Mixing study

Short description: Type of blood plasma screening test

Mixing studies are tests performed on blood plasma of patients or test subjects to distinguish factor deficiencies from factor inhibitors, such as lupus anticoagulant, or specific factor inhibitors, such as antibodies directed against factor VIII.[1] Mixing studies are screening tests widely performed in coagulation laboratories. The basic purpose of these tests is to determine the cause of prolongation of Prothrombin Time (PT), Partial Thromboplastin Time, or sometimes of thrombin time (TT). Mixing studies take advantage of the fact that factor levels that are 50 percent of normal should give a normal Prothrombin time (PT) or Partial thromboplastin time (PTT) result.[2]

## Contents

* 1 Test method
* 2 Adsorbed Plasma and Aged Plasma
* 2.1 Correction of prothrombin time
* 2.2 Correction of partial thromboplastin time
* 3 Time-dependent inhibitors
* 4 Abnormal coagulation test results
* 5 Inhibitor
* 5.1 Assessing correction of mixing study
* 6 References

## Test method

Fresh normal plasma has all the blood coagulation factors with normal levels.

If the problem is a simple factor deficiency, mixing the patient plasma 1:1 with plasma that contains 100% of the normal factor level results in a level ≥50% in the mixture (say the patient has an activity of 0%; the average of 100% + 0% = 50%).[3] The PT or PTT will be normal (the mixing study shows correction). Correction with mixing indicates factor deficiency. Failure to correct with mixing indicates an inhibitor. Performing a thrombin time on the test plasma can provide useful additional information for the interpretation of mixing tests, such as by demonstrating the presence of anticoagulants, hypofibrinogenemia or dysfibrinogenemia.[4]

## Adsorbed Plasma and Aged Plasma

Factor deficient plasmas (Adsorbed Plasma and Aged Plasma, etc.) have been used historically in mixing studies. Plasma with known factor deficiencies are commercially available but are very expensive, so they have been prepared in the laboratory and used for mixing tests. Adsorbed plasma or plasma from patients on oral anticoagulants (Warfarin etc.) for a week or more is deficient in Factor II, Factor VII, Factor IX, and Factor X. Plasma from patients on oral anticoagulants (Warfarin etc.) for 48–72 hours is deficient in Factor VII. Aged plasma is deficient in Factor V & Factor VIIIC. Serum is deficient in factors I, V & VIIIC.

### Correction of prothrombin time

Prothrombin time (PT) may be corrected as follows:[5][6]

Factor Deficiency/Abnormality | Prothrombin Time corrected by mixing with

|

Normal Plasma | Adsorbed Plasma | Aged Plasma | Coumarin Plasma
Factor I | Yes  | Yes  | Yes  | Yes
Factor II | Yes  | Partial  | Yes  | Yes
Factor V  | Yes  | Yes  | No  | Yes
Factor VII | Yes  | No  | Yes  | No
Factor X | Yes  | No  | Yes  | Yes
Anticoagulants | No  | No  | No  | No

### Correction of partial thromboplastin time

Partial thromboplastin time (PTT) may be corrected as follows:[5]

Factor Deficiency/Abnormality | Partial Thromboplastin Time corrected by mixing with

|

Normal Plasma | Adsorbed Plasma | Aged Plasma
Factor VIIIC  | Yes  | Yes  | No
Factor IX  | Yes  | No  | Yes
Factor XI  | Yes  | Yes  | Yes

## Time-dependent inhibitors

Some inhibitors are time dependent. In other words, it takes time for the antibody to react with and inactivate the added clotting factor. The clotting test performed immediately after the specimens are mixed may show correction because the antibody has not had time to inactivate its target factor. A test performed after the mixture is incubated for 1 to 2 hours at 37°C will show significant prolongation over the clotting time obtained after immediate mixing. Nonspecific inhibitors like the lupus anticoagulant usually are not time dependent; the immediate mixture will show prolongation. Many specific factor inhibitors are time dependent, and the inhibitor will not be detected unless the test is repeated after incubation (factor VIII inhibitors are notorious for this).[7]

## Abnormal coagulation test results

A common problem is an unexplained increase in the PT and/or PTT. If this is observed, the test should be repeated with a fresh sample. Another consideration is heparin. It is possible that the blood sample was mistakenly drawn though a running line. Interference by heparin can be detected by absorbing the heparin with a resin ("Heparsorb") or by using an enzyme to digest the heparin ("Hepzyme[8]"). Also, the patient's history should be checked, especially with regard to anticoagulant use or liver disease. Provided that the abnormal result is reproduced on a fresh specimen and there is no obvious explanation from the history, a mixing study should be performed. If the mixing study shows correction and no prolongation with incubation, factor deficiency should be looked for, starting with VIII and IX. Vitamin K-dependent and nonvitamin K–dependent factors should be considered to rule out vitamin K deficiency, or accidental or surreptitious warfarin ingestion.

