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PHILADELPHIA, PENNSYLVANIA


Acute Massive Pulmonary Embolism (AMPE)<br />

The Aria Health Experience:-<br />

Rapid Response and Two Surgical Techniques which resulted in<br />

100% positive out<strong>com</strong>e in the cardiac operating room.<br />

H.MOHAMED, CCP., J.SCHULTZ, CCP., T.ZOMBOLAS, CCP., R. METCALF, MD.


Recent National Incidents:<br />

February 2011:<br />

Transgender hip-hop singer from Philadelphia sought for the<br />

death of a young British female entertainer.<br />

March 2011:<br />

Tennis star Serena Williams, on a flight from NY to LA,<br />

suffered from a PE.


OBJECTIVE / PURPOSE:AMPE<br />

- Raise an awareness with causes and <strong>com</strong>plications<br />

- Review the multidisciplinary team approach to treatment:<br />

- <strong>Perfusion</strong>ist, Surgeon, Anesthesiologist, Intensivist,<br />

Radiologist<br />

- Stat admission to the Cardiac OR<br />

- Assessment of RV Function / Strain<br />

- Assessment of Lung Function<br />

- Review / Discuss our experience and treatment<br />

- Highlight a possible new treatment approach with new equipment


HISTORY<br />

1872 - Dr. Trendelenburg studied 9 hospitalized patients with PE. He<br />

performed 2 pulmonary embolectomies and both patients died within<br />

37 hours.<br />

1924 - Dr. Kirschner, a student of Trendelenburg, performed the first<br />

successful pulmonary embolectomy. This case was presented at the<br />

Berlin Surgical Conference. Dr. Oschner from the USA attended this<br />

conference and took note of the procedure.<br />

1932 - Drs. Oschner and Debakey advocated IVC ligation to prevent<br />

pulmonary embolus.<br />

1932 - While a surgical resident, Dr. Gibbon witnessed an<br />

unsuccessful open attempt to save the life of a young woman who had<br />

sustained a pulmonary embolus - this was the catalyst for the<br />

development of the Heart / Lung Machine.<br />

1934 - Dr. Homans performed the first prophylactic venous ligation.


HISTORY cont’d.<br />

1961 - Dr. Cooley attempted a pulmonary embolectomy<br />

using CPB.<br />

1962 - Dr. Sharp performed the first successful pulmonary<br />

embolectomy in the United States.<br />

Two surgical approaches ultimately evolved for the<br />

management of pulmonary embolus.<br />

1. Operations that focused on the removal of an embolus<br />

to the lung.<br />

2. Operations that were designed to prevent embolization.<br />

Note: Sudden interruption of vena cava flow caused a<br />

decreased cardiac output and severe peripheral edema


Background Information<br />

-“Pulmonary embolism is a life-threatening condition that occurs<br />

when a thrombus or other material blocks the pulmonary arterial<br />

system in your lungs”.<br />

-This is an extremely <strong>com</strong>mon and highly lethal condition that is a<br />

leading cause of death in all age groups.<br />

-One of the most prevalent disease processes responsible for<br />

in-patient mortality (30-50%)<br />

-Overlooked diagnosis.


Why is this clinical picture of PE so important?<br />

Prompt diagnosis and treatment can dramatically reduce the<br />

mortality and morbidity rate.<br />

Majority of the cases are unrecognised clinically.<br />

One third of the patients who survive an initial PE die of a future<br />

embolic episode.<br />

Many patients who die of PE have not had any diagnostic workup<br />

nor have they received any prophylaxis for the disease.<br />

In most cases, the CLINICIANS have not even considered the<br />

diagnosis of PE.


Pathophysiology<br />

PE is not a disease in and of itself.<br />

It is often a fatal <strong>com</strong>plication of underlying venous<br />

thrombosis.<br />

Normally microthrombi (RBC,Platelets and Fibrin) are formed<br />

and lysed within the venous circulatory system.<br />

Under pathological conditions, these microthrombi may<br />

escape, propagate and will block the pulmonary blood vessels<br />

causing PE.


Facts about PE.<br />

3 rd most <strong>com</strong>mon cause of death.<br />

2 nd most <strong>com</strong>mon cause of unexpected death in most age<br />

groups.<br />

60% of patients dying in the hospital have had a PE.<br />

Diagnosis has been missed in about 70% of the cases


National Statistics<br />

There are approximately 650,000 occurrences in the United States.<br />

400,000 of these patients go undiagnosed.<br />

The Center for Disease Control (CDC) estimated that about 250,000<br />

Americans annually suffer from a PE.<br />

About 100,000 deaths occur annually and these could have been<br />

prevented with proper diagnosis and treatment.


