Bleeding due to severe thrombocytopenia
The immediate goal is to stop the bleeding.
Close observation of respiratory and cardiovascular status is required. Intravenous fluid support and positive inotropic agents are given as required.
A thorough history and physical examination followed by a CBC and peripheral smear are usually sufficient to guide initial treatment. Prothrombin time, activated partial thromboplastin time, and fibrinogen can help distinguish disseminated intravascular coagulation from thrombotic thrombocytopenic purpura. CT head should be performed for suspected intracranial hemorrhage.
Any anticoagulant or antiplatelet drugs should be withdrawn.[24]Cooper N, Ghanima W. Immune thrombocytopenia. N Engl J Med. 2019 Sep 5;381(10):945-55.
https://www.doi.org/10.1056/NEJMcp1810479
http://www.ncbi.nlm.nih.gov/pubmed/31483965?tool=bestpractice.com
Patients with severe thrombocytopenia due to ITP often receive IV immunoglobulin and glucocorticoids. Antifibrinolytic agents may be used for life-threatening bleeding associated with ITP.[4]Provan D, Arnold DM, Bussel JB, et al. Updated international consensus report on the investigation and management of primary immune thrombocytopenia. Blood Adv. 2019 Nov 26;3(22):3780-817.
https://ashpublications.org/bloodadvances/article/3/22/3780/428877/Updated-international-consensus-report-on-the
http://www.ncbi.nlm.nih.gov/pubmed/31770441?tool=bestpractice.com
[24]Cooper N, Ghanima W. Immune thrombocytopenia. N Engl J Med. 2019 Sep 5;381(10):945-55.
https://www.doi.org/10.1056/NEJMcp1810479
http://www.ncbi.nlm.nih.gov/pubmed/31483965?tool=bestpractice.com
[25]Blanchette V, Imbach P, Andrew M, et al. Randomised trial of intravenous immunoglobulin G, intravenous anti-D, and oral prednisone in childhood acute immune thrombocytopenic purpura. Lancet. 1994;344:703-6.
http://www.ncbi.nlm.nih.gov/pubmed/7915773?tool=bestpractice.com
Platelet transfusion can be useful even in thrombocytopenia caused by immune platelet destruction.[24]Cooper N, Ghanima W. Immune thrombocytopenia. N Engl J Med. 2019 Sep 5;381(10):945-55.
https://www.doi.org/10.1056/NEJMcp1810479
http://www.ncbi.nlm.nih.gov/pubmed/31483965?tool=bestpractice.com
Sepsis
Sepsis is a spectrum of disease, where there is a systemic and dysregulated host response to an infection.[26]Singer M, Deutschman CS, Seymour CW, et al. The third international consensus definitions for sepsis and septic shock (Sepsis-3). JAMA. 2016 Feb 23;315(8):801-10.
https://jamanetwork.com/journals/jama/fullarticle/2492881
http://www.ncbi.nlm.nih.gov/pubmed/26903338?tool=bestpractice.com
Presentation ranges from subtle, non-specific symptoms (e.g., feeling unwell with a normal temperature) to severe symptoms with evidence of multi-organ dysfunction and septic shock. Patients may have signs of tachycardia, tachypnea, hypotension, fever or hypothermia, poor capillary refill, mottled or ashen skin, cyanosis, newly altered mental state, or reduced urine output.[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
Sepsis and septic shock are medical emergencies.
Risk factors for sepsis include: age under 1 year, age over 75 years, frailty, impaired immunity (due to illness or drugs), recent surgery or other invasive procedures, any breach of skin integrity (e.g., cuts, burns), intravenous drug misuse, indwelling lines or catheters, and pregnancy or recent pregnancy.[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
Early recognition of sepsis is essential because early treatment improves outcomes.[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
[28]Evans L, Rhodes A, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143.
https://journals.lww.com/ccmjournal/Fulltext/2021/11000/Surviving_Sepsis_Campaign__International.21.aspx
[Evidence C]4925f83c-bff3-4d25-ae87-3aa35d4b571aguidelineC What are the effects of early versus late initiation of empiric antimicrobial treatment in adults with or at risk of developing sepsis or severe sepsis?[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
[Evidence C]a27ae3fa-30e4-45d1-ad14-63b8ad481e40guidelineC What are the effects of early versus late initiation of empiric antimicrobial treatment in children with or at risk of developing sepsis or severe sepsis?[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
However, detection can be challenging because the clinical presentation of sepsis can be subtle and non-specific. A low threshold for suspecting sepsis is therefore important.
