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'''Critical care''' medicine is the "health care provided to a critically ill patient during a medical emergency or crisis".<ref name="MeSH-CriticalCare">{{cite web |url=http://www.nlm.nih.gov/cgi/mesh/2008/MB_cgi?term=Critical+care |title=Critical care |accessdate=2008-01-07 |author=Anonymous|publisher=National Library of Medicine |authorlink= |coauthors= |date= |format= |work=|pages= |language= |archiveurl= |archivedate= |quote=}}</ref>
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'''Critical care''' medicine is the "health care provided to a critically ill patient during a medical emergency or crisis".<ref name="MeSH-CriticalCare">{{cite web |url=http://www.nlm.nih.gov/cgi/mesh/2008/MB_cgi?term=Critical+care |title=Critical care |accessdate=2008-01-07 |author=Anonymous|publisher=National Library of Medicine |authorlink= |coauthors= |date= |format= |work=|pages= |language= |archiveurl= |archivedate= |quote=}}</ref> It may be provided in [[intensive care unit]]s, "stepdown" hospital wards, [[emergency room]]s, and in [[field medicine]].


==Monitoring==
==Monitoring the critically ill patient==
===Swan-Ganz catheterization===
Several measures are available based on [[blood gas analysis]].
 
===Circulation===
;Pulmonary  artery catheterization
Among patients with [[acute lung injury]], the use of [[pulmonary artery catheterization]] (Swan-Ganz catheterization) did not improve outcomes over monitoring with [[central venous catheterization]].<ref name="pmid16714768">{{cite journal| author=National Heart, Lung, and Blood Institute Acute Respiratory Distress Syndrome (ARDS) Clinical Trials Network. Wheeler AP, Bernard GR, Thompson BT, Schoenfeld D, Wiedemann HP et al.| title=Pulmonary-artery versus central venous catheter to guide treatment of acute lung injury. | journal=N Engl J Med | year= 2006 | volume= 354 | issue= 21 | pages= 2213-24 | pmid=16714768
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=16714768 | doi=10.1056/NEJMoa061895 }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=17080982 Review in: ACP J Club. 2006 Nov-Dec;145(3):70] <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
;Inferior vena cava ultrasonography
[[Ultrasonography]]  of the inferior [[vena cava]]  may help detect low central venous pressure. The caval index is the  relative decrease in diameter  between expiration and inspiration. If  the caval index is 50%, then a central venous pressure of < 8 mm Hg  is detected with:<ref  name="pmid19556029">{{cite journal|  author=Nagdev AD, Merchant RC, Tirado-Gonzalez A, Sisson CA, Murphy MC|  title=Emergency department bedside ultrasonographic measurement of the  caval index for noninvasive determination of low central venous  pressure. | journal=Ann Emerg Med | year= 2010 | volume= 55 | issue= 3 |  pages= 290-5 | pmid=19556029
| 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=19556029  | doi=10.1016/j.annemergmed.2009.04.021 }}  <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
* [[Sensitivity  and specificity|Sensitivity]] of 91%
* [[Sensitivity  and specificity|Specificity]] of 94%
 
===Respiration and oxygenation===
;PaO<sub>2</sub>/FiO2 ratio (PF ratio)
{{main|P:F ratio}}
:<math>{P/F\ ratio} = \left (\frac{PaO_2}{Fi0_2}\right) \times 100</math>
An example in a healthy person:
:<math>{476} = \left (\frac{100\ mm\ Hg}{21%}\right) \times 100</math>
 
A higher ratio indicates better gas exchange:
* Normal is 500
* [[Adult respiratory distress syndrome|ARDS]] is < 200
 
Comparative studies suggest this measure correlates better with pulmonary shunts than does the A-a gradient.<ref name="pmid6409506">{{cite journal |author=Covelli HD, Nessan VJ, Tuttle WK |title=Oxygen derived variables in acute respiratory failure |journal=Crit. Care Med. |volume=11 |issue=8 |pages=646–9 |year=1983 |pmid=6409506 |doi=}}</ref><ref name="pmid14769743">{{cite journal |author=El-Khatib MF, Jamaleddine GW |title=A new oxygenation index for reflecting intrapulmonary shunting in patients undergoing open-heart surgery |journal=Chest |volume=125 |issue=2 |pages=592–6 |year=2004 |pmid=14769743 |doi=}}</ref><ref name="pmid3191742">{{cite journal |author=Cane RD, Shapiro BA, Templin R, Walther K |title=Unreliability of oxygen tension-based indices in reflecting intrapulmonary shunting in critically ill patients |journal=Crit. Care Med. |volume=16 |issue=12 |pages=1243–5 |year=1988 |pmid=3191742 |doi=}}</ref>
 
;Oxygenation index
:<math>Oxygenation\ index =  \left(\frac{mean\ airway\ pressure}{P/F\ ratio}\right) \times 100</math>
or
:<math>Oxygenation\ index =  \left(mean\ airway\ pressure \times \left(\frac{Fi0_2}{PaO_2}\right)\right) \times 100</math>
A lower oxygenation index indicates better gas exchange. The oxygenation index, which includes the mean airway pressure<ref name="pmid1395670">{{cite journal| author=Marini JJ, Ravenscraft SA| title=Mean airway pressure: physiologic determinants and clinical importance--Part 1: Physiologic determinants and measurements. | journal=Crit Care Med | year= 1992 | volume= 20 | issue= 10 | pages= 1461-72 | pmid=1395670
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=1395670 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name="pmid1424706">{{cite journal| author=Marini JJ, Ravenscraft SA| title=Mean airway pressure: physiologic determinants and clinical importance--Part 2: Clinical implications. | journal=Crit Care Med | year= 1992 | volume= 20 | issue= 11 | pages= 1604-16 | pmid=1424706
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=1424706 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>, may better correlate with intrapulmonary shunting than the PF ratio<ref name="pmid14769743"/>


===Oxygenation===
;Alveolar-arterial oxygen (A-a) gradient (alveolar-arterial oxygen difference - AVO<sub>2</sub>D)
;Alveolar-arterial oxygen (A-a) gradient (alveolar-arterial oxygen difference - AVO<sub>2</sub>D)
The A-a gradient is harder to calculate, but accounts for changes in ventilation as measured by the partial pressure of carbon dioxide.
:<math>\mbox{A-a gradient} = {PAO_2}\  -\  {PaO_2}</math>
;PaO2/FiO2 ratio (PF ratio)
:<math>{PAO_2} = {Fi0_2} *\left ({760 - 47}\right) \  -\  \frac{PaCO_2}{0.8}</math>
This measure is easier to calculate.
* Normal is < 10 mm Hg
 
The A-a gradient is harder to calculate, but accounts for changes in respiration as measured by the [[partial pressure]] of carbon dioxide. However, this calculation relies on the respiratory quotient being constant in the prediction of alveolar CO<sub>2</sub> When compared to the PF ratio, the A-a gradient is found to correlate less well with pulmonary shunting.<ref name="pmid6409506">{{cite journal |author=Covelli HD, Nessan VJ, Tuttle WK |title=Oxygen derived variables in acute respiratory failure |journal=Crit. Care Med. |volume=11 |issue=8 |pages=646–9 |year=1983 |pmid=6409506 |doi=}}</ref><ref name="pmid14769743">{{cite journal |author=El-Khatib MF, Jamaleddine GW |title=A new oxygenation index for reflecting intrapulmonary shunting in patients undergoing open-heart surgery |journal=Chest |volume=125 |issue=2 |pages=592–6 |year=2004 |pmid=14769743 |doi=}}</ref><ref name="pmid3191742">{{cite journal |author=Cane RD, Shapiro BA, Templin R, Walther K |title=Unreliability of oxygen tension-based indices in reflecting intrapulmonary shunting in critically ill patients |journal=Crit. Care Med. |volume=16 |issue=12 |pages=1243–5 |year=1988 |pmid=3191742 |doi=}}</ref>
 
Among outpatients with possible pulmonary embolism, the A-a gradient may be a better test.<ref name="pmid8304364">{{cite journal |author=McFarlane MJ, Imperiale TF |title=Use of the alveolar-arterial oxygen gradient in the diagnosis of pulmonary embolism |journal=Am. J. Med. |volume=96 |issue=1 |pages=57–62 |year=1994 |pmid=8304364 |doi=}}</ref>
 
An online calculator for the A-a gradient is at http://www.mdcalc.com/aagrad.
 
