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[[Rudolf Virchow]] noted several factors affecting the clot formation, which are as follows:
'''Sticky platelet syndrome''' is a term used by some<ref name="pmid10548069">{{Cite journal|author=Mammen EF |title=Sticky platelet syndrome |journal=Semin. Thromb. Hemost. |volume=25 |issue=4 |pages=361–5 |year=1999 |pmid=10548069 |doi= 10.1055/s-2007-994939|url=}}</ref><ref name="pmid12627663">{{Cite journal|author=Frenkel EP, Mammen EF |title=Sticky platelet syndrome and thrombocythemia |journal=Hematol. Oncol. Clin. North Am. |volume=17 |issue=1 |pages=63–83 |date=February 2003 |pmid=12627663 |doi= 10.1016/S0889-8588(02)00096-5|url=}}</ref><ref name="pmid18662911">{{Cite journal|author=Mears KA, Van Stavern GP |title=Bilateral Simultaneous Anterior Ischaemic Optic Neuropathy Associated with Sticky Platelet Syndrome |journal=Br J Ophthalmol |volume= 93|issue= 7|pages= 885–6, 913|date=July 2008 |pmid=18662911 |doi=10.1136/bjo.2008.142919 |url=http://bjo.bmj.com/cgi/pmidlookup?view=long&pmid=18662911}}</ref><ref name="pmid2465231">{{Cite journal|author=Mammen EF, Barnhart MI, Selik NR, Gilroy J, Klepach GL |title="Sticky platelet syndrome": a congenital platelet abnormality predisposing to thrombosis? |journal=Folia Haematol. Int. Mag. Klin. Morphol. Blutforsch. |volume=115 |issue=3 |pages=361–5 |year=1988 |pmid=2465231 |doi= |url=}}</ref> to describe a disorder of [[platelet]] function.<ref name="pmid17532753">{{Cite journal|author=Mühlfeld AS, Ketteler M, Schwamborn K, ''et al'' |title=Sticky platelet syndrome: an underrecognized cause of graft dysfunction and thromboembolic complications in renal transplant recipients |journal=Am. J. Transplant. |volume=7 |issue=7 |pages=1865–8 |date=July 2007 |pmid=17532753 |doi=10.1111/j.1600-6143.2007.01835.x}}</ref> It was first described by Mammen in 1983.<ref name="isbn0-521-83953-X">{{Cite book|author=Bick, Rodger L |title=Hematological complications in obstetrics, pregnancy, and gynecology |publisher=Cambridge University Press |location=Cambridge, UK |year=2006 |pages=147  |isbn=0-521-83953-X |oclc= |doi= |accessdate=}}</ref> It is inherited in an [[autosomal dominant]] pattern.<ref name="isbn0-521-87082-8">{{Cite book|author=McKay, Robert; David R. Gambling |title=Obstetric anesthesia and uncommon disorders |publisher=Cambridge University Press |location=Cambridge, UK |year=2008 |pages=308  |isbn=0-521-87082-8 |oclc= |doi= |accessdate=}}</ref> It has not been associated with a specific gene, and it is not recognized as an entity in [[OMIM]].


1) Alterations in blood flow ([[stasis]]): Blood flows throughout the circulatory system, without significantly stopping or slowing any where. In certain pathological conditions where the blood flow slows down or stops, it causes:
Among researchers using the term, it has been described as a coagulation disorder that can present in conjunction with [[protein S deficiency]] and [[Factor V Leiden]].<ref name="pmid9973658">{{Cite journal|author=Chaturvedi S, Dzieczkowski JS |title=Protein S deficiency, activated protein C resistance and sticky platelet syndrome in a young woman with bilateral strokes |journal=Cerebrovasc. Dis. |volume=9 |issue=2 |pages=127–30 |year=1999 |pmid=9973658 |doi= 10.1159/000015911|url=http://content.karger.com/produktedb/produkte.asp?typ=fulltext&file=ced09127}}</ref> It is not currently known if sticky platelet syndrome is a distinct condition, or if it represents part of the presentation of a more well characterized coagulation disorder.
* Increase in platelet to endothelium contact
* Decrease the dilution of clotting factors
This increases the risk of clot formation and form microthrombi, which further grow and propagate.


