Dianne E. Tobias
Resident assessment and medication monitoring to optimize outcomes through prevention, detection, and resolution of medication-related problems lie at the heart of nursing facility-based pharmaceutical care. Consultant pharmacists have long desired a tool to more tightly integrate these fundamental processes. Now they have it. The MDS-Med Guide is a unique clinical tool for consultant pharmacists and other health professionals to promote the integration of resident assessment data with monitoring of medication therapy in the federally mandated resident assessment process. The MDS-Med Guide is intended to assist in the clinical decision-making process of evaluating complex medication regimens of nursing facility residents, monitoring the therapeutic outcomes of medication therapy, and identifying and preventing potential medication-related problems. This article describes the MDS-Med Guide, the methodology used in its development, and suggestions for use in clinical practice.
Resident AssessmentComprehensive resident assessment has been a federal requirement in all Medicare- and Medicaid-certified nursing facilities since 1991. The Resident Assessment Instrument (RAI) is a revolutionary health care tool that provides a comprehensive, standardized, reproducible assessment of each nursing facility resident’s cognitive, behavioral, functional, and medical status. The RAI is used to develop outcome-oriented resident care plans to maximize quality of care and residents’ quality of life through early recognition of problems and risk factors that can be avoided, managed, or reversed.
The RAI consists of the Minimum Data Set (MDS), Triggers, Resident Assessment Protocols (RAPs), and Utilization Guidelines.
Importance of MDS DataThe significance of the MDS to long-term care pharmacy cannot be overstated. The MDS is the basis for resident classification under the Medicare prospective payment system (PPS). State Medicaid programs use MDS data to determine case-mix reimbursement rates. State regulatory agencies use MDS data to target the facility survey process to problem areas. The Health Care Financing Administration (HCFA) has developed nursing home Quality Indicators (QIs), derived from items on the MDS, that indicate either the presence or absence of potentially poor care practices or outcomes in nursing facilities. On July 1, 1999, HCFA incorporated QIs into the nursing facility survey process. Many of these QIs are designed to evaluate the use of medications in the facility; others can be impacted by drug therapy.In addition, the MDS and QIs may also be used by managed care organizations to determine reimbursement levels and assess quality. For these reasons it is critical that long-term care pharmacy begin integrating MDS data into its systems and processes, and linking clinical services to these established resident-specific and facility-specific quality and outcome data. To advance the process of data integration, the ASCP Research and Education Foundation has developed the MDS-Med Guide.
Goals of the MDS-Med GuideThe MDS-Med Guide was developed to:
The MDS-Med Guide is a tool—not a definitive reference for medication side effects or adverse drug reactions—and it is not designed and should not be used as a rigid screen. The MDS-Med Guide was designed for the geriatric nursing facility resident with chronic diseases and conditions; acute or self-limiting conditions were not considered. The MDS-Med Guide relates specific MDS items, which may reflect potential positive and negative outcomes of medication therapy, to specific medications and medication classes. The consultant pharmacist can use this information when performing initial medication assessments and drug regimen reviews; when developing pharmaceutical care plans to establish and monitor progress toward achieving desired therapeutic goals; and to identify, resolve, and prevent medication-related problems. To use the MDS-Med Guide, the pharmacist must have expertise in geriatric pharmacotherapy and be thoroughly familiar with the resident assessment process and the components of the RAI: the MDS, Triggers, RAPs, and Utilization Guidelines. For complete information, see the Long Term Care Facility Resident Assessment Instrument User’s Manual, published by HCFA and available from various distributors.
Enhancing and Expanding the Role of the PharmacistIncreased involvement in resident assessment and care planning through the use of the MDS-Med Guide will enable pharmacists to see a resident’s medication regimen not in isolation, but rather as one component contributing to the physical, functional, and psychosocial status of the resident. This integrated approach is needed to effectively identify, resolve, and prevent medication-related problems.The MDS-Med Guide will also increase awareness and appreciation of the effect of medications on a resident’s physical, functional, and psychosocial status. Many MDS items use functional terminology familiar to nursing and other long-term care health professionals involved in care planning to describe the behavior, mood, cognition, psychosocial well-being, functional ability, and involvement in activities assessed as part of the resident assessment process. The MDS-Med Guide correlates this functional language to potential therapeutic and adverse effects of medications. This correlation will assist the pharmacist in incorporating the "language of resident assessment" into their problem identification process, clinical decision-making, and patient care recommendations. The ability to communicate in the common language of resident assessment will enhance the effectiveness of the pharmacist’s recommendations and facilitate incorporation of medication-related issues into the resident’s plan of care.
