DeserTortoise Home Page Providing Consultation and Education Since 1992

Previous Newsletters:
Vol. 1, No. 1, July-Sept 2000
Vol. 1, No. 2, Oct.-Dec. 2000
Vol. 2, No. 1,
Jan-Mar. 2001

    Quarterly Newsletter
Vol.1, No. 2, Oct.-Dec. 2000
www.desert-t.com © 2000

Topics: Our Website - Check us out, bookmark us
Be Prepared - U.S. Department of Labor, Wage and Hour Division visits
In the News - Medication Errors and your role in the War on Drug Errors
Medications - Newly Approved, New Names, New Warnings, New Formulations
Herbal Review - Cat’s Claw; Saw Palmetto
Clinical Reminders - The aging process and cold weather
Helpful Tips - Our elderly population, depression and the holidays
Comments and Suggestions

Our Website

Thank you all for your encouraging and supportive comments about both our website and the newsletter. Your comments and suggestions are much appreciated.

Be sure bookmark us and to keep an eye on our website. We are looking forward to expanding the site in order to more fully address and support the Assisted Living Facility industry needs.

Help us help you. Please take a few minutes to complete and return the attached survey form.


Be Prepared

U.S. Department of Labor, Wage and Hour Division Representatives plan to visit all of Arizona’s licensed Assisted Living Facilities. Be prepared! Is your payroll paper work complete and on site? Do your schedules, time cards and payroll sheets agree? Do you have W-4s or W-9s and I-9s on all employees? Do you have the Federal Minimum Wage rates posted? Fines as high as $10,000 per violation may assessed.

If you do not have current W-4s, W-9s, I-9s, A-4s or the Minimum Wage Poster, they may be obtained at the following websites:

I-9 http://www.ins.usdoj.gov
W-4 http://www.fedword.gov
W-9 http://www.irs.ustreas.gov
A-4 http://www.revenue.state.as.us
Minimum Wage Posters http://www.dol.gov./dol/esa/public/regs/compliance/posters/flsa.htm


In the News

Medication Errors

Have you noticed that it is almost impossible to read a medically oriented publication or visit a medical website without reading about medication errors and their, all too often fatal, effects?

The Washington Post, Monday, July 3, 2000, Page A01 (by Maria Glod) “Prescription Deaths Bring Call for Checks” cites specific cases of death due to medication errors, and reports the fact that in the Untied States there are no standard reporting methods to accurately compile statistics of medication errors and adverse reactions.

The Washington Post goes on to cite “Last year, pharmacists nationwide filled about 3 billion prescriptions, and that number is expected to hit 4 billion by 2004, said Carmen Catizone, executive director of the Illinois-based National Association of Board of Pharmacy. Although the number of prescriptions has grown rapidly, the number of pharmacists has risen only about 10 percent over the past five years.

State pharmacy boards estimate that between 2 percent and 5 percent of the prescriptions filled in 1999 included some sort of error, from simple misspellings to more serious dispensing or instruction mistakes.”

WebMD Medical News (http://my.webmd.com) has several related articles posted, “RX Errors on the Rise; As the number of prescriptions soars, so too does the number of mistakes. For patients, the consequences can be serious,” “Medical Mistakes; As a result of a medication error, the writer suffered a stroke. Could this happen to you?,” and “Precarious Prescriptions; Can your doctor’s handwriting kill you?,” all of which speak to the rising incidence of medication error caused death and injury which seems prevalent in the US today.

The FDA (www.fda.gov) and the CDC (www.cdc.gov) both have numerous articles about the rising problem and possible solutions to curb the errors.

The FDA hopes to reduce drug errors by working harder to prevent mix-ups caused by similar sounding drug names, by highlighting interactions and potential dosing errors on drug labels, by putting the most important information at the start of package inserts, and by hosting a national summit on ways to reduce drug errors. (The Pink Sheet, Vol. 62, No. 9), www.fdcreports.com.

“War on Drug Errors; Judging by budget requests from the Food and Drug (FDA), the war on drug errors has begun. As part of its nearly $16 million proposal, the FDA would focus on these areas: developing new standards for drug naming, packaging, and labeling--reportedly the source of about half of drug errors hiring more staff members to create or upgrade reporting systems and to interpret the resulting reports identifying drug errors more quickly by creating links to other government and private databases expanding the FDA's current drug safety program for consumers devoting added resources to policing Internet drug sales.

The Pharmaceutical Research & Manufacturers of America also plans to fight in the war on drug errors. The organization has convened a task force whose mission is to identify methods by which drug makers can help to reduce drug errors. Thus far, the task force is focusing on packaging, bar codes, labels, and confusion over drug names.” (The Pink Sheet, Vol. 62, No. 11), www.fdcreports.com.