2) Injury to the vascular endothelium: Intrinsic or secondary to external trauma (eg, catheterization) can cause [[Tunica intima|intimal]] damage and stimulates clot formation. See [[Coagulation]].
==Diagnosis==
SPS is diagnosed by demonstrating platelet hyperaggregability.  In a lab test called aggregometry platelet stickyness is stimulated with epinephrine (EPI) and/or adenosine diphosphate (ADP).<ref>http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1C-47T2D4S-4&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=fa06922a824e24db83382664b8659e30</ref>  This test is not possible for patients being treated with [[Aspirin|acetylsalicylic acid]] until that substance has sufficiently cleared from their system.


3) Alterations in the constitution of blood ([[hypercoagulability]]): It is the propensity to develop thrombosis due to an abnormality in the system of coagulation.  
==Treatment==
Those diagnosed are usually treated with taking a low dose (80–100&nbsp;mg) [[Aspirin]] a day.<ref>{{cite journal | pmid = 10548069 | doi=10.1055/s-2007-994939 | volume=25 | issue=4 | title=Sticky platelet syndrome | year=1999 | journal=Semin. Thromb. Hemost. | pages=361–5 | author=Mammen EF}}</ref>  [[Anticoagulant]]s (e.g. [[Warfarin]], [[Coumadin]]) or clopidogrel ([[Plavix]]) are often additionally prescribed following formation of a medically significant clot. Thrombelastography is more commonly being used to diagnose hypercoagulability and monitor anti-platelet therapy.


These three conditions are collectively known as [[Virchow's triad]] and lead to intravascular [[coagulation]], forming a mass of [[red blood cell]]s, [[leukocyte]]s, and [[fibrin]].
==Criticism==
 
Critics of the diagnosis complain that case evidence is spotty and lacking controlled clinical studies.<ref>http://www.fvleiden.org/ask/78.html</ref>
'''This video explains the process of thrombosis:'''
 
{{#ev:youtube|X_POCRsy7i4}}


==References==
{{Reflist|2}}




Revision as of 17:36, 7 May 2015


Sticky platelet syndrome is a term used by some[1][2][3][4] to describe a disorder of platelet function.[5] It was first described by Mammen in 1983.[6] It is inherited in an autosomal dominant pattern.[7] It has not been associated with a specific gene, and it is not recognized as an entity in OMIM.

Among researchers using the term, it has been described as a coagulation disorder that can present in conjunction with protein S deficiency and Factor V Leiden.[8] It is not currently known if sticky platelet syndrome is a distinct condition, or if it represents part of the presentation of a more well characterized coagulation disorder.

Diagnosis

SPS is diagnosed by demonstrating platelet hyperaggregability. In a lab test called aggregometry platelet stickyness is stimulated with epinephrine (EPI) and/or adenosine diphosphate (ADP).[9] This test is not possible for patients being treated with acetylsalicylic acid until that substance has sufficiently cleared from their system.

Treatment

Those diagnosed are usually treated with taking a low dose (80–100 mg) Aspirin a day.[10] Anticoagulants (e.g. Warfarin, Coumadin) or clopidogrel (Plavix) are often additionally prescribed following formation of a medically significant clot. Thrombelastography is more commonly being used to diagnose hypercoagulability and monitor anti-platelet therapy.