Structure of the MDS-Med GuideThe MDS-Med Guide is available in three formats: pocket guide, wall chart, and query software. The content and format of the MDS-Med Guide dramatically illustrate the scope and potential effect of medications on the cognitive, behavioral, functional, and medical status of nursing facility residents. The pharmacist’s experience and knowledge of geriatric pharmacotherapy provides the important and necessary expertise required to use the MDS-Med Guide appropriately.The MDS-Med Guide Pocket Guide and Wall Chart present both MDS-medication and RAP-medication data in a grid format. Medications/medication classes are listed vertically, and MDS items or RAP titles are arranged horizontally. MDS items and RAP titles are cross-indexed with medications/medication classes by color-coded cells. The medications/medication classes in the MDS-Med Guide represent
those commonly prescribed for geriatric nursing facility residents with
chronic diseases or conditions; topical agents and antineoplastic medications
are not included. The medications/medication classes are listed in the
MDS-Med Guide in the following manner (Table
3): The basis for the organization of medications/medication classes is the table of contents of the Handbook of Clinical Drug Data, 8th Edition;1 the list was adapted with permission. The user must be familiar with this format in order to efficiently use the MDS-Med Guide.
MDS GridThe MDS Grid (Figure 1) contains MDS Sections and relevant subsections, MDS item numbers, and MDS item descriptions from the MDS Version 2.0 Full Assessment. MDS item numbers mandated for quarterly assessment are indicated by an asterisk. If the MDS item is a RAP trigger, the applicable RAP number(s) appears in parentheses.
The following MDS Sections are not included in the MDS Grid: Section A. Identification and Background Information; Section O. Medications; Section P. Special Treatments and Procedures; Section Q. Discharge Potential and Overall Status; Section R. Assessment Information; Section T. Therapy Supplement for Medicare PPS. In addition, the MDS Grid does not include every item in the MDS; items with little or no applicability to the monitoring of medication therapy are not included. The MDS Grid identifies medications/medication classes that have the potential, over time, to improve or cause a decline in the disease, condition, sign, symptom, or function described by the MDS item. MDS items are cross-indexed with medication/medication class by red, green, or blue color-coded cells:
Assigning Green, Red, and Blue CellsIn developing the MDS-Med Guide, all medications of a class were, if possible, grouped together for purposes of assigning red and green cells. However, in many cases the assignment of red cells dictated that medications from the same class be listed individually because of different adverse effect profiles.The MDS-Med Guide does not present every documented adverse effect of every medication/medication class listed. The absence of a red cell does not mean a medication/medication class can be excluded as a possible cause of an adverse effect. This is especially true when the addition of the medication or a change in its dosage is closely related in time to the emergence of the adverse effect. Similarly, the association of a medication/medication class and adverse or therapeutic effect does not constitute evidence of a true cause-and-effect relationship. Illness of any sort is highly individualized, and residents may experience medication-related benefits or adverse effects in more or fewer MDS items than indicated. It is possible, and perhaps likely, that more than one medication in a resident’s regimen may contribute to an adverse effect or improvement in resident status. The potential effect of multiple medication therapy was not considered in the development of the MDS-Med Guide.
MDS Item Data SetsMDS items were identified that correlate with: (1) presenting features and functional signs and symptoms associated with diagnoses frequently encountered in nursing facility residents that may be improved with medication therapy; and (2) possible signs and symptoms of common or serious adverse medication effects.a These MDS items were grouped into data sets for possible therapeutic effect and possible adverse effect (Appendix 1).The correlations for possible therapeutic effect were determined through a review of gerontology nursing texts.2–5 For each diagnosis, the presenting features and functional signs and symptoms identified were then reviewed with therapeutics texts to determine which medications/medication classes might contribute to improvement of a given set of presenting features, signs, and symptoms.6, 7 The correlations for possible adverse effect were determined based on a review of side effects reference texts and review articles.1, 8–28 The MDS item data sets identified for a particular adverse drug effect (e.g., confusion) or clinical condition (e.g., heart failure) were made as inclusive as possible; not all medications/medication classes will necessarily affect all MDS items in a data set. Figure 2 presents a schematic of MDS item data set development.