The key to early recognition is the systematic identification of any patient who has signs or symptoms suggestive of infection and is at risk of deterioration due to organ dysfunction. Several risk stratification approaches have been proposed. All rely on a structured clinical assessment and recording of the patient’s vital signs.[27]National Institute for Health and Care Excellence. Suspected sepsis: recognition, diagnosis and early management. Mar 2024 [internet publication].
https://www.nice.org.uk/guidance/ng51
[29]Royal College of Physicians. National Early Warning Score (NEWS) 2. Dec 2017 [internet publication].
https://www.rcplondon.ac.uk/projects/outputs/national-early-warning-score-news-2
[30]American College of Emergency Physicians (ACEP) Expert Panel on Sepsis. DART: an evidence-driven tool to guide the early recognition and treatment of sepsis and septic shock [internet publication].
https://poctools.acep.org/POCTool/Sepsis(DART)/276ed0a9-f24d-45f1-8d0c-e908a2758e5a
[31]Academy of Medical Royal Colleges. Statement on the initial antimicrobial treatment of sepsis V2.0. Oct 2022 [internet publication].
https://www.aomrc.org.uk/wp-content/uploads/2022/10/Statement_on_the_initial_antimicrobial_treatment_of_sepsis_V2_1022.pdf
[32]Schlapbach LJ, Watson RS, Sorce LR, et al. International consensus criteria for pediatric sepsis and septic shock. JAMA. 2024 Feb 27;331(8):665-74.
https://jamanetwork.com/journals/jama/fullarticle/2814297
http://www.ncbi.nlm.nih.gov/pubmed/38245889?tool=bestpractice.com
It is important to check local guidance for information on which approach your institution recommends. The timeline of ensuing investigations and treatment should be guided by this early assessment.[31]Academy of Medical Royal Colleges. Statement on the initial antimicrobial treatment of sepsis V2.0. Oct 2022 [internet publication].
https://www.aomrc.org.uk/wp-content/uploads/2022/10/Statement_on_the_initial_antimicrobial_treatment_of_sepsis_V2_1022.pdf
Treatment guidelines have been produced by the Surviving Sepsis Campaign and remain the most widely accepted standards.[28]Evans L, Rhodes A, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143.
https://journals.lww.com/ccmjournal/Fulltext/2021/11000/Surviving_Sepsis_Campaign__International.21.aspx
[33]Surviving Sepsis Campaign. Hour-1 bundle: initial resuscitation for sepsis and septic shock. 2019 [internet publication].
https://www.sccm.org/sccm/media/PDFs/Surviving-Sepsis-Campaign-Hour-1-Bundle.pdf
Recommended treatment of patients with suspected sepsis is:
Measure lactate level, and remeasure lactate if initial lactate is elevated (>18 mg/dL [>2 mmol/L]).
Obtain blood cultures before administering antibiotics.
Administer broad-spectrum antibiotics (with methicillin-resistant Staphylococcus aureus [MRSA] coverage if there is a high risk of MRSA) for adults with possible septic shock or a high likelihood for sepsis.
For adults with sepsis or septic shock at high risk of fungal infection, empiric antifungal therapy should be administered.
Begin rapid administration of crystalloid fluids for hypotension or lactate level ≥36 mg/dL (≥4 mmol/L). Consult local protocols.
Administer vasopressors peripherally if hypotensive during or after fluid resuscitation to maintain MAP ≥65 mmHg, rather than delaying initiation until central venous access is secured. Norepinephrine (noradrenaline) is the vasopressor of choice.
For adults with sepsis-induced hypoxemic respiratory failure, high flow nasal oxygen should be given.
Ideally these interventions should all begin in the first hour after sepsis recognition.[33]Surviving Sepsis Campaign. Hour-1 bundle: initial resuscitation for sepsis and septic shock. 2019 [internet publication].
https://www.sccm.org/sccm/media/PDFs/Surviving-Sepsis-Campaign-Hour-1-Bundle.pdf
For adults with possible sepsis without shock, if concern for infection persists, antibiotics should be given within 3 hours from the time when sepsis was first recognized.[28]Evans L, Rhodes A, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143.
https://journals.lww.com/ccmjournal/Fulltext/2021/11000/Surviving_Sepsis_Campaign__International.21.aspx
For adults with a low likelihood of infection and without shock, antibiotics can be deferred while continuing to closely monitor the patient.[28]Evans L, Rhodes A, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143.
https://journals.lww.com/ccmjournal/Fulltext/2021/11000/Surviving_Sepsis_Campaign__International.21.aspx
For more information on sepsis, please see our topics [Related Topic: Sepsis in adults] and [Related Topic: Sepsis in children].