Criticism

Critics of the diagnosis complain that case evidence is spotty and lacking controlled clinical studies.[11]

References

  1. ↑ Mammen EF (1999). "Sticky platelet syndrome". Semin. Thromb. Hemost. 25 (4): 361–5. doi:10.1055/s-2007-994939. PMID 10548069.
  2. ↑ Frenkel EP, Mammen EF (February 2003). "Sticky platelet syndrome and thrombocythemia". Hematol. Oncol. Clin. North Am. 17 (1): 63–83. doi:10.1016/S0889-8588(02)00096-5. PMID 12627663.
  3. ↑ Mears KA, Van Stavern GP (July 2008). "Bilateral Simultaneous Anterior Ischaemic Optic Neuropathy Associated with Sticky Platelet Syndrome". Br J Ophthalmol. 93 (7): 885–6, 913. doi:10.1136/bjo.2008.142919. PMID 18662911.
  4. ↑ Mammen EF, Barnhart MI, Selik NR, Gilroy J, Klepach GL (1988). ""Sticky platelet syndrome": a congenital platelet abnormality predisposing to thrombosis?". Folia Haematol. Int. Mag. Klin. Morphol. Blutforsch. 115 (3): 361–5. PMID 2465231.
  5. ↑ Mühlfeld AS, Ketteler M, Schwamborn K; et al. (July 2007). "Sticky platelet syndrome: an underrecognized cause of graft dysfunction and thromboembolic complications in renal transplant recipients". Am. J. Transplant. 7 (7): 1865–8. doi:10.1111/j.1600-6143.2007.01835.x. PMID 17532753.
  6. ↑ Bick, Rodger L (2006). Hematological complications in obstetrics, pregnancy, and gynecology. Cambridge, UK: Cambridge University Press. p. 147. ISBN 0-521-83953-X.
  7. ↑ McKay, Robert; David R. Gambling (2008). Obstetric anesthesia and uncommon disorders. Cambridge, UK: Cambridge University Press. p. 308. ISBN 0-521-87082-8.
  8. ↑ Chaturvedi S, Dzieczkowski JS (1999). "Protein S deficiency, activated protein C resistance and sticky platelet syndrome in a young woman with bilateral strokes". Cerebrovasc. Dis. 9 (2): 127–30. doi:10.1159/000015911. PMID 9973658.
  9. ↑ http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1C-47T2D4S-4&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=fa06922a824e24db83382664b8659e30
  10. ↑ Mammen EF (1999). "Sticky platelet syndrome". Semin. Thromb. Hemost. 25 (4): 361–5. doi:10.1055/s-2007-994939. PMID 10548069.
  11. ↑ http://www.fvleiden.org/ask/78.html


Ventricular Tachycardia

Common causes of ventricular tachycardia include ischemic heart disease, illicit drugs (cocaine and methamphetamine), structural heart disease (including congenital heart diseases such as tetralogy of Fallot), inherited channelopathies, drug toxicity (digoxin, drugs that prolong the QT interval) and electrolyte disturbances (such as hypokalemia, hypomagnesemia, and hypocalcemia).




Table 1. Common Bacterial Pathogens in Neutropenic Patients
Gram-Positive Pathogens
  • Coagulase-negative staphylococci
  • Staphylococcus aureus, including methicillin-resistant strains
  • Enterococcus species, including vancomycin-resistant strains
  • Viridans group streptococci
  • Streptococcus pneumoniae
  • Streptococcus pyogenes
Gram-Negative Pathogens
  • Escherichia coli
  • Klebsiella species
  • Enterobacter species
  • Pseudomonas aeruginosa
  • Citrobacter species
  • Acinetobacter species
  • Stenotrophomonas maltophilia


Bloodstream infections caused by endogenous flora and reactivation of latent infections account for a majority of initial febrile episode in neutropenic patients with cancer. Common bacterial isolates that cause bacteremia in the setting of neutropenia are listed in Table 1.[1] Certain endogenous microorganisms may be reactivated and exit latency during immunosuppression. These include herpes simplex virus, varicella-zoster virus, Epstein-Barr virus, cytomegalovirus, hepatitis B and C viruses, and Mycobacterium tuberculosis. Exogenous pathogens carried by contaminated blood products, medical equipment and devices, water sources, and health care workers represent less common sources of infection. These include Clostridium difficile, respiratory syncytial virus, vancomycin-resistant enterococci, and other multidrug resistant bacteria.[2]

Fungal infections often take place in the setting of prolonged or profound neutropenia after administration of empirical therapy. Candidiasis may range in severity from mucosal or cutaneous infection to septicemia, endocarditis, or disseminated infection. Aspergillus, on the contrary, typically causes life-threatening infection of the sinuses and lungs, particularly after protracted neutropenia.[3]


