTSS scores that were nine points higher.” (Interian, Kline & Janal, 2014) This study revealed that the occurrence of home front stressors increased the risks of PTSS and that soldiers were more likely to develop precursors to PTSD if PTSS was present before and after the deployment. Overall, the issues that pertain to the lifestyle or family of individuals deployed are relevant to the mental health of the individual. The frustration that these people endure because they can’t be present to address issues at the home front due to being separated and having no control or involvement in the situation leaves a sense of powerlessness and creates a chain reaction of thought processes which I attribute to being the leading cause for increases in PTSS and PTSD as a result of multiple deployments. This causes undue hardships on the family structure and as a result makes reintegration into the home front & community after the deployment increasingly difficult for all involved. Biological and Molecular Effects as it Pertains to PTSD: The biological & molecular effects of psychological stressors have multiple effects that transpire throughout the endocrine system. Hormones are released in a series of different chain reactions that each have a distinct effect & chemical reactions are then set into motion that continue the chain of events that influence the response of the body’s endocrine & nervous system. This chemical reaction is a response to the stimulation & signals that the brain interprets & can vary on intensity based on different factors. The following examples of studies about the biological & molecular characteristics of PTSD are suspected to have neurological effects on the individual affected & could vary in degrees based on the severity of the trauma & the susceptibility of the individual involved in the trauma. Studies in animals have shown that exposure to severe stress can damage the hippocampus & similar studies in humans suggest a link exists in the amount of volume present in the hippocampus correlates with vulnerability to psychological trauma. The smaller hippocampal volume constitutes a risk factor for the development of stress related psychopathology & individuals with smaller hippocampal volume are more susceptible to instances of PTSD than those with larger levels of hippocampal volume. (Gilbertson, Shenton & Ciszewski, 2002) Another study of the Serotonergic & Noradrenergic markers of PTSD & Depression has shown that research on the biological pathophysiology of PTSD found evidence of the roles of catecholamine & serotonin (5-HT). This finding on the increases of the catecholaminergic or sympathetic nervous system (SNS) activity in PTSD patients is fairly consistent across studies. For example, combat veterans with PTSD have shown significantly higher 24-hour urinary excretion with plasma concentrations of catecholamine, noradrenaline (NE), adrenaline, & dopamine, versus the normal control group, other psychiatric patients, or combat veterans without PTSD. These combat veterans have shown significantly higher rise in plasma (NE) & peripheral (SNS) activity than normal volunteers following acute stressors within the laboratory with stimuli reminiscent of the trauma linked to their PTSD. PTSD patients also have significantly decreased platelet counts suggesting down-regulation of α2-adrenoceptors (α2ARs) on platelets within the bloodstream. Laboratory trials with yohimbine, a α2-AR antagonist that blocks the presynaptic α2-AR auto-receptor resulted in significantly higher plasma levels of 3-methoxy-4-hydroxyphenylglycol (MHPG), the major NE metabolite. This was more prominent in PTSD veterans than in control groups. These results suggest that central presynaptic α2-ARs are sub-sensitive in PTSD patients. No significant alterations in 24-hour urinary (NE) excretion & lower arterialized plasma (NE) concentrations have been found in other studies although no research has examined plasma tyrosine, the precursor of (NE), in patients or veterans with PTSD. Evidence of (NE) in the brain determined by tyrosine concentrations, are reflected in the plasma. This is measured by the molar ratio of tyrosine to other amino acids which compete for the same cerebral uptake site. The competing amino acids (CAA) are tryptophan, phenylalanine, leucine, isoleucine, & valine. During stressful events the plasma tyrosine & the tyrosine/CAA increase & the increases in the tyrosine/CAA ratio is related to increased brain noradrenergic turnover. (Maes, Lin & Verkerk, 1999) Other studies have tried to identify the implications & relationships between trauma memory for pharmacological treatments which have been proposed for the prevention of PTSD & the idea of reprocessing trauma memories to bring about recovery through treatments such as invasive exposure therapy. Psychological accounts of PTSD & the biological concept for reconsolidation of active memories suggest that physiological arousal enhances the reprocessing of traumatic memories. Use of drugs that influence arousal through chemical means may then have effects after the trauma & depend on the psychosocial context that they are used in, thus in theory helping to prevent the development of PTSD in some trauma victims, but impeding recovery in others who would do well without such treatments. This would mean that you would have to be preemptively treating someone with drug related therapies before they were exposed to the traumatic event in order to use some of these treatments successfully. (McCleery & Harvey, 2004) There are many things that can trigger a traumatic event activating a person’s fight-or-flight response which is the body’s instinctual reflex to possible trauma & works as a survival mechanism normally by increasing the biological output of molecular responses such as the increase of hormones such as adrenaline or body systems such as arterial blood pressure, oxygen