===Tissue perfusion===
;Central venous oxygen saturation (ScvO<sub>2</sub>)
In patients with [[septic shock]], maintaining the central venous oxygen saturation (ScvO<sub>2</sub>) <u>></u> 70% is a [[health care quality assurance]] measure for the Institute for Healthcare Improvement.<ref>[http://www.ihi.org/IHI/Topics/CriticalCare/Sepsis/Changes/IndividualChanges/Maintainadequatecentralvenousoxygensaturation.htm Maintain Adequate Central Venous Oxygen Saturation] Institute for Healthcare Improvement</ref>  This is measured from the [[superior vena cava]]. This is hard to predict by [[physical examination]].<ref name="pmid19885995">{{cite journal| author=Grissom CK, Morris AH, Lanken PN, Ancukiewicz M, Orme JF, Schoenfeld DA et al.| title=Association of physical examination with pulmonary artery  catheter parameters in acute lung injury. | journal=Crit Care Med | year= 2009 | volume= 37 | issue= 10 | pages= 2720-6 | pmid=19885995
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19885995 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
;Mixed venous oxygen saturation (SvO<sub>2</sub>)
In patients with [[septic shock]], maintaining the mixed venous oxygen saturation (ScvO<sub>2</sub>) <u>></u> 65% is a [[health care quality assurance]] measure for the Institute for Healthcare Improvement that is an alternative to the central venous oxygen saturation.<ref>[http://www.ihi.org/IHI/Topics/CriticalCare/Sepsis/Changes/IndividualChanges/Maintainadequatecentralvenousoxygensaturation.htm Maintain Adequate Central Venous Oxygen Saturation] Institute for Healthcare Improvement</ref> This is measured from a [[pulmonary artery catheter]].  This is hard to predict by [[physical examination]].<ref name="pmid19885995">{{cite journal| author=Grissom CK, Morris AH, Lanken PN, Ancukiewicz M, Orme JF, Schoenfeld DA et al.| title=Association of physical examination with pulmonary artery  catheter parameters in acute lung injury. | journal=Crit Care Med | year= 2009 | volume= 37 | issue= 10 | pages= 2720-6 | pmid=19885995
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19885995 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
The mixed venous pressure may be lower than the central venous pressure due to mixing with blood from the splanchnic circulation or carotid sinuses that has lower oxygen content.<ref name="pmid16100219">{{cite journal| author=Kopterides P, Mavrou I, Kostadima E| title=Central or mixed venous oxygen saturation? | journal=Chest | year= 2005 | volume= 128 | issue= 2 | pages= 1073-4; author reply 1074-5 | pmid=16100219
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=16100219 | doi=10.1378/chest.128.2.1073 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
;Tissue oxygen saturation (StO<sub>2</sub>)
Tissue oxygen saturation (StO<sub>2</sub>) at the thenar eminence may be an alternative, non-invasive measurement.<ref name="pmid17227587">{{cite journal| author=Podbregar M, Mozina H| title=Skeletal muscle oxygen saturation does not estimate mixed venous oxygen saturation in patients with severe left heart failure and additional severe sepsis or septic shock. | journal=Crit Care | year= 2007 | volume= 11 | issue= 1 | pages= R6 | pmid=17227587
| 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=17227587 | doi=10.1186/cc5153 | pmc=PMC2147710 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name="pmid19602965">{{cite journal| author=Leone M, Blidi S, Antonini F, Meyssignac B, Bordon S, Garcin F et al.| title=Oxygen tissue saturation is lower in nonsurvivors than in survivors after early resuscitation of septic shock. | journal=Anesthesiology | year= 2009 | volume= 111 | issue= 2 | pages= 366-71 | pmid=19602965
| 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=19602965 | doi=10.1097/ALN.0b013e3181aae72d }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
;Lactate clearance
Maintaining lactate clearance about 10% may be an easier alternative than invasive measurements of oxygenation according to a [[randomized controlled trial]] by [http://www.emshocknet.com/ EMShockNet].<ref name="pmid20179283"/>
:<math>\text{Lactate clearance} = \left(\frac{lactate_{initial} - lactate_{two\ hours}}{lactate_{initial}}\right) \times 100</math>
 
;Capnography
Capnography, which is "continuous recording of the [[carbon dioxide]] content of expired air,"<ref>{{MeSH|Capnography}}</ref> may detect respiratory depression before hypoxemia occurs.<ref name="pmid19783324">{{cite journal| author=Deitch K, Miner J, Chudnofsky CR, Dominici P, Latta D| title=Does end tidal CO2 monitoring during emergency department procedural sedation and analgesia with propofol decrease the incidence of hypoxic events? A randomized, controlled trial. | journal=Ann Emerg Med | year= 2010 | volume= 55 | issue= 3 | pages= 258-64 | pmid=19783324
| 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=19783324 | doi=10.1016/j.annemergmed.2009.07.030 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref> Proposed criteria for respiratory depression are:<ref name="pmid19783324"/>
* End tidal CO<sub>2</sub> (ETCO<sub>2</sub>)  level  50 mm Hg
* ETCO<sub>2</sub> change from baseline of 10%
* Loss of waveform for  15 seconds
 
===Real time glucose monitoring===
Real-time glucose monitoring does not clearly help control the blood glucose level.<ref name="pmid20007948">{{cite journal| author=Holzinger U, Warszawska J, Kitzberger R, Wewalka M, Miehsler W, Herkner H et al.| title=Real-Time Continuous Glucose Monitoring in Critically Ill Patients: A prospective randomized trial. | journal=Diabetes Care | year= 2010 | volume= 33 | issue= 3 | pages= 467-72 | pmid=20007948
| 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=20007948 | doi=10.2337/dc09-1352 | pmc=PMC2827490 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
 
==Treatments provided in the intensive care unit==
===Goal-directed  resuscitation===
Protocols for the resuscitation of [[septic shock]] are:<ref name="pmid20179283">{{cite journal| author=Jones AE, Shapiro NI, Trzeciak S, Arnold RC, Claremont HA, Kline JA et al.| title=Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial. | journal=JAMA | year= 2010 | volume= 303 | issue= 8 | pages= 739-46 | pmid=20179283
| 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=20179283 | doi=10.1001/jama.2010.158 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name="pmid11794169">{{cite journal| author=Rivers E, Nguyen B, Havstad S, Ressler J, Muzzin A, Knoblich B et al.| title=Early goal-directed therapy in the treatment of severe sepsis and septic shock. | journal=N Engl J Med | year= 2001 | volume= 345 | issue= 19 | pages= 1368-77 | pmid=11794169
| 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=11794169 }}  [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=11985431 Review in: ACP J Club. 2002 May-Jun;136(3):90] <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
# "Isotonic  crystalloid was administered in boluses to achieve a central  venous pressure of 8 mm Hg or higher"
# "Mean  arterial pressure goal of 65 mm Hg or higher, if not achieved  with fluid administration, was targeted by initiating and titrating vasopressors ([[dopamine]] or [[norepinephrine]])"<ref  name="pmid20179283"/> or goal of 65 mm Hg to 90 mm Hg<ref name="pmid11794169"/>
# If ScvO<sub>2</sub> < 70% or lactate clearance < 10%
:*If [[hematocrit]] is < 30%, packed red  blood cells were transfused
:*If hematocrit is > 30%, [[cardiotonic agent]]s such as [[dobutamine]]
 
===Circulatory support===
{{main|Vasoconstrictor agent|Cardiotonic agent}}
Goal-directed  resuscitation has been developed and so far studies for the resuscitation of [[septic shock]]:<ref  name="pmid20179283"></ref>
# "Isotonic crystalloid was administered in boluses to achieve a central venous pressure of 8 mm Hg or higher"
# "Mean  arterial pressure goal of 65 mm Hg or higher, if not achieved with fluid administration, was targeted by initiating and titrating [[vasoconstrictor agent|vasopressors]] ([[dopamine]]  or [[norepinephrine]])"<ref name="pmid20179283"/> or goal of 65  mm Hg to 90 mm Hg<ref name="pmid11794169"/>
# If ScvO<sub>2</sub> < 70% or lactate  clearance < 10%
:*If [[hematocrit]] is < 30%, packed red blood cells were transfused
:*If hematocrit is > 30%, [[cardiotonic agent]]s such as [[dobutamine]]
 
===Renal support===
{{Main|Renal replacement therapy}}
 
===Respiratory support===
{{main|Artificial respiration}}
==Surgical and trauma critical care==
The standard of care for fluid replacement after traumatic injury continues to evolve. [[Permissive hypotension]] is increasingly preferred in most situations: giving enough fluid to return the systolic blood pressure to approximately 100mm, but ''not'' to return it to normal. Raising the pressure to normal levels may also raise the pressure enough to disrupt clots and restart hemorrhaging.
 
