Icd 10 code for hx of breast cancer

Breast J. Author manuscript; available in PMC 2020 Jul 24.

Published in final edited form as:

PMCID: PMC7369243

NIHMSID: NIHMS1597903

Studying patterns of care and medical service utilization after the period of initial treatment of cancer using increasingly-available administrative claims data [1] can be challenging. [2, 3] Patients diagnosed early in their disease may be cured or their cancer may go into remission; therefore, it is possible that few, if any, medical claims remote from the initial treatment will contain a diagnosis code specifically indicating cancer. Patients previously treated for cancer may be overlooked in cancer-related studies of claims data or mistakenly included as a normal control. [4]

We wanted to understand how best to identify breast cancer (BC) patients in claims data during the first 5 years after treatment for the primary cancer. We also aimed to identify any additional diagnosis codes potentially related to the treatment of BC that could be used to identify BC patients whose claims lacked cancer-specific diagnosis codes (174.X family of ICD-9 codes and v10.3).

Using claims (“NCH” and “OUTSAF”) data of 51,278 (median 120 claims) newly diagnosed BC patients (females, age ≥ 65 years, first malignant non-metastatic BC, no non-BC, 6 years of consistent and exclusive enrollment in Medicare parts A and B) from the BC subset of the 2000-2014 Surveillance, Epidemiology and End Results (SEER)-Medicare linked database (N=51,278), we determined the fraction of BC patients who could be identified using BC-specific codes 174.x and v10.3 during the year of diagnosis/treatment and during each of the 5 years following treatment. Only 551 BC patients lacked a claim containing 174.x or v10.3 diagnosis codes (Table 1).

Table 1:

Demographics of Patients in the Breast Cancer (BC) and Non-Breast Cancer (non-BC) Groups Without Codes 174.x / v10.3

We then developed a list of diagnosis codes apart from 174.x and v10.3 found more often in claims of BC patients than in claims of a cohort of patients without BC (non-BC cohort of 174,903 patients of a 5% Medicare sample who did not appear in any SEER cancer registry (2000-2014) and did not have claims with 174.x or v10.3 diagnosis codes) using a patient-referenced odds ratio (OR):

OR=fBC(no174.x∕v10.3),IC D−9(XXX.X)fnonBC,ICD−9(XXX.X) fBC(no174.x∕v10.3),ICD−9(XXX.X)=N BC(no174.x∕v10.3)withICD−9(XXX.X )NBC(no174.x∕v10.3)withoutIC D−9(XXX.X)fnonBC,ICD−9(XXX.X)= NnonBCwithICD−9(XXX.X)NnonBCw ithoutICD−9(XXX.X)

where

fBC (no 174.x/v10.3),ICD–9(XXX.X) is the odds that the specific ICD-9 diagnosis code (XXX.X) is present in claims of BC patients who had medical claims but none of those claims contained 174.x/v10.3 codes; fnonBC,ICD–9(XXX.X) is the odds that the specific ICD-9 (XXX.X) is present in the claims of patients without BC; NBC (no 174.x/v10.3)with ICD–9(XXX.X) is the number of BC patients with a claim containing the specified ICD-9 code (XXX.X) but no claims containing 174.x/v10.3 codes; NBC (no 174.x/v10.3)without ICD–9(XXX.X) is the number of BC patients without a claim containing the specified ICD-9 code (XXX.X) and no claims containing 174.x/v10.3 codes; NnonBC with ICD–9(XXX.X) is the number of non-BC patients with a claim containing the specified ICD-9 code (XXX.X); and NnonBC without ICD–9(XXX.X) is the number of non-BC patients without a claim containing the specified ICD-9 code (XXX.X).

Diagnosis codes over the 5-year follow-up period that appeared in at least 0.1% of the population, provided O.R.>1.01, and were related to the management of BC are provided (Table 2).1

Table 2.

Diagnoses and codes related to breast cancer or treatment and more commonly associated with breast cancer patients than patients in the general population

For each year following the initial year of treatment and overall, BC patients were identified as belonging to one of 5 subgroups (Figure 1):

Subgroups of BC patients based on diagnosis codes contained in claims in the initial year of treatment and years 1-5 of follow-up after diagnosis.

1. Those with at least one utilization claim containing a diagnosis code indicating active, invasive BC (174.x)

2. Those without a 174.x code on claims, but with at least one utilization claim containing a diagnosis code indicating a personal past history of BC (v10.3)

3. Those without any 174.x or any v10.3 codes on claim, but with at least one utilization claim containing a diagnosis code more likely to be encountered in a claim from a patient with BC (O.R>1.01) and related to management of BC

4. Those with claims containing only diagnosis codes unrelated to management of BC

5. Those without any claims

In any single year during the 5-year follow-up period, 72.8 – 99.1% of BC patients had a claim with a 174.x diagnosis code. Another 0 – 11.1% of BC patients did not have a 174.x code but did have a v10.3 code. Of patients without a claim containing 174.x or v10.3, 0 – 0.62% had a claim containing one or more of the diagnosis codes in Table 2 in any given year following treatment.

We conclude that breast cancer patients can be robustly identified within claims databases using diagnosis codes specifically referring to “invasive breast cancer”, including the ICD-9 family of 174.X codes and v10.3, particularly in the treatment and early post-treatment periods.

Supplementary Material

Supplementary material

Acknowlegements:

This study used the linked SEER-Medicare database. The interpretation and reporting of these data are the sole responsibility of the authors. The authors acknowledge the efforts of the National Cancer Institute; the Office of Research, Development and Information, CMS; Information Management Services (IMS), Inc.; and the Surveillance, Epidemiology, and End Results (SEER) Program tumor registries in the creation of the SEER-Medicare database.

Funding: This work was funded by grant 1R01HS024936-01 from the Agency for Healthcare Research and Quality

Footnotes

Conflict of Interest Notification: None

1All diagnosis codes with O.R. > 1.01 in at least 0.1% of patients may be found in supplemental material 1

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