exchange in the lungs & many other effects. This natural response has given man many advantages over the course of evolution. There are instances though that this natural mechanism displays a dysfunction which happens when a functional impairment causes an individual to become psychologically traumatized creating PTSD within the individual because their normal defense mechanisms against trauma has failed to operate & process the information in a manner that is traditionally in line with the body’s normal functioning. These individuals are among the population that is biologically susceptible to the pathophysiology that causes PTSD. These pathological features found in patients with PTSD overlap similarly in patients with traumatic brain injury paralleling the shared signs & symptoms of these syndromes in clinical studies. The signs & symptoms of PTSD appear to reflect a persistent & abnormal adaptation of neurobiological systems to the stress of a witnessed traumatic event. The neurobiological systems that regulate stress responses include certain endocrine & neurotransmitter pathways as well the network of brain regions known to regulate fear & behavior at both conscious & unconscious levels. (Sherin & Nemeroff, 2011) Psychosocial & Behavioral Health Factors Influenced by PTSD: Public Health is concerned with the psychosocial and behavioral health factors of the community at large. There are various measures to discuss how public health can gauge these concerns but here we will focus on the ecological model of health behaviors which are identified as the five following factors. 1) Intrapersonal factors 2) Interpersonal relations 3) Institutional factors 4) Community factors & 5) Public policy. These factors along with the psychological model of health behavior or health belief model help explain how we interact with the world around us and how the world around us can influence our behaviors & our actions. When you associate these factors to the behavioral outcomes related to people who suffer from PTSD, we may finally be able to understand the relationship of the events leading to the patient’s behavior after being exposed to the traumatic event. (Schneider, 2012) One study that focuses on the specific symptom clusters of 1) hyper-arousal 2) reexperiencing 3) numbing and 4) avoidance as it pertains to reabuse of women exposed to intimate partner violence or (IPV) is of particular interest. I say that this is related to veterans with PTSD because there are different types of experiences that can cause PTSD and many of these symptoms are standard across all PTSD patients. Some are women veterans that experienced spousal abuse or rape, while others are combat related. These symptoms are common symptoms associated with PTSD. Hyper-arousal will be present in people that suffer from PTSD and sometimes cause an increase in the severity of the response to episodes where the patient is re-experiencing the traumatic scenario. The other symptoms numbing and avoidance will have different effects on the individuals and how they interact with others. All of these symptoms will affect the interpersonal relations of an individual that suffers from PTSD. The symptoms will also interfere with how an individual that suffers from PTSD will interact with all of the ecological factors at varying levels depending on the severity of the patient’s PTSD symptoms and whether they are controlled with medication & therapy or uncontrolled. (Krause, Kaltman & Goodman, 2006) Another study which focuses on smoking and anxiety in combat veterans from the Vietnam War has found a link in the behaviors of substance abuse and those that suffer from PTSD. (Beckham, 1999) This coincides with the amount of smoking or substance abuse that is done to help the patient avoid or numb the experience which is the subject of their pain. This link between PTSD and substance abuse or chemical dependency being more prevalent in this population of veterans along with the appearance of other negative health behaviors has an adverse effect on the degree in which ecological factors affect the veteran community. This will cause the veteran’s intrapersonal relationship to change thus causing a reaction within the community & changing their interpersonal relationships, thoughts and feelings toward institutions and the reactions they have toward changes in public policy or the failure of changes to be implemented in public policy. This cascade of events or domino effect can possibly be averted for the next generation of veterans that suffer from PTSD through the proper implementation of treatment establishing a healthy behavior model that engages the veteran with positive reinforcements. This study with further research can provide the information to help render advancements in the treatment of recent veterans who are beginning to experience similar circumstances and symptoms as those in the study. Treatments like group therapy and support groups are the key to establishing a positively structured environment that nurtures development of social skills through interpersonal relationships and helps to reintegrate the veterans into the community. A study that involves compulsive behaviors provides an example of how a health belief model can influence the psychosocial behaviors and influence the reintegration of veterans into the ecological model of society. The specific duties that a veteran has during a combat deployment creates a rehearsed response which becomes a learned behavior and influences a belief that things must be done according to this to have the desired health outcome which in many cases is survival or the survival of fellow soldiers, friends & comrades. This conditioning translates into difficulties in reintegrating back into the society here on the home front. With over 1.5 million soldiers deployed into the theater of operations and an estimate as high as 1020% of these