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'''Anaphylaxis''', often called '''anaphylactic shock''', is an acute allergic reaction caused by exposure to an antigen to which the patient is hypersensitive. It is characteristic of the condition that significant distress can begin within short minutes of exposure. While the patient may be aware of the hypersensitivity, it may trigger on a first exposure, as to an insect sting.
'''Anaphylaxis''', often called '''anaphylactic shock''', is "an acute [[immediate hypersensitivity|hypersensitivity]] reaction due to exposure to a previously encountered [[antigen]]. The reaction may include rapidly progressing [[urticaria]], respiratory distress, vascular collapse, systemic [[shock]], and death".<ref>{{MeSH}}</ref>


Signs of the reaction can include a raised red rash ("hives", [[urticaria]]), respiratory distress, cardiovascular failure, shock and death. While anaphylaxis can progress at a slower rate, it can take effect with frightening speed. Patients aware of sensitivities that could trigger anaphylaxis should carry an [[epinephrine]] autoinjector, and other recommended drugs. Emergency responder doing [[triage]] must place these patients in the highest priority, because the condition is usually controllable with prompt treatment.  
Signs of the reaction can include a raised red rash ("hives", [[urticaria]]), respiratory distress, cardiovascular failure, shock and death. While anaphylaxis can progress at a slower rate, it can take effect with frightening speed. Patients aware of sensitivities that could trigger anaphylaxis should carry an [[epinephrine]] autoinjector, and other recommended drugs. Emergency responder doing [[triage]] must place these patients in the highest priority, because the condition is usually controllable with prompt treatment.  
Consensus guidelines for the immediate and long-term management of anaphylaxis have been published,<ref name=JTF>{{citation
| title = The diagnosis and management of anaphylaxis: an updated practice parameter.
| url = http://www.guideline.gov/summary/summary.aspx?doc_id=6887
| author = Joint Task Force on Practice Parameters for Allergy and Immunology}}</ref> based on a 2005 paper in the Journal of Allergy and Clinical Immunology. <ref>{{citation
| journal = J Allergy Clin Immunol
| date = 2005 Mar
| volume = 115(3 Suppl 2)
| pages =S483-523
| title = The diagnosis and management of anaphylaxis: an updated practice parameter.
| author = Joint Task Force on Practice Parameters; American Academy of Allergy, Asthma and Immunology; American College of Allergy, Asthma and Immunology; Joint Council of Allergy, Asthma and Immunology}}</ref>


==Pathophysiology==
==Pathophysiology==
"Anaphylaxis" includes to mast cell and basophil degranulation, triggered either by an [[Immunoglobulin#Immunoglobulin E|immunoglobulin E (IgE)]] mediated "anaphylactic reaction", or by degranulation mediated by non-IgE factors, or "anaphylactoid reaction". <ref name=eMed-ana>{{citation
"Anaphylaxis" is a form of [[immediate hypersensitivity]] and includes [[mast cell]] and [[basophil]] degranulation, triggered either by an [[Immunoglobulin#Immunoglobulin E|immunoglobulin E (IgE)]] mediated "anaphylactic reaction", or by other factors, or "anaphylactoid reaction". <ref name=eMed-ana>{{citation
  | url = http://www.emedicine.com/med/topic128.htm
  | url = http://www.emedicine.com/med/topic128.htm
  | title = Anaphylaxis
  | title = Anaphylaxis
Line 25: Line 14:


In either case, the released cytokines include [[histamine]], which increases blood vessel permeability, as well as contraction of smooth muscles, such as the [[bronchi]].  The increased vascular permeability can cause [[shock]] by shifting as much as 50% of the body's fluids to the [[extravascular compartment]].
In either case, the released cytokines include [[histamine]], which increases blood vessel permeability, as well as contraction of smooth muscles, such as the [[bronchi]].  The increased vascular permeability can cause [[shock]] by shifting as much as 50% of the body's fluids to the [[extravascular compartment]].
==Evaluation==
==Evaluation==
The patient, if conscious, will be apprehensive and appear seriously ill.  If the patient or a companion can inform the treating clinician of known anaphylaxis, this is critical information. If there is no informant, search for an identifying bracelet, necklace, or identification card.
The patient, if conscious, will be apprehensive and appear seriously ill.  If the patient or a companion can inform the treating clinician of known anaphylaxis, this is critical information. If there is no informant, search for an identifying bracelet, necklace, or identification card.
Line 30: Line 20:
Assuming it is possible to get history, key questions included the existence of cardiac disease or [[hypertension]], and if the patient is taking [[beta-adrenergic antagonist]]s for any reason.
Assuming it is possible to get history, key questions included the existence of cardiac disease or [[hypertension]], and if the patient is taking [[beta-adrenergic antagonist]]s for any reason.


Bystander history of a possible trigger, sudden onset, and rapid progression is informative. The presence of urticaria or general flushing, hypotension, bronchospasm, laryngeal edema, back pain, dilation of the pupils, and convulsions, or combinations of them, are warning signs; ''the patient is at risk for immediate death''. Cardiac arrest, in suspected anaphylaxis, calls for vigorous resuscitation since it is a potentially reversable condition.
Bystander history of a possible trigger, sudden onset, and rapid progression is informative. The presence of urticaria or general flushing, hypotension, bronchospasm, laryngeal edema, back pain, dilation of the pupils, and convulsions, or combinations of them, are warning signs; ''the patient is at risk for immediate death''. Cardiac arrest, in suspected anaphylaxis, calls for vigorous resuscitation since it is a potentially reversible condition.


Any person or facility administering [[vaccine]]s<ref name=AuNT-Vac>{{citation
Any person or facility administering [[vaccine]]s<ref name=AuNT-Vac>{{citation
Line 36: Line 26:
| author = Northern Territory (Australia) Centre for Disease Control
| author = Northern Territory (Australia) Centre for Disease Control
|url = http://www.health.nt.gov.au/library/scripts/objectifyMedia.aspx?file=pdf/10/95.pdf&siteID=1&str_title=Anaphylaxis%20rural.pdf}}</ref> or [[immunologic desensitization]] must be immediately prepared to respond to anaphylaxis.  
|url = http://www.health.nt.gov.au/library/scripts/objectifyMedia.aspx?file=pdf/10/95.pdf&siteID=1&str_title=Anaphylaxis%20rural.pdf}}</ref> or [[immunologic desensitization]] must be immediately prepared to respond to anaphylaxis.  
==Treatment==
==Treatment==
Patients in anaphylaxis should be transported by advanced life support capable ambulance when available. If the trigger point of entry can be identified  (e.g., a bee sting), and it is on an extremity, a tourniquet, released every 5 minutes, can be applied. If a stinger or other source is present, remove it as quickly as possible.
Multiple [[clinical practice guideline]]s for the immediate and long-term management of anaphylaxis have been published<ref name="pmid17620061">{{cite journal| author=Alrasbi M, Sheikh A| title=Comparison of international guidelines for the emergency medical management of anaphylaxis. | journal=Allergy | year= 2007 | volume= 62 | issue= 8 | pages= 838-41 | pmid=17620061
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=17620061 | doi=10.1111/j.1398-9995.2007.01434.x }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>, including joint American guidelines<ref name="pmid15753926">{{cite journal| author=Joint Task Force on Practice Parameters. American Academy of Allergy, Asthma and Immunology. American College of Allergy, Asthma and Immunology. Joint Council of Allergy, Asthma and Immunology| title=The diagnosis and management of anaphylaxis: an updated practice parameter. | journal=J Allergy Clin Immunol | year= 2005 | volume= 115 | issue= 3 Suppl 2 | pages= S483-523 | pmid=15753926
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=15753926 | doi=10.1016/j.jaci.2005.01.010 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--> [http://www.guideline.gov/summary/summary.aspx?doc_id=6887  Summary at the National Guidelines Clearinghouse]</ref>


