Wednesday, June 25, 2014

Problematic Effects of a Pacifying Potion



For years I was a physician to members of his family and had known this 59-year-old executive.  I was surprised when he was admitted to our hospital for palpitations and weakness.  

I knew that he used to drink alcohol socially, and when that became a problem, he had quit sixteen years ago.  I was aware that he took pride in his health.  He was proud that he ate organic and natural foods.  At admission we learned that he consumed nearly a quart of yogurt each day, and also each day drank ten to twenty cups of herbal teas.

His personal physician had seen him regularly for routine health matters.  He prescribed a medication for anxiety.  He had found that his blood pressure was high, and it proved to be somewhat difficult to treat. Three drugs were used in a step-wide fashion during the next 18 months. 

Now, because of the palpitations and weakness, he had gone to the emergency room of our hospital where his serum potassium was found to be 2.2 millimoles per liter.  Such low levels of potassium (hypokalemia) are dangerous and can lead to ventricular fibrillation and death.  He was admitted to the hospital for close observation and treatment. 

Potassium was administered intravenously and his serum potassium level increased somewhat to 2.8 millmoles.  His palpitations disappeared.

His hypokalemia most certainly was the cause of his symptoms, but what was causing his potassium to be so low? As a thiazide had recently been added to his blood pressure medications, the hospital’s clinicians briefly considered that this might be the culprit.  However, he was on an appropriately low dose of the thiazide that ordinarily would not cause this level of hypokalemia. 

Over the next few days he remained markedly hypokalemic despite additional potassium.  Multiple physicians examined him for other conditions that might cause hypokalemia, particularly those which cause hypertension too.

Hyperaldosteronism was one such diagnostic hypothesis.  Although not common, this can be a serious disease.  Hyperaldosteronism is the over production of a salt retaining hormone, aldosterone, which may occur from an adrenal gland tumor or from severe narrowing of an artery to the kidney, i.e., renovascular disease.  Other less common causes of hypokalemia and hypertension were also considered, some of them seemingly benign, such as excessive amounts of licorice in the diet, but the patient denied a fondness for licorice.


After extensive testing, neither hyperaldosteronism nor any other cause was found.  He was a diagnostic puzzle, but, he felt well, and he was sent home when his potassium returned to normal. 

Shortly after discharge, at the request of his in-patient internist, he brought in his herbal teas.  In each licorice root was a major ingredient!  The mystery was solved.





As you recall, he had mentioned at the time of his admission to the hospital that he had been drinking ten to twenty cups of these teas per day for many months.   These were taken to calm his nerves after tense days at the office. Even though they were intrigued by the extraordinary amount of herbal teas that he drank each day, his clinicians were unaware that some herbal teas contain licorice.  He had denied licorice use. 

He stopped drinking the teas.  He was seen again in the clinic thirty days after discharge and he said he felt terrific.  His blood pressure was 104/64 and his serum potassium was 5.1 millimoles per liter.  Antihypertensive medications were reduced and eventually discontinued. 


Eating licorice is an uncommon cause of the syndrome of hypertension and hypokalemia. In the past few decades with the virtual disappearance in the United State of candy that contains true licorice root; it has virtually disappeared.   However, it is important to note that other sources of true licorice root are still available.  These sources, including herbal teas, should be considered in patients with unexplained hypertension and hypokalemia.  

Saturday, June 7, 2014

My Mother’s Last Weeks



Madolyn, my 98 year-old mother had been treated for her indolent B-cell lymphoma for about four years, first with neck and mediastinal irradiation and then retuximab.  

To digress from the central story, we were all together for Christmas 2009 in our home on the Oregon Coast when Mom confided to my wife, Beth, that her eyes had become increasingly more swollen each morning.  She now could not see when she awoke.  After she had been up for a few hours the swelling disappeared.  I found that she had prominent lymph nodes in her neck and above the collar bones.  It seemed likely that the mediastinum was similarly involved, and that she had a Superior Vena Cava Syndrome.  This is caused by lymph nodes compressing the veins  in the center of the chest.  A CT scan confirmed this.  She had irradiation and retuximab and the nodes grew smaller.  The neck and facial swelling subsided.

Then all went well until about four years later, when in August of 2013 she noted an increasing mass of lymph nodes in her right upper neck and a mass in the back of her throat on the same side.  She reluctantly consented to another round of irradiation.  The therapist carefully constructed a hard plastic mask that fit over her face and neck.  The x-ray beam was then directed upward from the front of right side of her neck to the mass on her palate. The irradiation was was finished in early October.  

Adamant that she would accept no more treatment, she signed up for hospice care in early November.  In mid-November she complained of fatigue, and she decreased her activities.  On November 16th she did not get up from bed and had become very somnolent.  She was worse on Monday, and Beth drove to the Coast to help care for her.  She was bedfast and unresponsive.  Beth activated hospice care and a team worked with the family.
   
We had our Thanksgiving meal at the Coast, and Mom was in her hospital bed near us as we ate.  She was unresponsive.

  In early December although still bedfast, she responded to voices and was able to identify us.  She asked “what happened?”.  I had to tell her that I did not know.  She then lapsed back into sleep.  She awoke for sips of water, coffee and custard.  Her somnolence continued and by early February she was unable to take any food or nutrition.  She died February 6th.

A few weeks later I was making hospital teaching rounds, and an eighty-eight year-old woman was discussed.  She had had total cranial irradiation for lymphomatous meningitis.  Approximately a month after her treatment ended she became somnolent and then unresponsive.  She was now recovering. Her oncologist discussed her case with us and confided that he thought that she had had the syndrome of post-irradiation encephalopathy or somnolence.  My colleagues with me on rounds had never heard of this syndrome, and I had not either.


Post brain-irradiation encephalopathy is more commonly seen in children because they more often than adults get brain irradiation for their leukemias.  It comes on suddenly four to six weeks after radiation therapy.  After a variable time, most  patients recover.   My mother was frail and her prolonged coma made her more frail.  It was not possible for her to recover.