veterans experiencing some type or form of PTSD symptoms, it is of particular interest to better understand how PTSD can be displayed or induce other forms of mental health disorders such as OCD or anxiety disorders. These disorders and the symptoms of PTSD are presenting with different clinical outcomes compared to other instances of PTSD and will thus complicate the treatment process and possibly creates a concern for the public health in how to best address the treatment of this increasing population and return them into active members of the community. (Tuerk, Grubaugh & Hamner, 2009) Conclusion Summary: The reintegration of veterans with PTSD back into the community through public health initiatives is a lengthy and time consuming process. It is not something that happens over the course of a night, through 1 meeting, or the application & use of medications. There is no cure all or instant fix solutions. It is not completed with just a shot in the arm, a pill to pop, or the duration of a course of a prescription drug. It is a life-long process with success being measured in varying degrees. The public’s health has been sustained in part through the contributions and sacrifices of the veteran community allowing for the continuation of the American lifestyle. PTSD is perhaps the most painful mental disorder to have treatment for and it can be a life-long process of treatment through either therapy or medication to manage and control the symptoms. The reintegration of these veterans into being active and participating members of society is paramount to the overall success of the community. They have valuable skills and experience that contribute to the success of a sustainable economy and in order for the structure of society to remain intact, the public health community needs to accommodate planning and strategies to address how to best help reintegrate these individuals into the home front. Works Cited: http://www.ptsd.va.gov/professional/newsletters/research-quarterly/V20N1.pdf Litz, B., & Schlenger, W. (2009). PTSD in service members and new veterans of the Iraq and Afghanistan wars: A bibliography and critique. PTSD Research Quarterly, 20(1), 1-8. Retrieved from http://www.ptsd.va.gov/professional/newsletters/research-quarterly/V20N1.pdf (Litz & Schlenger, 2009) http://www.veteransandptsd.com/PTSD-statistics.html Veterans & PTSD. (2013). Veterans statistics: PTSD, depression, TBI, suicide. Retrieved from http://www.veteransandptsd.com/PTSD-statistics.html (Veterans & PTSD, 2013) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891773/ Aust, N. (2010). Prevalence estimates of combat-related PTSD: A critical review. NIHPA Author Manuscripts, 44(1), 4-19. Retrieved from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891773/ (Aust, 2010) http://epirev.oxfordjournals.org/content/27/1/78.full Galea, S., Nandi, A., & Vlahov, D. (2004). The epidemiology of post-traumatic stress disorder after disasters. Oxford Journals, 27(1), 78-91. Retrieved from http://epirev.oxfordjournals.org/content/27/1/78.full (Galea, Nandi & Vlahov, 2004) Interian, A., Kline, A., & Janal, M. (2014). Multiple deployments and combat trauma: Do homefront stressors increase the risk for posttraumatic stress symptoms?. Journal of traumatic stress, 27(1), 90-97. doi: 10.1002/jts.21885 (Interian, Kline & Janal, 2014) Thomas, B. (2012, September 19). Strong star: South Texas research organizational network guiding studies on trauma and resilience. Retrieved from http://psychiatry.uthscsa.edu/Research/STRONG_STAR_A.asp (Thomas, 2012) For more information on STRONG STAR and its research projects, visit www.strongstar.org Sherin, J., & Nemeroff, C. (2011). Post-traumatic stress disorder: the neurobiological impact of psychological trauma. Dialogues in clinical neuroscience, 13(3), 263-278. doi: PMC3182008 (Sherin & Nemeroff, 2011) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182008/ Yehuda, R., Koenen, K., & Galea, S. (2011). The role of genes in defining a molecular biology of PTSD. Disease Markers, 30(2-3), 67-76. doi: 10.3233/DMA-2011-0794 (Yehuda, Koenen & Galea, 2011) http://iospress.metapress.com/content/w77t770111456543/ McCleery, J., & Harvey, A. (2005). Integration of psychological & biological approaches to trauma memory: Implications for pharmacological prevention of PTSD. Journal of traumatic stress, 17(6), 485-496. doi: 10.1007/s10960-004-5797-5 (McCleery & Harvey, 2005) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182008/ Maes, M., Lin, A., & Verkerk, R. (1999). Serotonergic & noradrenergic markers of posttraumatic stress disorder with & without major depression. Neuropsychopharmacology , (20), 188-197. doi: 10.1016/S0893-133X(98)00058-X (Maes, Lin & Verkerk, 1999) http://www.nature.com/npp/journal/v20/n2/full/1395241a.html Schneider, M. (2012). Introduction to public health. (4th ed., pp. 221-236). Burlington, MA: Jones & Bartlett Learning. (Schneider, 2012) Beckham, J. (1999). Smoking and anxiety in combat veterans with chronic posttraumatic stress disorder: A review. Journal of Psychoactive Drugs, 31(2), 103-110. doi: 10.1080/02791072.1999.10471731 (Beckham, 1999) http://www.tandfonline.com/doi/abs/10.1080/02791072.1999.10471731#.U0Su7jjD_ip Tuerk, P., Grubaugh, A., & Hamner, M. (2009). Diagnosis and treatment of PTSD-related compulsive checking behaviors in veterans of the Iraq war: The influence of military context on the expression of PTSD symptoms. The American Journal of Psychiarty, 166(7), 762-767. doi: 10.1176/appi.ajp.2009.08091315 (Tuerk, Grubaugh & Hamner, 2009) http://journals.psychiatryonline.org/article.aspx?articleid=100938 Krause, E., Kaltman, S., & Goodman, L. (2006). Role of distinct PTSD symptoms in intimate partner reabuse: A prospective study. Journal of traumatic stress, 19(4), 507-516. doi: 10.1002/jts.20136 (Krause, Kaltman & Goodman, 2006) http://onlinelibrary.wiley.com/doi/10.1002/jts.20136/abstract