Epinephrine is the critical component of therapy. While some physicians are reluctant to administer it due to possible side effects, only the most extreme and confirmed reasons can justify withholding it. In mild to moderate cases, it is given intramuscularly in 1:1,000 solution, 0.3 to 0.5 ml for adults. Repeat every 5-10 minutes until the signs disappear. Obvious care must be taken in patients with cardiac or hypertensive disease, but a patient is likelier to die quickly from anaphylaxis than the effects of epinephrine.
===Immediate management===
Patients with a history of anaphylaxis, or a strong risk thereof, may self-administer an epinephrine autoinjector. Depending on local protocols, Basic Life Support emergency personnel, not normally authorized to administer drugs, may assist the patient with self-administration.
{|align="right" cellpadding="10"  style="background-color:#FFFFCC; width:50%; border: 1px  solid #aaa; margin:20px; font-size: 92%;"
|'''Medical errors in dosing [[epinephrine]]'''


In all cases, intravenous access should be gained immediately, giving adults 500 ml to 1 L of normal saline over 30 minutes, with additional fluids given to support the clinical situation, which is likely to involve shock. Wnen anaphylaxis is severe, give epinephrine intravenously or by endotracheal tube, 1.0 ml. of 1:10,000 solution. A continuous infusion may be needed.
As the dose of [[epinephrine]] is sometimes expressed as a  ratio only (1 mL  of 1:1000) or a concentration only (1 mg in 1 mL), [[medical error]]s  in administration may be made.<ref  name="pmid18166759">{{cite  journal |author=Wheeler DW, Carter  JJ, Murray LJ, ''et  al'' |title=The effect of drug  concentration expression on epinephrine dosing errors: a randomized  trial |journal=Ann. Intern. Med. |volume=148 |issue=1 |pages=11–4  |year=2008 |month=January |pmid=18166759 |doi= |url=http://www.annals.org/cgi/pmidlookup?view=long&pmid=18166759    |issn=}}</ref>


<center>'''note well: 1:1,000 solution intramuscular, 1:10,000 intravenous or endotracheal'''</center>
'''Which concentration of epinephrine to use?'''
*  '''1:1,000 solution is for intramuscular'''
* '''1:10,000 intravenous or endotracheal'''
|}


Patients in anaphylaxis should be transported by advanced life support capable ambulance when available. If the trigger point of entry can be identified  (e.g., a bee sting), and it is on an extremity, a tourniquet, released every 5 minutes, can be applied. If a stinger or other source is present, remove it as quickly as possible.


[[Epinephrine]] is given intramuscularly in 1:1,000 solution, 0.3 to 0.5 ml for adults.  When  anaphylaxis is severe, give epinephrine intravenously or by  endotracheal tube, 1.0 ml. of 1:10,000 solution.  A continuous infusion  may be needed. Repeat every 5-10 minutes until the signs disappear. While some physicians frequently do not administer epinephrine, possibly due to concern about [[drug toxicity]]<ref name="pmid20094000">{{cite journal| author=Russell S, Monroe K, Losek JD| title=Anaphylaxis management in the pediatric emergency department: opportunities for improvement. | journal=Pediatr Emerg Care | year= 2010 | volume= 26 | issue= 2 | pages= 71-6 | pmid=20094000
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=20094000 | doi=10.1097/PEC.0b013e3181ce2e1c }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>, only the most extreme and confirmed reasons can justify withholding it. Obvious care must be taken in patients with cardiac or hypertensive disease, but a patient is likelier to die quickly from anaphylaxis than the effects of epinephrine. In the presence of laryngeal swelling, nebulized epinephrine may help,  but evidence of such swelling will usually justify epinephrine.  Bronchospasm, if present, should be treated with a nebulized  short-acting [[beta-adrenergic agonist|β<sub>2</sub> agonist]]  such as [[albuterol]].