Causes by Organ System

Cardiovascular No underlying causes
Chemical/Poisoning No underlying causes
Dental No underlying causes
Dermatologic No underlying causes
Drug Side Effect Acetaminophen and Oxycodone, Aclarubicin, Albendazole, Alemtuzumab, Alkylating antineoplastic agent, Alkylators, Arsenicals, Auranofin, Azathioprine, Aztreonam, Boceprevir, Busulphan, carbamazepine, Carboplatin, Cefadroxil, Ceftazidime, Certolizumab pegol, Chlorpromazine, Chloramphenicol, Chlorpropamide, Cidofovir, Clomipramine, Colchicine toxicity, Cytotoxic drugs and radiation, Dactinomycin, Doxorubicin, Ethosuximide, Febuxostat, Flucytosine, Gold, Gemifloxacin mesylate, Idarubicin, indomethacin , Interferon beta- 1a, Lincomycin Hydrochloride Minocycline hydrochloride, Non steroidal anti-inflammatory drugs, Ofatumumab, Omacetaxine, Oxaprozin, Oxcarbazepine, Penicillamine, phenacemide , Phenylbutazone, Piperacillin, Pralatrexate, propylthiouracil , Pyrimethamine, Rabeprazole, Radium chloride, sulfonamides, Tamoxifen, Tolbutamide, Tolazamide, Trifluoperazine, Trimethadione, Thiothixene, Valganciclovir hydrochloride
Ear Nose Throat No underlying causes
Endocrine Thyroid carcinoma
Environmental Tobacco use, Environmental/occupational (eg, benzene)
Gastroenterologic Portal hypertension, Intestinal lymphangiectasia, Hepatitis
Genetic Ataxia telangiectasia, Barth syndrome, Chediak-Higashi disease, defect in synthesis of adenosylcobalamin, DNA repair deficiencies, Down syndrome, Dubowitz syndrome, familial monosomy 7, Fanconi anaemia, genotoxic therapy, glutathione synthase deficiency, glycogen storage diseases, mutagen exposure, mutagen-detoxification (GSTq1-null), neurofibromatosis 1, Niemann-Pick disease, Nijmege breakage syndrome, Noonan syndrome, organic acid metabolism defect, Pearson syndrome, Seckel syndrome, Severe combined immunodeficiency, T- B+ due to JAK3 deficiency, trisomy 8 mosaicism, Wiskott-Aldrich syndrome
Hematologic Sickle cell disease, Reticular dysgenesis, Paroxysmal nocturnal haemoglobinuria, Non-Hodgkin lymphoma, Myelpathic anemia,

Myeloma, Myelofibrosis, Myelodysplastic syndrome, Megaloblastic anaemia, Malignant histiocytosis, Leucoerythroblastic anaemia,

Large granular lymphocytic leukemia, Langerhans cell histiocytosis, Ineffective erythropoiesis, Hypoplastic myelodysplastic syndromes ,

Hypersplenism, Hodgkin lymphoma, Histiocytosis X, Hepatosplenic T-cell lymphoma, Hemoglobin H disease, Hematopoietic cell transplantation, Hairy cell leukaemia, Haemoglobin SC disease, Haemoglobin E disease, Graft versus host disease, Familial myelofibrosis, Familial histiocytic reticulosis, Eosinophilic fasciitis , Cyclical neutropenia, Congenital neutropenia (Kostmann's or Shwachman-Diamond syndrome), Common variable hypogammaglobulinaemia, Chronic myeloid leukaemia, Chronic lymphocytic leukaemia, Bleeding (Excessive), Autoimmune lymphoproliferative syndrome type 2, Autoimmune lymphoproliferative syndrome type 1, Aplastic anemia, Amegakaryocytic thrombocytopenia, Aggressive NK-cell leukemia, Acute lymphoblastic leukemia