Routine use of vasopressors in trauma uncomplicated by disease is discouraged; a surgical maxim is that the treatment for traumatic hypotension is surgery, not drugs.
 
An important exception to permissive hypotension is the field management of [[crush injury]]. In this case, fluid overload, as well as alkalinization, is necessary to protect the kidneys and other organs from the rush of muscle breakdown products when the flow-occluding pressure of a heavy object is removed.


Comparative studies provide mixed recommendations regarding which measure is best.<ref name="pmid6409506">{{cite journal |author=Covelli HD, Nessan VJ, Tuttle WK |title=Oxygen derived variables in acute respiratory failure |journal=Crit. Care Med. |volume=11 |issue=8 |pages=646–9 |year=1983 |pmid=6409506 |doi=}}</ref><ref name="pmid14769743">{{cite journal |author=El-Khatib MF, Jamaleddine GW |title=A new oxygenation index for reflecting intrapulmonary shunting in patients undergoing open-heart surgery |journal=Chest |volume=125 |issue=2 |pages=592–6 |year=2004 |pmid=14769743 |doi=}}</ref>
==Complications==
===Abdominal compartment syndrome===
Abdominal compartment syndrome is associated with increased mortality.<ref name="pmid15699833">{{cite journal |author=Malbrain ML, Chiumello D, Pelosi P, ''et al'' |title=Incidence and prognosis of intraabdominal hypertension in a mixed population of critically ill patients: a multiple-center epidemiological study |journal=Crit. Care Med. |volume=33 |issue=2 |pages=315–22 |year=2005 |month=February |pmid=15699833 |doi= |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=33&issue=2&spage=315 |issn=}}</ref>
 
===Medical error===
{{main|Medical error}}
Examining errors in administration of parenteral [[medication]]s, a study found:<ref name="pmid19282436">{{cite journal |author=Valentin A, Capuzzo M, Guidet B, ''et al'' |title=Errors in administration of parenteral drugs in intensive care units: multinational prospective study |journal=BMJ |volume=338 |issue= |pages=b814 |year=2009 |pmid=19282436 |doi= |url=http://bmj.com/cgi/pmidlookup?view=long&pmid=19282436 |issn=}}</ref>
* 74 errors per 100 patient-days
* Independent risk factors were:
** Patient complexity as measured by
*** number of organ failures
*** number of parenteral administrations
** Work load as measured by
*** Larger intensive care unit
*** Increased ratio of patient turnover to the size of the unit
*** Number of patients per nurse
*** Occupancy rate of the unit
 
==Preventing complications in the critically ill patient==
===Delirium===
{| class="wikitable" align="right"
|+ [[Antipsychotic agent]]s to reduce the number of days mechanically ventilated patients were alive without [[delirium]]<ref name="pmid20095068">{{cite journal| author=Girard TD, Pandharipande PP, Carson SS, Schmidt GA, Wright PE, Canonico AE et al.| title=Feasibility, efficacy, and safety of antipsychotics for intensive care unit delirium: the MIND randomized, placebo-controlled trial. | journal=Crit Care Med | year= 2010 | volume= 38 | issue= 2 | pages= 428-37 | pmid=20095068
| 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=20095068 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
! Drug!! Number of days
|-
| [[Haloperidol]] || 14.0
|-
| [[Ziprasidone]] || 15.0
|-
| [[Placebo]]|| 12.5
|-
| colspan="2"| P = 0.66
|}
 
[[Antipsychotic agent]]s, in a small study, found that an average of 15 mgs per day of [[haloperidol]] and 113 mg per day of [[ziprasidone]] increased [[akathisia]] (see table for benefits which did not have [[statistical significance]]).<ref name="pmid20095068"/>
===Glucose control===
Two [[clinical practice guideline]]s are available for patients with ; however, both of these guidelines were developed without broad representation of stakeholders.<ref name="pmid11330080">{{cite journal |author=Mulrow CD, Lohr KN |title=Proof and policy from medical research evidence |journal=J Health Polit Policy Law |volume=26 |issue=2 |pages=249–66 |year=2001 |month=April |pmid=11330080 |doi= |url=http://jhppl.dukejournals.org/cgi/pmidlookup?view=long&pmid=11330080 |issn=}}</ref> This may lead to overly aggressive clinical recommendations. In addition, these guidelines were published before the two recent negative trials.
 
The [[American Association of Clinical Endocrinologists]] (AACE) recommends the following target blood glucose levels:<ref name="pmid17613449">{{cite journal |author= |title=American Association of Clinical Endocrinologists medical guidelines for clinical practice for the management of diabetes mellitus |journal=Endocr Pract |volume=13 Suppl 1 |issue= |pages=1–68 |year=2007 |pmid=17613449 |doi= |url=http://aace.metapress.com/openurl.asp?genre=article&issn=1530-891X&volume=13%20Suppl%201&issue=&spage=1 |issn=|author=AACE Diabetes Mellitus Clinical Practice Guidelines Task Force}} [http://ngc.gov/summary/summary.aspx?ss=15&doc_id=11100 Complete summary from National Guidelines Clearinghouse]</ref>
* "Critically ill patients, between 80 to 110 mg/dL (grade A recommendation)"
 
The [[American Diabetes Association]] (ADA) states<ref name="pmid18165335">{{cite journal |author= |title=Standards of medical care in diabetes--2008 |journal=Diabetes Care |volume=31 Suppl 1 |issue= |pages=S12–54 |year=2008 |month=January |pmid=18165335 |doi=10.2337/dc08-S012 |url=http://care.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=18165335 |issn=|author=American Diabetes Association}} [http://ngc.gov/summary/summary.aspx?ss=15&doc_id=10403 Complete summary from National Guidelines Clearinghouse]</ref>
* "Critically ill patients: blood glucose levels should be kept as close to 110 mg/dl (6.1 mmol/l) as possible and generally <140 mg/dl (7.8 mmol/l). (A) These patients require an intravenous insulin protocol that has demonstrated efficacy and safety in achieving the desired glucose range without increasing risk for severe hypoglycemia. (E)"
 
====Evidence====
[[Randomized controlled trial]]s of tight glucose control in the critical care and [[perioperative care]] settings have produced mixed results. See Table.
 
