Patient Education Blog

Psychological Impact of Having a Blood Clot

Beth Waldron, Program Director of Clot Connect writes…

The person diagnosed with a blood clot may develop depression and anxiety, particularly if the clot was extensive and life-threatening.  This can be difficult to deal with.  Emotional states (such as depression, anxiety, happiness and optimism) have been shown to influence health outcomes in many medical conditions. ([1],[2],[3])  However, very little research has been done examining the psychological impact of a blood clot on a patient’s health outcome.

What is known about the psychological impact of having a blood clot? 

High levels of anxiety, depression and psychological stress have been reported among patients with deep vein thrombosis-DVT or pulmonary embolism-PE (DVT and PE are referred to collectively as VTE or venous thromboembolism).([4],[5]) This may be attributed to several factors:

  1. VTE is an acute and potentially life-threatening medical event.  Anxiety and depression are common mood responses early after diagnosis of acute conditions in general.(3,4)
  2. Both DVT and PE affect daily functioning, which can induce anxiety and depression. It is not uncommon for VTE patients to report pain, limited mobility, perceptions of impairments at home and work, and general feelings of stress associated with these impairments.(5)
  3. The use of warfarin and other blood thinners is a factor leading to anxiety and depression.(4) This may occur due to the lifestyle impact and management challenges of blood thinners or may be due to a patient worrying about bleeding risk.([6],[7])  Being on warfarin has unique management issues which impact lifestyle and, therefore, may induce additional anxiety—such as with the need for frequent (INR monitoring), and close attention to diet and medication interactions. Having to self-inject blood thinners underneath the skin, such as low-molecular weight heparins (Enoxaparin = Lovenox®, Dalteparin = Fragmin®, Tinzaparin = Innohep®) or Fondaparinux (Arixtra®) can also be anxiety provoking for some patients. While, to my knowledge self-injection fears have not been examined specifically among VTE patients, the fear of medication self-injection and its relationship to anxiety has been well-documented in other diseases states, such as diabetes and multiple sclerosis.
  4. Patients with post-thrombotic syndrome (i.e. the long-term damage in an extremity which occurs in approximately 40% of DVT patients) report lowered quality of life. This may be due to chronic pain, swelling and decreased mobility.([8])
  5. Patients with pulmonary embolism have been shown to have significantly lower quality of life, impairment of physical performance and social activities, even among PE patients who do not experience chronic lung damage (such as pulmonary hypertension).(2)  Additionally, difficulty breathing and lowered blood oxygen saturation levels that patients may experience when they have an acute PE may lead to anxiety and depression.(4,[9]The association between shortness of breath and anxiety has been documented in a number of other diseases.
  6. The psychological impact of being diagnosed with a clotting disorder (thrombophilia) following a VTE event is unclear. While there have been studies examining the psychological impact of thrombophilia testing, results have been inconsistent or of limited scope to be widely applicable.([10],[11]) Additional studies are needed to more fully understand the emotional impact of thrombophilia testing on patients and family members, particularly if a strong clotting disorder is identified.
  7. The fear of a clot recurrence is common among VTE patients. However, to the best of my knowledge, a gap in the literature exists directly examining this fear perception and its impact on quality of life and health outcomes.
  8. Patients with unprovoked VTE and patients with VTE who have a permanent risk factor (such as chronic immobility, strong clotting disorder, strong family history) have been shown to experience lower quality of life than patients whose clots were caused by transient risk factors (such as major surgery or major trauma).(2) This may be because patients with clots caused by transient risk factors may view the VTE as a ‘one-time event’ with a clearly identified cause which can be avoided in the future. Patients with an unexplained (=idiopathic) clot, on the other hand, in whom no reason for the clot has been found, may worry more about a recurrent out-of-the blue event, as they do not have any modifiable/avoidable risk factors.

The psychological impact of VTE on patient health is an understudied area.  The limited studies which have been done reinforce what is often experienced by patients: that DVT and PE do have a significant emotional impact on patients and their quality of life, not just immediately after diagnosis, but for years afterwards.

 What can patients do to address the emotional impact of a blood clot? 

  • Patients should know that feelings of anxiety and depressed mood following VTE are normal responses.  They and their family members should be alert to changes in mood that do not improve or are accompanied by a withdrawal from activities or increased negative thoughts and tearfulness, as this may indicate a more severe depression requiring treatment.
  • Patients should mention these symptoms to their health care professional.
  • Sometimes, the use of anti-depressant medication for some period of time is appropriate and should be considered.  Referral to a social worker who helps with work related problems or financial issues that contribute to depression might be appropriate. And referral to a psychologist may, at times, also be helpful.
  • Treatment should also be geared towards trying to prevent and manage post-thrombotic syndrome (PTS), as presence of PTS has been shown to be the principal determinant of quality of life 2 years after DVT.(8) Compression stockings should be started as soon as possible after DVT for maximum effectiveness and should be consistently used.
  • Connecting socially to other people with shared experiences has been shown to have positive health effects([12]). Unfortunately, very few formal support groups for the VTE patients exist in the U.S. Some online groups exist. Clot Connect provides an online discussion and support forum where patients and families can connect to share information and experiences, and find support. The support forum can be found at:


 Patients’ comments reflecting the emotional impact of a blood clot

Below are excerpts from posts by VTE patients on Clot Connect’s discussion board and social media forums, which reflect the emotional impact of VTE:


