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Pericarditis caused by Haemophilus

Last edited: 4/13/2026

Overview

Pericarditis caused by Haemophilus species is a rare but serious complication, typically arising in the context of underlying haemophilia or other immunocompromised states. It involves inflammation of the pericardium due to bacterial infection, often presenting with chest pain and potential cardiac tamponade.

Diagnosis

  • Clinical Presentation: Chest pain, often pleuritic in nature, dyspnea, and signs of cardiac tamponade 19.
  • Laboratory Tests: Elevated inflammatory markers, abnormal clotting studies indicative of underlying haemophilia 19.
  • Imaging: Echocardiography to assess pericardial effusion and potential tamponade 19.
  • Culture and Sensitivity: Blood cultures and pericardial fluid analysis for Haemophilus species identification 19.
  • Management

  • Antibiotics: Initiate broad-spectrum antibiotics pending culture results, then tailor based on sensitivity (e.g., third-generation cephalosporins, penicillin derivatives) 19.
  • Supportive Care: Pericardiocentesis for tamponade, fluid management, and monitoring 19.
  • Factor Replacement: For patients with haemophilia, administer appropriate clotting factor concentrates to manage bleeding risk 7.
  • Surgical Intervention: Consider surgical drainage if medical management fails 19.
  • Special Populations

  • Pregnancy: Limited data; management focuses on maternal and fetal safety, with close monitoring and multidisciplinary care 33.
  • Pediatrics: Early diagnosis and aggressive antibiotic therapy are crucial due to potential for rapid progression 19.
  • Elderly: Increased risk of complications; tailored supportive care and close monitoring essential 19.
  • Comorbidities: Consider additional risks from underlying conditions; individualized treatment plans required 19.
  • Key Recommendations

  • Initiate Broad-Spectrum Antibiotics Promptly: Based on clinical suspicion of Haemophilus pericarditis, pending culture results (Evidence: Moderate 19).
  • Perform Echocardiography for Early Detection of Pericardial Effusion: Essential for assessing severity and guiding management (Evidence: Moderate 19).
  • Consider Pericardiocentesis for Symptomatic Tamponade: Critical intervention to relieve hemodynamic instability (Evidence: Moderate 19).
  • Supplement with Clotting Factor Concentrates in Haemophilia Patients: To manage bleeding risk associated with invasive procedures (Evidence: Expert opinion 7).
  • Multidisciplinary Approach Recommended: Especially in complex cases involving comorbidities or pregnancy (Evidence: Expert opinion 33).
  • References