National Statistics cont’d.<br />

This type of obstruction can manifest itself into a myriad of<br />

physiologic events which can ultimately result in cardiac arrest and<br />

death of up to 70-90% of these patients in the first hour.<br />

Approximately 75% of autopsy-proven Pulmonary Embolisms (PE)<br />

are not detected clinically.


National Statistics cont’d.<br />

African Americans are the highest risk group with a 50%<br />

higher incidence than American Whites.<br />

Asian/Pacific Islanders/American Indian patients have a<br />

markedly lower risk.<br />

The risk factor is increased in pregnancy and during the<br />

postpartum period.<br />

The mortality rate remains 20-30% higher in men than in<br />

women.


RECOMMENDATIONS<br />

CPB for pulmonary embolism should be utilized for those<br />

patients who are hypotensive (systolic pressure


Definition<br />

A pulmonary embolus is described as a blockage of the:<br />

- Main Pulmonary Artery (PA).<br />

- The Right and/or Left Pulmonary Arteries.<br />

- The Segmental Pulmonary Arteries.<br />

…by either a blood clot (thrombus), fat, gas (nitrogen, air, CO 2),<br />

tumor cells, amniotic fluid, septic embolism, talc or elemental<br />

mercury and more recently silicone.


Silicone Embolus<br />

Former Miss. Argentina (1994) died in December 2009 from<br />

silicone <strong>com</strong>plications of a “gluteal plasty” which involved<br />

injection of liquid silicone.<br />

In November 2006, this occurrence (44 patients) was presented at<br />

the annual meeting of the Radiological Society of North America<br />

(RSNA) where the idea of “Pump Up” parties was discussed for the<br />

very first time.<br />

Often members of the male-to-female transgender <strong>com</strong>munity<br />

gather for liquid silicone injections in hopes of feminizing their<br />

appearance.


Definition cont’d.<br />

Medically, AMPE is defined as an occlusion of the PA that exceeds<br />

50% of its cross sectional area, resulting in progressive<br />

hemodynamic <strong>com</strong>promise.<br />

Massive PE is also defined as the presence of persistent systemic<br />

hypotension or cardiogenic shock and signs of right ventricular<br />

dysfunction (RVD).<br />

A sub-massive PE is defined as moderate to large clot, presence of<br />

RVD, and normal arterial blood pressure.


SIGNS AND SYMPTOMS:<br />

Signs and symptoms of PE may include any or all of the<br />

following:<br />

∙chest pain at rest ∙anxiety<br />

∙S.O.B. at rest ∙dizziness<br />

∙hyperventilation ∙diaphoresis<br />

∙syncope ( B/P, CO, PAP) ∙tachycardia (>100 b/p/m) ∙clammy<br />

skin ∙hemoptysis (13%)<br />

∙swollen/painful legs ∙wheezing/crackles<br />

∙apnea ∙peripheral cyanosis<br />

∙dyspnea (73%) ∙painful respirations<br />

∙cough (37%) ∙fever<br />

∙pleuritic chest pain (66%) ∙T wave inversions (leads V1-4)


TESTS USED TO CONFIRM PE:<br />

∙Quantitative D-dimer assay test* ∙Ventilation/perfusion Scan ( V/Q) ∙Pulse Oximetry ∙CT Angiography<br />

∙Pulmonary Arteriogram ∙CT Scan (helical)<br />

∙Doppler Ultrasonography ∙Hemodynamics<br />

∙Venogram of the leg ∙Arteriogram of the leg<br />

∙Arterial Blood Gas (ABG) ∙EKG (S-T in V1- 4)<br />

∙Physical exam/family history or prior Deep Vein Thrombosis (DVT)/PE<br />

∙Echocardiography<br />

<br />

*D-dimer ASSAY TEST:<br />

The Quantitative D-dimer assay test is also referred to as the “Fibrin<br />

Degradation test” or “Fragment D-dimer”. The Fragment D-dimer assesses both<br />

thrombin and plasmin activity. Related tests may include; Fibrin Split Products<br />

(FSP), Fibrin Degradation Products (FDP), Prothrombin Time (PT), Partial<br />

Thromboplastin Time (PTT); Fibrinogen, and or Platelet count.