Iatrogenic No underlying causes
Infectious Disease Q fever, Parvovirus B19 infection, Oklahoma tick fever, Mycobacterium tuberculosis, Legionella pneumophila, Lassa fever, Human immunodeficiency virus , Epstein-Barr virus Seronegative, Dengue, Brucellosis
Musculoskeletal/Orthopedic No underlying causes
Neurologic No underlying causes
Nutritional/Metabolic Vitamin C deficiency, Vitamin B12 deficiency, Marasmus, Malabsorption syndrome, Kwashiorkor, Iron deficiency,

Intrinsic factor deficiency, Folate deficiency, Copper deficiency

Obstetric/Gynecologic Pregnancy
Oncologic Thymoma , Prostate cancer, Metastatic neoplasm, Melanoma, Germ cell tumors (embryonal dysgenesis), Ewing sarcoma, Chondrosarcoma, Cancer treatment
Ophthalmologic No underlying causes
Overdose/Toxicity No underlying causes
Psychiatric Anorexia nervosa
Pulmonary No underlying causes
Renal/Electrolyte Renal failure, chronic
Rheumatology/Immunology/Allergy Systemic lupus erythematosus, Rheumatoid disease, Osteopetrosis autosomal recessive 2, Osteopetrosis lethal

Osteoclastoma, Ankylosing spondylitis

Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous Topoisomerase II interactive agents, Plummer-Vinson syndrome, Obesity, Idiopathic , Glue vapors, Dyskeratosis congenita Shwachman-Diamond syndrome, Diamond-Blackfan anemia, Castleman disease, Bloom's syndrome