Meta-analyses of these trials exist:
* Meta-analysis in 2011 of 21 trials was negative.<ref name="pmid21320942">{{cite journal| author=Kansagara D, Fu R, Freeman M, Wolf F, Helfand M| title=Intensive insulin therapy in hospitalized patients: a systematic review. | journal=Ann Intern Med | year= 2011 | volume= 154 | issue= 4 | pages= 268-82 | pmid=21320942 | doi=10.1059/0003-4819-154-4-201102150-00008 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21320942  }} </ref>
* Meta-analysis in 2010 of 7 trials was negative.<ref name="pmid20018803">{{cite journal| author=Marik PE, Preiser JC| title=Toward understanding tight glycemic control in the ICU: a systematic review and metaanalysis. | journal=Chest | year= 2010 | volume= 137 | issue= 3 | pages= 544-51 | pmid=20018803 | doi=10.1378/chest.09-1737 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20018803  }} </ref>
* Meta-analysis in 2009 of 26 trials was negative.<ref name="pmid19318387">{{cite journal| author=Griesdale DE, de Souza RJ, van Dam RM, Heyland DK, Cook DJ, Malhotra A et al.| title=Intensive insulin therapy and mortality among critically ill patients: a meta-analysis including NICE-SUGAR study data. | journal=CMAJ | year= 2009 | volume= 180 | issue= 8 | pages= 821-7 | pmid=19318387 | doi=10.1503/cmaj.090206 | pmc=PMC2665940 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19318387  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19687478 Review in: Ann Intern Med. 2009 Aug 18;151(4):JC2-4, JC2-5] </ref>
* Meta-analysis in 2009 of 29 trials was negative.<ref name="pmid18728267">{{cite journal| author=Wiener RS, Wiener DC, Larson RJ| title=Benefits and risks of tight glucose control in critically ill adults: a meta-analysis. | journal=JAMA | year= 2008 | volume= 300 | issue= 8 | pages= 933-44 | pmid=18728267 | doi=10.1001/jama.300.8.933 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18728267  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19321828 Review in: Evid Based Nurs. 2009 Apr;12(2):51]  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19172710 Review in: Ann Intern Med. 2009 Jan 20;150(2):JC1-5] </ref>
 
{| class="wikitable"
|+ Selected randomized controlled trials of glucose control in critical care<ref name="pmid20103758">{{cite journal| author=COIITSS Study Investigators. Annane D, Cariou A, Maxime V, Azoulay E, D'honneur G et al.| title=Corticosteroid treatment and intensive insulin therapy for septic shock in adults: a randomized controlled trial. | journal=JAMA | year= 2010 | volume= 303 | issue= 4 | pages= 341-8 | pmid=20103758
| 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=20103758 | doi=10.1001/jama.2010.2 }}</ref><ref name="pmid19318384">{{cite journal |author=The NICE-SUGAR Study Investigators|title=Intensive versus conventional glucose control in critically ill patients |journal=N. Engl. J. Med. |volume=360 |issue=13 |pages=1283–97 |year=2009 |month=March |pmid=19318384 |doi=10.1056/NEJMoa0810625 |url=http://content.nejm.org/cgi/pmidlookup?view=short&pmid=19318384&promo=ONFLNS19 |issn=}}</ref><ref name="pmid18936702">{{cite journal |author=Arabi YM, Dabbagh OC, Tamim HM, ''et al'' |title=Intensive versus conventional insulin therapy: a randomized controlled trial in medical and surgical critically ill patients |journal=Crit. Care Med. |volume=36 |issue=12 |pages=3190–7 |year=2008 |month=December |pmid=18936702 |doi=10.1097/CCM.0b013e31818f21aa |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?doi=10.1097/CCM.0b013e31818f21aa |issn=}}</ref><ref name="pmid18184958">{{cite journal |author=Brunkhorst FM, Engel C, Bloos F, ''et al'' |title=Intensive insulin therapy and pentastarch resuscitation in severe sepsis |journal=N. Engl. J. Med. |volume=358 |issue=2 |pages=125–39 |year=2008 |pmid=18184958 |doi=10.1056/NEJMoa070716 |issn=}}</ref>
<ref name="pmid16452557">{{cite journal |author=Van den Berghe G, Wilmer A, Hermans G, ''et al'' |title=Intensive insulin therapy in the medical ICU |journal=N. Engl. J. Med. |volume=354 |issue=5 |pages=449–61 |year=2006 |pmid=16452557 |doi=10.1056/NEJMoa052521|url=http://content.nejm.org/cgi/content/full/354/5/449}}</ref><ref name="pmid11794168">{{cite journal |author=van den Berghe G, Wouters P, Weekers F, ''et al'' |title=Intensive insulin therapy in the critically ill patients |journal=N. Engl. J. Med. |volume=345 |issue=19 |pages=1359–67 |year=2001 |pmid=11794168 |doi=|url=http://content.nejm.org/cgi/content/full/345/19/1359}}</ref>
! rowspan="2"|Trial !!rowspan="2"| Patients !!rowspan="2"| Intervention !!rowspan="2"| Comparison !!rowspan="2"| Outcomes !!colspan="2"| Results!!rowspan="2"| Authors' conclusions
|-
! Intensive control !! Control group
|-
| COIITSS Study<ref name="pmid20103758"/><br/>2010||509 adults with septic shock||Insulin targeting serum glucose of 80 to 110 mg/dl|| 2004 Surviving Sepsis Campaign guidelines<ref name="pmid15090974">{{cite journal| author=Dellinger RP, Carlet JM, Masur H, Gerlach H, Calandra T, Cohen J et al.| title=Surviving Sepsis Campaign guidelines for management of severe sepsis and septic shock. | journal=Crit Care Med | year= 2004 | volume= 32 | issue= 3 | pages= 858-73 | pmid=15090974
| 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=15090974 }}</ref>||In-hospital mortality||align="center"  style="background-color:red"|45.9% *||align="center"|42.9%||"intensive insulin therapy did not improve in-hospital mortality "
|-
| NICE-SUGAR<ref name="pmid19318384"/><br/>2009||6104 patients in medical and surgical ICU||Insulin drip targeting serum glucose of 81 to 108 mg/dl||Insulin drip targeting serum glucose of 144 - 180 mg/dl||Mortality at 90 days||align="center"  style="background-color:red"|27.5% *||align="center"|24.9%||"intensive glucose control increased mortality among adults in the ICU"
|-
| Arabi et al<ref name="pmid18936702"/><br/>2008|| 523 patients in medical and surgical ICU||Insulin drip targeting serum glucose of 80 to 110 mg/dl||Insulin drip targeting serum glucose of 180 to 200 mg/dl||Mortality in the intensive care unit||align="center"|13.5%||align="center"|17.1||"Intensive insulin therapy was not associated with improved survival...and was associated with increased occurrence of hypoglycemia"
|-
| SepNet<ref name="pmid18184958"/><br/>2008|| 537 patients with severe sepsis||Insulin drip if needed to target serum glucose of 80 to 110 mg/dl||Insulin drip if needed to target serum glucose of < 200 mg/dl||Mortality in the intensive care unit||align="center"|24.7%||align="center"|26%||"intensive insulin therapy placed critically ill patients with sepsis at increased risk for serious adverse events"
|-
| Van den Berghe<ref name="pmid16452557"/><br/>2006||1200 patients in medical ICU||Insulin drip targeting serum glucose of 80 to 110 mg/dl||Insulin drip targeting serum glucose of 180 to 200 mg/dl||Hospital mortality||align="center"|37.3%||align="center"|40%||"Intensive insulin therapy significantly reduced morbidity but not mortality"
|-
| Van den Berghe<ref name="pmid11794168"/><br/>2001||1548 patients in surgical ICU|||Insulin drip targeting serum glucose of 80 to 110 mg/dl||Insulin drip targeting serum glucose of 180 to 200 mg/dl||Mortality in the intensive care unit||align="center" style="background-color:lightgreen"|4.6% *||align="center"|8%||"Intensive insulin therapy...reduces morbidity and mortality"
|-
| colspan="8"|Notes:<br/>* Significantly different from the control group.
|}
 
Two of the trials in the Table suggested benefit (see green cells):
*Van den Berghe 2006<ref name="pmid16452557"/>. Although this trial concluded "intensive insulin therapy significantly reduced morbidity but not mortality among all patients in the medical ICU. Although the risk of subsequent death and disease was reduced in patients treated for three or more days" the trial stated "these patients could not be identified before therapy."<ref name="pmid16452557">{{cite journal |author=Van den Berghe G, Wilmer A, Hermans G, ''et al'' |title=Intensive insulin therapy in the medical ICU |journal=N. Engl. J. Med. |volume=354 |issue=5 |pages=449–61 |year=2006 |pmid=16452557 |doi=10.1056/NEJMoa052521|url=http://content.nejm.org/cgi/content/full/354/5/449}}</ref>
* Van den Berghe 2002<ref name="pmid11794168"/>. This trial has been criticized for the following reasons:<ref name="pmid18380987">{{cite journal| author=Gandhi GY, Murad MH, Flynn DN, Erwin PJ, Cavalcante AB, Bay Nielsen H et al.| title=Effect of perioperative insulin infusion on surgical morbidity and mortality: systematic review and meta-analysis of randomized trials.7. | journal=Mayo Clin Proc | year= 2008 | volume= 83 | issue= 4 | pages= 418-30 | pmid=18380987 | doi= | pmc= | url= }} </ref><br/>
# "The trial was stopped early for an unexpectedly large treatment effect, which can overestimate the efficacy of treatment or result in a false-positive finding;"
# "The relative reduction in mortality for a decrease of 50 mg/dL in morning glucose levels seems biologically implausible and exceeds that for any other intervention in critically ill patients;"
# "The mortality rate in the control group was much higher than that noted in tertiary care medical centers in the United States. On admission to the ICU, all patients received 200 to 300 g/d of intravenous dextrose followed by enteral or parenteral nutrition, an unusual practice considering the deleterious effects of parenteral nutrition; at least in part, the difference in outcomes between the 2 arms in this study might have reflected the harm of maintaining the control group as hyperglycemic rather than the benefit of strict glucose control in the intervention group."
 