Antihistamines support epinephrine, but do not replace it. The combination of a histamine H<sub>1</sub> antagonist (e.g., [[diphenhydramine]]) and H<sub>2</sub> antagonist (e.g., [[ranitidine]]) has been demonstrated to be superior to a single type. <ref name=CEDT-09>{{citation
[[Intravenous infusion]] of  saline or other crystalloid should be started immediately, giving adults 500 ml to 1 L of normal saline over 30 minutes, with additional fluids given as needed. If the episode is prolonged, treatment in an [[critical care|intensive care unit]] may be needed with invasive monitoring of [[cardiac output]] and [[central venous pressure]].  
| editor = Stone, CK and Humphries R
| title = Current Emergency Diagnosis & Treatment
| publisher = Lange Medical Books/McGraw-Hill
| edition = 5th
| year = 2004
| id = CEDT-09
| contribution = Chapter 9, Shock
| first1 = Peter W | last1 = Greenwald}}, pp. 207-208</ref>


In the presence of laryngeal swelling, nebulized epinephrine may help, but evidence of such swelling will usually justify epinephrine. Bronchospasm, if present, should be treated with a nebulized short-acting [[beta-adrenergic agonist|β<sub>2</sub> agonist]] such as [[albuterol]]
[[Vasoconstrictor agent]]s to support blood pressure can include continuous [[epinephrine]] infusion, as well as [[dopamine]].


While they will not have a short-term effect, [[corticosteroid]]s should be started early in the incident; anaphylaxis may have a late-phase component.<ref name=CEDT-09 />
[[Histamine antagonist|Antihistamine]]s  support epinephrine, but do not replace it. The combination of a histamine H<sub>1</sub> antagonist (e.g., [[diphenhydramine]]) and [[histamine H2 antagonist]] (e.g., [[ranitidine]]) may be better than either drug alone in some settings.<ref name="pmid2863224">{{cite journal| author=Ring J, Rothenberger KH, Clauss W| title=Prevention of anaphylactoid reactions after radiographic contrast media infusion by combined histamine H1- and H2-receptor antagonists: results of a prospective controlled trial. | journal=Int Arch Allergy Appl Immunol | year= 1985 | volume= 78 | issue= 1 | pages= 9-14 | pmid=2863224
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=2863224 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name="pmid1536481">{{cite journal| author=Runge JW, Martinez JC, Caravati EM, Williamson SG, Hartsell SC| title=Histamine antagonists in the treatment of acute allergic reactions. | journal=Ann Emerg Med | year= 1992 | volume= 21 | issue= 3 | pages= 237-42 | pmid=1536481
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=1536481 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name=CEDT-09>{{citation
| editor = Stone, CK and Humphries R
| title =  Current Emergency Diagnosis & Treatment
| publisher =  Lange Medical Books/McGraw-Hill
| edition = 5th
| year = 2004
| id =  CEDT-09
| contribution = Chapter 9, Shock
| first1 =  Peter W | last1 = Greenwald}},  pp. 207-208</ref>


It has become understood that maintaining adequate blood pressure can be the most difficult part of treatment, in an [[critical care|intensive care unit]] if the episode is prolonged. Fluid replacement is the first part of therapy for [[hypotension]], which may require very aggressive volumes of saline or other crystalloid. Fluids must be individualized, based on blood pressure and urine volume; in severe cases, invasive monitoring of [[cardiac output]] and [[central venous pressure]] are appropriate.  
While they will not have a short-term effect, [[corticosteroid]]s should be started early in the incident; anaphylaxis may have a late-phase component.<ref name=CEDT-09 />


Pharmacologic support of blood pressure can include continuous epinephrine infusion, as well as [[dopamine]]. This is one of the few remaining indications for [[military antishock trousers]]. <ref name=Brown>{{citation | 
If the patient is taking a [[Adrenergic beta-antagonist|beta-blocker]], reversing its effect with [[glucagon]] may help if the patient has not responded to epinephrine and fluids. There is anecdotal<ref>{{citation
| journal = J Accid Emerg Med.  (now J. Emergency Medicine)
| title = Glucagon infusion in anaphylactic shock in patients on beta-blockers
| date=1995 June
|first = Martin | last =Thomas
| volume = 12(2)
| date = April 12, 2005  
| pages = 89–100
| journal = Bestbets
| pmid = PMC1342543
| title = Anaphylactic shock: mechanisms and treatment.
| first = A F | last = Brown
| url = http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1342543}}</ref>.
 