Causes in Alphabetical Order










Causes of Hypotension

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

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Common Causes

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Causes by Organ System

Cardiovascular Aortic aneurysm rupture, aortic arch syndrome, aortic isthmus stenosis, aortic regurgitation, aortic stenosis, aortocaval compression syndrome, atrial myxoma, atrioventricular node conduction block, B type natriuretic peptide, baroceptor dysfunction in the elderly, capillary leak syndrome, cardiac tamponade, cardiogenic shock, carotid sinus hypersensitivity, carotid sinus syndrome, coarctation of aorta, complete heart block, constrictive pericarditis, cor triatriatum, dehydration, dissecting aortic aneurysm, distributive shock, Eisenmenger's syndrome, embolism, endotoxic shock, gray baby syndrome, heart arrhythmia, heart block, heart failure, heart injury, hemorrhagic shock, hemorrhagic shock and encephalopathy syndrome, hypertrophic obstructive cardiomyopathy, hypovolemic shock, idiopathic hypotension, iliac artery aneurysm rupture, internal bleeding, ischaemic heart disease, myocardial infarction, myocardial ischemia, obstructive shock, orthostatic hypotension, pericardial effusion, pericarditis, perimyocarditis, post-tussive syncope, postural hypotension, pulmonary embolism, shock, sick sinus syndrome, supraventricular tachycardia , syncope, tetralogy of Fallot, traumatic shock, tricuspid stenosis, vasovagal syncope, ventricular fibrillation, WPW syndrome
Chemical / poisoning Acetaldehyde, adiponitrile , copper, cyanides, demeton-S-methyl, diazinon , dioxathion, disulfoton , ethion , fensulfothion, fenthion, honey bee bite, indian tobacco, malathion, methidathion, methiocarb, methomyl, mushroom poisoning , parathion, phosdrin, poison hemlock, profenofos, scorpion bite, sodium nitrite, terbufos, tetraethyl pyrophosphate , tetrodotoxin, tobacco , wasp bite
Dermatologic Gray baby syndrome, mastocytosis
Drug Side Effect Acetophenazine, alcuronium, alfuzosin, aliskiren, alseroxylon, ambenonium, ambrisentan, amifostine, aminoglutethimide, amitriptyline, amlodipine, amoxapine, amphotericin B, amrinone, amyl nitrate, antipsychotic agents, apomorphine, azilsartan medoxomil, B type natriuretic peptide, baclofen, beta blockers, bethanechol, bethanidine, bortezomib, bosentan, bretylium, bromocriptine, bupivacaine, cabergoline, calcium channel blockers, candesartan, captopril, chloroquine, chlorpheniramine, chlorpromazine, chlorthalidone, cilazapril, cinacalcet, cinnarizine, clevidipine, clomipramine, clonidine, colchicine, cyclobenzaprine, deserpidine, desferrioxamine, desipramine, dexmedetomidine, diazoxide, dichlorvos , dicobalt edetate, dicrotophos , diltiazem, diphenhydramine, dipyridamole, disopyramide, distigmine, diuretics, donepezil , dothiepin, doxazosin, doxepin, enalapril, epidural anaesthesia, eplerenone, epoprostenol, etoposide, felodipine , fenoldopam, fentanyl, fosinopril, general anaesthesia, glyceryl trinitrate, granulocyte-macrophage colony stimulating factor, gray baby syndrome, guanadrel, guanethidine, guanfacine, haloperidol, hexamethonium, hydralazine, hydroxyzine, imipramine, indapamide, indoramin, interleukin 2, iodine containing radiocontrast media, irbesartan, isosorbide dinitrate, isosorbide mononitrate, isoxsuprine, isradipine, ketanserin, labetalol, l-dopa, levomepromazine, levosimendan, lidocaine , lisinopril, lithium, lofexidine, losartan, mecamylamine, methyldopa, metirosine, metolazone, minoxidil, morphine, moxonidine, nefazodone, neostigmine, niacin, nicorandil, nifedipine, nimodipine, nitroprusside, nortriptyline, olanzapine, olmesartan, omapatrilat, opioid poisoning, paliperidone, pentamidine, perazine, pergolide, phenothiazines, phenoxybenzamine, phentolamine, pimobendan, pinacidil, pipothiazine, piribedil, pramipexole, prazosin, protamine sulfate, protriptyline, quetiapine, ramipril, rasagiline, reboxetine, reserpine, rilmenidine, risperidone, rituximab, ropinirole, rotigotine, sassafras oil, serotonin syndrome, sildenafil, silodosin, sodium nitroprusside, spironolactone, streptokinase, sulphonamides, tacrine, tadalafil, tamsulosin, terazosin, tetrabenazine, tizanidine, tolazoline, tramadol, treprostinil, trifluperidol, trimethaphan, trimipramine, tubocurarine, urapidil, valerian, valsartan, vardenafil, verapamil, ziconotide, zotepine
Ear Nose Throat No underlying causes
Endocrine Achalasia-addisonianism-alacrima syndrome, ACTH deficiency, Addison's disease, addisonian crisis, adrenal hemorrhage, adrenogenital syndrome, adrenoleukodystrophy , Allgrove syndrome, APECED syndrome , B type natriuretic peptide, carcinoid syndrome , congenital adrenal hyperplasia, diabetes insipidus, diabetic autonomic neuropathy, diabetic ketoacidosis, hyperosmolar hyperglycemic nonketotic coma, hypoaldosteronism, hyporeninemic hypoaldosteronism, hypothyroidism, Myxedema, myxedema coma, panhypopituitarism, pituitary insufficiency, pseudohypoaldosteronism, Renon-Delille syndrome, serotonin syndrome, triple-A syndrome
Environmental Snake bite, zero gravity
Gastroenterologic Achalasia-addisonianism-alacrima syndrome, acute liver failure , acute pancreatitis, acute viral gastroenteritis, Allgrove syndrome, bowel strangulation, deglutition syncope, diarrhea, duodenal ulcer bleeding, gastric ulcer bleeding, gastric volvulus, hepatic vein thrombosis, hepatitis, intususception, mastocytosis , necrotizing enterocolitis, paralytic ileus, peritonitis , postprandial hypotension, retroperitoneal haemorrhage, small bowel obstruction, splenic rupture, superior mesenteric artery occlusion, triple A syndrome, tropical sprue , variceal bleeding, vomiting