How Were Green Cells Assigned?Medications/medication classes that are considered therapeutic for a disease or condition, or that may improve a sign or symptom, are coded green for all items in the applicable MDS item data set. If a medication/medication class is known to be therapeutic only for certain signs or symptoms, only those MDS items were coded green. In most cases, all items in the MDS item data set were coded green for all therapeutic medications/medication classes because it is often difficult to delineate which symptoms benefit from which medications. For example, various antipsychotic agents are indicated for the treatment of schizophrenia/psychosis. These medications are coded green for the disease diagnosis schizophrenia (MDS Item I1gg) and for the MDS data set that correlates with signs or symptoms of schizophrenia/psychosis: B4; B5a-f; B6; E1a,d-l,n-p; E3; E4a-e; E5; F1a-f; I1gg; J1e,i; N1; N2 (Table 4).
How Were Red Cells Assigned?Medications/medication classes known to cause an adverse effect were coded red for all items in the applicable MDS item data set. For example, various medications may cause diarrhea. These medications are coded red for the bowel elimination pattern, diarrhea (MDS Item H2c), and for the MDS data set that correlates with signs or symptoms of diarrhea: H2c; J1a,c (Table 5).
How Were Blue Cells Assigned?A blue cell indicates that the medication/medication class has the potential to either improve or worsen the disease, condition, sign, or symptom described by the MDS item. MDS items are coded blue for medications/medication classes that were independently coded red and green for an MDS item based on the therapeutic effect, adverse effects, or MDS item data sets.
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Table 5. MDS Item Adverse Effect Data Set (Red Cells) for Diarrhea |
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| MDS Items: H2c; J1a,c | ||
| MDS Section | MDS Item | |
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| H. Continence | 2. Bowel Elimination Pattern | c. Diarrhea |
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| J. Health Conditions | 1. Problem Conditions | a. Weight gain/loss 3 or more pounds within 7 day period c. Dehydrated; output exceeds input |
The MDS-Med Guide RAP Grid (Figure 3) identifies medications/ medication classes that have the potential to contribute to or aggravate a RAP problem. RAP titles are cross-indexed with medication/medication class by red cells. A red cell indicates that the medication/medication class may cause or aggravate the problem addressed by the RAP. The RAP Grid contains only red cells because it focuses exclusively on the potential negative effects of medications on a resident’s problem.
In addition, correlations were made between the RAPs and signs and symptoms of potential adverse medication effects from the MDS item data sets. If there is a correlation between the signs and symptoms of an adverse medication effect and a RAP problem, all medications/medication classes in the applicable data set are coded red for that RAP (Appendix 1).
The Feeding Tubes and Physical Restraints RAPs do not list or discuss specific medications/medication classes in the RAP Guidelines, and no MDS item data set correlations were made; therefore, there are no red cells for the Feeding Tubes and Physical Restraints RAPs.
Genesis of the MDS-Med GuideThe concept for the MDS-Med Guide was fostered by the 1995–96 ASCP Organizational Affairs Council, which was charged with developing a Statement and Guidelines on The Role of the Consultant Pharmacist in Resident Assessment and Care Planning. The Guidelines were intended to identify specific areas where consultant pharmacists could contribute to the resident assessment and care planning process for individual residents, including the evaluation of drug therapy as a cause or aggravating factor contributing to the resident’s problem that can be avoided, managed, or reversed. The ultimate goal was to develop a “product” to be used by consultant pharmacists to achieve this end. With the MDS-Med Guide this goal has now been reached.1995–96 ASCP Organizational Affairs Council |