Tight control may protect renal function.<ref name="pmid18235100">{{cite journal |author=Schetz M, Vanhorebeek I, Wouters PJ, Wilmer A, Van den Berghe G |title=Tight blood glucose control is renoprotective in critically ill patients |journal=J. Am. Soc. Nephrol. |volume=19 |issue=3 |pages=571-8 |year=2008 |pmid=18235100 |doi=10.1681/ASN.2006101091 |url=http://jasn.asnjournals.org/cgi/pmidlookup?view=long&pmid=18235100}}</ref>
 
Regarding [[perioperative care|intraoperative]] control of glucose, a [[randomized controlled trial]] concluded "the increased incidence of death and stroke in the intensive treatment group raises concern about routine implementation of this intervention."<ref name="pmid17310047">{{cite journal |author=Gandhi GY, Nuttall GA, Abel MD, ''et al'' |title=Intensive intraoperative insulin therapy versus conventional glucose management during cardiac surgery: a randomized trial |journal=Ann. Intern. Med. |volume=146 |issue=4 |pages=233–43 |year=2007 |pmid=17310047 |doi= |issn=|url=http://www.annals.org/cgi/content/full/146/4/233}}</ref>
 
===Preventing anemia===
====Blood transfusion====
;Clinical practice guidelines
[[Clinical practice guideline]]s by the Eastern Association for Surgery of Trauma and the American College of Critical Care Medicine include [[blood transfusion]]s recommendations for:<ref name="pmid19773646">{{cite journal| author=Napolitano LM, Kurek S, Luchette FA, Corwin HL, Barie PS, Tisherman SA et al.| title=Clinical practice guideline: red blood cell transfusion in adult trauma and critical care. | journal=Crit Care Med | year= 2009 | volume= 37 | issue= 12 | pages= 3124-57 | pmid=19773646
| 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=19773646 | doi=10.1097/CCM.0b013e3181b39f1b }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
# "patients with evidence of hemorrhagic shock"
# "patients with evidence of acute hemorrhage and hemodynamic instability or inadequate" oxygenation
# "A “restrictive” strategy of RBC transfusion (transfuse when Hb < 7 g/dL) is as effective as a 'liberal' transfusion strategy (transfusion when Hb < 10 g/dL) in critically ill patients with hemodynamically stable anemia, except possibly in patients with acute myocardial ischemia."
# "The use of only Hb level as a 'trigger' for transfusion should be avoided"
# "In the absence of acute hemorrhage, RBC transfusion should be given as single units"
# "Consider transfusion if Hb is <7 g/dL in critically ill patients requiring mechanical ventilation"
# "Consider transfusion if Hb is <7 g/dL in resuscitated critically ill trauma patients"
# "Consider transfusion if Hb is <7 g/dL in critically ill patients with stable cardiac disease"
# "RBC transfusion should not be considered as an absolute method to improve tissue oxygen consumption in critically ill patients."
# "RBC transfusion may be beneficial in patients with acute coronary syndromes (ACS) who are anemic (Hb <u><</u> 8 g/dL) on hospital admission"
# "The transfusion needs for each septic patient must be assessed individually because optimal transfusion triggers in sepsis patients are not known and there is no clear evidence that blood transfusion increases tissue oxygenation"
# "All efforts should be initiated to avoid RBC transfusion in patients at risk for ALI and ARDS after completion of resuscitation."
 
;Trials
There may not be a meaningful difference in outcomes between transfusing blood to maintain a hemoglobin > 7.0 g/dl versus a hemoglobin > 10.0 g/dl.<ref name="pmid9971864">{{cite journal |author=Hébert PC, Wells G, Blajchman MA, ''et al'' |title=A multicenter, randomized, controlled clinical trial of transfusion requirements in critical care. Transfusion Requirements in Critical Care Investigators, Canadian Critical Care Trials Group |journal=N. Engl. J. Med. |volume=340 |issue=6 |pages=409–17 |year=1999 |pmid=9971864 |doi= |issn=}}</ref>
 
====Erythropoietin====
A [[randomized controlled trial]] reported "epoetin alfa does not reduce the incidence of red-cell transfusion among critically ill patients, but it may reduce mortality in patients with trauma. Treatment with epoetin alfa is associated with an increase in the incidence of thrombotic events."<ref name="pmid17804841">{{cite journal |author=Corwin HL, Gettinger A, Fabian TC, ''et al'' |title=Efficacy and safety of epoetin alfa in critically ill patients |journal=N. Engl. J. Med. |volume=357 |issue=10 |pages=965–76 |year=2007 |pmid=17804841 |doi=10.1056/NEJMoa071533}}</ref>


==Preventing complications in critically ill patients==
===Selective gastrointestinal decontamination===
===Selective gastrointestinal decontamination===
[[Systematic review]]s conclude that selective decontamination of the digestive tract may reduce morbidity in critically ill patients<ref name="pmid17387118">{{cite journal |author=Chan EY, Ruest A, Meade MO, Cook DJ |title=Oral decontamination for prevention of pneumonia in mechanically ventilated adults: systematic review and meta-analysis |journal=BMJ |volume=334 |issue=7599 |pages=889 |year=2007 |pmid=17387118 |doi=10.1136/bmj.39136.528160.BE}}</ref><ref name="pmid17244516">{{cite journal |author=Silvestri L, van Saene HK, Milanese M, Gregori D, Gullo A |title=Selective decontamination of the digestive tract reduces bacterial bloodstream infection and mortality in critically ill patients. Systematic review of randomized, controlled trials |journal=J. Hosp. Infect. |volume=65 |issue=3 |pages=187–203 |year=2007 |pmid=17244516 |doi=10.1016/j.jhin.2006.10.014}}</ref><ref name="pmid15895205">{{cite journal |author=Silvestri L, van Saene HK, Milanese M, Gregori D |title=Impact of selective decontamination of the digestive tract on fungal carriage and infection: systematic review of randomized controlled trials |journal=Intensive Care Med |volume=31 |issue=7 |pages=898–910 |year=2005 |pmid=15895205 |doi=10.1007/s00134-005-2654-9}}</ref> although some [[randomized controlled trial]]s have<ref name="pmid14522530">{{cite journal |author=de Jonge E, Schultz MJ, Spanjaard L, ''et al'' |title=Effects of selective decontamination of digestive tract on mortality and acquisition of resistant bacteria in intensive care: a randomised controlled trial |journal=Lancet |volume=362 |issue=9389 |pages=1011–6 |year=2003 |pmid=14522530 |doi=}}</ref><ref name="pmid1524328">{{cite journal |author=Cockerill FR, Muller SR, Anhalt JP, ''et al'' |title=Prevention of infection in critically ill patients by selective decontamination of the digestive tract |journal=Ann. Intern. Med. |volume=117 |issue=7 |pages=545–53 |year=1992 |pmid=1524328 |doi=}}</ref><ref name="pmid17146635">{{cite journal |author=Stoutenbeek CP, van Saene HK, Little RA, Whitehead A |title=The effect of selective decontamination of the digestive tract on mortality in multiple trauma patients: a multicenter randomized controlled trial |journal=Intensive Care Med |volume=33 |issue=2 |pages=261–70 |year=2007 |pmid=17146635 |doi=10.1007/s00134-006-0455-4}}</ref> and others have not found benefit<ref name="pmid1734249">{{cite journal |author=Gastinne H, Wolff M, Delatour F, Faurisson F, Chevret S |title=A controlled trial in intensive care units of selective decontamination of the digestive tract with nonabsorbable antibiotics. The French Study Group on Selective Decontamination of the Digestive Tract |journal=N. Engl. J. Med. |volume=326 |issue=9 |pages=594–9 |year=1992 |pmid=1734249 |doi=}}</ref>.