## Inhibitor

If the mixing study fails to correct, then an inhibitor should be suspected.[9][10] The most common inhibitor is a nonspecific inhibitor such as a lupus anticoagulant.[9] Perform a test to demonstrate a phospholipid-dependent antibody, such as a platelet neutralization procedure. Spontaneous specific inhibitors against clotting factors occur (i.e. not in hemophiliacs), most often against factor VIII.[11] This can occur in patients with systemic lupus erythematosus, monoclonal gammopathies, other malignancies, during pregnancy and for no apparent reason (idiopathic). These patients can have devastating bleeding. The thing to do is identify the specific factor involved and find out how high the titer is. If the patient has a low titer inhibitor, try to overwhelm it with high doses of the factor. If the patient has a high titer antibody against factor VIII, try porcine factor VIII, activated prothrombin complex concentrate FEIBA (Factor Eight Inhibitor Bypassing Agent),[12] or NovoSeven[13] to stop the bleeding. Prednisone will often lower the titer over time. Intravenous immunoglobulin has been reported to also help but it does not seem to work for hemophiliacs with an inhibitor. Rituximab, cyclophosphamide or other immunosuppressive therapy may be required.[14]

### Assessing correction of mixing study

In order to provide specific cutoffs to distinguish an inhibitor defect from a factor deficiency, the "Rosner index" (index of circulating anticoagulant)[15] and/or the "Chang percentage" (percent correction method) can be used:[16]

Rosnerindex=(aPTTof1:1mix)−(aPTTofnormalpooledplasma)aPTTofnonmixedpatientplasmax100

Results are: ≤10 is classified as correction, ≥15 indicates presence of an inhibitor, and 11-15 is classified as "indeterminate".[17]

Changpercentage=(aPTTofnonmixedpatientplasma)−(aPTTof1:1mix)(aPTTofnonmixedpatientplasma)−(aPTTofnormalpooledplasma)x100

Results are classified as follows: <58% as inhibitor and >70% as correction.[18]>

Alternatively, correction into the reference range can be used to define complete correction.[19]

A fourth method is known as Estimated Factor Correction (EFC). This method involves four steps. First, determine the most likely factor suspected to be deficient, based on PT, aPTT, and clinical history. Next, choose the appropriate curve — single factor deficiency, vitamin K-dependent factor deficient, or all factor-deficient. Use this curve to estimate the factor level in the patient sample. Then, predict the factor level and PT or aPTT that will occur after 1:1 mix in case of deficiency. Finally, compare the actual mix results with the predicted results for deficiency.[19]

