Pulmonary Embolism: Difference between revisions

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;Non-invasive imaging
;Non-invasive imaging
[[CT pulmonary angiogram|CT pulmonary angiography]] (CTPA) is a [[pulmonary angiogram]] obtained using [[computed tomography]] (CT) with [[radiocontrast]] rather than right heart catheterization. Its advantages are clinical equivalence, its non-invasive nature, its greater availability to patients, and the possibility of identifying other lung disorders from the [[differential diagnosis]] in case there is no pulmonary embolism. Assessing the accuracy of CT pulmonary angiography is hindered by the rapid changes in the number of rows of detectors available in multidetector CT (MDCT) machines.<ref name=pmid16479644>{{cite journal |author=Schaefer-Prokop C, Prokop M |title=MDCT for the diagnosis of acute pulmonary embolism |journal=European radiology |volume=15 Suppl 4 |issue= |pages=D37–41 |year=2005 |pmid=16479644 |doi=}}</ref> According to a [[cohort study]], single-slice [[spiral CT]] may help diagnose detection among patients with suspected pulmonary embolism .<ref name="pmid15634261">{{cite journal| author=|title=Accuracy of single-detector spiral CT in the diagnosis of pulmonary embolism: a prospective multicenter cohort study of consecutive patients with abnormal perfusion scintigraphy|year=2005|journal=Journal of thrombosis and haemostasis : JTH |pmid=15634261|pmc=|doi=10.1111/j.1538-7836.2004.01064.x| last1=Van Strijen| first1=MJ| last2=De Monye| first2=W| last3=Kieft| first3=GJ| last4=Pattynama| first4=PM| last5=Prins| first5=MH| last6=Huisman| first6=MV| volume=3| issue=1| pages=17–25}}</ref> In this study, the [[sensitivity (tests)|sensitivity]] was 69% and [[specificity (tests)|specificity]] was 84%. In this study which had a prevalence of detection was 32%, the [[positive predictive value]] of 67.0% and [[negative predictive value]] of 85.2% ([http://medinformatics.uthscsa.edu/calculator/calc.shtml?calc_dx_SnSp.shtml?prevalence=32&sensitivity=69&specificity=84 click here] to adjust these results for patients at higher or lower risk of detection). However, this study's results may be biased due to possible incorporation bias, since the CT scan was the final diagnostic tool in patients with pulmonary embolism. The authors noted that a negative single slice CT scan is insufficient to rule out pulmonary embolism on its own. A separate study with a mixture of 4 slice and 16 slice scanners reported a [[sensitivity (tests)|sensitivity]] of 83% and a [[specificity (tests)|specificity]] of 96%. This study noted that additional testing is necessary when the clinical probability is inconsistent with the imaging results.<ref name=pmid16738268>{{cite journal |author=Stein PD, Fowler SE, Goodman LR, ''et al.'' |title=Multidetector computed tomography for acute pulmonary embolism |journal=N. Engl. J. Med. |volume=354 |issue=22 |pages=2317–27 |year=2006 |pmid=16738268 |doi=10.1056/NEJMoa052367 |last12=Tapson |first12=VF |last13=Wakefield |first13=TW |last14=Weg |first14=JG |last15=Woodard |first15=PK |last16=Pioped Ii |first16=Investigators}}</ref> CTPA is non-inferior to VQ scanning, and identifies more emboli (without necessarily improving the outcome) compared to VQ scanning.<ref name=Anderson2007>{{cite journal|author=Anderson DR, Kahn SR, Rodger MA ''et al.''|year=2007|title=Computed tomographic pulmonary angiography vs ventilation-perfusion lung scanning in patients with suspected pulmonary embolism|journal=JAMA|volume=298|issue=23|pages=2743–53|doi= 10.1001/jama.298.23.2743|pmid=18165667|last12=Cartier|first12=Y|last13=Barnes|first13=D|last14=Burton|first14=E|last15=Pleasance|first15=S|last16=Skedgel|first16=C|last17=O'rouke|first17=K|last18=Wells|first18=PS}}</ref>
[[CT pulmonary angiogram|CT pulmonary angiography]] (CTPA) is a [[pulmonary angiogram]] obtained using [[computed tomography]] (CT) with [[radiocontrast]] rather than right heart catheterization. Its advantages are clinical equivalence, its non-invasive nature, its greater availability to patients, and the possibility of identifying other lung disorders from the [[differential diagnosis]] in case there is no pulmonary embolism. Assessing the accuracy of CT pulmonary angiography is hindered by the rapid changes in the number of rows of detectors available in multidetector CT (MDCT) machines. <cite>REFNAME16</cite> According to a [[cohort study]], single-slice [[spiral CT]] may help diagnose detection among patients with suspected pulmonary embolism. <cite>REFNAME17</cite> In this study, the [[sensitivity (tests)|sensitivity]] was 69% and [[specificity (tests)|specificity]] was 84%. In this study which had a prevalence of detection was 32%, the [[positive predictive value]] of 67.0% and [[negative predictive value]] of 85.2% ([http://medinformatics.uthscsa.edu/calculator/calc.shtml?calc_dx_SnSp.shtml?prevalence=32&sensitivity=69&specificity=84 click here] to adjust these results for patients at higher or lower risk of detection). However, this study's results may be biased due to possible incorporation bias, since the CT scan was the final diagnostic tool in patients with pulmonary embolism. The authors noted that a negative single slice CT scan is insufficient to rule out pulmonary embolism on its own. A separate study with a mixture of 4 slice and 16 slice scanners reported a [[sensitivity (tests)|sensitivity]] of 83% and a [[specificity (tests)|specificity]] of 96%. This study noted that additional testing is necessary when the clinical probability is inconsistent with the imaging results. <cite>REFNAME18</cite> CTPA is non-inferior to VQ scanning, and identifies more emboli (without necessarily improving the outcome) compared to VQ scanning. <cite>Anderson2007</cite>


