Chapter 27 Plasmaphoresis Flashcards

1
Q

What is plasmapheresis?

A

A procedure involving the extracorporeal separation of blood components to obtain a filtered plasma product.

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2
Q

What is the basis for therapeutic plasmapheresis (TP)?

A

The removal of proteins, protein-bound or high molecular weight solutes including autoantibodies, immune complexes, excess lipids, hormones, aromatic amino acids, ammonia, bilirubin, endotoxin, lipids, phenols, and exogenous toxins.

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3
Q

What are the two common methods for preparing plasma products in equine medicine?

A

Manual blood centrifugation and gravity sedimentation.

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4
Q

What is automated plasmapheresis?

A

A procedure using in-line blood cell separators to remove whole blood, infuse anticoagulant, and separate blood components via centrifugation, returning concentrated cells to the donor.

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5
Q

What are the advantages of automated plasmapheresis over manual methods?

A

It is more efficient, reduces erythrocyte and leukocyte counts, minimizes the risk of immunological and non-immunological adverse reactions, and maintains normal coagulation activity.

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6
Q

What is the main goal of apheresis?

A

To separate one or more blood components and return the remaining products to the patient or donor, with or without extracorporeal treatment or replacement of the separated component.

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7
Q

What are the categories of apheresis applications according to the American Society of Apheresis?

A

Category I: first-line therapy, Category II: second-line therapy, Category III: uncertain role, Category IV: ineffective or harmful.

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8
Q

What is the primary use of therapeutic plasmapheresis in human and veterinary medicine?

A

To remove disease-causing or disease-related plasma components from circulation and replace them with harmless plasma.

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9
Q

What types of solutes does therapeutic plasmapheresis primarily remove?

A

Protein-bound or high molecular weight solutes such as circulating protein-bound toxins, autoantibodies, immune complexes, and abnormally occurring molecules.

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10
Q

What are the conditions for which therapeutic plasmapheresis has been used in human medicine?

A

Immune-mediated diseases, neoplasia, infectious diseases, sepsis, hyperlipidemia, thyrotoxicosis, and removal of toxins.

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11
Q

What are the indications for using therapeutic plasmapheresis in equine medicine?

A

Conditions such as immune-mediated hemolytic anemia, immune-mediated dermatoses, purpura hemorrhagica, hypertriglyceridemia, liver failure, kernicterus, sepsis, and multiple organ dysfunction syndrome.

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12
Q

What is the role of therapeutic plasmapheresis in immune-mediated hemolytic anemia?

A

It removes circulating autoantibodies, immune complexes, and activated complement components in patients with poor response to blood transfusions and life-threatening hemolysis.

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13
Q

What is pemphigus foliaceus and its treatment challenge?

A

A common autoimmune skin disease in horses that may take weeks to months to control with glucocorticoids and/or azathioprine.

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14
Q

What was the author’s experience using TP in equine patients with pemphigus foliaceus?

A

TP was applied to four adult equine patients unresponsive to high doses of dexamethasone, showing clinical improvement with lower doses of dexamethasone after TP.

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15
Q

What is purpura hemorrhagica?

A

An immune-mediated severe necrotizing vasculitis causing lesions of the skin and mucous membranes, with larger hemorrhagic and edematous damage in muscles and subcutaneous tissues.

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16
Q

What was the author’s experience using TP for purpura hemorrhagica?

A

TP was used in two severe cases unresponsive to glucocorticoids, with TP helping remove antibody-antigen complexes until immunosuppressive therapy became effective.

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17
Q

What conditions can lead to hypertriglyceridemia in equids?

A

Secondary to primary systemic diseases such as septicemia, colitis, esophageal obstruction, gastric impaction or rupture, fecalith, excessive parasitism, and pituitary adenoma, more frequent in miniature horses and donkeys.

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18
Q

What was the author’s approach using TP for hypertriglyceridemia in equids?

A

TP was considered for animals unresponsive to conventional treatment, with plasma removal volumes of 15-20 ml/kg body weight and potential repeat TP with donor plasma transfusion.

19
Q

What are the therapeutic goals of TP in liver failure and kernicterus?

A

To reverse hepatic coma, improve coagulation, and manage kernicterus and neurological signs, although success in equine patients is limited.

20
Q

What are the benefits of TP in treating sepsis and multiple organ dysfunction syndrome?

A

TP removes multiple toxic mediators of sepsis, potentially more effective than blocking single components, and randomized clinical trials in humans showed reduced mortality rates.

21
Q

What complications can arise from therapeutic plasmapheresis in horses?

A

Inadvertent return of concentrated blood cells into subcutaneous tissue, neurological abnormalities, citrate toxicity, hypercoagulability, hypogammaglobulinemia, hypotension (foals), and inflammatory responses to extracorporeal devices.