If the patient is taking a beta-blocker, its effects must be reversed. There is anecdotal<ref>{{citation
| title = Glucagon infusion in anaphylactic shock in patients on beta-blockers
|first = Martin | last =Thomas
| date = April 12, 2005  
| journal = Bestbets
| url = http://www.bestbets.org/bets/bet.php?id=148
| url = http://www.bestbets.org/bets/bet.php?id=148
}}</ref> and animal<ref>{{citation
}}</ref> and animal<ref>{{citation
| journal = Br J Pharmacol
| journal = Br J Pharmacol
| date = 1982 July
| date = 1982 July
| volume = 76(3)
| volume = 76(3)
| pages =483–489.
| pages =483–489.
| pmcid= PMC2071802
| pmcid= PMC2071802
| title  =Protective effects of glucagon during the anaphylactic response in guinea-pig isolated heart
| title  =Protective effects of glucagon during the anaphylactic response in guinea-pig isolated heart
|first1 = Ivan | last1 = Andjelkovic| first2=Berislav |last2=Zlokovic
|first1 = Ivan | last1 = Andjelkovic| first2=Berislav |last2=Zlokovic
| url = http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2071802
| url = http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2071802
}}</ref> evidence that glucagon can be helpful. It also provides inotropic effects and chronotropic effects on the heart by increasing intracellular levels of [[Cyclic adenosine monophosphate|cAMP]].  
}}</ref> evidence that glucagon can be helpful. It also provides inotropic effects and chronotropic effects on the heart by increasing intracellular levels of [[Cyclic adenosine monophosphate|cAMP]].
 
Anaphylaxis is one of the few remaining indications for [[military  antishock trousers]]. <ref name=Brown>{{citation | 
| journal = J  Accid Emerg Med.  (now J. Emergency Medicine)
| date=1995  June
|  volume = 12(2)
| pages = 89–100
| pmid =  PMC1342543
| title = Anaphylactic shock: mechanisms  and treatment.
| first = A F | last = Brown
| url = http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1342543}}</ref>.
 
Relapse of shock after treatment is rare.<ref name="pmid24239340">{{cite journal| author=Grunau BE, Li J, Yi TW, Stenstrom R, Grafstein E, Wiens MO et al.| title=Incidence of clinically important biphasic reactions in emergency department patients with allergic reactions or anaphylaxis. | journal=Ann Emerg Med | year= 2014 | volume= 63 | issue= 6 | pages= 736-744.e2 | pmid=24239340 | doi=10.1016/j.annemergmed.2013.10.017 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24239340  }} </ref>
24239340


==Long-term management==
===Long-term management===
Obviously, the patient should avoid antigens to which they know they are sensitive. If, for example, there is hypersensitivity to latex, all medical personnel should be informed, and the patient should wear an alerting bracelet or necklace. When insect stings are a trigger, the patient must take precautions to avoid attracting insects while outside, such as wearing strong perfumes.
Obviously, the patient should avoid antigens to which they know they are sensitive. If, for example, there is hypersensitivity to latex, all medical personnel should be informed, and the patient should wear an alerting bracelet or necklace. When insect stings are a trigger, the patient must take precautions to avoid attracting insects while outside, such as wearing strong perfumes.


It is also advisable to carry an emergency drug kit, which minimally consists of an epinephrine autoinjector, and perhaps [[antihistamine]]s.
It is also advisable to carry an emergency drug kit, which minimally consists of an epinephrine autoinjector, and perhaps [[antihistamine]]s.


[[Allergic desensitization]] should be considered seriously if feasible.  
[[Allergic desensitization]] should be considered seriously if feasible.
 