''[[Ventilation/perfusion scan]]'' (or ''V/Q scan'' or ''lung [[scintigraphy]]''), which shows that some areas of the lung are being [[Ventilation (physiology)|ventilated]] but not [[Perfusion|perfused]] with blood (due to obstruction by a clot). This type of examination is used less often because of the more widespread availability of CT technology, however, it may be useful in patients who have an allergy to [[iodinated contrast]] or in [[pregnancy]] due to lower radiation exposure than CT.<ref>{{cite journal |author=Scarsbrook AF, Gleeson FV |title=Investigating suspected pulmonary embolism in pregnancy |journal=BMJ |volume=334 |issue=7590 |pages=418–9 |year=2007 |pmid=17322258 |doi=10.1136/bmj.39071.617257.80|url=http://www.bmj.com/cgi/content/full/334/7590/418 |pmc=1804186}}</ref>
''[[Ventilation/perfusion scan]]'' (or ''V/Q scan'' or ''lung [[scintigraphy]]''), which shows that some areas of the lung are being [[Ventilation (physiology)|ventilated]] but not [[Perfusion|perfused]] with blood (due to obstruction by a clot). This type of examination is used less often because of the more widespread availability of CT technology, however, it may be useful in patients who have an allergy to [[iodinated contrast]] or in [[pregnancy]] due to lower radiation exposure than CT. <cite>REFNAME19</cite>


;Low probability diagnostic tests/non-diagnostic tests
;Low probability diagnostic tests/non-diagnostic tests
Tests that are frequently done that are not [[sensitivity (tests)|sensitive]] for PE, but can be diagnostic.
Tests that are frequently done that are not [[sensitivity (tests)|sensitive]] for PE, but can be diagnostic.
*''[[Chest X-ray]]s'' are often done on patients with shortness of breath to help rule-out other causes, such as [[congestive heart failure]] and [[rib fracture]]. Chest X-rays in PE are rarely normal,<ref>{{cite journal | author = Worsley D, Alavi A, Aronchick J, Chen J, Greenspan R, Ravin C | title = Chest radiographic findings in patients with acute pulmonary embolism: observations from the PIOPED Study | journal = Radiology | volume = 189 | issue = 1 | pages = 133–6 | year = 1993 | pmid = 8372182}}</ref> but usually lack [[radiologic sign|sign]]s that suggest the diagnosis of PE (e.g. [[Westermark sign]], [[Hampton's hump]]).
*''[[Chest X-ray]]s'' are often done on patients with shortness of breath to help rule-out other causes, such as [[congestive heart failure]] and [[rib fracture]]. Chest X-rays in PE are rarely normal, <cite>REFNAME20</cite> but usually lack [[radiologic sign|sign]]s that suggest the diagnosis of PE (e.g. [[Westermark sign]], [[Hampton's hump]]).
*''[[medical ultrasound|Ultrasonography]] of the legs'', also known as ''leg doppler'', in search of [[deep venous thrombosis]] (DVT). The presence of [[deep venous thrombosis|DVT]], as shown on [[ultrasonography]] of the legs, is in itself enough to warrant anticoagulation, without requiring the V/Q or spiral CT scans (because of the strong association between DVT and PE). This may be valid approach in [[pregnancy]], in which the other modalities would increase the risk of birth defects in the unborn child. However, a negative scan does not rule out PE, and low-radiation dose scanning may be required if the mother is deemed at high risk of having pulmonary embolism. {{Citation needed|date=August 2011}}
*''[[medical ultrasound|Ultrasonography]] of the legs'', also known as ''leg doppler'', in search of [[deep venous thrombosis]] (DVT). The presence of [[deep venous thrombosis|DVT]], as shown on [[ultrasonography]] of the legs, is in itself enough to warrant anticoagulation, without requiring the V/Q or spiral CT scans (because of the strong association between DVT and PE). This may be valid approach in [[pregnancy]], in which the other modalities would increase the risk of birth defects in the unborn child. However, a negative scan does not rule out PE, and low-radiation dose scanning may be required if the mother is deemed at high risk of having pulmonary embolism. {{Citation needed|date=August 2011}}


===Electrocardiogram===
===Electrocardiogram===
[[File:Pulmonary embolism ECG.jpg|thumb|Electrocardiogram of a patient with pulmonary embolism showing [[sinus tachycardia]] of approximately 150 beats per minute and [[right bundle branch block]].]]
[[File:Pulmonary embolism ECG.jpg|thumb|Electrocardiogram of a patient with pulmonary embolism showing [[sinus tachycardia]] of approximately 150 beats per minute and [[right bundle branch block]].]]
An [[electrocardiogram]] (ECG) is routinely done on patients with chest pain to quickly diagnose [[myocardial infarction]]s (heart attacks). An ECG may show signs of right heart strain or acute ''[[cor pulmonale]]'' in cases of large PEs - the classic signs are a large S wave in lead I, a large Q wave in lead III and an inverted [[T wave]] in lead III ("S1Q3T3").<ref>{{cite journal |author=McGinn S, [[Paul Dudley White|White PD]] | title=Acute cor pulmonale resulting from pulmonary embolism |journal=J Am Med Assoc |year=1935 |volume=104 | pages=1473–80}}</ref> This is occasionally (up to 20%) present, but may also occur in other acute lung conditions and has therefore limited diagnostic value. The most commonly seen signs in the ECG is [[sinus tachycardia]], right axis deviation and [[right bundle branch block]].<ref>{{cite journal |author=Rodger M, Makropoulos D, Turek M, ''et al.'' |title=Diagnostic value of the electrocardiogram in suspected pulmonary embolism |journal=Am. J. Cardiol. |volume=86 |issue=7 |pages=807–9, A10 |year=2000 |month= October|pmid=11018210 |doi=10.1016/S0002-9149(00)01090-0}}</ref>  Sinus tachycardia was however still only found in 8 - 69% of people with PE.<ref>{{cite book |author=Amal Mattu; Deepi Goyal; Barrett, Jeffrey W.; Joshua Broder; DeAngelis, Michael; Peter Deblieux; Gus M. Garmel; Richard Harrigan; David Karras; Anita L'Italien; David Manthey |title=Emergency medicine: avoiding the pitfalls and improving the outcomes |publisher=Blackwell Pub./BMJ Books |location=Malden, Mass |year=2007 |pages=10 |isbn=1-4051-4166-2 |oclc= |doi= |accessdate=}}</ref>
An [[electrocardiogram]] (ECG) is routinely done on patients with chest pain to quickly diagnose [[myocardial infarction]]s (heart attacks). An ECG may show signs of right heart strain or acute ''[[cor pulmonale]]'' in cases of large PEs - the classic signs are a large S wave in lead I, a large Q wave in lead III and an inverted [[T wave]] in lead III ("S1Q3T3").<ref>{{cite journal |author=McGinn S, [[Paul Dudley White|White PD]] | title=Acute cor pulmonale resulting from pulmonary embolism |journal=J Am Med Assoc |year=1935 |volume=104 | pages=1473–80}}</ref> This is occasionally (up to 20%) present, but may also occur in other acute lung conditions and has therefore limited diagnostic value. The most commonly seen signs in the ECG is [[sinus tachycardia]], right axis deviation and [[right bundle branch block]]. <cite>REFNAME21</cite>  Sinus tachycardia was however still only found in 8 - 69% of people with PE. <cite>REFNAME22</cite>


