Advances in the management of posttraumatic stress disorder after critical illness: a narrative review

Evanthia Asimakopoulou , Panagiotis Theodosis-Nobelos , Charalampos Triantis

Emergency and Critical Care Medicine ›› 2024, Vol. 4 ›› Issue (4) : 174 -182.

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Emergency and Critical Care Medicine ›› 2024, Vol. 4 ›› Issue (4) :174 -182. DOI: 10.1097/EC9.0000000000000139
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Advances in the management of posttraumatic stress disorder after critical illness: a narrative review

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Abstract

Illness requiring critical care can lead to the development of posttraumatic stress disorder (PTSD), a complex mental health condition resulting from exposure to traumatic events. In the intensive care unit (ICU), the nature of interventions often contributes to a high incidence of PTSD, which is a significant component of post-intensive care syndrome (PICS). This article provides a comprehensive overview of the pathophysiological mechanisms underlying PTSD and explores various intervention strategies, emphasizing the importance of a multidisciplinary and holistic approach. Although prevention remains the best therapy, pharmacotherapy is a key component in the management of PTSD symptoms. Antidepressants, particularly selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs), have demonstrated efficiency in alleviating symptoms. 3,4-Methylenedioxymethamphetamine-assisted therapy is the most promising approach, and the results of the clinical trials are encouraging. Furthermore, medications targeting specific neurotransmission systems involved in fear responses and emotional regulation are being explored, offering promising avenues for future treatment. Nonpharmacological interventions are integral to PTSD treatment. These are often employed alone or in conjunction with pharmacotherapy. Evidence-based psychotherapies, such as cognitive-behavioral therapy and exposure therapies, are effective in addressing maladaptive thought patterns and facilitating trauma processing. Beyond interventions, lifestyle modifications have emerged as significant contributors to resilience and recovery. Regular physical exercise, adequate sleep, and robust social support networks are integral to the overall well-being of patients who have developed PTSD after critical illness. By integrating pharmacological and nonpharmacological approaches within a holistic framework, clinicians and researchers could better address the complex nature of PTSD and enhance the quality of care for individuals affected by this debilitating condition.

Keywords

Critical illness / Management / Nonpharmacological interventions / Pharmacological interventions / Posttraumatic stress disorder

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Evanthia Asimakopoulou, Panagiotis Theodosis-Nobelos, Charalampos Triantis. Advances in the management of posttraumatic stress disorder after critical illness: a narrative review. Emergency and Critical Care Medicine, 2024, 4(4): 174-182 DOI:10.1097/EC9.0000000000000139

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Conflict of interest statement

The authors declare no conflict of interest.

Author contributions

Asimakopoulou E conceived the topic and scope of the study. Triantis C and Asimakopoulou E wrote the manuscript. Theodosis-Nobelos P and Triantis C critically revised the manuscript. All the authors have read and approved the final version of the manuscript.

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Not applicable.

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References

[1]

American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders. 5th ed. https://doi.org/10.1176/appi.books.9780890425596

[2]

Yehuda R.Post-traumatic stress disorder. N Engl J Med. 2002; 346(2):108-114. doi:10.1056/NEJMra012941

[3]

Pitman RK, Rasmusson AM, Koenen KC, et al. Biological studies of post-traumatic stress disorder. Nat Rev Neurosci. 2012; 13(11):769-787. doi:10.1038/nrn3339

[4]

Kessler RC, Sonnega A, Bromet E, Hughes M, Nelson CB. Posttraumatic stress disorder in the National Comorbidity Survey. Arch Gen Psychiatry. 1995; 52(12):1048-1060. doi:10.1001/archpsyc.1995.03950240066012

[5]

Asimakopoulou E, Madianos M. Posttraumatic stress disorder after discharge from intensive care units in greater Athens area. J Trauma Nurs. 2015; 22(4):209-217. doi:10.1097/JTN.0000000000000142

[6]