TREATMENT OF PE:<br />

First Line Treatment: NON-ACUTE SITUATION<br />

∙O 2 Therapy<br />

∙Intubation/Ventilation<br />

∙Insertion of Vena Caval Filter<br />

Bird’s nest filter (Infrarenal)<br />

Greenfield filter (Suprarenal)<br />

∙Sildenafil (Viagra)<br />

∙Anticoagulant/Thrombolysis<br />

-Heparin<br />

-Coumadin<br />

-Tissue Plasminogen Activators (TPA)<br />

∙Low Molecular Weight Heparin


TREATMENT OF PE: cont’d<br />

Second Line Treatment: ACUTE SITUATION<br />

∙Surgical removal with the use of CPB<br />

∙*Surgical removal with the Vortex Angiovac cannula<br />

(new technique)<br />

∙Intubation / Ventilation<br />

∙O 2 Therapy<br />

∙Insertion of Vena Caval Filter<br />

Bird’s nest filter (Infrarenal)<br />

Greenfield filter (Suprarenal)<br />

∙Anticoagulant/Thrombolysis<br />

-Heparin<br />

-Coumadin<br />

-TPA<br />

-Low Molecular Weight Heparin


AngioVac System<br />

Right Femoral 22 fr.to Left Femoral 18 fr. venous bypass.<br />

Utilizing a centrifugal pump and no oxygenator in line.<br />

Tracking over an Amplatz stiff wire, the AngioVac cannula is<br />

positioned first in the main PA. The balloon actuated funnel tip on<br />

the AngioVac is then opened and the pump flow is initiated and<br />

then optimized.


Vortex Medical Inc.<br />

AngioVac System


∙Sudden Cardiac death<br />

COMPLICATIONS OF PE:<br />

∙Long term anticoagulant prophylaxis potentially leading to<br />

bleeding problems<br />

∙Right Ventricular Hypertophy (RVH) / Cor Pulmonale<br />

∙Respiratory Failure<br />

∙Cardiogenic shock ( C.O., B/P)<br />

∙Palpitations


Regular exercise<br />

Anticoagulant prophylaxis<br />

Hydration<br />

Alcohol intake (decrease)<br />

Use of <strong>com</strong>pression stockings<br />

PREVENTION OF PE:<br />

Mobilization when taking long travel trips<br />

Use professionals for cosmetic surgeries


Chest X-Ray of PE


Pulmonary Angiogram


Pulmonary Angiogram X-Ray


Contrast CT showing Pulmonary Embolus


The Aria Experience<br />

Methods: Two Cardiopulmonary Bypass Techniques<br />

- Deep Hypothermic Circulatory Arrest (DHCA)<br />

with Cold Retrograde Cerebral <strong>Perfusion</strong> (RCP)<br />

(n=7)<br />

- Normothermic (Tepid)<br />

(n=13)


DHCA Technique (Group A)<br />

Cannulation: Aortic & Bi-Caval Venous Cannulation<br />

Cardioplegia administration: Antegrade/Retrograde (warm/cold)<br />

Systemic cooling: As per protocol to 18 o C<br />

Circulatory Arrest: Initiation<br />

Initiation of RCP: Flow & pressure as per protocol<br />

Surgical removal of PE<br />

Cessation of RCP<br />

Rewarm as per protocol<br />

Administration of warm retrograde blood only to the heart<br />

TEE Assessment<br />

Termination of CPB (See table 1-Group A)


Population<br />

Group A (Circ. Arrest)<br />

7<br />

Average Age Male = 48.8 /Female = 33<br />

Sex Male = 6 Female = 1<br />

Mean Arterial Pressure 80 (mmHg)<br />

Mean PA Pressure n /a* (mmHg)<br />

Mean CVP (20-30 mmHg) (SVC)<br />

Average Retrograde<br />

Cerebral Blood flow<br />

260 mL/min (180-350)<br />

Mean SvO2 (CPB) 82<br />

Mean Pre Bypass rSO2<br />

52<br />

Mean Cooling rSO2<br />

77<br />

Mean RCP rSO2<br />

85<br />

Mean Warming rSO2<br />

73<br />

Cannulation Same<br />

(AO/IVC/SVC)<br />

Average Pump Time 135 Min.<br />

Average Crossclamp 41Min.<br />

Time<br />

Average Circ Arrest 41 Min. (30-66)<br />

Time<br />

Lowest temperature<br />

13<br />

during Circ. Arrest<br />

o C<br />

Average Cooling Time 52 Min.<br />

Average Rewarming 77 Min.<br />

Time<br />

* = No PA line was inserted into the Pulmonary Artery pre-CPB.