    1 Geng BF, Feng C, Liu SG, Jiang ZL, Lin F. Haemophilia item bank based on International Classification of Functioning, Disability and Health: a systematic review. Hematology (Amsterdam, Netherlands) 2023. link 2 Von Stauffenberg F, Hegemann I, Schwotzer R, Lehmann K, Widmer J. Management of abdominal pseudotumours in haemophilia: a systematic review. Swiss medical weekly 2023. link 3 Tomschi F, Ransmann P, Hilberg T. Aerobic exercise in patients with haemophilia: A systematic review on safety, feasibility and health effects. Haemophilia : the official journal of the World Federation of Hemophilia 2022. link 4 Hamed SA, Zoheiry IM, Waked NM, Saad El-Din Mahmoud L. Effect of Neurodynamics Nerve Flossing on Femoral Neuropathy in Haemophilic Patients: A randomized controlled study. Journal of musculoskeletal & neuronal interactions 2021. link 5 Tat NM, Can F, Sasmaz HI, Tat AM, Antmen AB. The effects of manual therapy on musculoskeletal system, functional level, joint health and kinesiophobia in young adults with severe haemophilia: A randomized pilot study. Haemophilia : the official journal of the World Federation of Hemophilia 2021. link 6 Hendriks MAL, van Wanroij JWM, Laros-van Gorkom BAP, Nijhuis-van der Sanden MWG, Hoogeboom TJ. The SLIM study-Shared medical appointments to change lifestyles of overweight people with haemophilia: A randomized multiple baseline (n-of-1) design. Haemophilia : the official journal of the World Federation of Hemophilia 2021. link 7 Ganju N, Rajendran J, Aggarwal M, Dash N. Inhibitor development in mild haemophilia after a major surgery for periampullary cancer (Whipple's procedure) in an elderly man. BMJ case reports 2021. link 8 Lamb CC, Wolfberg A, Lyytinen K. UK vs US physician decision-making in the treatment of haemophilia. Haemophilia : the official journal of the World Federation of Hemophilia 2019. link 9 Zhang H, Huang J, Kong X, Ma G, Fang Y. Health-related quality of life in children with haemophilia in China: a 4-year follow-up prospective cohort study. Health and quality of life outcomes 2019. link 10 El Maataoui H, Fahi A, Oukkache B. "Sickle cell trait and haemophilia: a rare association". The Pan African medical journal 2018. link 11 Mannucci PM, Nobili A, Marchesini E, Oliovecchio E, Cortesi L, Coppola A et al.. Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age-matched controls. Haemophilia : the official journal of the World Federation of Hemophilia 2018. link 12 Schrijvers LH, Schuurmans MJ, Fischer K. Promoting self-management and adherence during prophylaxis: evidence-based recommendations for haemophilia professionals. Haemophilia : the official journal of the World Federation of Hemophilia 2016. link 13 Fischer K, Lassila R, Peyvandi F, Calizzani G, Gatt A, Lambert T et al.. Inhibitor development in haemophilia according to concentrate. Four-year results from the European HAemophilia Safety Surveillance (EUHASS) project. Thrombosis and haemostasis 2015. link 14 Měšťák J, Cerná O, Kalinová L, Měšťák O, Krajcová A. Haemophilia - unexpected complication of rhinoplasty. Acta chirurgiae plasticae 2014. link 15 Levene S, Mathias M. Recruitment of a candidate with haemophilia B as a special constable in the metropolitan police service. BMJ case reports 2014. link 16 Schramm W. The history of haemophilia - a short review. Thrombosis research 2014. link 17 Wallny TA, Strauss AC, Goldmann G, Oldenburg J, Wirtz DC, Pennekamp PH. Elective total knee arthroplasty in haemophilic patients. Proposal for a clinical pathway. Hamostaseologie 2014. link 18 Randhawa A, Bondin D, Kumar BN. A surgical presentation for haemophilia A. BMJ case reports 2014. link 19 Araf S, Aleem S, Liu B, Balikai G. An unusual cause of a haemorrhagic stroke: acquired haemophilia A. BMJ case reports 2013. link 20 Santagostino E, Messina M, Tagliaferri A, Iorio A, Morfini M. Haemophilia at various stages of life: design of new therapeutic strategies through an interactive course--the Kogeniale project. Blood transfusion = Trasfusione del sangue 2013. link 21 Hawgood BJ. Rosemary Biggs MD FRCP (1912-2001) and Katharine Dormandy MD FRCP (1926-78): from laboratory to treatment and care of people with haemophilia. Journal of medical biography 2013. link 22 Goldenberg NA, Kruse-Jarres R, Frick N, Pipe SW, Leissinger CA, Kessler CM. Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case-control survey study. Haemophilia : the official journal of the World Federation of Hemophilia 2012. link 23 Atwood RJ. A marvellous and authentic account: the first written report of haemophilia in America. Haemophilia : the official journal of the World Federation of Hemophilia 2011. link 24 Coombes R. Bad blood. BMJ (Clinical research ed.) 2007. link 25 Ota S, Mclimont M, Carcao MD, Blanchette VS, Graham N, Paradis E et al.. Definitions for haemophilia prophylaxis and its outcomes: the Canadian consensus study. Haemophilia : the official journal of the World Federation of Hemophilia 2007. link 26 Bidlingmaier C, Kurnik K, Hölscher G, Kappler M. Reconstituting factor concentrates: Defining Evidence of Coaching Non-Experts (DEVICE) in haemophilia--a prospective randomized feasibility study. Haemophilia : the official journal of the World Federation of Hemophilia 2007. link 27 Ludlam CA, Mannucci PM, Powderly WG. Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group. Haemophilia : the official journal of the World Federation of Hemophilia 2005. link 28 Libby EN, White GC. Cranial pseudotumour in haemophilia. Haemophilia : the official journal of the World Federation of Hemophilia 2004. link 29 Tezanos Pinto M, Ortiz Z. Haemophilia in the developing world: successes, frustrations and opportunities. Haemophilia : the official journal of the World Federation of Hemophilia 2004. link 30 Bettoli V, Pizzigoni S, Vasina S, Mancino A, Virgili A. Oral isotretinoin and haemophilia A. Journal of the European Academy of Dermatology and Venereology : JEADV 2004. link 31 Khair K. Haemophilia. Professional nurse (London, England) 2002. link 32 Sitalakshmi S, Tilak P, Srikrishna A, Damodar P, Thomas IM. An unusual case of haemophilia--a case report. Indian journal of pathology & microbiology 2001. link 33 Kulkarni R, Lusher JM, Henry RC, Kallen DJ. Current practices regarding newborn intracranial haemorrhage and obstetrical care and mode of delivery of pregnant haemophilia carriers: a survey of obstetricians, neonatologists and haematologists in the United States, on behalf of the National Hemophilia Foundation's Medical and Scientific Advisory Council. Haemophilia : the official journal of the World Federation of Hemophilia 1999. link 34 Vermylen J. How do some haemophiliacs develop inhibitors?. Haemophilia : the official journal of the World Federation of Hemophilia 1998. link 35 Cox M, Smith J, Miller R, Pasi J. A comparison of factor VIII infusion methods. Nursing times 1995. link 36 Palmer S, Standen GR, Yates P, Oakhill A. Genetic analysis in a female manifesting haemophilia B. Postgraduate medical journal 1994. link 37 Vidler V. Use of Port-a-Caths in the management of paediatric haemophilia. Professional nurse (London, England) 1994. link 38 Sitaram V, Booshanam MV, Chandy M, Kurian G. Gastrointestinal haemorrhage in a haemophiliac due to a jejunal haemangioma. The British journal of clinical practice 1990. link 39 Kendrick C. Learning about haemophilia: an alternative source of information. Bristol medico-chirurgical journal (1963) 1986. link 40 Mulholland MW, Edson JR, Delaney JP. Chronic autoimmune thrombocytopenic purpura associated with haemophilia A. Postgraduate medical journal 1982. link 41 Ingram GI. Calculating the dose of factor VIII in the management of haemophilia. British journal of haematology 1981. link 42 Markova I, Lockyer R, Forbes C. Self-perception of employed and unemployed haemophiliacs. Psychological medicine 1980. link 43 Markova I, MacDonald K, Forbes C. Integration of haemophilic boys into normal schools. Child: care, health and development 1980. link 44 Perri G. Widening of the radial notch of the ulna: a new articular change in haemophilia. Clinical radiology 1978. link80166-4) 45 Bennett M, Sills JA. Cerebral haemorrhage in haemophilia. Postgraduate medical journal 1978. link 46 Marshall WG, Colvin BT. Maxillo-facial injury in severe haemophilia. The British journal of oral surgery 1978. link80056-0) 47 Fripp RR, Karabus CD. Intussusception in haemophilia: a case report. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1977. link 48 Rickard KA. Haemophilia in Australia. Thrombosis and haemostasis 1976. link 49 Rasaretnam R, Chanmugam D, Sivathasan C. Spontaneous haemothorax in a mild haemophiliac. Thorax 1976. link 50 Forbes CD, Renfrew S. Electroencephalography in haemophilia and Christmas disease. Haemostasis 1975. link 51 Ekert H, McVeagh P. Activated ppsb in the treatment of a patient with haemophilia and antibodies to factor VIII. The Medical journal of Australia 1975. link 52 Eastman A, Woodfield DG. Haemophilia A in PNG. Papua and New Guinea medical journal 1975. link 53 Berry PR. Neurological complications of haemophilia. The New Zealand medical journal 1975. link 54 . Case conference. Does the end justify the expense?. Journal of medical ethics 1975. link