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| Michele Arling, RPh, FASCP St. Charles, Illinois |
Ronald Kennedy, RPh Northglenn, Colorado |
| Board Liaison Diane Darling, RPh, FASCP Hilliard, Ohio |
Annamary A. Kisic, RPh, FASCP Ebensburg, Pennsylvania |
| Allen Ezelle, RPh, FASCP Prattville, Alabama |
Jeffrey Reist, RPh, FASCP Cedar Rapids, Iowa |
| Quentin C. Florence, RPh, FASCP Albuquerque, New Mexico |
Chairman Robert Warnock, DPh, FASCP Conyers, Georgia |
| Chuck Hunt, RPh, FASCP Dublin, Ohio |
|
MDS-Med Guide Advisory Board |
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| Maude Babington, PharmD, FASCP Babington Consulting, LLC Boulder, Colorado |
Nancy L. Losben, RPh, FASCP NeighborCare Cherry Hill, New Jersey |
| Sandra Brownstein, PharmD, FASCP, CGP SeniorCare Strategies Aurora, Illinois |
Mark Sey, PharmD, FASCP Mark Sey & Associates Woodbridge, California |
| Sharon F. Clackum, PharmD, FASCP PharMerica Cumming, Georgia |
Rachelle Spiro, RPh Vencare Pharmacy Services Louisville, Kentucky |
| Diane Darling, RPh, FASCP NCS HealthCare Hilliard, Ohio |
Dianne E. Tobias, PharmD, FASCP Dianne E. Tobias Consulting Services Davis, California |
| Stephen M. Feldman, RPh, FASCP The ICPS Group Boston, Massachusetts |
Robert Warnock, DPh, FASCP Medical Arts Health Care, Inc. Conyers, Georgia |
| Susan Klem, RPh, FASCP Omnicare, Inc. Livonia, Michigan |
Lynn Williams, RPh, FASCP Solutions Boulder, Colorado |
The appropriate use of the MDS-Med Guide requires a thorough understanding of the resident assessment process and resident assessment instrument, how the MDS-Med Guide grids were developed, and expertise in geriatric pharmacotherapy. Before using the MDS-Med Guide, pharmacists should become familiar with the resident assessment process and procedures, the role of the MDS coordinator, and the MDS software system and capabilities in the different facilities they serve. The MDS-Med Guide will be most valuable when incorporated into the pharmaceutical care process. For information on how to establish a pharmaceutical care practice and implement the pharmaceutical care process, see Cipolle RJ, Strand LM, Morley PC. Pharmaceutical care practice. New York: McGraw-Hill; 1998.
At least initially, pharmacists may want to target residents to receive formalized pharmaceutical care planning based on high risk for medication-related problems,29 high risk for RAP problems, or RAP problem areas of concern to specific facilities (e.g., falls, nutrition, pressure ulcers).
Use information in the RAP Grid to identify: (1) potential problem areas where medications may be a cause or contributing factor; (2) residents at high risk for developing a RAP problem; and (3) medications/medication classes that may be implicated in a triggered RAP.
This information should be incorporated into the pharmaceutical care plan, and the pharmacist’s assessment of this information should be shared with the MDS coordinator and interdisciplinary team for incorporation into the resident’s care plan. Specific interventions may include:
To begin, evaluate the resident’s medication regimen against the MDS and RAP Grids:
This process allows the pharmacist to see the potential cumulative effect of medications on MDS items/Sections.
This process allows the pharmacist to see the potential cumulative effect of medications on RAP problem areas and can be used to identify residents who may be at higher risk for developing a RAP problem. The data may initially appear overwhelming, but in a short time the pharmacist should become familiar with the MDS and be able to easily organize the information by MDS Section. The MDS-Med Guide Query Software automates this process and provides data in five report formats: Med/MDS, MDS/Med, Med/RAP, RAP/Med, Triggered RAPs/Med.
It may be useful to develop MDS item monitoring forms for specific diseases or conditions for which medications should provide a therapeutic benefit (e.g., depression, congestive heart failure), medications/medication classes known to be problematic in nursing facility residents, or residents at high risk for specific RAP problem areas. The use of forms should facilitate the monitoring of MDS items over time and aid in clinical decision-making.