Parotto M, Herridge MS. Recovery after prolonged treatment in the intensive care unit. CMAJ. 2020; 192(48):E1637. doi:10.1503/cmaj.201356

[7]

Harvey MA, Davidson JE. Postintensive care syndrome: right care, right now…and later. Crit Care Med. 2016; 44(2):381-385. doi:10.1097/CCM.0000000000001531

[8]

Kosinski S, Mohammad RA, Pitcher M, et al. What is post-intensive care syndrome (PICS)?. Am J Respir Crit Care Med. 2020; 201(8):P15-P16. doi:10.1164/rccm.2018P15

[9]

Asimakopoulou E, Theodosis-Nobelos P, Triantis C. Pain assessment and management in intensive care unit: pharmacological and non-pharmacological approaches. Hell J Nurs. 2018; 57(4):349-361

[10]

Asimakopoulou E, Zavridis P. Rehabilitation of chronic pain in post-critical care patients. A narrative review. OBM Neurobiol. 2023; 7(4):194. doi:10.21926/obm.neurobiol.2304194

[11]

Franks ZM, Alcock JA, Lam T, Haines KJ, Arora N, Ramanan M. Physical restraints and post-traumatic stress disorder in survivors of critical illness. A systematic review and meta-analysis. Ann Am Thorac Soc. 2021; 18(4):689-697. doi:10.1513/AnnalsATS.202006-738OC

[12]

Hatch R, Young D, Barber V, Griffiths J, Harrison DA, Watkinson P. Anxiety, depression and post traumatic stress disorder after critical illness: a UK-wide prospective cohort study. Crit Care. 2018; 22(1):310. doi:10.1186/s13054-018-2223-6

[13]

Long AC, Kross EK, Davydow DS, Curtis JR. Posttraumatic stress disorder among survivors of critical illness: creation of a conceptual model addressing identification, prevention, and management. Intensive Care Med. 2014; 40(6):820-829. doi:10.1007/s00134-014-3306-8

[14]

Foa EB, Riggs DS, Dancu CV, Rothbaum BO. Reliability and validity of a brief instrument for assessing post-traumatic stress disorder. J Trauma Stress. 1993; 6(4):459-473

[15]

Weiss DS, Marmar CR. The Impact of Event Scale—Revised. In: JP Wilson, TM Keane, eds. Assessing Psychological Trauma and PTSD vol. 1995. New York: The Guilford Press; 1997:399-411.

[16]

Rosendahl J, Kisyova H, Gawlytta R, Scherag A. Comparative validation of three screening instruments for posttraumatic stress disorder after intensive care. J Crit Care. 2019; 53:149-154. doi:10.1016/j.jcrc.2019.06.016

[17]

Yaribeygi H, Panahi Y, Sahraei H, Johnston TP, Sahebkar A. The impact of stress on body function: a review. EXCLI J. 2017; 16:1057-1072. doi:10.17179/excli2017-480

[18]

James KA, Stromin JI, Steenkamp N, Combrinck MI. Understanding the relationships between physiological and psychosocial stress, cortisol and cognition. Front Endocrinol (Lausanne). 2023; 14:1085950. doi:10.3389/fendo.2023.1085950

[19]

Dunlop BW, Wong A. The hypothalamic-pituitary-adrenal axis in PTSD: pathophysiology and treatment interventions. Prog Neuropsychopharmacol Biol Psychiatry. 2019; 89:361-379. doi:10.1016/j.pnpbp.2018.10.010

[20]

Castro-Vale I, van Rossum EFC, Machado JC, Mota-Cardoso R, Carvalho D. Genetics of glucocorticoid regulation and posttraumatic stress disorder—what do we know?. Neurosci Biobehav Rev. 2016; 63:143-157. doi:10.1016/j.neubiorev.2016.02.005

[21]

Heim C, Nemeroff CB. Neurobiology of posttraumatic stress disorder. CNS Spectr. 2009; 14(1Suppl 1): 13-24

[22]