===Echocardiography===
===Echocardiography===
In massive and submassive PE, dysfunction of the right side of the heart can be seen on [[echocardiography]], an indication that the [[pulmonary artery]] is severely obstructed and the heart is unable to match the pressure. Some studies (see below) suggest that this finding may be an indication for [[thrombolysis]]. Not every patient with a (suspected) pulmonary embolism requires an echocardiogram, but elevations in [[troponin|cardiac troponins]] or [[brain natriuretic peptide]] may indicate heart strain and warrant an echocardiogram.<ref>{{cite journal |author=Kucher N, Goldhaber SZ |title=Cardiac biomarkers for risk stratification of patients with acute pulmonary embolism |journal=Circulation |volume=108 |issue=18 |pages=2191–4 |year=2003 |pmid=14597581 |doi=10.1161/01.CIR.0000100687.99687.CE}}</ref>
In massive and submassive PE, dysfunction of the right side of the heart can be seen on [[echocardiography]], an indication that the [[pulmonary artery]] is severely obstructed and the heart is unable to match the pressure. Some studies (see below) suggest that this finding may be an indication for [[thrombolysis]]. Not every patient with a (suspected) pulmonary embolism requires an echocardiogram, but elevations in [[troponin|cardiac troponins]] or [[brain natriuretic peptide]] may indicate heart strain and warrant an echocardiogram. <cite>REFNAME23</cite>


The specific appearance of the right ventricle on echocardiography is referred to as the ''McConnell's sign''. This is the finding of akinesia of the mid-free wall but normal motion of the apex. This phenomenon has a 77% sensitivity and a 94% specificity for the diagnosis of acute pulmonary embolism in the setting of right ventricular dysfunction.<ref>{{cite journal |author=McConnell MV, Solomon SD, Rayan ME, Come PC, Goldhaber SZ, Lee RT |title=Regional right ventricular dysfunction detected by echocardiography in acute pulmonary embolism |journal=Am. J. Cardiol. |volume=78 |issue=4 |pages=469–73 |year=1996 |pmid=8752195 |doi=10.1016/S0002-9149(96)00339-6}}</ref>
The specific appearance of the right ventricle on echocardiography is referred to as the ''McConnell's sign''. This is the finding of akinesia of the mid-free wall but normal motion of the apex. This phenomenon has a 77% sensitivity and a 94% specificity for the diagnosis of acute pulmonary embolism in the setting of right ventricular dysfunction. <cite>REFNAME24</cite>


===Algorithms===
===Algorithms===
Recent recommendations for a diagnostic algorithm have been published by the PIOPED investigators; however, these recommendations do not reflect research using 64 slice MDCT.<ref name=pmid17185658/> These investigators recommended:
Recent recommendations for a diagnostic algorithm have been published by the PIOPED investigators; however, these recommendations do not reflect research using 64 slice MDCT. <cite>REFNAME25</cite> These investigators recommended:
* Low clinical probability. If negative D-dimer, PE is excluded. If positive D-dimer, obtain MDCT and based treatment on results.
* Low clinical probability. If negative D-dimer, PE is excluded. If positive D-dimer, obtain MDCT and based treatment on results.
* Moderate clinical probability. If negative D-dimer, PE is excluded. ''However'', the authors were not concerned that a negative MDCT with negative D-dimer in this setting has an 5% probability of being false. Presumably, the 5% error rate will fall as 64 slice MDCT is more commonly used. If positive D-dimer, obtain MDCT and based treatment on results.
* Moderate clinical probability. If negative D-dimer, PE is excluded. ''However'', the authors were not concerned that a negative MDCT with negative D-dimer in this setting has an 5% probability of being false. Presumably, the 5% error rate will fall as 64 slice MDCT is more commonly used. If positive D-dimer, obtain MDCT and based treatment on results.
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The Pulmonary Embolism Rule-out Criteria, or PERC rule, helps assess people in whom pulmonary embolism is suspected, but unlikely. Unlike the Wells Score and Geneva score, which are clinical prediction rules intended to risk stratify patients with suspected PE, the PERC rule is designed to rule out risk of PE in patients when the physician has already stratified them into a low-risk category.
The Pulmonary Embolism Rule-out Criteria, or PERC rule, helps assess people in whom pulmonary embolism is suspected, but unlikely. Unlike the Wells Score and Geneva score, which are clinical prediction rules intended to risk stratify patients with suspected PE, the PERC rule is designed to rule out risk of PE in patients when the physician has already stratified them into a low-risk category.