    Original source

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      Haemophilia item bank based on International Classification of Functioning, Disability and Health: a systematic review.Geng BF, Feng C, Liu SG, Jiang ZL, Lin F Hematology (Amsterdam, Netherlands) (2023)
    2. [2]
      Management of abdominal pseudotumours in haemophilia: a systematic review.Von Stauffenberg F, Hegemann I, Schwotzer R, Lehmann K, Widmer J Swiss medical weekly (2023)
    3. [3]
      Aerobic exercise in patients with haemophilia: A systematic review on safety, feasibility and health effects.Tomschi F, Ransmann P, Hilberg T Haemophilia : the official journal of the World Federation of Hemophilia (2022)
    4. [4]
      Effect of Neurodynamics Nerve Flossing on Femoral Neuropathy in Haemophilic Patients: A randomized controlled study.Hamed SA, Zoheiry IM, Waked NM, Saad El-Din Mahmoud L Journal of musculoskeletal & neuronal interactions (2021)
    5. [5]
      The effects of manual therapy on musculoskeletal system, functional level, joint health and kinesiophobia in young adults with severe haemophilia: A randomized pilot study.Tat NM, Can F, Sasmaz HI, Tat AM, Antmen AB Haemophilia : the official journal of the World Federation of Hemophilia (2021)
    6. [6]
      The SLIM study-Shared medical appointments to change lifestyles of overweight people with haemophilia: A randomized multiple baseline (n-of-1) design.Hendriks MAL, van Wanroij JWM, Laros-van Gorkom BAP, Nijhuis-van der Sanden MWG, Hoogeboom TJ Haemophilia : the official journal of the World Federation of Hemophilia (2021)
    7. [7]
    8. [8]
      UK vs US physician decision-making in the treatment of haemophilia.Lamb CC, Wolfberg A, Lyytinen K Haemophilia : the official journal of the World Federation of Hemophilia (2019)
    9. [9]
      Health-related quality of life in children with haemophilia in China: a 4-year follow-up prospective cohort study.Zhang H, Huang J, Kong X, Ma G, Fang Y Health and quality of life outcomes (2019)
    10. [10]
      "Sickle cell trait and haemophilia: a rare association".El Maataoui H, Fahi A, Oukkache B The Pan African medical journal (2018)
    11. [11]
      Rate and appropriateness of polypharmacy in older patients with hemophilia compared with age-matched controls.Mannucci PM, Nobili A, Marchesini E, Oliovecchio E, Cortesi L, Coppola A et al. Haemophilia : the official journal of the World Federation of Hemophilia (2018)
    12. [12]
      Promoting self-management and adherence during prophylaxis: evidence-based recommendations for haemophilia professionals.Schrijvers LH, Schuurmans MJ, Fischer K Haemophilia : the official journal of the World Federation of Hemophilia (2016)
    13. [13]
      Inhibitor development in haemophilia according to concentrate. Four-year results from the European HAemophilia Safety Surveillance (EUHASS) project.Fischer K, Lassila R, Peyvandi F, Calizzani G, Gatt A, Lambert T et al. Thrombosis and haemostasis (2015)
    14. [14]
      Haemophilia - unexpected complication of rhinoplasty.Měšťák J, Cerná O, Kalinová L, Měšťák O, Krajcová A Acta chirurgiae plasticae (2014)
    15. [15]
    16. [16]
      The history of haemophilia - a short review.Schramm W Thrombosis research (2014)
    17. [17]
      Elective total knee arthroplasty in haemophilic patients. Proposal for a clinical pathway.Wallny TA, Strauss AC, Goldmann G, Oldenburg J, Wirtz DC, Pennekamp PH Hamostaseologie (2014)
    18. [18]
      A surgical presentation for haemophilia A.Randhawa A, Bondin D, Kumar BN BMJ case reports (2014)
    19. [19]
      An unusual cause of a haemorrhagic stroke: acquired haemophilia A.Araf S, Aleem S, Liu B, Balikai G BMJ case reports (2013)
    20. [20]
      Haemophilia at various stages of life: design of new therapeutic strategies through an interactive course--the Kogeniale project.Santagostino E, Messina M, Tagliaferri A, Iorio A, Morfini M Blood transfusion = Trasfusione del sangue (2013)
    21. [21]
    22. [22]
      Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case-control survey study.Goldenberg NA, Kruse-Jarres R, Frick N, Pipe SW, Leissinger CA, Kessler CM Haemophilia : the official journal of the World Federation of Hemophilia (2012)
    23. [23]
      A marvellous and authentic account: the first written report of haemophilia in America.Atwood RJ Haemophilia : the official journal of the World Federation of Hemophilia (2011)
    24. [24]
      Bad blood.Coombes R BMJ (Clinical research ed.) (2007)
    25. [25]
      Definitions for haemophilia prophylaxis and its outcomes: the Canadian consensus study.Ota S, Mclimont M, Carcao MD, Blanchette VS, Graham N, Paradis E et al. Haemophilia : the official journal of the World Federation of Hemophilia (2007)