==References==
==References==
{{reflist|2}}
{{reflist|2}}[[Category:Suggestion Bot Tag]]

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Anaphylaxis, often called anaphylactic shock, is "an acute hypersensitivity reaction due to exposure to a previously encountered antigen. The reaction may include rapidly progressing urticaria, respiratory distress, vascular collapse, systemic shock, and death".[1]

Signs of the reaction can include a raised red rash ("hives", urticaria), respiratory distress, cardiovascular failure, shock and death. While anaphylaxis can progress at a slower rate, it can take effect with frightening speed. Patients aware of sensitivities that could trigger anaphylaxis should carry an epinephrine autoinjector, and other recommended drugs. Emergency responder doing triage must place these patients in the highest priority, because the condition is usually controllable with prompt treatment.

Pathophysiology

"Anaphylaxis" is a form of immediate hypersensitivity and includes mast cell and basophil degranulation, triggered either by an immunoglobulin E (IgE) mediated "anaphylactic reaction", or by other factors, or "anaphylactoid reaction". [2]

In either case, the released cytokines include histamine, which increases blood vessel permeability, as well as contraction of smooth muscles, such as the bronchi. The increased vascular permeability can cause shock by shifting as much as 50% of the body's fluids to the extravascular compartment.

Evaluation

The patient, if conscious, will be apprehensive and appear seriously ill. If the patient or a companion can inform the treating clinician of known anaphylaxis, this is critical information. If there is no informant, search for an identifying bracelet, necklace, or identification card.

Assuming it is possible to get history, key questions included the existence of cardiac disease or hypertension, and if the patient is taking beta-adrenergic antagonists for any reason.

Bystander history of a possible trigger, sudden onset, and rapid progression is informative. The presence of urticaria or general flushing, hypotension, bronchospasm, laryngeal edema, back pain, dilation of the pupils, and convulsions, or combinations of them, are warning signs; the patient is at risk for immediate death. Cardiac arrest, in suspected anaphylaxis, calls for vigorous resuscitation since it is a potentially reversible condition.

Any person or facility administering vaccines[3] or immunologic desensitization must be immediately prepared to respond to anaphylaxis.

Treatment

Multiple clinical practice guidelines for the immediate and long-term management of anaphylaxis have been published[4], including joint American guidelines[5]

Immediate management

Patients with a history of anaphylaxis, or a strong risk thereof, may self-administer an epinephrine autoinjector. Depending on local protocols, Basic Life Support emergency personnel, not normally authorized to administer drugs, may assist the patient with self-administration.

Medical errors in dosing epinephrine

As the dose of epinephrine is sometimes expressed as a ratio only (1 mL of 1:1000) or a concentration only (1 mg in 1 mL), medical errors in administration may be made.[6]

Which concentration of epinephrine to use?

  • 1:1,000 solution is for intramuscular
  • 1:10,000 intravenous or endotracheal

Patients in anaphylaxis should be transported by advanced life support capable ambulance when available. If the trigger point of entry can be identified (e.g., a bee sting), and it is on an extremity, a tourniquet, released every 5 minutes, can be applied. If a stinger or other source is present, remove it as quickly as possible.

Epinephrine is given intramuscularly in 1:1,000 solution, 0.3 to 0.5 ml for adults. When anaphylaxis is severe, give epinephrine intravenously or by endotracheal tube, 1.0 ml. of 1:10,000 solution. A continuous infusion may be needed. Repeat every 5-10 minutes until the signs disappear. While some physicians frequently do not administer epinephrine, possibly due to concern about drug toxicity[7], only the most extreme and confirmed reasons can justify withholding it. Obvious care must be taken in patients with cardiac or hypertensive disease, but a patient is likelier to die quickly from anaphylaxis than the effects of epinephrine. In the presence of laryngeal swelling, nebulized epinephrine may help, but evidence of such swelling will usually justify epinephrine. Bronchospasm, if present, should be treated with a nebulized short-acting β2 agonist such as albuterol.

Intravenous infusion of saline or other crystalloid should be started immediately, giving adults 500 ml to 1 L of normal saline over 30 minutes, with additional fluids given as needed. If the episode is prolonged, treatment in an intensive care unit may be needed with invasive monitoring of cardiac output and central venous pressure.

Vasoconstrictor agents to support blood pressure can include continuous epinephrine infusion, as well as dopamine.