Patients in this low risk category without any of these criteria may undergo no further diagnostic testing for PE: Hypoxia - Sa0<sub>2</sub> <95%, unilateral leg swelling, hemoptysis, prior DVT or PE, recent surgery or trauma, age >50, hormone use, tachycardia. The rationale behind this decision is that further testing (specifically CT angiogram of the chest) may cause more harm (from radiation exposure and contrast dye) than the risk of PE.<ref>{{Cite journal | last = Kline | first =  Jeffrey A | year = 2004 | title = Clinical criteria to prevent unnecessary diagnostic testing in emergency department patients with suspected pulmonary embolism | journal = Journal of Thrombosis and Haemostasis | volume = 2 | issue = 8 | pages = 1247–1255 | doi = 10.1111/j.1538-7836.2004.00790.x | url = http://piedmontfayetteed.org/PERC%20rule.pdf | pmid = 15304025 | last1 = Kline | first1 = JA | last2 = Mitchell | first2 = AM | last3 = Kabrhel | first3 = C | last4 = Richman | first4 = PB | last5 = Courtney | first5 = DM}}</ref> The PERC rule has a sensitivity of 97.4% and specificity of 21.9% with a false negative rate of 1.0% (16/1666).<ref>{{Cite journal | last = Kline | first =  Jeffrey A | year = 2008 | title = Prospective multicenter evaluation of the pulmonary embolism rule-out criteria | journal = Journal of Thrombosis and Haemostasis | volume = 6 | issue = 5 | pages = 772–780 | doi = 10.1111/j.1538-7836.2008.02944.x | url = http://www.ingentaconnect.com/content/bsc/jth/2008/00000006/00000005/art00010 | pmid = 18318689 | last1 = Kline | first1 = JA | last2 = Courtney | first2 = DM | last3 = Kabrhel | first3 = C | last4 = Moore | first4 = CL | last5 = Smithline | first5 = HA | last6 = Plewa | first6 = MC | last7 = Richman | first7 = PB | last8 = O'Neil | first8 = BJ | last9 = Nordenholz | first9 = K}}</ref>
Patients in this low risk category without any of these criteria may undergo no further diagnostic testing for PE: Hypoxia - Sa0<sub>2</sub> <95%, unilateral leg swelling, hemoptysis, prior DVT or PE, recent surgery or trauma, age >50, hormone use, tachycardia. The rationale behind this decision is that further testing (specifically CT angiogram of the chest) may cause more harm (from radiation exposure and contrast dye) than the risk of PE. <cite>REFNAME26</cite> The PERC rule has a sensitivity of 97.4% and specificity of 21.9% with a false negative rate of 1.0% (16/1666). <cite>REFNAME27</cite>


==Treatment==
==Treatment==
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===Anticoagulation===
===Anticoagulation===
{{main|anticoagulant}}
{{main|anticoagulant}}
In most cases, [[anticoagulant]] therapy is the mainstay of treatment. [[Heparin]], [[low molecular weight heparin]]s (such as [[enoxaparin]] and [[dalteparin]]), or [[fondaparinux]] is administered initially, while [[warfarin]], [[acenocoumarol]], or [[phenprocoumon]] therapy is commenced (this may take several days, usually while the patient is in the hospital). [[Low molecular weight heparin]] may reduce bleeding among patients with pulmonary embolism as compared to heparin according to a [[systematic review]] of [[randomized controlled trial]]s by the [[Cochrane Collaboration]].<ref name="pmid15495007">{{cite journal |author=Erkens PM, Prins MH |title=Fixed dose subcutaneous low molecular weight heparins versus adjusted dose unfractionated heparin for venous thromboembolism |journal=Cochrane Database Syst Rev |volume= |issue=9 |pages=CD001100 |year=2010 |pmid=20824828 |doi=10.1002/14651858.CD001100.pub3 |url=http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD001100.pub3/abstract |editor1-last=Prins |editor1-first=Martin H}} [http://pubmed.gov/15862070 ACPJC Review]</ref> The [[relative risk reduction]] was 40.0%. For patients at similar risk to those in this study (2.0% had bleeding when not treated with low molecular weight heparin), this leads to an [[absolute risk reduction]] of 0.8%. 125.0 patients [[number needed to treat|must be treated for one to benefit]].
In most cases, [[anticoagulant]] therapy is the mainstay of treatment. [[Heparin]], [[low molecular weight heparin]]s (such as [[enoxaparin]] and [[dalteparin]]), or [[fondaparinux]] is administered initially, while [[warfarin]], [[acenocoumarol]], or [[phenprocoumon]] therapy is commenced (this may take several days, usually while the patient is in the hospital). [[Low molecular weight heparin]] may reduce bleeding among patients with pulmonary embolism as compared to heparin according to a [[systematic review]] of [[randomized controlled trial]]s by the [[Cochrane Collaboration]]. <cite>REFNAME28</cite> The [[relative risk reduction]] was 40.0%. For patients at similar risk to those in this study (2.0% had bleeding when not treated with low molecular weight heparin), this leads to an [[absolute risk reduction]] of 0.8%. 125.0 patients [[number needed to treat|must be treated for one to benefit]].


It is possible to treat low risk patients (risk class I or class II) as [[Patient#Outpatients_and_inpatients|outpatients]].<ref name="Aujesky2011">{{cite journal
It is possible to treat low risk patients (risk class I or class II) as [[Patient#Outpatients_and_inpatients|outpatients]].<ref name="Aujesky2011">{{cite journal
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| format=
| format=
| date = January 22, 2007
| date = January 22, 2007
| accessdate = July 4, 2011}}</ref> This confirms the findings of an earlier [[systematic review]] of [[observational study|observational studies]].<ref>{{Cite journal
| accessdate = July 4, 2011}}</ref> This confirms the findings of an earlier [[systematic review]] of [[observational study|observational studies]]. <cite>REFNAME29</cite>
| title = Outpatient treatment and early discharge of symptomatic pulmonary embolism: a systematic review
| year = 2009
| journal = Eur Respir J
| pages = 1148–55
| volume = 33
| issue = 5
| pmid = 19407049
| last1 = Squizzato  | first1 =  A.
| last2 =  Galli  | first2 =  M.
| last3 =  Dentali  | first3 =  F.
| last4 =  Ageno  | first4 =  W.
| doi = 10.1183/09031936.00133608
}}</ref>