“Ways and Means to Curtail Medical Errors; Alarmed by recent reports citing high rates of medical errors in the American health care system, government officials are discussing several ways to reduce them. Indeed, the Institute of Medicine has set a goal to reduce medical errors by 50% over the next 5 years. How to do it? Here are some of the proposals: President Clinton's budget for fiscal year 2001 would give $20 million to the Agency for Healthcare Research and Quality to research the best ways to reduce errors. California Congressman Pete Stark proposed a Medicare-sponsored prescription drug benefit in which computers could detect and prevent inappropriate or dangerous drug prescriptions. Stark also proposed beefing up Medicare's existing Peer Review Organization as a reporting system. California Congressman Bill Thomas proposed an amendment to the patient's bill of rights that encourages voluntary reporting of errors. Pennsylvania Senator Arlen Specter introduced the Medical Error Reduction Act (S 2038) that proposes to test error-reducing strategies through demonstration projects involving 15 hospitals. The projects would test the effects of hand-held electronic prescription pads, bar codes on prescription drugs, and bar codes on patient ID bracelets. The projects would also compare differences among three reporting protocols: Five participating hospitals would voluntarily report errors to the Department of Health and Human Services (DHHS), five would be required to report errors to DHHS, and five would be required to report errors not only to DHHS but also to patients and their families.” (The Pink Sheet, Vol. 62, No. 7), www.fdcreports.com.

As caregivers what can you do? What is your part in the war on drug errors? You are the bottom line, the final filter, if you will, between errors and your residents. As caregivers we are tasked with knowing our residents, their needs and the medications they take. If you assist with or administer medications you must be aware of the drug which is being prescribed and make sure that the medication received is the medication that was prescribed. It is up to you to know the medication and the indication of use. If the medication does not seem to couple with your resident’s diagnoses, or if the medication received is not the one you anticipated, check with the physician’s office for verification or clarification. Please, go to the source, not to the pharmacist who filled the prescription.

I have seen medication errors by physicians, by pharmacists, and by caregivers alike. We are all human. However, in light of the current volume of mistakes, we must all be more vigilant. I have seen pharmacies fill prescriptions for one person and have them delivered to a person with a similar name at an entirely different address. I have seen pharmacies fill the wrong drug and the right drug filled at the wrong dose. I have known of physicians being interrupted while writing a prescription for one person then writing the wrong drug on the prescription pad. And, I have seen caregivers give the wrong medication to the wrong resident. Unfortunately many of these mistakes were not noticed immediately and the resident received the medication as delivered. I also have had caregivers ask me what a particular medication is and what it is used for. I do not mind the questions but am very concerned that the questions were not posed to the physician. By the time I am asked the resident has been receiving the medication for days or even weeks.

Always know your residents and their medical status. Know the medications they are taking, check for drug-drug or drug-food interactions, (even when you think you know, check) know why the medications are prescribed, and what the expected outcome of taking the medication is. And, have this knowledge before giving the medication.

In this regard the old adage ‘when in doubt ask’ is definitely sage. The only stupid or foolish questions are the unasked questions. Be your residents final safety net. If you do not know, ask, ask, ask.

And remember, chronic illnesses or the physiologic effects of aging may alter a drug’s action. Dosages for geriatric patients must be adjusted individually. Because of the individual nature of aging and unique medical history of each patient, assess each geriatric patient’s response to drugs individually.


Medications

Newly Approved Medications

Rivastigmine tartrate (Exelon), approved April 2000. Pharmacologic classification, cholinesterase inhibitor; therapeutic classification, cholinergic enhancer; pregnancy risk, category B. Pharmaceutical company, Novartis Pharmaceuticals Corp., www.novartis.com.

Exelon indicated for symptomatic treatment of patients with mild to moderate Alzheimer’s disease.

Exelon is contraindicated in patients with hypersensitivity to drug or its components or to other carbamate derivatives. Use cautiously in patients with history of ulcers or GI bleed, sick sinus syndrome or other supraventricular cardiac conditions, asthma or obstructive pulmonary disease (COPD), or seizures and in those taking nonsteroidal anti-inflammatory drugs.

Interactions: Multiple, see package insert.

Common adverse reactions, dizziness, headache, nausea, vomiting, diarrhea, anorexia, abdominal pain and accidental trauma.

Be sure to review drug information on web site, from physician or package inserts for full information.