Genetic Achalasia-addisonianism-alacrima syndrome, acute intermittent porphyria, Allgrove syndrome, APECED syndrome, Bartter syndrome, corticosteroid-binding globulin deficiency , familial juvenile hyperuricemic nephropathy type 2, hereditary peripheral nervous disorder, hereditary sensory and autonomic neuropathy type 3, pseudohypoaldosteronism, Renon-Delille syndrome, Riley-Day syndrome, triple A syndrome, Wohlwill-Andrade syndrome
Hematologic Acute intermittent porphyria, anemia
Iatrogenic After a major surgery, blood transfusion , dialyzer hypersensitivity syndrome, epidural anesthesia, gastric acid stimulation test using histamines, general anesthesia, mechanical ventilation, post-operative, renal dialysis, transfusion reaction
Infectious Disease Acute viral gastroenteritis, botulism, cholera, dengue hemorrhagic fever, hantavirus, lassa fever, rocky mountain spotted fever , septic shock, septicemia , toxic shock syndrome, vibrio vulnificus, Waterhouse-Friederichsen syndrome, Weil syndrome
Musculoskeletal / Ortho Cervical spine injury, fracture of bone, vertebral fracture
Neurologic Autonomic failure, autonomic neuropathy, Binswanger's disease , Bradbury-Eggleston syndrome, diabetic autonomic neuropathy, DOPA decarboxylase deficiency, dopamine beta hydroxylase deficiency, dysautonomia, glossopharyngeal neuralgia, Guillain-Barre syndrome, hemorrhagic shock and encephalopathy syndrome, hereditary peripheral nervous disorder, hereditary sensory and autonomic neuropathy type 3, multiple system atrophy, neurogenic shock, Parkinson's disease, polyradiculitis, Riley-Day syndrome, seizures, Shy-Drager syndrome, syringomyelia, tabes dorsalis, vasovagal syncope, Wohlwill-Andrade syndrome
Nutritional / Metabolic Dehydration,excessive dieting,kwashiorkor
Obstetric/Gynecologic Aortocaval compression syndrome, ectopic pregnancy rupture, ovarian hyperstimulation syndrome, postpartum haemorrhage, pregnancy, puerpural shock, septic abortion , uterine rupture
Oncologic Atrial myxoma, carcinoid syndrome , mastocytosis , pheochromocytoma, serotonin-secreting tumor
Opthalmologic No underlying causes
Overdose / Toxicity Acetophenazine, alcuronium, alfuzosin, aliskiren, alseroxylon, ambenonium, ambrisentan, amifostine, aminoglutethimide, amitriptyline, amlodipine, amoxapine, amphotericin B, amrinone, antipsychotic agents, apomorphine, azilsartan medoxomil, baclofen, beta blockers, bethanechol, bethanidine, bortezomib, bosentan, bretylium, bromocriptine, bupivacaine, cabergoline, calcium channel blockers, candesartan, captopril, chloroquine, chlorpheniramine, chlorpromazine, chlorthalidone, cilazapril, cinnarizine, clevidipine, clomipramine, clonidine, colchicine, cyclobenzaprine, deserpidine, desferrioxamine, desipramine, dexmedetomidine, diazoxide, dichlorvos , dicobalt edetate, dicrotophos , diltiazem, diphenhydramine, dipyridamole, disopyramide, distigmine, diuretics, donepezil , dothiepin, doxazosin, doxepin, enalapril, epidural anaesthesia, eplerenone, epoprostenol, etoposide, felodipine , fenoldopam, fentanyl, fosinopril, general anaesthesia, glyceryl trinitrate, granulocyte-macrophage colony stimulating factor, guanadrel, guanethidine, guanfacine, haloperidol, hexamethonium, hydralazine, hydroxyzine, imipramine, indapamide, indoramin, interleukin 2, irbesartan, isosorbide dinitrate, isosorbide mononitrate, isoxsuprine, isradipine, ketanserin, labetalol, l-dopa, levomepromazine, levosimendan, lidocaine , lisinopril, lithium, lofexidine, losartan, magnesium overdose, mecamylamine, methyldopa, metirosine, metolazone, minoxidil, morphine, moxonidine, nefazodone, neostigmine, niacin, nicorandil, nifedipine, nimodipine, nitroprusside, nortriptyline, olanzapine, , olmesartan, omapatrilat, opioid poisoning, paliperidone, pentamidine, perazine, pergolide, phenothiazines, phenoxybenzamine, phentolamine, pimobendan, pinacidil, pipothiazine, piribedil, pramipexole, prazosin, protamine sulfate, protriptyline, quetiapine, ramipril, rasagiline, reboxetine, reserpine, rilmenidine, risperidone, rituximab, ropinirole, rotigotine, sassafras oil, sildenafil, silodosin, sodium nitroprusside, spironolactone, streptokinase, sulphonamides, tacrine, tadalafil, tamsulosin, terazosin, tetrabenazine, tizanidine, tolazoline, tramadol, treprostinil, trifluperidol, trimethaphan, trimipramine, tubocurarine, urapidil, valerian, valsartan, vardenafil, verapamil, ziconotide, zotepine
Psychiatric Anorexia nervosa, depression
Pulmonary Post-tussive syncope, pulmonary edema, pulmonary embolism, tension pneumothorax
Renal / Electrolyte Bartter syndrome, dehydration, familial juvenile hyperuricemic nephropathy type 2, hypermagnesaemia, hypokalemia, hyponatremia
Rheum / Immune / Allergy Amyloidosis, anaphylactic shock, anaphylactoid reaction, blood transfusion , dialyzer hypersensitivity syndrome, food additive allergy, Guillain-Barre syndrome, honey bee bite, mastocytosis, scorpion bite, transfusion reaction, urticaria, wasp bite, Wohlwill-Andrade syndrome, x-ray studies using contrast media
Sexual Renon-Delille syndrome
Trauma Blood vessel trauma, burns, cervical spine injury, chemical burn, fracture of bone, heart injury, pericardial effusion, shaken baby syndrome, tension pneumothorax, traumatic shock
Urologic No underlying causes
Dental No underlying causes
Miscellaneous Alcohol, alcohol withdrawal syndrome, decompression sickness, deglutition syncope, dehydration, fatigue, heat exhaustion, hypothermia, insufficient fluid intake, low salt diet, micturition syncope, prolonged bed rest, snake bite, syncope, volume depletion , zero gravity