Antihistamines support epinephrine, but do not replace it. The combination of a histamine H1 antagonist (e.g., diphenhydramine) and histamine H2 antagonist (e.g., ranitidine) may be better than either drug alone in some settings.[8][9][10]

While they will not have a short-term effect, corticosteroids should be started early in the incident; anaphylaxis may have a late-phase component.[10]

If the patient is taking a beta-blocker, reversing its effect with glucagon may help if the patient has not responded to epinephrine and fluids. There is anecdotal[11] and animal[12] evidence that glucagon can be helpful. It also provides inotropic effects and chronotropic effects on the heart by increasing intracellular levels of cAMP.

Anaphylaxis is one of the few remaining indications for military antishock trousers. [13].

Relapse of shock after treatment is rare.[14] 24239340

Long-term management

Obviously, the patient should avoid antigens to which they know they are sensitive. If, for example, there is hypersensitivity to latex, all medical personnel should be informed, and the patient should wear an alerting bracelet or necklace. When insect stings are a trigger, the patient must take precautions to avoid attracting insects while outside, such as wearing strong perfumes.

It is also advisable to carry an emergency drug kit, which minimally consists of an epinephrine autoinjector, and perhaps antihistamines.

Allergic desensitization should be considered seriously if feasible.

References

  1. Anonymous (2024), Anaphylaxis (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. Dreskin, Stephen C & G William Palmer (October 7, 2005), "Anaphylaxis", eMedicine
  3. Northern Territory (Australia) Centre for Disease Control, Management of anaphylaxis in the rural NT setting
  4. Alrasbi M, Sheikh A (2007). "Comparison of international guidelines for the emergency medical management of anaphylaxis.". Allergy 62 (8): 838-41. DOI:10.1111/j.1398-9995.2007.01434.x. PMID 17620061. Research Blogging.
  5. Joint Task Force on Practice Parameters. American Academy of Allergy, Asthma and Immunology. American College of Allergy, Asthma and Immunology. Joint Council of Allergy, Asthma and Immunology (2005). "The diagnosis and management of anaphylaxis: an updated practice parameter.". J Allergy Clin Immunol 115 (3 Suppl 2): S483-523. DOI:10.1016/j.jaci.2005.01.010. PMID 15753926. Research Blogging. Summary at the National Guidelines Clearinghouse
  6. Wheeler DW, Carter JJ, Murray LJ, et al (January 2008). "The effect of drug concentration expression on epinephrine dosing errors: a randomized trial". Ann. Intern. Med. 148 (1): 11–4. PMID 18166759[e]
  7. Russell S, Monroe K, Losek JD (2010). "Anaphylaxis management in the pediatric emergency department: opportunities for improvement.". Pediatr Emerg Care 26 (2): 71-6. DOI:10.1097/PEC.0b013e3181ce2e1c. PMID 20094000. Research Blogging.
  8. Ring J, Rothenberger KH, Clauss W (1985). "Prevention of anaphylactoid reactions after radiographic contrast media infusion by combined histamine H1- and H2-receptor antagonists: results of a prospective controlled trial.". Int Arch Allergy Appl Immunol 78 (1): 9-14. PMID 2863224.
  9. Runge JW, Martinez JC, Caravati EM, Williamson SG, Hartsell SC (1992). "Histamine antagonists in the treatment of acute allergic reactions.". Ann Emerg Med 21 (3): 237-42. PMID 1536481.
  10. 10.0 10.1 Greenwald, Peter W (2004), Chapter 9, Shock, in Stone, CK and Humphries R, Current Emergency Diagnosis & Treatment (5th ed.), Lange Medical Books/McGraw-Hill, CEDT-09, pp. 207-208
  11. Thomas, Martin (April 12, 2005), "Glucagon infusion in anaphylactic shock in patients on beta-blockers", Bestbets
  12. Andjelkovic, Ivan & Berislav Zlokovic (1982 July), "Protective effects of glucagon during the anaphylactic response in guinea-pig isolated heart", Br J Pharmacol 76(3): 483–489.
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