Meloxicam (Mobic), approved April 14, 2000. Pharmacologic classification, enolic acid nonsteroidal anti-inflammatory (NSAID); therapeutic classification, anti-inflammatory, analgesic; pregnancy risk, category C. Pharmaceutical company, Boehringer Ingelheim Pharmaceuticals, Inc. www.boehringer-ingelheim.com.

Mobic is indicated for relief of signs and symptoms of osteoarthritis.

Mobic is contraindicated in patients with hypersensitivity to drug and in those with history of asthma, uticaria, or allergic-type reactions after taking aspirin or other NSAIDs. Avoid use in late pregnancy. Use with extreme caution in patients with history of ulcers or GI bleeding, in patients with dehydration, anemia, hepatic disease, renal disease, hypertension, fluid retention, heart failure or preexisting asthma. Also use cautiously in elderly and debilitated patients because of increased risk of fatal GI bleeding.

Interactions: Multiple, see package insert.

Life-threatening adverse reactions: arrhythmias, myocardial infarction, hemorrhage, pancreatitis, renal failure, leukopenia, thrombocytopenia, hepatitis, bronchospasms or angioedema.

Be sure to review drug information on web site, from physician or package inserts for full information.


Linezolid (Zyvox), approved April 18, 2000. Pharmacologic classification, oxazolidinone; therapeutic classification, antibiotic; pregnancy risk, category C. Pharmaceutical company, Pharmacia & Upjohn Co., www.pnu.com/home.asp.

Zyvox is indicated for vancomycin-resistant Enterococcus faecium infections, including cases with concurrent bacteremia.

Contraindicated in patients with hypersensitivity to drug or other components of formulation.

Interactions: Multiple, see package insert.

Life-threatening adverse reactions: leukopenia, neutropenia, thrombocytopenia.

Be sure to review drug information on web site, from physician or package inserts for full information.


Insulin glargine (rDNA) injection (Lantus), approved April 24, 1000. Pharmacologic classification, pancreatic hormone; therapeutic classification, antidiabetic; pregnancy risk, category C. Pharmaceutical company, Aventis Pharmaceuticals, Inc., www.aventis.com.

Lantus is indicated for management of type I diabetes mellitus in patients who need basal (long-acting) insulin for control of hyperglycemia.

Contraindicated in patients with hypersensitivity to insulin glarine or its components. Do not use during episodes of hypoglycemia and use cautiously in patients with renal or hepatic impairment.

Interactions: Multiple, see package insert.

Be sure to review drug information on web site, from physician or package inserts for full information.


Insulin aspart (rDNA) injection (NovoLog), approved June 7, 2000. Pharmacologic classification, hormone and synthetic substitute; therapeutic classification, antidiabetic; pregnancy risk, category C. Pharmaceutical company, Novo Nordisk Pharmaceuticals, www.nova-nordisk.com.

NovoLog is indicated for the control of hyperglycemia in patients with diabetes mellitus.

Contraindicated during episodes of hypoglycemia and in patients hypersensitive to NovoLog or one of its excipients. Use cautiously in patients who are prone to hypoglycemia and hypokalemia, such as patients who are fasting, have autonomic neuropathy, or who are using potassium-lowering drugs or drugs sensitive to serum potassium levels.

Warning: NovoLog may be incompatible with crystalline zinc insulin preparations. Do not mix together.

Interactions: Multiple, see package insert.

Be sure to review drug information on web site, from physician or package inserts for full information.


Name Change

Amrinone (Inocor),
issued July 1, 2000, pharmaceutical company, Sanofi Pharmaceuticals, www.sanofi-synthelabous.com.

Sanofi Pharmaceuticals announced that amrinone has been renamed as of July 1, 2000. The company has renamed the product because of confusion with amiodarone. The new name for amrinone is inamrinone.


New Warnings

Thioridazine Hydrochloride (Mellaril),
issued July 2000, pharmaceutical company, Novartis Pharmaceuticals Corp., www.novartis.com.

Novartis Pharmaceuticals has issued a statement that important changes have been made to the labeling of Mellaril. A warning has been added to the label advising clinicians that Mellaril may prolong the QTc interval in a dose-related manner, and may be associated with torsades de pointes and sudden death.

In addition, the package labeling has been updated to reflect a change in the indication for use of Mellaril.

Be sure to review drug information on web site, from physician or package inserts for full information.


Zanamivir (Relenza), issued July, 2000, pharmaceutical company, Glaxo Wellcome, Inc., www.glaxowellcome.com.

Glaxo Wellcome, Inc., has issued a warning that Relenza may cause serious respiratory adverse reactions in patients with our without known underlying respiratory disease. The package labeling has been revised to state that Relenza is not recommended for patients with underlying airway diseases, such as asthma or chronic obstructive pulmonary disease (COPD) because of reports of bronchospasm and decline in lung function in some patients.