Warfarin therapy often requires frequent dose adjustment and monitoring of the [[international normalized ratio|INR]]. In PE, INRs between 2.0 and 3.0 are generally considered ideal. If another episode of PE occurs under warfarin treatment, the INR window may be increased to e.g. 2.5-3.5 (unless there are contraindications) or anticoagulation may be changed to a different anticoagulant e.g. [[low molecular weight heparin]]. In patients with an underlying malignancy, therapy with a course of [[low molecular weight heparin]] may be favored over warfarin based on the results of the CLOT trial.<ref>{{cite journal | author=Lee AY, Levine MN, Baker RI, Bowden C, [[Ajay Kakkar, Baron Kakkar|Kakkar AK]], Prins M, Rickles FR, Julian JA, Haley S, Kovacs MJ, Gent M | title=Low-molecular-weight heparin versus a coumarin for the prevention of recurrent venous thromboembolism in patients with cancer | journal=N Engl J Med | year=2003 | pages=146–53 | volume=349 | issue=2  | pmid=12853587 | doi=10.1056/NEJMoa025313 | last12=Randomized Comparison Of Low-Molecular-Weight Heparin Versus Oral Anticoagulant Therapy For The Prevention Of Recurrent Venous Thromboembolism In Patients With Cancer (Clot) | first12=Investigators}}</ref>
Warfarin therapy often requires frequent dose adjustment and monitoring of the [[international normalized ratio|INR]]. In PE, INRs between 2.0 and 3.0 are generally considered ideal. If another episode of PE occurs under warfarin treatment, the INR window may be increased to e.g. 2.5-3.5 (unless there are contraindications) or anticoagulation may be changed to a different anticoagulant e.g. [[low molecular weight heparin]]. In patients with an underlying malignancy, therapy with a course of [[low molecular weight heparin]] may be favored over warfarin based on the results of the CLOT trial. <cite>REFNAME30</cite>


Similarly, pregnant women are often maintained on low molecular weight heparin to avoid the known [[teratogenic]] effects of warfarin, especially in the early stages of pregnancy. {{Citation needed|date=August 2011}}
Similarly, pregnant women are often maintained on low molecular weight heparin to avoid the known [[teratogenic]] effects of warfarin, especially in the early stages of pregnancy. {{Citation needed|date=August 2011}}


People are usually admitted to hospital in the early stages of treatment, and tend to remain under inpatient care until INR has reached therapeutic levels. Increasingly, low-risk cases are managed on an outpatient basis in a fashion already common in the treatment of DVT.<ref>{{cite journal |author=Davies CW, Wimperis J, Green ES, ''et al.'' |title=Early discharge of patients with pulmonary embolism: a two-phase observational study |journal=Eur. Respir. J. |volume=30 |issue=4 |pages=708–14 |year=2007 |month= October|pmid=17567672 |doi=10.1183/09031936.00140506}}</ref>
People are usually admitted to hospital in the early stages of treatment, and tend to remain under inpatient care until INR has reached therapeutic levels. Increasingly, low-risk cases are managed on an outpatient basis in a fashion already common in the treatment of DVT. <cite>REFNAME31</cite>


Warfarin therapy is usually continued for 3–6 months, or "lifelong" if there have been previous DVTs or PEs, or none of the usual risk factors is present. An abnormal [[D-dimer]] level at the end of treatment might signal the need for continued treatment among patients with a first unprovoked pulmonary embolus.<ref name=pmid17065639>{{cite journal |author=Palareti G, Cosmi B, Legnani C, ''et al.'' |title=D-dimer testing to determine the duration of anticoagulation therapy |journal=N. Engl. J. Med. |volume=355 |issue=17 |pages=1780–9 |year=2006 |pmid=17065639 |doi=10.1056/NEJMoa054444 |last12=Tripodi |first12=A |last13=Prolong |first13=Investigators}}</ref>
Warfarin therapy is usually continued for 3–6 months, or "lifelong" if there have been previous DVTs or PEs, or none of the usual risk factors is present. An abnormal [[D-dimer]] level at the end of treatment might signal the need for continued treatment among patients with a first unprovoked pulmonary embolus. <cite>REFNAME32</cite>


===Thrombolysis===
===Thrombolysis===

Revision as of 15:10, 14 January 2012

Pulmonary embolism (PE) is a blockage of the main artery of the lung or one of its branches by a substance that has travelled from elsewhere in the body through the bloodstream (embolism). Usually this is due to embolism of a thrombus (blood clot) from the deep veins in the legs, a process termed venous thromboembolism. A small proportion is due to the embolization of air, fat, talc in drugs of intravenous drug abusers or amniotic fluid. The obstruction of the blood flow through the lungs and the resultant pressure on the right ventricle of the heart leads to the symptoms and signs of PE. The risk of PE is increased in various situations, such as cancer or prolonged bed rest.[1]

Symptoms of pulmonary embolism include difficulty breathing, chest pain on inspiration, and palpitations. Clinical signs include low blood oxygen saturation and cyanosis, rapid breathing, and a rapid heart rate. Severe cases of PE can lead to collapse, abnormally low blood pressure, and sudden death.[1]

Diagnosis is based on these clinical findings in combination with laboratory tests (such as the D-dimer test) and imaging studies, usually CT pulmonary angiography. Treatment is typically with anticoagulant medication, including heparin and warfarin. Severe cases may require thrombolysis with drugs such as tissue plasminogen activator (tPA) or may require surgical intervention via pulmonary thrombectomy.[1]