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Causes in Alphabetical Order

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Primary treatment option
Atropine
❑ Administer a first dose 0.5 mg IV bolus
❑ Repeat every 3-5 minutes
❑ Administer a maximum dose of 3 mg
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Secondary treatment options
If atropine ineffective:
❑ Administer dopamine infusion (2-10 mcg/kg/min)
OR
❑ Administer epinephrine infusion (2-10 mcg/min)
OR
❑ Proceed with transcutaneous pacing
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Consult a cardiologist
❑ Consider transvenous pacing
 
 
 
 
 
 






References

  1. ↑ Pagano, L. (2012-05). "A prospective survey of febrile events in hematological malignancies". Annals of Hematology. 91 (5): 767–774. doi:10.1007/s00277-011-1373-2. ISSN 1432-0584. PMID 22124621. Unknown parameter |coauthors= ignored (help); Check date values in: |date= (help)
  2. ↑ MD, John E. Niederhuber (2013-11-05). Abeloff's Clinical Oncology: Expert Consult Premium Edition - Enhanced Online Features and Print, 5e (5 edition ed.). Philadelphia, Pennsylvania: Saunders. ISBN 9781455728657. Unknown parameter |coauthors= ignored (help)
  3. ↑ Freifeld, Alison G. (2011-02-15). "Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 Update by the Infectious Diseases Society of America". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (4): 427–431. doi:10.1093/cid/ciq147. ISSN 1537-6591. PMID 21205990. Unknown parameter |coauthors= ignored (help)

Overview

Causes

Life Threatening Causes

Common Causes

Diagnosis

Focused Initial Rapid Evaluation

Complete Evaluation

 
 
 
 
 
 
 
 
A01
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
B01
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
C01
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
D01
 
 
 
 
 
 
 
 
 
 
 
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E02
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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Treatment

Do's

Don'ts

References

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