22
Q

What was the observed outcome of neurological abnormalities in horses undergoing automated plasmapheresis?

A

Temporary resolution within hours to days, except for one horse that had bilateral blindness.

23
Q

What are the reported complications of plasmapheresis in human patients?

A

Transient hypercoagulable state, hypogammaglobulinemia, and non-specific inflammatory response to the extracorporeal circulation filter and/or drains.

24
Q

What is the author’s recommended frequency for safe TP in equine patients without exchange plasma transfusions?

A

Removal of 22 ml of plasma/kg body weight every 14 days.

25
Q

What are the additional monitoring requirements for foals undergoing TP?

A

Monitoring vital signs and urine production to adjust colloid or crystalloid therapy and prevent hypovolemia.

26
Q

What was the author’s approach to plasma collection using manual methods?

A

Using a 12 or 10 gauge indwelling catheter in a jugular vein, collecting 15 ml/kg body weight of blood into anticoagulant citrate dextrose (ACD) solution, and allowing sedimentation for 24 hours at 4°C.

27
Q

What is the efficiency of automated plasmapheresis compared to manual methods?

A

Harvests one liter of plasma in 20 minutes, with significantly reduced erythrocytes and leukocytes, minimizing immunological and non-immunological adverse reactions.

28
Q

What are the main criteria for assessing plasma quality in plasmapheresis?

A

Low blood cell counts and normal coagulation activity.

29
Q

What is the impact of using glass bottles for plasma harvesting in coagulation factor substitution?

A

Reduces platelets and coagulation factors VII, VIII, and XII, making glass bottles unsuitable for this purpose.

30
Q

What are some diseases treated with plasma harvested from equine donors?

A

Coagulopathies, protein-losing enteropathies, endotoxemia, failure of passive transfer, and protection against infections like Rhodococcus equi, Salmonella, Clostridium difficile, and Clostridium perfringens.

31
Q

What was the observed increase in plasma albumin levels with plasma administration in horses?

A

An increase of 0.1–0.2 g/dl per 1 L of plasma administered.

32
Q

What was the outcome of septic foals receiving hyperimmune plasma rich in antiendotoxin antibodies?

A

Higher survival rates to discharge and greater overall survival in septic foals.

33
Q

What are the main adverse effects of therapeutic plasmapheresis in human patients?

A

Hypercoagulability, hypogammaglobulinemia, and non-specific inflammatory responses to the extracorporeal circulation devices.

34
Q

What was the primary therapeutic aim of TP in treating immune-mediated diseases?

A

Rapidly decreasing plasma concentrations of antibodies or immune complexes while using other immunosuppressive measures to prolong the effect.

35
Q

What are some indications for apheresis in human medicine?

A

First-line therapy for Guillain-Barre Syndrome and myasthenia gravis, second-line therapy for multiple sclerosis and mushroom poisoning, and individualized decision-making for immune-mediated hemolytic anemia.

36
Q

What are the reported benefits of TP in treating hypertriglyceridemia in human patients?

A

Reductions in triglyceride levels by 46–80% and improvement of symptoms following one to three TP procedures.

37
Q

What was the author’s approach to using TP in foals with kernicterus?

A

Removing 15–20 ml of plasma/kg body weight with concurrent administration of an equivalent volume of donor plasma, though not yet successful in preventing death.

38
Q

What are the potential benefits of TP in treating sepsis in equine patients?

A

Removal of multiple toxic mediators of sepsis, potentially reducing mortality rates similar to findings in human randomized clinical trials.

39
Q

What was the author’s experience with adverse events during automated plasmapheresis?

A

Temporary neurological abnormalities such as ataxia, inability to stand, unilateral or bilateral blindness, and one case of bilateral blindness.

40
Q

What is the significance of automated plasmapheresis in minimizing adverse reactions?

A

Thorough removal of erythrocytes and leukocytes reduces the risk of immunological and non-immunological adverse reactions.

41
Q

What are some of the toxic mediators of sepsis targeted by TP?

A

Tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-1, IL-2, IL-6, IL-8, leukotrienes, prostaglandins, endotoxin, and tumor necrosis factor beta (TGF-beta).

42
Q

What are the clinical outcomes of using TP for purpura hemorrhagica?

A

Aided removal of antibody-antigen complexes, allowing immunosuppressive therapy to become effective.

43
Q

What is the main challenge in using TP for liver failure and kernicterus in equine patients?

A

The need for a large volume of normal plasma as a substitute during TP.

44
Q

What is the rationale for using TP in immune-mediated dermatoses like pemphigus foliaceus?

A

TP helps remove pathogenic autoantibodies, aiding in the management of patients unresponsive to high doses of glucocorticoids.