The package labeling has also been revised to state that allergic reactions may occur in patients receiving Relenza, and that serious bacterial infections may occur with influenza-like symptoms. The clinician is reminded that Relenza does not prevent bacterial infections associated with influenza.

Be sure to review drug information on web site, from physician or package inserts for full information.


New Formulations

Also watch for:

A new patch in a controlled release form from Novartis Pharmaceuticals Corp. “Vivelle” for the prevention of postmenopausal osteoporosis which was approved August 16, 2000. http://www.novartis.com/

“Depakote ER” tablets for the prophylaxis of migraine headaches in adults, from Abbott Laboratories, approved August 4, 2000. http://www.abbott.com/

“Rescula” eye drops from Ciba Vision Corp Div Novartis Co. for the lowering of intraocular pressure in patients with open-angle glaucoma or ocular hypertension who are intolerant of other interocular pressure lowering medications or insufficiently responsive to other intraocular pressure lowering medications, approved August 3, 2000. http://www.novartis.com/

“Atacand HCT” tablets for the treatment of hypertension from Astrazeneca LP, approved September 5, 2000. http://www.astrazeneca-us.com/products/pibs_tradename.asp

As always check pharmaceutical websites or with the physician or pharmacist for package insert and full information.


Herbal Review

“If the results of a small Texas study hold true nationwide, abut 4 in 10 people use herbal supplements, more than half as first-line treatments for various ailments. But only about 1 in 10 of the people who use herbal supplements discuss their choice with a physician or pharmacist. Worse yet, of the 135 HMO members who responded to the survey, at least 2 in 10 took both herbal supplements and prescribed or over-the-counter drugs at the same time.

As these figures make clear, the risk of mysterious adverse effects and interactions may be substantial. The risk may be compounded by the finding that about half of herbal supplement users obtain information about herbs from their friends or family. Another 1 in 5 rely on the media or advertisements. Most users confess that they don’t know how dependable herbal products are in strength or quality. Even so, at least two-thirds of them say they’ll bet that the supplements are safe,” from FDC (The Green Sheet, Vol.49, No19), www.fdcreports.com.

Although Arizona’s Assisted Living Facilities are required to obtain Primary Care Provider orders to assist or administer any prescribed or over-the-counter preparation, many caregivers are not familiar with herbal supplements and they frequently are not listed in our drug reference books. Therefor, the DeserTortoise Quarterly Newsletter will review one or two herbs in each issue beginning with a couple I have recently seen prescribed, Cats Claw and Saw Palmetto.


Cat’s Claw (Scientific Name, Uncaria tomentosa):

Reported medical uses: Treatment of systemic inflammatory diseases such as arthritis and rheumatism and inflammatory diseases such as diverticulitis, gastritis, Chron’s disease, dysentery, ulcerations and for immune system stimulation.

As with most herbal supplements, information is as diverse as it is sketchy. Be sure to know why the preparation has been ordered and what the primary care provider would like you to watch for.

Contraindications and precautions: Contraindicated in patients undergoing skin grafts and organ transplants and in those who have coagulation (bleeding) disorders or who are receiving anticoagulants. Avoid use in pregnant or breast-feeding patients as its effects are unknown.

Adverse reactions: Potential hypotension.

Interactions: Antihypertensives; may potentate effects, avoid concomitant use.

Sources: Professional’s Handbook of Complementary & Alternative Medicines, by C.W. Fetrow and J.R. Avila, Springhouse Corporation, 1999; The A to Z Guide to Healing Herbal Remedies, by Jason Elias, M.A., L.Ac., and Shelagh Ryan Masline, Dell Publishing, 1995; Nurses Handbook of Alternative & Complementary Therapies, Springhouse Corporation, 1999; Herbal information Center, www.kcweb.com/herb/catsclaw.htm; Tropical Plant Database, www.rain-tree.com/plants.htm; Purdue University, www.hort.purdue.edu/newcrop/CropFactSheets/catsclaw.html;
Alternative Medicine Foundation HerbMed, www.herbmed.org/herbs/Uncaria_CatClaw.htm


Saw Palmetto (Scientific Name, Serenoa serrulata & repens [arecaceae]):

Reported medical uses: Treatment of conditions associated with benign prostatic hypertrophy (BPH). It is chiefly used as a diuretic and to tone the bladder by improving urinary flow and relieving strain. It also inhibits androgen and estrogen receptor activity and may be beneficial for both sexes in balancing the hormones thereby (possibly) increasing sperm production, breast size and sexual vigor.