===Preventing gastrointestinal tract ulceration===
===Preventing gastrointestinal tract ulceration===
[[Systematic review]]s conclude that selective decontamination of the digestive tract may reduce morbidity in critically ill patients<ref name="pmid17387118">{{cite journal |author=Chan EY, Ruest A, Meade MO, Cook DJ |title=Oral decontamination for prevention of pneumonia in mechanically ventilated adults: systematic review and meta-analysis |journal=BMJ |volume=334 |issue=7599 |pages=889 |year=2007 |pmid=17387118 |doi=10.1136/bmj.39136.528160.BE}}</ref><ref name="pmid17244516">{{cite journal |author=Silvestri L, van Saene HK, Milanese M, Gregori D, Gullo A |title=Selective decontamination of the digestive tract reduces bacterial bloodstream infection and mortality in critically ill patients. Systematic review of randomized, controlled trials |journal=J. Hosp. Infect. |volume=65 |issue=3 |pages=187–203 |year=2007 |pmid=17244516 |doi=10.1016/j.jhin.2006.10.014}}</ref><ref name="pmid15895205">{{cite journal |author=Silvestri L, van Saene HK, Milanese M, Gregori D |title=Impact of selective decontamination of the digestive tract on fungal carriage and infection: systematic review of randomized controlled trials |journal=Intensive Care Med |volume=31 |issue=7 |pages=898–910 |year=2005 |pmid=15895205 |doi=10.1007/s00134-005-2654-9}}</ref> although some [[randomized controlled trial]]s have<ref name="pmid14522530">{{cite journal |author=de Jonge E, Schultz MJ, Spanjaard L, ''et al'' |title=Effects of selective decontamination of digestive tract on mortality and acquisition of resistant bacteria in intensive care: a randomised controlled trial |journal=Lancet |volume=362 |issue=9389 |pages=1011–6 |year=2003 |pmid=14522530 |doi=}}</ref><ref name="pmid1524328">{{cite journal |author=Cockerill FR, Muller SR, Anhalt JP, ''et al'' |title=Prevention of infection in critically ill patients by selective decontamination of the digestive tract |journal=Ann. Intern. Med. |volume=117 |issue=7 |pages=545–53 |year=1992 |pmid=1524328 |doi=}}</ref><ref name="pmid17146635">{{cite journal |author=Stoutenbeek CP, van Saene HK, Little RA, Whitehead A |title=The effect of selective decontamination of the digestive tract on mortality in multiple trauma patients: a multicenter randomized controlled trial |journal=Intensive Care Med |volume=33 |issue=2 |pages=261–70 |year=2007 |pmid=17146635 |doi=10.1007/s00134-006-0455-4}}</ref> and others have not found benefit<ref name="pmid1734249">{{cite journal |author=Gastinne H, Wolff M, Delatour F, Faurisson F, Chevret S |title=A controlled trial in intensive care units of selective decontamination of the digestive tract with nonabsorbable antibiotics. The French Study Group on Selective Decontamination of the Digestive Tract |journal=N. Engl. J. Med. |volume=326 |issue=9 |pages=594–9 |year=1992 |pmid=1734249 |doi=}}</ref>.


===Preventing deep venous thrombosis===
===Preventing deep venous thrombosis===
{{main|Deep venous thrombosis}}


===Preventing healthcare-associated pneumonia===
===Preventing healthcare-associated pneumonia===
===Preventing posttraumatic stress disorder===
Light sedation (patient awake and cooperative) may be more effective than deep sedation (patient asleep, awakening upon physical stimulation).<ref name="pmid19602975">{{cite journal| author=Treggiari MM, Romand JA, Yanez ND, Deem SA, Goldberg J, Hudson L et al.| title=Randomized trial of light versus deep sedation on mental health after critical illness. | journal=Crit Care Med | year= 2009 | volume= 37 | issue= 9 | pages= 2527-34 | pmid=19602975
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19602975 | doi=10.1097/CCM.0b013e3181a5689f }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
==Medical error in the intensive care==
{{main|medical error}}
Regarding overlooked diagnosis among patients receiving [[artificial respiration]] in the intensive care, an [[autopsy]] study concluded "abdominal pathologic conditions--abscesses, bowel perforations, or infarction--were as frequent as pulmonary emboli as a cause of class I errors. While patients with abdominal pathologic conditions generally complained of abdominal pain, results of examination of the abdomen were considered unremarkable in most patients, and the symptom was not pursued." <ref name="pmid1992186">{{cite journal |author=Papadakis MA, Mangione CM, Lee KK, Kristof M |title=Treatable abdominal pathologic conditions and unsuspected malignant neoplasms at autopsy in veterans who received mechanical ventilation |journal=JAMA |volume=265 |issue=7 |pages=885–7 |year=1991 |pmid=1992186 |doi=}}</ref>
==Predicting outcomes of adult patients==
Although there is much research into prognosing patients in intensive care, patients are not very confident in thei accuracy of prognoses.<ref name="pmid18596630">{{cite journal |author=Zier LS, Burack JH, Micco G, ''et al'' |title=Doubt and belief in physicians' ability to prognosticate during critical illness: the perspective of surrogate decision makers |journal=Crit. Care Med. |volume=36 |issue=8 |pages=2341–7 |year=2008 |month=August |pmid=18596630 |doi=10.1097/CCM.0b013e318180ddf9 |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?doi=10.1097/CCM.0b013e318180ddf9 |issn=}}</ref>
===Apache II score===
{{main|APACHE II}}
The APACHE II is available at http://www.sfar.org/scores2/apache22.html.
===SAPS II===
*[http://www.sfar.org/scores2/saps2.html SAPS II]<ref name="pmid8254858">{{cite journal |author=Le Gall JR, Lemeshow S, Saulnier F |title=A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study |journal=JAMA |volume=270 |issue=24 |pages=2957–63 |year=1993 |pmid=8254858 |doi= |url= |issn=}}</ref>
*[http://www.sfar.org/scores2/saps2_expanded.html SAPS II (expanded)]
===CIS===
The cellular injury score (CIS) can describe multiple organ dysfunction syndrome.<ref name="pmid11271086">{{cite journal| author=Oda S, Hirasawa H, Sugai T, Shiga H, Nakanishi K, Kitamura N et al.| title=Comparison of Sepsis-related Organ Failure Assessment (SOFA) score and CIS (cellular injury score) for scoring of severity for patients with multiple organ dysfunction syndrome (MODS). | journal=Intensive Care Med | year= 2000 | volume= 26 | issue= 12 | pages= 1786-93 | pmid=11271086
| 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=11271086 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>
===FOUR===
The FOUR (Full Outline of UnResponsiveness) score may be better than the [[Glasgow Coma Scale]] (GCS) in prognosticating patients in [[coma]].<ref name="pmid19648386">{{cite journal| author=Iyer VN, Mandrekar JN, Danielson RD, Zubkov AY, Elmer JL, Wijdicks EF| title=Validity of the FOUR score coma scale in the medical intensive care unit. | journal=Mayo Clin Proc | year= 2009 | volume= 84 | issue= 8 | pages= 694-701 | pmid=19648386
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19648386 | doi=10.4065/84.8.694 | pmc=PMC2719522 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref> The FOUR Score tests:
* eye response
* motor response
* brainstem reflexes
* respiration pattern
===SOFA===
The Sepsis-related Organ Failure Assessment (SOFA) score can describe multiple organ dysfunction syndrome.<ref name="pmid8844239">{{cite journal| author=Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H et al.| title=The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. | journal=Intensive Care Med | year= 1996 | volume= 22 | issue= 7 | pages= 707-10 | pmid=8844239
| 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=8844239 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref name="pmid11271086">{{cite journal| author=Oda S, Hirasawa H, Sugai T, Shiga H, Nakanishi K, Kitamura N et al.| title=Comparison of Sepsis-related Organ Failure Assessment (SOFA) score and CIS (cellular injury score) for scoring of severity for patients with multiple organ dysfunction syndrome (MODS). | journal=Intensive Care Med | year= 2000 | volume= 26 | issue= 12 | pages= 1786-93 | pmid=11271086
| 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=11271086 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref>