McFarlane AC, Barton CA, Yehuda R, Wittert G. Cortisol response to acute trauma and risk of posttraumatic stress disorder. Psychoneuroendocrinology. 2011; 36(5):720-727. doi:10.1016/j.psyneuen.2010.10.007

[23]

Mutesa L. Predictive evidence of the relevance of epigenetics to PTSD. Nat Rev Genet. 2023; 24(12):807. doi:10.1038/s41576-023-00646-1

[24]

Wang Z, Baker DG, Harrer J, Hamner M, Price M, Amstadter A. The relationship between combat-related posttraumatic stress disorder and the 5-HTTLPR/rs25531 polymorphism. Depress Anxiety. 2011; 28(12):1067-1073. doi:10.1002/da.20872

[25]

Gressier F, Calati R, Balestri M, et al. The 5-HTTLPR polymorphism and posttraumatic stress disorder: a meta-analysis. J Trauma Stress. 2013; 26(6):645-653. doi:10.1002/jts.21855

[26]

Rothbaum BO, Kearns MC, Reiser E, et al. Early intervention following trauma may mitigate genetic risk for PTSD in civilians: a pilot prospective emergency department study. J Clin Psychiatry. 2014; 75(12):1380-1387. doi:10.4088/JCP.13m08715

[27]

Banerjee SB, Morrison FG, Ressler KJ. Genetic approaches for the study of PTSD: advances and challenges. Neurosci Lett. 2017; 649:139-146. doi:10.1016/j.neulet.2017.02.058

[28]

Alexandra Kredlow M, Fenster RJ, Laurent ES, Ressler KJ, Phelps EA. Prefrontal cortex, amygdala, and threat processing: implications for PTSD. Neuropsychopharmacology. 2022; 47(1):247-259. doi:10.1038/s41386-021-01155-7

[29]

Govindula A, Ranadive N, Nampoothiri M, Rao CM, Arora D, Mudgal J. Emphasizing the crosstalk between inflammatory and neural signaling in post-traumatic stress disorder (PTSD). J Neuroimmune Pharmacol. 2023; 18(3):248-266. doi:10.1007/s11481-023-10064-z

[30]

Michopoulos V, Powers A, Gillespie CF, Ressler KJ, Jovanovic T. Inflammation in fear- and anxiety-based disorders: PTSD, GAD, and beyond. Neuropsychopharmacology. 2017; 42(1):254-270. doi:10.1038/npp.2016.146

[31]

Smoller JW. The genetics of stress-related disorders: PTSD, depression, and anxiety disorders. Neuropsychopharmacology. 2016; 41(1):297-319. doi:10.1038/npp.2015.266

[32]

Simons KS, van den Boogaard M, de Jager CPC. Impact of intensive care unit light and noise exposure on critically ill patients. Netherlands J Crit Care. 2019; 27(4):145-149

[33]

Baldwin DS, Anderson IM, Nutt DJ, et al. Evidence-based pharmacological treatment of anxiety disorders, post-traumatic stress disorder and obsessive-compulsive disorder: a revision of the 2005 guidelines from the British Association for Psychopharmacology. J Psychopharmacol. 2014; 28(5):403-439. doi:10.1177/0269881114525674

[34]

Feduccia AA, Holland J, Mithoefer MC. Progress and promise for the MDMA drug development program. Psychopharmacology (Berl). 2018; 235(2):561-571. doi:10.1007/s00213-017-4779-2

[35]

Guina J, Rossetter SR, DeRHODES BJ, Nahhas RW, Welton RS. Benzodiazepines for PTSD: a systematic review and meta-analysis. J Psychiatr Pract. 2015; 21(4):281-303. doi:10.1097/PRA.0000000000000091

[36]

Campos B, Vinder V, Passos RBF, et al. To BDZ or not to BDZ? That is the question! Is there reliable scientific evidence for or against using benzodiazepines in the aftermath of potentially traumatic events for the prevention of PTSD? A systematic review and meta-analysis. J Psychopharmacol. 2022; 36(4):449-459. doi:10.1177/02698811221080464

