Audra Zachman testified about how conflicting serial HCG reports affected a pregnancy assessment and why Theranos's correction and follow-up study did not restore her confidence. Cross-examination narrowed her expertise to clinical interpretation and examined the limited number of other questionable results found in her chart review.
Audra Zachman
Nurse practitioner who provided prenatal care to Brittany Gould.
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Audra Zachman testified for the government about evaluating Theranos for a Phoenix-area obstetrics practice and interpreting HCG results used in pregnancy care. The court permitted her to offer expert opinions on the clinical interpretation of those results and instructed jurors that they could accept, reject, or assign weight to her opinions.
Zachman reviewed Brittany Gould's serial laboratory reports and explained that a reported decline from 12,558 to 125.58 suggested a possible pregnancy loss, leading her to say the pregnancy appeared nonviable. Results from another laboratory later rose in a pattern that she considered consistent with viability. Theranos corrected the 125.58 result to 12,558 and attributed the original report to human entry error, but Zachman said the correction did not restore her confidence because identical values two days apart remained clinically unusual. She testified that she stopped referring patients to Theranos for HCG testing.
Cross-examination established that Zachman's expertise was limited to clinical interpretation rather than immunoassay mechanics, variability among assays, or technical report language. She explained that HCG trends must be considered alongside pregnancy timing, symptoms, ultrasound findings, and repeat testing. She also acknowledged Theranos's apology, stated corrective measures, offers of assistance, a comparative study, continued patient-submitted Theranos results, and a government-requested chart review that found few apparent issues. She denied that prosecutors expected her to identify additional problems.
The court struck Zachman's initial answer that she had never encountered a similar discrepancy because additional foundation was required. After further questioning, she described her estimate of testing volume as approximate and said cautiously that another comparable event likely would have stood out. On redirect, she maintained that the comparative study did not restore her confidence and did not recall resuming referrals to Theranos.
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