==References==
==References==
<references/>
{{reflist|2}}[[Category:Suggestion Bot Tag]]
 
[[Category:CZ Live]] [[Category:Health Sciences Workgroup]]

Latest revision as of 06:00, 3 August 2024

This article is developing and not approved.
Main Article
Discussion
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Critical care medicine is the "health care provided to a critically ill patient during a medical emergency or crisis".[1] It may be provided in intensive care units, "stepdown" hospital wards, emergency rooms, and in field medicine.

Monitoring the critically ill patient

Several measures are available based on blood gas analysis.

Circulation

Pulmonary artery catheterization

Among patients with acute lung injury, the use of pulmonary artery catheterization (Swan-Ganz catheterization) did not improve outcomes over monitoring with central venous catheterization.[2]

Inferior vena cava ultrasonography

Ultrasonography of the inferior vena cava may help detect low central venous pressure. The caval index is the relative decrease in diameter between expiration and inspiration. If the caval index is 50%, then a central venous pressure of < 8 mm Hg is detected with:[3]

Respiration and oxygenation

PaO2/FiO2 ratio (PF ratio)
For more information, see: P:F ratio.

An example in a healthy person:

A higher ratio indicates better gas exchange:

  • Normal is 500
  • ARDS is < 200

Comparative studies suggest this measure correlates better with pulmonary shunts than does the A-a gradient.[4][5][6]

Oxygenation index

or

A lower oxygenation index indicates better gas exchange. The oxygenation index, which includes the mean airway pressure[7][8], may better correlate with intrapulmonary shunting than the PF ratio[5]

Alveolar-arterial oxygen (A-a) gradient (alveolar-arterial oxygen difference - AVO2D)
  • Normal is < 10 mm Hg

The A-a gradient is harder to calculate, but accounts for changes in respiration as measured by the partial pressure of carbon dioxide. However, this calculation relies on the respiratory quotient being constant in the prediction of alveolar CO2 When compared to the PF ratio, the A-a gradient is found to correlate less well with pulmonary shunting.[4][5][6]

Among outpatients with possible pulmonary embolism, the A-a gradient may be a better test.[9]

An online calculator for the A-a gradient is at http://www.mdcalc.com/aagrad.

Tissue perfusion

Central venous oxygen saturation (ScvO2)

In patients with septic shock, maintaining the central venous oxygen saturation (ScvO2) > 70% is a health care quality assurance measure for the Institute for Healthcare Improvement.[10] This is measured from the superior vena cava. This is hard to predict by physical examination.[11]

Mixed venous oxygen saturation (SvO2)

In patients with septic shock, maintaining the mixed venous oxygen saturation (ScvO2) > 65% is a health care quality assurance measure for the Institute for Healthcare Improvement that is an alternative to the central venous oxygen saturation.[12] This is measured from a pulmonary artery catheter. This is hard to predict by physical examination.[11]

The mixed venous pressure may be lower than the central venous pressure due to mixing with blood from the splanchnic circulation or carotid sinuses that has lower oxygen content.[13]

Tissue oxygen saturation (StO2)

Tissue oxygen saturation (StO2) at the thenar eminence may be an alternative, non-invasive measurement.[14][15]

Lactate clearance

Maintaining lactate clearance about 10% may be an easier alternative than invasive measurements of oxygenation according to a randomized controlled trial by EMShockNet.[16]

Capnography

Capnography, which is "continuous recording of the carbon dioxide content of expired air,"[17] may detect respiratory depression before hypoxemia occurs.[18] Proposed criteria for respiratory depression are:[18]

  • End tidal CO2 (ETCO2) level 50 mm Hg
  • ETCO2 change from baseline of 10%
  • Loss of waveform for 15 seconds

Real time glucose monitoring

Real-time glucose monitoring does not clearly help control the blood glucose level.[19]

Treatments provided in the intensive care unit

Goal-directed resuscitation

Protocols for the resuscitation of septic shock are:[16][20]

  1. "Isotonic crystalloid was administered in boluses to achieve a central venous pressure of 8 mm Hg or higher"
  2. "Mean arterial pressure goal of 65 mm Hg or higher, if not achieved with fluid administration, was targeted by initiating and titrating vasopressors (dopamine or norepinephrine)"[16] or goal of 65 mm Hg to 90 mm Hg[20]
  3. If ScvO2 < 70% or lactate clearance < 10%

Circulatory support

For more information, see: Vasoconstrictor agent and Cardiotonic agent.

Goal-directed resuscitation has been developed and so far studies for the resuscitation of septic shock:[16]

  1. "Isotonic crystalloid was administered in boluses to achieve a central venous pressure of 8 mm Hg or higher"
  2. "Mean arterial pressure goal of 65 mm Hg or higher, if not achieved with fluid administration, was targeted by initiating and titrating vasopressors (dopamine or norepinephrine)"[16] or goal of 65 mm Hg to 90 mm Hg[20]
  3. If ScvO2 < 70% or lactate clearance < 10%

Renal support

For more information, see: Renal replacement therapy.


Respiratory support

For more information, see: Artificial respiration.

Surgical and trauma critical care

The standard of care for fluid replacement after traumatic injury continues to evolve. Permissive hypotension is increasingly preferred in most situations: giving enough fluid to return the systolic blood pressure to approximately 100mm, but not to return it to normal. Raising the pressure to normal levels may also raise the pressure enough to disrupt clots and restart hemorrhaging.

Routine use of vasopressors in trauma uncomplicated by disease is discouraged; a surgical maxim is that the treatment for traumatic hypotension is surgery, not drugs.

An important exception to permissive hypotension is the field management of crush injury. In this case, fluid overload, as well as alkalinization, is necessary to protect the kidneys and other organs from the rush of muscle breakdown products when the flow-occluding pressure of a heavy object is removed.

Complications

Abdominal compartment syndrome

Abdominal compartment syndrome is associated with increased mortality.[21]

Medical error

For more information, see: Medical error.

Examining errors in administration of parenteral medications, a study found:[22]

  • 74 errors per 100 patient-days
  • Independent risk factors were:
    • Patient complexity as measured by
      • number of organ failures
      • number of parenteral administrations
    • Work load as measured by
      • Larger intensive care unit
      • Increased ratio of patient turnover to the size of the unit
      • Number of patients per nurse
      • Occupancy rate of the unit

Preventing complications in the critically ill patient

Delirium

Antipsychotic agents to reduce the number of days mechanically ventilated patients were alive without delirium[23]
Drug Number of days
Haloperidol 14.0
Ziprasidone 15.0
Placebo 12.5
P = 0.66

Antipsychotic agents, in a small study, found that an average of 15 mgs per day of haloperidol and 113 mg per day of ziprasidone increased akathisia (see table for benefits which did not have statistical significance).[23]

Glucose control

Two clinical practice guidelines are available for patients with ; however, both of these guidelines were developed without broad representation of stakeholders.[24] This may lead to overly aggressive clinical recommendations. In addition, these guidelines were published before the two recent negative trials.