[37]

Cuninghame S, Jerath A, Gorsky K, et al. Effect of inhaled anaesthetics on cognitive and psychiatric outcomes in critically ill adults: a systematic review and meta-analysis. Br J Anaesth. 2023; 131(2):314-327. doi:10.1016/j.bja.2023.05.004

[38]

PTSD: National Center for PTSD. Medications for PTSD. Accessed December 13, 2023. https://www.ptsd.va.gov/understand_tx/meds_for_ptsd.asp

[39]

Cipriani A, Williams T, Nikolakopoulou A, et al. Comparative efficacy and acceptability of pharmacological treatments for post-traumatic stress disorder in adults: a network meta-analysis. Psychol Med. 2018; 48(12):1975-1984. doi:10.1017/S003329171700349X

[40]

Abdallah CG, Averill LA, Akiki TJ, et al. The neurobiology and pharmacotherapy of posttraumatic stress disorder. Annu Rev Pharmacol Toxicol. 2019; 59:171-189. doi:10.1146/annurev-pharmtox-010818-021701

[41]

Watts BV, Schnurr PP, Mayo L, Young-Xu Y, Weeks WB, Friedman MJ. Meta-analysis of the efficacy of treatments for posttraumatic stress disorder. J Clin Psychiatry. 2013; 74(6):e541-e550. doi:10.4088/JCP.12r08225

[42]

Ipser JC, Stein DJ. Evidence-based pharmacotherapy of post-traumatic stress disorder (PTSD). Int J Neuropsychopharmacol. 2012; 15(6):825-840. doi:10.1017/S1461145711001209

[43]

Crapanzano C, Damiani S, Casolaro I, Amendola C. Quetiapine treatment for post-traumatic stress disorder: a systematic review of the literature. Clin Psychopharmacol Neurosci. 2023; 21(1):49-56. doi:10.9758/cpn.2023.21.1.49

[44]

Krystal JH, Rosenheck RA, Cramer JA, et al; Veterans Affairs Cooperative Study no. 504 Group. Adjunctive risperidone treatment for antidepressant-resistant symptoms of chronic military service-related PTSD: a randomized trial. JAMA. 2011; 306(5):493-502. doi:10.1001/jama.2011.1080

[45]

Williams T, Phillips NJ, Stein DJ, Ipser JC. Pharmacotherapy for post traumatic stress disorder (PTSD). Cochrane Database Syst Rev. 2022; 3(3):CD002795. doi:10.1002/14651858.CD002795.pub3

[46]

de Moraes CG, Zanatta FB, Ziegelmann PK, Soares Barros AJ, Mello CF. Pharmacological treatments for adults with post-traumatic stress disorder: a network meta-analysis of comparative efficacy and acceptability. J Psychiatr Res. 2020; 130:412-420. doi:10.1016/j.jpsychires.2020.07.046

[47]

Jerome L, Feduccia AA, Wang JB, et al. Long-term follow-up outcomes of MDMA-assisted psychotherapy for treatment of PTSD: a longitudinal pooled analysis of six phase 2 trials. Psychopharmacology (Berl). 2020; 237(8):2485-2497. doi:10.1007/s00213-020-05548-2

[48]

Madero S, Alvarez OD. Premise, promise and challenges of MDMA assisted therapy for PTSD. Eur Neuropsychopharmacol. 2023; 70:19-20. doi:10.1016/j.euroneuro.2023.02.002

[49]

Mullard A. MDMA-assisted therapy for PTSD passes phase III trial. Nat Rev Drug Discov. 2023; 22(11):863. doi:10.1038/d41573-023-00165-y

[50]

Mitchell JM, Ot'alora GM, van der Kolk B, et al; MAPP2 Study Collaborator Group. MDMA-assisted therapy for moderate to severe PTSD: a randomized, placebo-controlled phase 3 trial. Nat Med. 2023; 29(10):2473-2480. doi:10.1038/s41591-023-02565-4

[51]