Contraindications and precautions: Contraindicated in women of childbearing age because of the herb’s potential hormonal effects. Should be used cautiously for conditions other than BPH due to data regarding the herb’s effects are sketchy at best.

Adverse reactions: abdominal pain, back pain, constipation, decreased libido, diarrhea, dysuria, headache, hypertension, impotence, nausea and urine retention.

Interactions: None reported.

Sources: Professional’s Handbook of Complementary & Alternative Medicines, by C.W. Fetrow and J.R. Avila, Springhouse Corporation, 1999; The A to Z Guide to Healing Herbal Remedies, by Jason Elias, M.A., L.Ac., and Shelagh Ryan Masline, Dell Publishing, 1995; Nurses Handbook of Alternative & Complementary Therapies, Springhouse Corporation, 1999; Alternative Medicine Foundation HerbMed, www.herbmed.org/ herbs/serenoa.htm; Herbal Information Center, www.kcweb.com/herb/sawpalm.htm; National Library of Medicine, www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?form=4&db=m&term=saw+palmetto.

As with most herbal supplements, readily available information on Cat’s Claw and Saw Palmetto is as diverse as it is sketchy. Be sure to know why the preparation has been ordered and what the Primary Care Provider hopes to achieve by adding the herb to the resident’s medication profile, also know what the Primary Care Provider would like you to watch for.


The Aging Process And Cold Weather

Just as a decrease in blood supply, perspiration, skin thickness causes our older population to become more sensitive in hot weather, age related changes effect the way they respond to cold weather.

As we age our systems experiences a skin cell replacement decline of about 50% of the epidermis and the dermis, which combined with age related connective tissue loss causes thinning of the skin. Blood supply to the skin decreases and subcutaneous fat is lost, both with the greatest decrease/loss occurring in the arms and legs. Men loose more subcutaneous fat than women. The thinning of the skin combined with the reduced blood supply and loss of insulating subcutaneous fat tissue causes a reduced ability to regulate body temperature.

Although The State of Arizona’s Department of Health Services requires Assisted Living Facilities to maintain an indoor temperature range of 68-85ºF (R9-10-718-A3), we should be alert to the fact that what is comfortable or warm for us may not be adequate for our residents. Be sure your residents have warm shoes and socks on (don’t forget warm socks when wearing slippers), that their arms and legs are covered and be prepared to add warm sweaters and serve warm drinks. Be careful, with the warm drinks, their thin skin makes them more susceptible to burns and at lower temperatures.


Our Elderly Population, Depression And The Holidays

Depression is the most common psychological consequence of disability and the frequency and intensity of depression increases with age. And once joyous holidays become lonely times to many of our older adults adding to the depression risk. To understand our elderly population’s propensity for depression we need to look at attitudes and beliefs.

Attitudes are learned through one’s culture. American cultural attitudes are diverse yet we share many similarities. We value performance, productivity, appearance, self-reliance, independence and individuality. And we are youth-oriented viewing older adults as obsolete and expendable, thus leaving older adults with feelings of worthless.

Beliefs affect attitudes and feelings. Beliefs vary with experience, culture and religious values causing many people to fear changes associated with aging. Older adults are the most stereotyped age group due to negative stereotyping of older adults in literature, jokes and on television, thus perpetuating the problem.

Physical, psychological and social losses combine with loneliness due to actual loss of (or separation from) family, friends and significant others sets our elderly up for depression. And depression increases the risk of suicide.

In the U.S. the suicide rate of older adult men is seven times that of older adult women. Older adults account for about 25% of suicides. Suicide among our older adults is rarely an impulsive act. Our older adults have less fear of death than younger people. Their greatest fears are dependency, pain and loss of function and control. And most older adult suicide attempts are not gestures or threats, they are real.

To support our older population be watchful for loneliness and depression and intervene to counter act it and increase the older adult’s socialization. Recruit family members, peer groups, community programs, pet therapy and crisis intervention.

To determine if your resident has considered suicide or has a plan for doing so, ask. Keep in mind that someone with a well-planned method (especially a lethal one) is at higher risk for suicide. Refer your resident with unresolved grief, depression, or thoughts of suicide for counseling. Support and encourage active participation in life (ie., suggest substitute for lost companionship, a pet or new social connection), group activities, perhaps even reestablishing contact with religious groups and activities.


Contact Us With Your Comments And Suggestions

Website www.desert-t.com

Email trudy@desert-t.com

Voice Mail (520) 733-6191

Fax (520) 733-6191 (remember to hang up the
handset on your phone before faxing)

Desert Tortoise
1440 N. Sonoita Ave.
Tucson, AZ 85712

 

 
 

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