MDS-Med Guide Editorial Review Board |
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| Lisa J. Adams, PharmD, BCPS, BCFE, BCFM, FASCP Veterans Affairs Medical Center Fresno, California |
Susan J. Klem, RPh, FASCP Omnicare, Inc. Livonia, Michigan |
| Al Barber, RPh, FASCP Ritzman Natural Health Pharmacy Wadsworth, Ohio |
James Kuchta, RPh South Dakota Department of Health Pierre, South Dakota |
| Barbara Baylis, MSN, RN Paragon Health Network Houston, Texas |
Ivan Lambert, RPh, FASCP National Institutional Pharmacy Services, Inc. Las Vegas, Nevada |
| Darryl Chutka, MD Mayo Clinic Rochester, Minnesota |
Donna M. Lisi, PharmD, FASCP New Jersey VA Healthcare System Somerset, New Jersey |
| Allen Ezelle, RPh, FASCP Unicare, Inc. Prattville, Alabama |
Nancy L. Losben, RPh, FASCP NeighborCare Cherry Hill, New Jersey |
| Stephen M. Feldman, RPh, FASCP ICPS Group Boston, Massachusetts |
Harlan Martin, RPh, CCP, FASCP Pharma-Care, Inc. Clark, New Jersey |
| Edward C. Fisher, Jr., MHA, CNHA Kennedy Living Center Martinsville, Indiana |
Dean A. Pedalino, RPh, CPH, FASCP Medi-Save Pharmacy St. Petersburg, Florida |
| Darlene Fujimoto, PharmD, FASCP Capstone Clinical Care Laguna Niguel, California |
Mildred G. Simmons, RN Sequoia Health Consultants, Inc. Castle Rock, Colorado |
| Chuck Hunt, RPh, FASCP Ohio State University Medical Center Dublin, Ohio |
Kathy Stevenson NCS HealthCare Billings, Montana |
| Annamary A. Kisic, RPh, FASCP NCS HealthCare Ebensburg, Pennsylvania |
Robert Warnock, DPh, FASCP Medical Arts Health Care, Inc. Conyers, Georgia |
With the information provided in the MDS-Med Guide, the pharmacist can begin to see how a resident’s medications, both individually and cumulatively, may affect various areas of functioning, then incorporate this information into the problem identification process and clinical decision-making. For example, if a resident is receiving a medication that is coded red for an MDS item and that MDS item has declined over time (i.e., since the last assessment), further investigation may be warranted to determine if the medication may have caused or contributed to the decline. This determination is a complex task requiring—in addition to knowledge of the potential effects of the medication—knowledge of the resident’s condition; disease progression, generally and in the individual resident specifically; and typical and atypical manifestations of the resident’s diseases or conditions.
After assessment, problem identification, and clinical decision-making, the pharmacist is ready to design and implement a pharmaceutical care plan. The pharmaceutical care plan includes therapeutic goals, monitoring parameters (including MDS items and RAP information), appropriate monitoring intervals, specific interventions, expected outcomes of intervention, schedule for follow-up, and actual outcomes during follow-up evaluation. For more information on pharmaceutical care planning, see Cipolle RJ, Strand LM, Morley PC. Pharmaceutical care practice. New York: McGraw-Hill; 1998.
The development of the MDS-Med Guide Version 1.0 established a methodology for correlating medications to MDS items and RAPs through the identification of data sets and the assigning of therapeutic or adverse effect potential to medications/medication classes commonly used in geriatric nursing facility residents. The next step is the incorporation of the MDS-Med Guide into practice and validity testing.
The MDS-Med Guide is a powerful clinical tool that can revolutionize the way consultant pharmacists practice. Increased involvement in resident assessment and care planning through the use of the MDS-Med Guide will shift the pharmacist’s focus from the medication regimen in isolation to the medication regimen as one component contributing to a resident’s physical, functional, and psychosocial status.
The MDS-Med Guide enables pharmacists to see how a resident’s medications, both individually and cumulatively, may impact on various areas of functioning, and to incorporate the "language of resident assessment" into their problem solving process, clinical decision-making, and recommendations.
Re-engineering one’s practice is a daunting task, but it can be done—one patient at a time. The MDS-Med Guide is the clinical tool to advance this process.