The American Association of Clinical Endocrinologists (AACE) recommends the following target blood glucose levels:[25]

  • "Critically ill patients, between 80 to 110 mg/dL (grade A recommendation)"

The American Diabetes Association (ADA) states[26]

  • "Critically ill patients: blood glucose levels should be kept as close to 110 mg/dl (6.1 mmol/l) as possible and generally <140 mg/dl (7.8 mmol/l). (A) These patients require an intravenous insulin protocol that has demonstrated efficacy and safety in achieving the desired glucose range without increasing risk for severe hypoglycemia. (E)"

Evidence

Randomized controlled trials of tight glucose control in the critical care and perioperative care settings have produced mixed results. See Table.

Meta-analyses of these trials exist:

  • Meta-analysis in 2011 of 21 trials was negative.[27]
  • Meta-analysis in 2010 of 7 trials was negative.[28]
  • Meta-analysis in 2009 of 26 trials was negative.[29]
  • Meta-analysis in 2009 of 29 trials was negative.[30]
Selected randomized controlled trials of glucose control in critical care[31][32][33][34] [35][36]
Trial Patients Intervention Comparison Outcomes Results Authors' conclusions
Intensive control Control group
COIITSS Study[31]
2010
509 adults with septic shock Insulin targeting serum glucose of 80 to 110 mg/dl 2004 Surviving Sepsis Campaign guidelines[37] In-hospital mortality 45.9% * 42.9% "intensive insulin therapy did not improve in-hospital mortality "
NICE-SUGAR[32]
2009
6104 patients in medical and surgical ICU Insulin drip targeting serum glucose of 81 to 108 mg/dl Insulin drip targeting serum glucose of 144 - 180 mg/dl Mortality at 90 days 27.5% * 24.9% "intensive glucose control increased mortality among adults in the ICU"
Arabi et al[33]
2008
523 patients in medical and surgical ICU Insulin drip targeting serum glucose of 80 to 110 mg/dl Insulin drip targeting serum glucose of 180 to 200 mg/dl Mortality in the intensive care unit 13.5% 17.1 "Intensive insulin therapy was not associated with improved survival...and was associated with increased occurrence of hypoglycemia"
SepNet[34]
2008
537 patients with severe sepsis Insulin drip if needed to target serum glucose of 80 to 110 mg/dl Insulin drip if needed to target serum glucose of < 200 mg/dl Mortality in the intensive care unit 24.7% 26% "intensive insulin therapy placed critically ill patients with sepsis at increased risk for serious adverse events"
Van den Berghe[35]
2006
1200 patients in medical ICU Insulin drip targeting serum glucose of 80 to 110 mg/dl Insulin drip targeting serum glucose of 180 to 200 mg/dl Hospital mortality 37.3% 40% "Intensive insulin therapy significantly reduced morbidity but not mortality"
Van den Berghe[36]
2001
1548 patients in surgical ICU Insulin drip targeting serum glucose of 80 to 110 mg/dl Insulin drip targeting serum glucose of 180 to 200 mg/dl Mortality in the intensive care unit 4.6% * 8% "Intensive insulin therapy...reduces morbidity and mortality"
Notes:
* Significantly different from the control group.

Two of the trials in the Table suggested benefit (see green cells):

  • Van den Berghe 2006[35]. Although this trial concluded "intensive insulin therapy significantly reduced morbidity but not mortality among all patients in the medical ICU. Although the risk of subsequent death and disease was reduced in patients treated for three or more days" the trial stated "these patients could not be identified before therapy."[35]
  • Van den Berghe 2002[36]. This trial has been criticized for the following reasons:[38]
  1. "The trial was stopped early for an unexpectedly large treatment effect, which can overestimate the efficacy of treatment or result in a false-positive finding;"
  2. "The relative reduction in mortality for a decrease of 50 mg/dL in morning glucose levels seems biologically implausible and exceeds that for any other intervention in critically ill patients;"
  3. "The mortality rate in the control group was much higher than that noted in tertiary care medical centers in the United States. On admission to the ICU, all patients received 200 to 300 g/d of intravenous dextrose followed by enteral or parenteral nutrition, an unusual practice considering the deleterious effects of parenteral nutrition; at least in part, the difference in outcomes between the 2 arms in this study might have reflected the harm of maintaining the control group as hyperglycemic rather than the benefit of strict glucose control in the intervention group."

Tight control may protect renal function.[39]

Regarding intraoperative control of glucose, a randomized controlled trial concluded "the increased incidence of death and stroke in the intensive treatment group raises concern about routine implementation of this intervention."[40]

Preventing anemia

Blood transfusion

Clinical practice guidelines

Clinical practice guidelines by the Eastern Association for Surgery of Trauma and the American College of Critical Care Medicine include blood transfusions recommendations for:[41]

  1. "patients with evidence of hemorrhagic shock"
  2. "patients with evidence of acute hemorrhage and hemodynamic instability or inadequate" oxygenation
  3. "A “restrictive” strategy of RBC transfusion (transfuse when Hb < 7 g/dL) is as effective as a 'liberal' transfusion strategy (transfusion when Hb < 10 g/dL) in critically ill patients with hemodynamically stable anemia, except possibly in patients with acute myocardial ischemia."
  4. "The use of only Hb level as a 'trigger' for transfusion should be avoided"
  5. "In the absence of acute hemorrhage, RBC transfusion should be given as single units"
  6. "Consider transfusion if Hb is <7 g/dL in critically ill patients requiring mechanical ventilation"
  7. "Consider transfusion if Hb is <7 g/dL in resuscitated critically ill trauma patients"
  8. "Consider transfusion if Hb is <7 g/dL in critically ill patients with stable cardiac disease"
  9. "RBC transfusion should not be considered as an absolute method to improve tissue oxygen consumption in critically ill patients."
  10. "RBC transfusion may be beneficial in patients with acute coronary syndromes (ACS) who are anemic (Hb < 8 g/dL) on hospital admission"
  11. "The transfusion needs for each septic patient must be assessed individually because optimal transfusion triggers in sepsis patients are not known and there is no clear evidence that blood transfusion increases tissue oxygenation"
  12. "All efforts should be initiated to avoid RBC transfusion in patients at risk for ALI and ARDS after completion of resuscitation."
Trials

There may not be a meaningful difference in outcomes between transfusing blood to maintain a hemoglobin > 7.0 g/dl versus a hemoglobin > 10.0 g/dl.[42]

Erythropoietin

A randomized controlled trial reported "epoetin alfa does not reduce the incidence of red-cell transfusion among critically ill patients, but it may reduce mortality in patients with trauma. Treatment with epoetin alfa is associated with an increase in the incidence of thrombotic events."[43]

Selective gastrointestinal decontamination

Systematic reviews conclude that selective decontamination of the digestive tract may reduce morbidity in critically ill patients[44][45][46] although some randomized controlled trials have[47][48][49] and others have not found benefit[50].

Preventing gastrointestinal tract ulceration

Preventing deep venous thrombosis

For more information, see: Deep venous thrombosis.


Preventing healthcare-associated pneumonia

Preventing posttraumatic stress disorder

Light sedation (patient awake and cooperative) may be more effective than deep sedation (patient asleep, awakening upon physical stimulation).[51]

Medical error in the intensive care

For more information, see: medical error.

Regarding overlooked diagnosis among patients receiving artificial respiration in the intensive care, an autopsy study concluded "abdominal pathologic conditions--abscesses, bowel perforations, or infarction--were as frequent as pulmonary emboli as a cause of class I errors. While patients with abdominal pathologic conditions generally complained of abdominal pain, results of examination of the abdomen were considered unremarkable in most patients, and the symptom was not pursued." [52]

Predicting outcomes of adult patients

Although there is much research into prognosing patients in intensive care, patients are not very confident in thei accuracy of prognoses.[53]

Apache II score

For more information, see: APACHE II.

The APACHE II is available at http://www.sfar.org/scores2/apache22.html.

SAPS II

CIS

The cellular injury score (CIS) can describe multiple organ dysfunction syndrome.[55]

FOUR

The FOUR (Full Outline of UnResponsiveness) score may be better than the Glasgow Coma Scale (GCS) in prognosticating patients in coma.[56] The FOUR Score tests:

  • eye response
  • motor response
  • brainstem reflexes
  • respiration pattern

SOFA

The Sepsis-related Organ Failure Assessment (SOFA) score can describe multiple organ dysfunction syndrome.[57][55]

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