Wiki Heterozygous Factor V Leiden

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Code: D68.5
Primary thrombophilia

Excludes 1: antiphospholipid syndrome (D68.61)
lupus anticoagulant (D68.62)
secondary activated protein C resistance (D68.69)
secondary antiphospholipid antibody syndrome (D68.69)
secondary lupus anticoagulant with hypercoagulable state (D68.69)
secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69)
systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0)
systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312)
thrombotic thrombocytopenic purpura (M31.1)
Primary hypercoagulable states
Parent Code Notes: D68
Excludes1: abnormal coagulation profile (R79.1)
coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

Block Notes
Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)

Coding Guidelines
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
Excludes 2: autoimmune disease (systemic) NOS (M35.9)
certain conditions originating in the perinatal period (P00-P96)
complications of pregnancy, childbirth and the puerperium (O00-O9A)
congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
endocrine, nutritional and metabolic diseases (E00-E88)
human immunodeficiency virus [HIV] disease (B20)
injury, poisoning and certain other consequences of external causes (S00-T88)
neoplasms (C00-D49)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)

kewing

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I'm looking for opinions/suggestions regarding the most appropriate ICD 10 code for a patient who is heterozygous for the Factor V Leiden mutation. I'm hesitant to use D68.51, especially when the physician documents that heterozygosity does not necessarily increase thrombophilia risk. Q99.8? Other ideas?

Thanks much.

Karen
 

hunters

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Factor V Leiden heterozygosity

I see no one ever responded to your thread. Did you ever find an answer? I've just come across a note with this same diagnosis and here is what I found. I use EncoderPro and if you go to D68.51 (or the ICD 9 code 289.81), under the code it lists problems that fall within that code category and Factor V Leiden Mutation is in the list. But, I then researched the difference between "mutation vs heterozygosity". I found that heterozygosity just refers to a specific genotype, but there is a mutation either way. So based on this, I went with the D68.51.

Sharon Hunter, CPC, CGSC
 
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I see no one ever responded to your thread. Did you ever find an answer? I've just come across a note with this same diagnosis and here is what I found. I use EncoderPro and if you go to D68.51 (or the ICD 9 code 289.81), under the code it lists problems that fall within that code category and Factor V Leiden Mutation is in the list. But, I then researched the difference between "mutation vs heterozygosity". I found that heterozygosity just refers to a specific genotype, but there is a mutation either way. So based on this, I went with the D68.51.

Sharon Hunter, CPC, CGSC

Thanks, I just was researching this as well. Appreciate the help.
 

kewing

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Sharon, I did not ever get a definitive answer for this. Thanks for your input. Karen
 
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