Appendix 1. MDS-Med Guide MDS Item Data Sets1-28Notes: MDS item data sets (Column 2) were identified that correlate with (1) presenting features and functional signs and symptoms for diagnoses frequently encountered in nursing facility residents that may be improved with medication therapy; and (2) possible signs and symptoms of common or serious adverse medication effects (Column 1). Medications/medication classes that are considered therapeutic for a diagnosis or that may improve a sign/symptom are coded green for all items in the applicable MDS data set (Column 3). Medications/medication classes known to cause an adverse effect (Column 4) were coded red for (1) all items in the applicable MDS data set; and (2) RAPs in which the adverse effect is implicated (Column 5). Data sets were made as inclusive as possible; not all medications/medication classes will necessarily affect all MDS items in a data set. |
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| Diagnosis/Condition Sign/Symptom |
MDS Item Data Set | Possible Therapeutic Effect (Green Cells) |
Possible Adverse Effect (Red Cells) |
RAP No. |
| Agitation | B5a,d; E1b-d,i,k,n, E2; F2a-d | clozapine, haloperidol, olanzapine, phenothiazines, risperidone, barbiturates, benzodiazepines,buspirone, chloral hydrate, zolpidem | bupropion, MAOI, benzodiazepines, chloral hydrate, zolpidem, H2 blockers | 9 |
| Allergies | I1nn | corticosteroids, antihistamines | ||
| Alzheimer’s Disease | B2a,b, B3, B4, B5a-d,f, B6; C4,6; E1b,c,k,n,o,p, E2, E3, E4a,b,c, E4d;
I1q; J1e,i; N2
E4b,c,d; J1e,I |
donepezil
|
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| Anemia | B5e; G1c-j, G2; I1oo | iron dextran, ferrous salts, epoetin alfa | chloramphenicol, amphotericin B | |
| Anticholinergic | B5a-f; C5; D1, D2a; E3, E4a-c,e, E5; H1b, H2b; I1ll; J1i; N1, N2 | disopyramide, clonidine, heterocyclic antidepressants clozapine, haloperidol, olanzapine, phenothiazines, amantadine, anticholinergics, GI antispasmodics, diphenoxylate/atropine, oxybutynin, antihistamines, cyproheptadine | 1,3,4,7,15 | |
| Anorexia | J1a; K3a, K4c | amiodarone, digitalis glycosides, disopyramide, mexiletine, tocainide, hydralazine, felbamate, SSRI, levodopa, sulfasalazine, metformin, sulfonylureas, loop diuretics, sodium poly sulfonate, theophylline, sulfonamides | 12 | |
| Anxiety | B5a,d; E1b-i,k,n, E2; F2a-d,g; I1dd; N2 | barbiturates, benzodiazepines, buspirone, chloral hydrate, zolpidem | clonidine, bupropion, SSRI, haloperidol, amantadine, metoclopramide, potassium, B2 agonists, theophylline, phenylpropanolamine, pseudoephedrine | 9 |
| Arrhythmia | B5e; I1e; J1f,m | amiodarone, digitalis glycosides, disopyramide, flecainide, lidocaine, mexiletine, procainmide, quinidine, tocainide | amiodarone, digitalis glycosides, disopyramide, flecainide, lidocaine, mexiletine, procainamide, quinidine, tocainide, a1-adrenergic antagonists, Ca-channel blockers, nitrates, heterocyclic antidepressants, dopaminergics, levodopa, octreotide, epoetin alfa, levothyroxine, amiloride, thiazides, triamterene, magnesium, potassium, sodium poly sulfonate, non-sedating antihistamines, B2 agonists, theophylline | |
| Arthritis | G1a-j, G2, G4, G7, G9; I1l; J1n, J2a,b, J3a,b,e,g, J4a,b; N2 | acetaminophen, NSAIDs, celecoxib, indomethacin, salicylates, methotrexate, corticosteroids, chloroquine | ||
| Bleeding, Internal | I1i,oo; J1j | NSAIDs, indomethacin, salicylates, mesalamine, heparin, clopidogrel, ticlopidine, warfarin, cephalosporins | ||
| Blood Disorders Hemolytic anemia | I1oo | salicylates, quinidine, quinine, sulfonamides | ||
| Blood Disorders Macrocytic anemia | I1oo | phenytoin, phenobarbital, trimethoprim | ||
| Blood Disorders Thrombocytopenia | I1oo; J1j; M4a | quinidine, dipryidamole, heparin, quinine, rifampin, ganciclovir | ||
| Blood Disorders Agranulocytosis/Neutropenia | I1oo; J1h | indomethacin, methotrexate, procainamide, tocainide, carbamazepine, clozapine, phenothiazines, propylthiouracil, trimetrexate, flucytosine, foscarnet, ganciclovir | ||
| Blood Disorders Aplastic anemia | I1oo, I2; J1h,j; M4a | felbamate, chloramphenicol | ||
| Bone fractures | I1m,p | estrogens, raloxifene, alendronate, calcitonin | corticosteroids | |
1. Anderson PO, Knoben JE, Troutman WG et al., eds. Handbook of clinical drug
data. 8th ed. Norwalk, CT: Appleton & Lange; 1997.