Signs and symptoms

Symptoms of PE are sudden-onset dyspnea (shortness of breath), tachypnea (rapid breathing), chest pain of a "pleuritic" nature (worsened by breathing), cough and hemoptysis (coughing up blood). More severe cases can include signs such as cyanosis (blue discoloration, usually of the lips and fingers), collapse, and circulatory instability due to decreased blood flow through the lungs and into the left side of the heart. About 15% of all cases of sudden death are attributable to PE.[1]

On physical examination, the lungs are usually normal. Occasionally, a pleural friction rub may be audible over the affected area of the lung (mostly in PE with infarct) . A pleural effusion is sometimes present that is transudative, detectable by decreased percussion note, audible breath sounds and vocal resonance. Strain on the right ventricle may be detected as a left parasternal heave, a loud pulmonary component of the second heart sound, and raised jugular venous pressure.[1] A low-grade fever may be present, particularly if there is associated pulmonary hemorrhage or infarction.[2]

More rarely, inability of the right ventricle to remove fluid from the tissues leads to fluid accumulation in the legs (peripheral edema), congestion of the liver with mild jaundice and tenderness, and ascites (fluid in the abdominal cavity).Template:Citation needed

Risk factors

The most common sources of embolism are proximal leg deep venous thrombosis (DVTs) or pelvic vein thromboses. Any risk factor for DVT also increases the risk that the venous clot will dislodge and migrate to the lung circulation, which happens in up to 15% of all DVTs. The conditions are generally regarded as a continuum termed venous thromboembolism (VTE).

The development of thrombosis is classically due to a group of causes named Virchow's triad (alterations in blood flow, factors in the vessel wall and factors affecting the properties of the blood). Often, more than one risk factor is present.

Diagnosis

The diagnosis of PE is based primarily on validated clinical criteria combined with selective testing because the typical clinical presentation (shortness of breath, chest pain) cannot be definitively differentiated from other causes of chest pain and shortness of breath. The decision to do medical imaging is usually based on clinical grounds, i.e. the medical history, symptoms and findings on physical examination, followed by an assessment of clinical probability.[1]

The most commonly used method to predict clinical probability, the Wells score, is a clinical prediction rule, whose use is complicated by multiple versions being available. In 1995, Wells et al. initially developed a prediction rule (based on a literature search) to predict the likelihood of PE, based on clinical criteria.[3] The prediction rule was revised in 1998 [4] This prediction rule was further revised when simplified during a validation by Wells et al. in 2000. [5] In the 2000 publication, Wells proposed two different scoring systems using cutoffs of 2 or 4 with the same prediction rule. [5] In 2001, Wells published results using the more conservative cutoff of 2 to create three categories.[6] An additional version, the "modified extended version", using the more recent cutoff of 2 but including findings from Wells's initial studies[7] [8] were proposed. [9] Most recently, a further study reverted to Wells's earlier use of a cutoff of 4 points [5] to create only two categories. [10]

There are additional prediction rules for PE, such as the Geneva rule. More importantly, the use of any rule is associated with reduction in recurrent thromboembolism. [11]

The Wells score: [12]

  • clinically suspected DVT - 3.0 points
  • alternative diagnosis is less likely than PE - 3.0 points
  • tachycardia - 1.5 points
  • immobilization/surgery in previous four weeks - 1.5 points
  • history of DVT or PE - 1.5 points
  • hemoptysis - 1.0 points
  • malignancy (treatment for within 6 months, palliative) - 1.0 points

Traditional interpretation [5][6] [13]

  • Score >6.0 - High (probability 59% based on pooled data [14])
  • Score 2.0 to 6.0 - Moderate (probability 29% based on pooled data [14])
  • Score <2.0 - Low (probability 15% based on pooled data [14])

Alternative interpretation [5][10]

  • Score > 4 - PE likely. Consider diagnostic imaging.
  • Score 4 or less - PE unlikely. Consider D-dimer to rule out PE.

Blood tests

Early primary research has shown that in low/moderate suspicion of PE, a normal D-dimer level (shown in a blood test) is enough to exclude the possibility of thrombotic PE. [15] This has been corroborated by a recent systematic review of studies of patients with low pre-test probability (PTP) of PE and negative D-dimer results that found the three month risk of thromboembolic events in patients excluded in this manner was 0.14%, with 95% confidence intervals from 0.05 to 0.41%, though this review was limited by its use of only one randomized-controlled clinical trial, the remainder of studies being prospective cohorts. [16] D-dimer is highly sensitive but not very specific (specificity around 50%). In other words, a positive D-dimer is not synonymous with PE, but a negative D-dimer is, with a good degree of certainty, an indication of absence of a PE. [17]

When a PE is being suspected, a number of blood tests are done, in order to exclude important secondary causes of PE. This includes a full blood count, clotting status (PT, aPTT, TT), and some screening tests (erythrocyte sedimentation rate, renal function, liver enzymes, electrolytes). If one of these is abnormal, further investigations might be warranted.

Imaging

Selective pulmonary angiogram revealing significant thrombus (labelled A) causing a central obstruction in the left main pulmonary artery. ECG tracing shown at bottom.
CT pulmonary angiography (CTPA) showing a saddle embolus and substantial thrombus burden in the lobar branches of both main pulmonary arteries.
Ventilation-perfusion scintigraphy in a woman taking hormonal contraceptives and valdecoxib.
(A) After inhalation of 20.1 mCi of Xenon-133 gas, scintigraphic images were obtained in the posterior projection, showing uniform ventilation to lungs.
(B) After intravenous injection of 4.1 mCi of Technetium-99m-labeled macroaggregated albumin, scintigraphic images were obtained, shown here in the posterior projection. This and other views showed decreased activity in multiple regions.

The gold standard for diagnosing pulmonary embolism (PE) is pulmonary angiography. Pulmonary angiography is used less often due to wider acceptance of CT scans, which are non-invasive. CT pulmonary angiography is the recommended first line diagnostic imaging test in most people.

