practice of Medicine
Orthopedic Surgery Toolkit
Weak on-call handoff and discharge instructions botch patient’s Coumadin therapy
A 46- year-old obese Caucasian female, underwent aortic heart valve surgery for aortic insufficiency with left sided ventricular enlargement on June 6, 2005.
During the post-operative hospital stay, the attending cardiologist periodically adjusted the patient’s Coumadin dose over three days. The cardiologist increased the dose each day, beginning with 5 mg/day, then 7.5 mg/day and finally 10 mg/day by the third day.
Starting on Friday, June 10, three different practitioners covered for the cardiologist. On that day, one of the nurse practitioners rounded on all of the inpatients that would likely be discharged during the weekend, including the subject patient. After visiting her, the nurse practitioner called the Coumadin clinic nurse to inform her that the patient would be discharged on a Coumadin dose of 10 mg/day.
On Saturday, another cardiologist from the same practice saw the patient in the hospital and reduced the Coumadin to 2.5 mg/day based on his assessment of the clotting studies, which showed increasing INRs. The patient was discharged on Sunday on a 2.5 mg/day dose. When she reported to the Coumadin clinic on Monday, her INR was 3.49.
The Coumadin clinic nurse phoned the results to the attending cardiologist without realizing that the patient's Coumadin discharge dose had decreased. The nurse instructed the patient to continue taking the 10 mg dose, and return to the clinic in a week. The actual hospital discharge orders with the lower dose of Coumadin were never communicated to the attending cardiologist's office.
A week later at the recheck visit, the patient’s INR measured 18. The attending cardiologist immediately admitted the patient to the hospital for monitoring. He also terminated the Coumadin, and ordered vitamin K administration and a head CT to rule out intracranial bleeding. The CT came back normal.
The patient remained stable until Tuesday, June 21, 10:05 PM. At that point, she became diaphoretic and tachycardic, and went into cardiac arrest. Full resuscitative measures were initiated. The resuscitation efforts failed, and the patient was pronounced dead at 11:45 PM. An autopsy was performed. The medical examiner concluded that the patient died of cardiac tamponade resulting from an accumulation of hemorrhagic fluid in the pericardium as a result of anti-coagulant usage.
Risk Management Commentary & Advice
- Avoid verbal communication of orders unless absolutely necessary. Use written instructions and written orders. If verbal orders are unavoidable, then implement a “read back” policy to decrease the likelihood an error.
- Develop a policy and procedure for documenting and communicating discharge instructions to the physician that will follow the patient once they arrive home.
- Provide the patient with a written copy of the attending’s discharge instructions, along with verbal instructions for reinforcement.
- On-call communications should always be documented and placed in the patient’s chart, then reported back to the attending physician.
- When multiple physicians, nurse practitioners and physician assistants follow patients, it is crucial to update the medication and problem sheets at each visit and communicate any changes to the attending physician.
The case settled for very large amount.
Multiple providers named in failure to diagnose case
A 61 year old female with a long history of smoking, hypertension and significant osteoporosis suffered a hip fracture. In addition to other studies, the emergency physician ordered a chest x-ray and admitted her to see an orthopedic surgeon. The patient did well with her ORIF and was discharged.
Neither the emergency room physician or the orthopedist reviewed the chest x-ray and report. Copies were sent to the primary care physician (PCP) and were filed in the chart without the PCP's review.
The PCP continued to treat the patient for hypertension, well-woman care and acute illnesses. Nearly 21 months after her ORIF, the patient developed hemoptysis. The PCP ordered a chest x-ray. In his report, the radiologist identified a large mass in the right upper lobe. At this time, the PCP also became aware of the previous chest x-ray report in her records. In that report the radiologist had identified a smaller but apparent mass in the same position, and had suggested a follow-up CT scan of the chest. The cancer had metastasized and the patient was now considered terminal.
All of the physicians involved in this case were named in a lawsuit for failure to diagnose lung cancer for a period of 21 months.
It was alleged that if the first report had been acted on earlier, the patient would have had a better prognosis.
- The emergency physician ordered the study, so his name appears on the report. It is alleged that he failed to review the study and relay the information to the subsequent provider.
- The orthopedist's name was included in the chest x-ray report and appeared in the hospital chart as the treating physician. He was named in the suit for not communicating the information to the patient or following up.
- The PCP was named in the suit as she saw the patient on several occasions during the delay period, and her chart contained the positive chest x-ray report filed but was not initialed.
- The radiologist who interpreted the report was named for not further communicating the finding to the other three physicians.
Risk Management Commentary & Advice
All physicians named in this lawsuit had the opportunity at different levels to see, act upon and/or to communicate the serious abnormal finding.
- If you order a study, you could be held responsible for its result.
- If a critical lab result comes to your office, the information should be reviewed, initialed and appropriate follow-up documented before the report is filed.
- Each office should have a standardized manner in which information flows to the provider, to ensure that reports are not filed prior to the provider's review. Everyone in the office should be aware of the process, and the provider should have a standardized method for indicating the review, whether the report is paper or electronic.
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