Griffiths RR, Johnson MW, Richards WA, Richards BD, McCann U, Jesse R. Psilocybin occasioned mystical-type experiences: immediate and persisting dose-related effects. Psychopharmacology (Berl). 2011; 218(4):649-665. doi:10.1007/s00213-011-2358-5

[52]

Krediet E, Bostoen T, Breeksema J, van Schagen A, Passie T, Vermetten E. Reviewing the potential of psychedelics for the treatment of PTSD. Int J Neuropsychopharmacol. 2020; 23(6):385-400. doi:10.1093/ijnp/pyaa018

[53]

Singewald N, Sartori SB, Reif A, Holmes A. Alleviating anxiety and taming trauma: novel pharmacotherapeutics for anxiety disorders and posttraumatic stress disorder. Neuropharmacology. 2023; 226:109418. doi:10.1016/j.neuropharm.2023.109418

[54]

Feder A, Costi S, Rutter SB, et al. A randomized controlled trial of repeated ketamine administration for chronic posttraumatic stress disorder. Am J Psychiatry. 2021; 178(2):193-202. doi:10.1176/appi.ajp.2020.20050596

[55]

Ragnhildstveit A, Roscoe J, Bass LC, Averill CL, Abdallah CG, Averill LA. The potential of ketamine for posttraumatic stress disorder: a review of clinical evidence. Ther Adv Psychopharmacol. 2023; 13:20451253231154125. doi:10.1177/20451253231154125

[56]

Sbarski B, Akirav I.Cannabinoids as therapeutics for PTSD. Pharmacol Ther. 2020; 211:107551. doi:10.1016/j.pharmthera.2020.107551

[57]

Ney LJ, Matthews A, Bruno R, Felmingham KL. Cannabinoid interventions for PTSD: where to next? Prog Neuropsychopharmacol Biol Psychiatry. 2019; 93:124-140. doi:10.1016/j.pnpbp.2019.03.017

[58]

Florido A, Velasco ER, Monari S, et al.Glucocorticoid-based pharmacotherapies preventing PTSD. Neuropharmacology. 2023; 224:109344. doi:10.1016/j.neuropharm.2022.109344

[59]

Golier JA, Li X, Bizien M, et al. Efficacy and safety of mifepristone in the treatment of male US veterans with posttraumatic stress disorder: a phase 2a randomized clinical trial. JAMA Netw Open. 2023; 6(5):e2310223. doi:10.1001/jamanetworkopen.2023.10223

[60]

Gasparyan A, Navarro D, Navarrete F, Manzanares J. Pharmacological strategies for post-traumatic stress disorder (PTSD): from animal to clinical studies. Neuropharmacology. 2022; 218:109211. doi:10.1016/j.neuropharm.2022.109211

[61]

Lago TR, Brownstein MJ, Page E, et al. The novel vasopressin receptor (V1aR) antagonist SRX246 reduces anxiety in an experimental model in humans: a randomized proof-of-concept study. Psychopharmacology (Berl). 2021; 238(9):2393-2403. doi:10.1007/s00213-021-05861-4

[62]

“FDA grants Breakthrough Therapy Designation for Roche's balovaptan in autism spectrum disorder” (Press release).https://www.reuters.com/article/business/roche-wins-fda-s-breakthrough-therapy-label-for-autism-drug-idUSKBN1FI0HS/. Accessed December 13, 2023

[63]

Raskind MA, Peterson K, Williams T, et al. A trial of prazosin for combat trauma PTSD with nightmares in active-duty soldiers returned from Iraq and Afghanistan. Am J Psychiatry. 2013; 170(9):1003-1010. doi:10.1176/appi.ajp.2013.12081133

[64]

Raskind MA, Peskind ER, Chow B, et al. Trial of prazosin for post-traumatic stress disorder in military veterans. N Engl J Med. 2018; 378(6):507-517. doi:10.1056/NEJMoa1507598

[65]