## References

1. ↑ Lanzkowsky, Philip (2005-06-06). Manual of Pediatric Hematology and Oncology. Elsevier. ISBN 978-0-08-049731-0. https://books.google.com/books?id=hU-xd9xDGxMC&q=coagulation+mixing+studies&pg=PA303.
2. ↑ "Interpretation of normal plasma mixing studies in the laboratory diagnosis of lupus anticoagulants". Thrombosis Research 119 (3): 369–76. 2007. doi:10.1016/j.thromres.2006.03.012. PMID 16704874. https://biblio.ugent.be/publication/742294/file/763496.
3. ↑ Hoffman, Ronald; Benz, Edward J.; Silberstein, Leslie E.; Heslop, Helen; Anastasi, John; Weitz, Jeffrey (2013-01-01). Hematology: Basic Principles and Practice. Elsevier Health Sciences. ISBN 978-1-4377-2928-3. https://books.google.com/books?id=a1estSuaQ6kC&q=coagulation+mixing+studies&pg=PA1863.
4. ↑ "International council for standardisation in haematology recommendations on fibrinogen assays, thrombin clotting time and related tests in the investigation of bleeding disorders". Int J Lab Hematol 46 (1): 20–32. February 2024. doi:10.1111/ijlh.14201. PMID 37984807.
5. ↑ 5.0 5.1 Gupta, Piyush; Menon, P. S. N.; Ramji, Siddarth; Lodha, Rakesh (2015-08-31). PG Textbook of Pediatrics: Volume 2: Infections and Systemic Disorders. JP Medical. ISBN 978-93-5152-955-2. https://books.google.com/books?id=krlEDwAAQBAJ&q=adsorbed+plasma+aged+plasma+correction&pg=PA1600.
6. ↑ Med Lab Tech Vol 1, 2/e. Tata McGraw-Hill Education. 2010. ISBN 978-0-07-007659-4. https://books.google.com/books?id=z_8hBAAAQBAJ&q=adsorbed+plasma+aged+plasma+correction&pg=PA344.
7. ↑ Bain, Barbara J.; Bates, Imelda; Laffan, Mike A. (2016-08-11). Dacie and Lewis Practical Haematology E-Book. Elsevier Health Sciences. ISBN 978-0-7020-6925-3. https://books.google.com/books?id=rEPUDAAAQBAJ&q=adsorbed+plasma+aged+plasma+correction&pg=PA385.
8. ↑ "Heparin Neutralization". 15 January 2017. http://www.clinlabnavigator.com/heparin-neutralization.html.
9. ↑ 9.0 9.1 "Making Sense of Mixing Studies". George King Bio-Medical, Inc.. 2016-01-07. https://kingbiomed.com/blog/making-sense-of-mixing-studies/.
10. ↑ McPherson, Richard A.; Pincus, Matthew R. (2011-09-06). Henry's Clinical Diagnosis and Management by Laboratory Methods E-Book. Elsevier Health Sciences. ISBN 978-1-4557-2684-4. https://books.google.com/books?id=-97J-8Zh2hkC&q=If+the+mixing+study+fails+to+correct,+then+you+need+to+think+about+an+inhibitor&pg=PA794.
11. ↑ "Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management". Blood Transfusion 13 (3): 498–513. July 2015. doi:10.2450/2015.0141-15. PMID 26192778.
12. ↑ "Inhibitor antibodies to factor VIII and factor IX: management". Seminars in Thrombosis and Hemostasis 26 (2): 179–88. 2000. doi:10.1055/s-2000-9821. PMID 10919411.
13. ↑ "Current status and future prospects of activated recombinant coagulation factor VIIa, NovoSeven®, in the treatment of haemophilia and rare bleeding disorders". Ann Hematol 103 (8): 2647–58. August 2024. doi:10.1007/s00277-023-05287-2. PMID 37391649.
14. ↑ "First-line immunosuppressive therapies for acquired hemophilia A: A 25-year cohort experience and network meta-analysis". Thromb Res 241. June 2024. doi:10.1016/j.thromres.2024.109067. PMID 38970991.
15. ↑ "Coagulation mixing studies: Utility, algorithmic strategies and limitations for lupus anticoagulant testing or follow up of abnormal coagulation tests". Am J Hematol 95 (1): 117–128. January 2020. doi:10.1002/ajh.25669. PMID 31674066.
16. ↑ Baig MA, Swamy KB (2021). "Comparative analysis of chromogenic vs clot.based one stage APTT assay for determination of factor VIII level.". Indian J Pathol Microbiol 64 (1): 123–7. doi:10.4103/IJPM.IJPM_900_19. PMID 33433421.
17. ↑ Rosner, Esther; Pauzner, Rachel; Lusky, Ayala; Modan, Michaela; Many, Amira (1987). "Detection and Quantitative Evaluation of Lupus Circulating Anticoagulant Activity". Thrombosis and Haemostasis 57 (2): 144–7. doi:10.1055/s-0038-1651083. ISSN 0340-6245. PMID 3110995.
18. ↑ Chang, Sheng-hsiung; Tillema, Veronica; Scherr, Doris (January 2002). "A "Percent Correction" Formula for Evaluation of Mixing Studies". American Journal of Clinical Pathology 117 (1): 62–73. doi:10.1309/rrek-8l6m-d2kc-hwlh. ISSN 0002-9173. PMID 11789732.
19. ↑ 19.0 19.1 "Evaluation of prothrombin time and activated partial thromboplastin time mixing studies using an estimated factor correction method". Blood Coagul Fibrinolysis 27 (1): 90–6. January 2016. doi:10.1097/MBC.0000000000000375. PMID 26397883.

* v
* t
* e

Common for blood tests (CPT 82000–84999)

Electrolytes|

* Sodium
* Potassium
* Chloride
* Calcium
* Renal function
* Creatinine
* Urea
* BUN-to-creatinine ratio
* Plasma osmolality
* Serum osmolal gap

Acid-base|

* Anion gap
* Arterial blood gas
* Base excess
* Bicarbonate
* CO2 content

Iron tests|

* Ferritin
* Serum iron
* Transferrin saturation
* Total iron-binding capacity
* Transferrin
* Transferrin receptor

Hormones|

* ACTH stimulation test
* Thyroid function tests
* Thyroid-stimulating hormone

Metabolism|

* Blood lipids

Cardiovascular|

* Cardiac marker
* Troponin test
* CPK-MB test
* Lactate dehydrogenase
* Myoglobin
* Glycogen phosphorylase isoenzyme BB

Liver function tests|

* Proteins
* Human serum albumin
* Serum total protein
* ALP
* transaminases
* ALT
* AST
* AST/ALT ratio
* Bilirubin
* Unconjugated
* Conjugated

Pancreas|

* Amylase
* Lipase
* Pancreatic lipase

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Mixing study. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Medicine:Mixing_study&oldid=4016594"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template