  • “I didn’t realize the mental burden the clot would have. Five years later and anytime I have a symptom – my mind automatically thinks there’s the possibility it could be a clot!”
  • “It was one of the scariest things I’ve had happen to me, not to mention all of the things you have to go through afterwards (i.e. the injections). I cried for the first week.”
  •  “While I’ve fully recovered, play sports, do stuff with my family, and live a normal life, it never leaves you completely, the details, the memory of not being able to take a breath. I still get a little chill when I think about it. What a thing.”
  • It is “is a constant worry it will happen again. The fact is that this event takes a huge emotional toll on you!”
  • “Knowing I had a clot put me in an emotional whirlwind and I just wish I had someone telling me ‘it is going to be ok, we’re doing everything we can to make this better’ but I never got that.”
  •  “It’s good to know that I’m not the only one who was overwhelmed after being diagnosed with a DVT; it was truly life changing.”
  • I have a “fear of dying suddenly”.
  • “I have been struggling with dealing with the aftermath of this life changing event.”
  •  Immediately after diagnosis “you don’t really have time to assess the emotions. You’re kind of on auto pilot. Couple of years later, it catches up with you.”
  • “I think of my husband witnessing my collapse in our home, an image that still haunts him even now.”


[1] Enga KF, Brækkan SK, Hansen-Krone IJ, Hansen JB. Emotional states and future risk of venous thromboembolism. The Tromsø Study. Thromb Haemost. 2012 Feb 8;107(3). [Epub ahead of print]

[2] Klok FA, van Kralingen KW, van Dijk AP, Heyning FH, Vliegen HW, Kaptein AA, Huisman MV. Quality of life in long-term survivors of acute pulmonary embolism. Chest. 2010 Dec;138(6):1432-40. Epub 2010 May 21.

 [3] Chida Y, Steptoe A. Positive psychological well-being and mortality: a quantitative review of prospective observational studies. Psychosom Med. 2008 Sep;70(7):741-56. Epub 2008 Aug 25.

 [4] Liu CP, Li XM, Chen HW, Cui JY, Niu LL, He YB, Tian XL. Depression, anxiety and influencing factors in patients with acute pulmonary embolism. Chin Med J (Engl). 2011 Aug;124(16):2438-42.

 [5] Lukas PS, Krummenacher R, Biasiutti FD, Begré S, Znoj H, von Känel R. Association of fatigue and psychological distress with quality of life in patients with a previous venous thromboembolic event. J Thromb Haemost. 2009 Dec;102(6):1219-26.

 [6] Abray KD, Paul DW, Oliver JC, Robert MW. The impact of long-term warfarin on the quality of life of elderly people with atrial fibrillation. Age and Ageing. 2007;36:95–97.

 [7] Geisa de Queiroz Almeida, Lúcia de ACB Noblat, Luiz Carlos Santana Passos, and Harrison Floriano do Nascimento Quality of Life analysis of patients in chronic use of oral anticoagulant: an observational study Health Qual Life Outcomes 2011; 9: 91.

 [8] Kahn SR, Shbaklo H, Lamping DL, Holcroft CA, Shrier I, Miron MJ, Roussin A, Desmarais S, Joyal F, Kassis J, Solymoss S,Desjardins L, Johri M, Ginsberg JS. Determinants of health-related quality of life during the 2 years following deep vein thrombosis. J Thromb Haemost 2008; 6: 1105–12.

 [9] Banzett RB, Pedersen SH, Schwartzstein RM, Lansing RW. The affective dimension of laboratory dyspnea: air hunger is more unpleasant than work/effort. Am J Respir Crit Care Med. 2008 Jun 15;177(12):1384-90.

 [10] Cohn DM, Vansenne F, Kaptein AA, De Borgie CA, Middeldorp S.The psychological impact of testing for thrombophilia: a systematic review. J Thromb Haemost. 2008 Jul;6(7):1099-104.

 [11] Hellman EA, Leslie N, Moll S: Knowledge and Information Satisfaction of Individuals with Factor V Leiden Mutation. J Thromb Haemost. 2003;1:2335-9

 [12] Umberson D, Montez JK. Social relationships and health: a flashpoint for health policy. J Health Soc Behav. 2010;51 Suppl:S54-66.


Written by Beth Wadron, MA; Reviewed by Stephan Moll, MD

Disclosures: I have no financial disclosures relevant to this blog post.
Last updated: Feb 28th, 2012

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One Response to “Psychological Impact of Having a Blood Clot”

  1. Lisa Copeland says:

    Oh my Goodness! I’ve been a silent partner on this DVT site. I do read all of the feeds, but the “psychological” part really got my attention. It has been a little over 2 years since my DVT-PE. Just a refresher for those that may not remember my story. When I finally decided I needed to go to the Dr. I had a massive clot from my belly to my foot on my left side. I had clots that had traveled to both lungs. I am on 325 aspirin daily now and have my leg ultrasounded every 6 months. Being followed up with a Vascular Surgeon who is very knowledgable in MTS. He came to Heart Hospital OKC from Dallas, Dr. Lenny Stubbs. Wonderful man. The last 6 months it has hit me, didn’t realize until reading the post, thought maybe it was Menopausal, maybe it was losing my mom not quite 5 years ago. But, after reading I’m thinking this is what it is. I was on anti-depressants and we were weaning me when I had my DVT, so we stayed on them for awhile. When I was over the hump, I was ready to come off of them. Haven’t been on anti depressants for over 2 years. My family has strongly urged me to seek help, but I hate the side effects of anti-depressants. I’m really close to seeking help, but such an emotional wreck that I think all I would do is cry. I am in constant pain in my leg, any pain that is above and beyond I think, What if?

    Lisa Copeland