Ehlers A, Clark DM, Hackmann A, McManus F, Fennell M. Cognitive therapy for post-traumatic stress disorder: development and evaluation. Behav Res Ther. 2005; 43(4):413-431. doi:10.1016/j.brat.2004.03.006

[66]

Roberts NP, Kitchiner NJ, Kenardy J, Robertson L, Lewis C, Bisson JI. Multiple session early psychological interventions for the prevention of post-traumatic stress disorder. Cochrane Database Syst Rev. 2019; 8(8):CD006869. doi:10.1002/14651858.CD006869.pub3

[67]

Foa EB, McLean CP, Zang Y, et al. Effect of prolonged exposure therapy delivered over 2 weeks vs 8 weeks vs present-centered therapy on PTSD symptom severity in military personnel: a randomized clinical trial. JAMA. 2018; 319(4):354-364. doi:10.1001/jama.2017.21242

[68]

Seidler GH, Wagner FE. Comparing the efficacy of EMDR and trauma-focused cognitive-behavioral therapy in the treatment of PTSD: a meta-analytic study. Psychol Med. 2006; 36(11):1515-1522. doi:10.1017/S0033291706007963

[69]

Kothgassner OD, Goreis A, Kafka JX, Van Eickels RL, Plener PL, Felnhofer A. Virtual reality exposure therapy for posttraumatic stress disorder (PTSD): a meta-analysis. Eur J Psychotraumatol. 2019; 10(1):1654782. doi:10.1080/20008198.2019.1654782

[70]

Hofmann SG, Gómez AF. Mindfulness-based interventions for anxiety and depression. Psychiatr Clin North Am. 2017; 40(4):739-749. doi:10.1016/j.psc.2017.08.008

[71]

Sarris J, McIntyre E, Camfield DA. Plant-based medicines for anxiety disorders, part 2: a review of clinical studies with supporting preclinical evidence. CNS Drugs. 2013; 27(4):301-319. doi:10.1007/s40263-013-0059-9

[72]

Chen XD, Wei JX, Wang HY, et al. Effects and mechanisms of salidroside on the behavior of SPS-induced PTSD rats. Neuropharmacology. 2023; 240:109728. doi:10.1016/j.neuropharm.2023.109728

[73]

Hediger K, Wagner J, Künzi P, et al. Effectiveness of animal-assisted interventions for children and adults with post-traumatic stress disorder symptoms: a systematic review and meta-analysis. Eur J Psychotraumatol. 2021; 12(1):1879713. doi:10.1080/20008198.2021.1879713

[74]

Pezzin LE, Larson ER, Lorber W, McGinley EL, Dillingham TR. Music-instruction intervention for treatment of post-traumatic stress disorder: a randomized pilot study. BMC Psychol. 2018; 6(1):60. doi:10.1186/s40359-018-0274-8

[75]

Baker FA, Metcalf O, Varker T, O'Donnell M. A systematic review of the efficacy of creative arts therapies in the treatment of adults with PTSD. Psychol Trauma. 2018; 10(6):643-651. doi:10.1037/tra0000353

[76]

Streeter CC, Gerbarg PL, Saper RB, Ciraulo DA, Brown RP. Effects of yoga on the autonomic nervous system, gamma-aminobutyric-acid, and allostasis in epilepsy, depression, and post-traumatic stress disorder. Med Hypotheses. 2012; 78(5):571-579. doi:10.1016/j.mehy.2012.01.021

[77]

Gazzato A, Scquizzato T, Imbriaco G, et al. The effect of intensive care unit diaries on posttraumatic stress disorder, anxiety, and depression: a systematic review and meta-analysis of randomized controlled trials. Dimens Crit Care Nurs. 2022; 41(5):256-263. doi:10.1097/DCC.0000000000000539

[78]

Hu RF, Jiang XY, Chen J, et al. Non-pharmacological interventions for sleep promotion in the intensive care unit. Cochrane Database Syst Rev. 2015; 2015(10): CD008808. doi:10.1002/14651858.CD008808.pub2

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