2. Berkow R, editor. Merck manual of diagnosis and therapy. 16th ed. Rahway,
NJ: Merck Research Laboratories; 1992.
3. Jaffe M. Geriatric nursing care plans. Aurora, CO: Skidmore-Roth Publishing;
1996.
4. McFarland GK, McFarlane EA. Nursing diagnosis and intervention. 3rd ed. St
Louis, MO: Mosby; 1997.
5. Needham JF. Gerontological nursing. Albany, NY: Delmar Publishers; 1995.
6. Delafuetne JC, Steward RB, eds. Therapeutics in the elderly. 2nd ed. Cincinnati,
OH: Harvey Whitney Books; 1995.
7. Dipiro JT, Talbert RL, Yee GC et al, eds. Pharmacotherapy. 3rd ed. Stamford,
CT: Appleton & Lange; 1997.
8. Bartalena L, Bogazzi F, Martino E. Adverse effects of thyroid hormone preparations
and antithyroid drugs. Drug Safety 1996;15:53–63.
9. Brunet L, Miranda J, Farré M et al. Gingival enlargement due to drugs. Drug
Saf 1996;15:219–31.
10. Carter GL, Dawson AH, Lopert R. Drug-induced delirium. Incidence, management
and prevention. Drug Saf 1996;15:291–301.
11. Cherin P, Colvez A, Deville de Periere G et al. Risk of syncope in the elderly
and consumption of drugs: a case-control study. J Clin Epidemiol 1997;50:313–20.
12. Curtis JL, Love RC. Drug-induced aggression and violent behavior. Pharmaguide
Hosp Med 1996;9(3):1–4,9,10.
13. Dukes MNG, editor. Meyler’s side effects of drugs. 13th ed. Amsterdam: Elsevier;
1996.
14. Frauman AG. An overview of the adverse reactions to corticosteroids. Adverse
Drug React Toxicol Rev 1996;15:203–6.
15. Gittoes NJL, Franklyn JA. Drug-induced thyroid disorders. Drug Saf 1995;13:46–55.
16. Griffin JP. Drug-induced disorders of taste. Adverse Drug React Toxicol
Rev 1992;11:229–39.
17. Hawkey CJ. Adverse drug reactions in the gastrointestinal tract. Adverse
Drug React Toxicol Rev 1988;3:153–9.
18. Jiménez-Jiménez FJ, García-Ruiz PJ, Molina JA. Drug-induced movement disorders.
Drug Saf 1997;16:180–204.
19. Jones G, Sambrook PN. Drug-induced disorders of bone metabolism. Incidence,
management and avoidance. Drug Saf 1994;10:480–9.
20. Kunisaki TA, Augenstein WL. Drug- and toxin-induced seizures. Emerg Med
Clin North Am 1993;12:1027–56.
21. Maxwell CJ, Neutel CI, Hirdes JP. A prospective study of falls after benzodiazepine
use; a comparison of new and repeat use. Pharmacoepidemiol Drug Saf 1997;6:27–35.
22. Morrow JI, Routledge PA. Drug-induced neurologic disorders. Adverse Drug
React Toxicol Rev 1988;3:105–33.
23. Novak M, Shapiro CM. Drug-induced sleep disturbances. Focus on nonpsychotropic
medications. Drug Saf 1997;16:133–49.
24. Starr JM, Whalley LJ. Drug-induced dementia. Incidence, management and prevention.
Drug Saf 1994;11:310–7.
25. Sultzer DL, Cummings JL. Drug-induced mania—causative agents, clinical characteristics
and management. A retrospective analysis of the literature. Med Toxicol Adverse
Drug Exp 1989;4:127–43.
26. Troupin AS. Dose-related adverse effects of anticonvulsants. Drug Saf 1996;14:299–328.
27. USP DI-volume I. Drug information for the health care professional. 17th
ed. Rockville, MD: United States Pharmacopeial Convention; 1997.
28. Zaccara G, Muscas GC, Messori A. Clinical features, pathogenesis and management
of drug-induced seizures. Drug Saf 1990;5:109–51.
29. Fouts M, Hanlon J, Pieper C et al. Identification of elderly nursing facility
residents at high risk for drug-related problems. Consult Pharm 1997;12:1103–11.