Non-invasive imaging

CT pulmonary angiography (CTPA) is a pulmonary angiogram obtained using computed tomography (CT) with radiocontrast rather than right heart catheterization. Its advantages are clinical equivalence, its non-invasive nature, its greater availability to patients, and the possibility of identifying other lung disorders from the differential diagnosis in case there is no pulmonary embolism. Assessing the accuracy of CT pulmonary angiography is hindered by the rapid changes in the number of rows of detectors available in multidetector CT (MDCT) machines. [18] According to a cohort study, single-slice spiral CT may help diagnose detection among patients with suspected pulmonary embolism. [19] In this study, the sensitivity was 69% and specificity was 84%. In this study which had a prevalence of detection was 32%, the positive predictive value of 67.0% and negative predictive value of 85.2% (click here to adjust these results for patients at higher or lower risk of detection). However, this study's results may be biased due to possible incorporation bias, since the CT scan was the final diagnostic tool in patients with pulmonary embolism. The authors noted that a negative single slice CT scan is insufficient to rule out pulmonary embolism on its own. A separate study with a mixture of 4 slice and 16 slice scanners reported a sensitivity of 83% and a specificity of 96%. This study noted that additional testing is necessary when the clinical probability is inconsistent with the imaging results. [20] CTPA is non-inferior to VQ scanning, and identifies more emboli (without necessarily improving the outcome) compared to VQ scanning. [21]

Ventilation/perfusion scan (or V/Q scan or lung scintigraphy), which shows that some areas of the lung are being ventilated but not perfused with blood (due to obstruction by a clot). This type of examination is used less often because of the more widespread availability of CT technology, however, it may be useful in patients who have an allergy to iodinated contrast or in pregnancy due to lower radiation exposure than CT. [22]

Low probability diagnostic tests/non-diagnostic tests

Tests that are frequently done that are not sensitive for PE, but can be diagnostic.

  • Chest X-rays are often done on patients with shortness of breath to help rule-out other causes, such as congestive heart failure and rib fracture. Chest X-rays in PE are rarely normal, [23] but usually lack signs that suggest the diagnosis of PE (e.g. Westermark sign, Hampton's hump).
  • Ultrasonography of the legs, also known as leg doppler, in search of deep venous thrombosis (DVT). The presence of DVT, as shown on ultrasonography of the legs, is in itself enough to warrant anticoagulation, without requiring the V/Q or spiral CT scans (because of the strong association between DVT and PE). This may be valid approach in pregnancy, in which the other modalities would increase the risk of birth defects in the unborn child. However, a negative scan does not rule out PE, and low-radiation dose scanning may be required if the mother is deemed at high risk of having pulmonary embolism. Template:Citation needed

Electrocardiogram

Electrocardiogram of a patient with pulmonary embolism showing sinus tachycardia of approximately 150 beats per minute and right bundle branch block.

An electrocardiogram (ECG) is routinely done on patients with chest pain to quickly diagnose myocardial infarctions (heart attacks). An ECG may show signs of right heart strain or acute cor pulmonale in cases of large PEs - the classic signs are a large S wave in lead I, a large Q wave in lead III and an inverted T wave in lead III ("S1Q3T3").[1] This is occasionally (up to 20%) present, but may also occur in other acute lung conditions and has therefore limited diagnostic value. The most commonly seen signs in the ECG is sinus tachycardia, right axis deviation and right bundle branch block. [24] Sinus tachycardia was however still only found in 8 - 69% of people with PE. [25]

Echocardiography

In massive and submassive PE, dysfunction of the right side of the heart can be seen on echocardiography, an indication that the pulmonary artery is severely obstructed and the heart is unable to match the pressure. Some studies (see below) suggest that this finding may be an indication for thrombolysis. Not every patient with a (suspected) pulmonary embolism requires an echocardiogram, but elevations in cardiac troponins or brain natriuretic peptide may indicate heart strain and warrant an echocardiogram. [26]

The specific appearance of the right ventricle on echocardiography is referred to as the McConnell's sign. This is the finding of akinesia of the mid-free wall but normal motion of the apex. This phenomenon has a 77% sensitivity and a 94% specificity for the diagnosis of acute pulmonary embolism in the setting of right ventricular dysfunction. [27]

Algorithms

Recent recommendations for a diagnostic algorithm have been published by the PIOPED investigators; however, these recommendations do not reflect research using 64 slice MDCT. [28] These investigators recommended:

  • Low clinical probability. If negative D-dimer, PE is excluded. If positive D-dimer, obtain MDCT and based treatment on results.
  • Moderate clinical probability. If negative D-dimer, PE is excluded. However, the authors were not concerned that a negative MDCT with negative D-dimer in this setting has an 5% probability of being false. Presumably, the 5% error rate will fall as 64 slice MDCT is more commonly used. If positive D-dimer, obtain MDCT and based treatment on results.
  • High clinical probability. Proceed to MDCT. If positive, treat, if negative, additional tests are needed to exclude PE.
Pulmonary Embolism Rule-out Criteria

The Pulmonary Embolism Rule-out Criteria, or PERC rule, helps assess people in whom pulmonary embolism is suspected, but unlikely. Unlike the Wells Score and Geneva score, which are clinical prediction rules intended to risk stratify patients with suspected PE, the PERC rule is designed to rule out risk of PE in patients when the physician has already stratified them into a low-risk category.

Patients in this low risk category without any of these criteria may undergo no further diagnostic testing for PE: Hypoxia - Sa02 <95%, unilateral leg swelling, hemoptysis, prior DVT or PE, recent surgery or trauma, age >50, hormone use, tachycardia. The rationale behind this decision is that further testing (specifically CT angiogram of the chest) may cause more harm (from radiation exposure and contrast dye) than the risk of PE. [29] The PERC rule has a sensitivity of 97.4% and specificity of 21.9% with a false negative rate of 1.0% (16/1666). [30]

Treatment

In most cases, anticoagulant therapy is the mainstay of treatment. Acutely, supportive treatments, such as oxygen or analgesia, are often required.