Normothermic (Tepid) Technique<br />

Cannulation: Aortic & Bi-Caval venous cannulation (Mitral valve)<br />

Cardioplegia administration: Antegrade/Retrograde (warm/cold)<br />

15 minutes intervals<br />

Systemic temperature: Drift to no less than 34 o C<br />

Surgical removal of PE<br />

Rewarm to 37 o C<br />

Administration of warm retrograde blood only to the heart<br />

TEE Assessment<br />

Termination of CPB (See table 1-Group B)


Group B (Normothermic)<br />

-Drift to 34 o Population<br />

C<br />

13<br />

Average Age Male = 54.2 /Female = 49.3<br />

Sex Male = 5 Female = 8<br />

Mean Arterial Pressure 95 (mmHg)<br />

Mean PA Pressure n /a* (mmHg)<br />

Mean CVP ?<br />

Average Retrograde<br />

Cerebral Blood flow<br />

0<br />

Mean SvO2 (CPB) 72<br />

Mean Pre Bypass rSO2<br />

52<br />

Mean Cooling rSO2<br />

NA<br />

Mean RCP rSO2<br />

NA<br />

Mean Warming rSO2<br />

68<br />

Cannulation Same<br />

Average Pump Time 64 Min.<br />

Average Crossclamp Time 45 Min.<br />

Lowest temperature<br />

during CPB<br />

34 o C<br />

Average Cooling Time 0<br />

Average Rewarming Time 15<br />

* = No PA line was inserted into the Pulmonary Artery pre-CPB.


Group A (Circ. Arrest) Group B (Normothermic)<br />

-Drift to 34 o C<br />

Population 7 13<br />

Average Age Male = 48.8 /Female = 33 Male = 54.2 /Female = 49.3<br />

Sex Male = 6 Female = 1 Male = 5 Female = 8<br />

Mean Arterial Pressure 80 (mmHg) 95 (mmHg)<br />

Mean PA Pressure n /a* (mmHg) n /a* (mmHg)<br />

Mean CVP (20-30 mmHg) (SVC) ?<br />

Average Retrograde 260 mL/min (180-350)<br />

0<br />

Cerebral Blood flow<br />

Mean SvO2 (CPB) 82 72<br />

Mean Pre Bypass rSO2 52 52<br />

Mean Cooling rSO2 77 NA<br />

Mean RCP rSO2 85 NA<br />

Mean Warming rSO2 73 68<br />

Cannulation Same<br />

Same<br />

(AO/IVC/SVC)<br />

Average Pump Time 135 Min. 64 Min.<br />

Average Crossclamp Time 41Min. 45 Min.<br />

Average Circ Arrest Time 41 Min. (30-66) 0<br />

Lowest temperature<br />

13 o C 34 o C<br />

during CPB<br />

Average Cooling Time 52 Min. 0<br />

Average Rewarming Time 77 Min. 15<br />

* = No PA line was inserted into the Pulmonary Artery pre-CPB.


BLOOD GASES<br />

Pre Intubation pH CO 2 O 2<br />

Normothermic 7.436 (7.37-7.52) 35 (27-56) 70.2 (56-86)<br />

Circ. Arrest 7.325 (7.25-7.40) 41 (27-55) 75.5 (58-93)**<br />

On CPB pH CO 2 O 2<br />

Normothermic 7.352 (7.27-7.41) 40.9 (31-53) 328.7 (173-488)<br />

Circ. Arrest 7.281 (7.10-7.47) 52.4 (40-70) 539 (408-696)<br />

Post Bypass pH CO 2 O 2<br />

Normothermic 7.376 (7.30-7.47) 40.5 (29-48) 305.2 (105-487)<br />

Circ. Arrest 7.314 (7.25-7.37) 44.1 (36-59) 126 (64-218)***<br />

** = Demonstrating gas exchange problems<br />

*** = Still denoting gas exchange problems


Summary<br />

The Keys to Our Management Strategy<br />

- Mandatory multidisciplinary approach.<br />

- 24/7 availability.<br />

- Rapid and a precise diagnosis with an immediate transfer to the<br />

CTOR (resembling Rescue Therapy) (LIKE VAD/ECMO)<br />

- Execution of a precise care plan by - <strong>Perfusion</strong>ist<br />

- Surgeon<br />

- Intensivist<br />

- Radiologist<br />

- Anesthesiologist<br />

- ICU staff<br />

- Results - 100% survival rate in the CTOR


Summary cont’d<br />

In a nonrandomized <strong>com</strong>parison of surgical and medical treatment<br />

in hemodynamically <strong>com</strong>promised patients with massive PE, the<br />

medical group had an increased mortality rate, increased number<br />

of hemorrhagic events and a higher incidence of recurrent PE.<br />

Gulba DC, Schmid C, Borst HG, Lichtlen P, Dietz R, Luft FC. Medical <strong>com</strong>pared with Surgical Treatment for<br />

Massive Pulmonary Embolism. Lancet. 1994:343:576-577.<br />

Currently our practice uses only the “tepid” CPB approach when<br />

we treat Acute Massive Pulmonary Embolism.


Thank You<br />

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