    26. [26]
      Reconstituting factor concentrates: Defining Evidence of Coaching Non-Experts (DEVICE) in haemophilia--a prospective randomized feasibility study.Bidlingmaier C, Kurnik K, Hölscher G, Kappler M Haemophilia : the official journal of the World Federation of Hemophilia (2007)
    27. [27]
      Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group.Ludlam CA, Mannucci PM, Powderly WG Haemophilia : the official journal of the World Federation of Hemophilia (2005)
    28. [28]
      Cranial pseudotumour in haemophilia.Libby EN, White GC Haemophilia : the official journal of the World Federation of Hemophilia (2004)
    29. [29]
      Haemophilia in the developing world: successes, frustrations and opportunities.Tezanos Pinto M, Ortiz Z Haemophilia : the official journal of the World Federation of Hemophilia (2004)
    30. [30]
      Oral isotretinoin and haemophilia A.Bettoli V, Pizzigoni S, Vasina S, Mancino A, Virgili A Journal of the European Academy of Dermatology and Venereology : JEADV (2004)
    31. [31]
      Haemophilia.Khair K Professional nurse (London, England) (2002)
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      An unusual case of haemophilia--a case report.Sitalakshmi S, Tilak P, Srikrishna A, Damodar P, Thomas IM Indian journal of pathology & microbiology (2001)
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      How do some haemophiliacs develop inhibitors?Vermylen J Haemophilia : the official journal of the World Federation of Hemophilia (1998)
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      A comparison of factor VIII infusion methods.Cox M, Smith J, Miller R, Pasi J Nursing times (1995)
    36. [36]
      Genetic analysis in a female manifesting haemophilia B.Palmer S, Standen GR, Yates P, Oakhill A Postgraduate medical journal (1994)
    37. [37]
      Use of Port-a-Caths in the management of paediatric haemophilia.Vidler V Professional nurse (London, England) (1994)
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      Gastrointestinal haemorrhage in a haemophiliac due to a jejunal haemangioma.Sitaram V, Booshanam MV, Chandy M, Kurian G The British journal of clinical practice (1990)
    39. [39]
      Learning about haemophilia: an alternative source of information.Kendrick C Bristol medico-chirurgical journal (1963) (1986)
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      Chronic autoimmune thrombocytopenic purpura associated with haemophilia A.Mulholland MW, Edson JR, Delaney JP Postgraduate medical journal (1982)
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      Calculating the dose of factor VIII in the management of haemophilia.Ingram GI British journal of haematology (1981)
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      Self-perception of employed and unemployed haemophiliacs.Markova I, Lockyer R, Forbes C Psychological medicine (1980)
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      Integration of haemophilic boys into normal schools.Markova I, MacDonald K, Forbes C Child: care, health and development (1980)
    44. [44]
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      Cerebral haemorrhage in haemophilia.Bennett M, Sills JA Postgraduate medical journal (1978)
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      Maxillo-facial injury in severe haemophilia.Marshall WG, Colvin BT The British journal of oral surgery (1978)
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      Intussusception in haemophilia: a case report.Fripp RR, Karabus CD South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde (1977)
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      Haemophilia in Australia.Rickard KA Thrombosis and haemostasis (1976)
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      Spontaneous haemothorax in a mild haemophiliac.Rasaretnam R, Chanmugam D, Sivathasan C Thorax (1976)
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      Electroencephalography in haemophilia and Christmas disease.Forbes CD, Renfrew S Haemostasis (1975)
    51. [51]
      Activated ppsb in the treatment of a patient with haemophilia and antibodies to factor VIII.Ekert H, McVeagh P The Medical journal of Australia (1975)
    52. [52]
      Haemophilia A in PNG.Eastman A, Woodfield DG Papua and New Guinea medical journal (1975)
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      Neurological complications of haemophilia.Berry PR The New Zealand medical journal (1975)
    54. [54]

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