Anticoagulation

Template:Main In most cases, anticoagulant therapy is the mainstay of treatment. Heparin, low molecular weight heparins (such as enoxaparin and dalteparin), or fondaparinux is administered initially, while warfarin, acenocoumarol, or phenprocoumon therapy is commenced (this may take several days, usually while the patient is in the hospital). Low molecular weight heparin may reduce bleeding among patients with pulmonary embolism as compared to heparin according to a systematic review of randomized controlled trials by the Cochrane Collaboration. [31] The relative risk reduction was 40.0%. For patients at similar risk to those in this study (2.0% had bleeding when not treated with low molecular weight heparin), this leads to an absolute risk reduction of 0.8%. 125.0 patients must be treated for one to benefit.

It is possible to treat low risk patients (risk class I or class II) as outpatients.[2] A randomised trial of 344 patients (171 outpatients and 168 inpatients) found that outcomes were equivalent whether patients were treated in hospital or at home (there was one death at 90 days in each group).[2][3] This confirms the findings of an earlier systematic review of observational studies. [32]

Warfarin therapy often requires frequent dose adjustment and monitoring of the INR. In PE, INRs between 2.0 and 3.0 are generally considered ideal. If another episode of PE occurs under warfarin treatment, the INR window may be increased to e.g. 2.5-3.5 (unless there are contraindications) or anticoagulation may be changed to a different anticoagulant e.g. low molecular weight heparin. In patients with an underlying malignancy, therapy with a course of low molecular weight heparin may be favored over warfarin based on the results of the CLOT trial. [33]

Similarly, pregnant women are often maintained on low molecular weight heparin to avoid the known teratogenic effects of warfarin, especially in the early stages of pregnancy. Template:Citation needed

People are usually admitted to hospital in the early stages of treatment, and tend to remain under inpatient care until INR has reached therapeutic levels. Increasingly, low-risk cases are managed on an outpatient basis in a fashion already common in the treatment of DVT. [34]

Warfarin therapy is usually continued for 3–6 months, or "lifelong" if there have been previous DVTs or PEs, or none of the usual risk factors is present. An abnormal D-dimer level at the end of treatment might signal the need for continued treatment among patients with a first unprovoked pulmonary embolus. [35]

Thrombolysis

Template:Main

Massive PE causing hemodynamic instability (shock and/or hypotension, defined as a systolic blood pressure <90 mmHg or a pressure drop of 40 mmHg for>15 min if not caused by new-onset arrhythmia, hypovolemia or sepsis) is an indication for thrombolysis, the enzymatic destruction of the clot with medication. It is the best available medical treatment in this situation and is supported by clinical guidelines.[4][5][6]

The use of thrombolysis in non-massive PEs is still debated. The aim of the therapy is to dissolve the clot, but there is an attendant risk of bleeding or stroke.[7] The main indication for thrombolysis is in submassive PE where right ventricular dysfunction can be demonstrated on echocardiography, and the presence of visible thrombus in the atrium.[8]

Surgery

Used inferior vena cava filter.

Surgical management of acute pulmonary embolism (pulmonary thrombectomy) is uncommon and has largely been abandoned because of poor long-term outcomes. However, recently, it has gone through a resurgence with the revision of the surgical technique and is thought to benefit selected patients.[9]

Chronic pulmonary embolism leading to pulmonary hypertension (known as chronic thromboembolic hypertension) is treated with a surgical procedure known as a pulmonary thromboendarterectomy.

Inferior vena cava filter

Template:Main If anticoagulant therapy is contraindicated and/or ineffective, or to prevent new emboli from entering the pulmonary artery and combining with an existing blockage, an inferior vena cava filter may be implanted.[10]

Prognosis

Large saddle embolus seen at PA.

Mortality from untreated PE is said to be 26%. This figure comes from a trial published in 1960 by Barrit and Jordan,[11] which compared anticoagulation against placebo for the management of PE. Barritt and Jordan performed their study in the Bristol Royal Infirmary in 1957. This study is the only placebo controlled trial ever to examine the place of anticoagulants in the treatment of PE, the results of which were so convincing that the trial has never been repeated as to do so would be considered unethical. That said, the reported mortality rate of 26% in the placebo group is probably an overstatement, given that the technology of the day may have detected only severe PEs.

Prognosis depends on the amount of lung that is affected and on the co-existence of other medical conditions; chronic embolisation to the lung can lead to pulmonary hypertension. After a massive PE, the embolus must be resolved somehow if the patient is to survive. In thrombotic PE, the blood clot may be broken down by fibrinolysis, or it may be organized and recanalized so that a new channel forms through the clot. Blood flow is restored most rapidly in the first day or two after a PE.[12] Improvement slows thereafter and some deficits may be permanent. There is controversy over whether or not small subsegmental PEs need to be treated at all[13] and some evidence exists that patients with subsegmental PEs may do well without treatment.[14][15]

Once anticoagulation is stopped, the risk of a fatal pulmonary embolism is 0.5% per year.[16]

Predicting mortality

The PESI and Geneva prediction rules can estimate mortality and so may guide selection of patients who can be considered for outpatient therapy.[17]

Underlying causes

After a first PE, the search for secondary causes is usually brief. Only when a second PE occurs, and especially when this happens while still under anticoagulant therapy, a further search for underlying conditions is undertaken. This will include testing ("thrombophilia screen") for Factor V Leiden mutation, antiphospholipid antibodies, protein C and S and antithrombin levels, and later prothrombin mutation, MTHFR mutation, Factor VIII concentration and rarer inherited coagulation abnormalities. Template:Citation needed

References

  1. ISBN:0071391401 [Goldhaber]
  2. Stein PD, Sostman HD, Hull RD, Goodman LR, Leeper KV Jr, Gottschalk A, Tapson VF, and Woodard PK. Diagnosis of pulmonary embolism in the coronary care unit. Am J Cardiol. 2009 Mar 15;103(6):881-6. DOI:10.1016/j.amjcard.2008.11.040 | PubMed ID:19268750 | HubMed [Stein]