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swallow for treatment of her oral thrush infection. On follow-up at as inhibition of cyclooxygenase by aspirin may shunt the arachidonic
day 4 in the clinic, her lungs are clear without wheezing; her respira- acid pathway away from prostaglandin synthesis and toward leuko-
tory rate is 16 breaths per minute; and her pulse oximetry is 97% on triene production. Although inhaled corticosteroids are still the pre-
room air. Her peak flow readings have improved to 300 L/min. ferred anti-inflammatory medications for patients with asthma and
known aspirin sensitivity, leukotriene modifiers may also be useful in
such patients based on this theoretical mechanism.
QUESTIONS
REFERENCES
Problem Identification
1.a. Create a list of the patient’s drug therapy problems. 1. National Asthma Education and Prevention Program. Executive sum-
mary of the NAEPP expert panel report 3: guidelines for the diagnosis
1.b. What information indicates the presence of uncontrolled and management of asthma. Bethesda, MD: U.S. Department of
chronic asthma and an acute asthma exacerbation? Health and Human Services, Public Health Service, National Institutes
1.c. What factors may have contributed to this patient’s poorly of Health, National Heart, Lung, and Blood Institute, Full Report 2007.
controlled asthma and acute exacerbation? Available at http://www.nhlbi.nih.gov/guidelines/asthma/index.htm.
2. Global Initiative for Asthma (GINA). Global strategy for asthma man-
1.d. How would you classify this patient’s level of asthma control agement and prevention (updated 2006). Available at http://www.
(well controlled, not well controlled, or very poorly con- ginasthma.org; 2006.
trolled), according to NIH guidelines? 3. Greening AP, Ind PW, Northfield M, et al. Added salmeterol versus
high-dose corticosteroid in asthma patients with symptoms on existing
Desired Outcome inhaled corticosteroid. Lancet 1994;344:219–224.
4. Busse W, Raphael GD, Galant S, et al. Fluticasone Propionate Clinical
2. What are the goals of pharmacotherapy in this case? Research Study Group. Low-dose fluticasone propionate compared
with montelukast for first-line treatment of persistent asthma: a
Therapeutic Alternatives randomized clinical trial. J Allergy Clin Immunol 2001;107:461–468.
5. Busse W, Nelson H, Wolfe J, et al. Comparison of inhaled salmeterol
3.a. What nonpharmacologic therapies might be useful for this and oral zafirlukast in patients with asthma. J Allergy Clin Immunol
patient? 1999;103:1075–1080.
3.b. What feasible pharmacotherapeutic alternatives are available 6. Humbert M, Beasley R, Ayres J, et al. Benefits of omalizumab as add-
for treatment of this patient’s chronic asthma? on therapy in patients with severe persistent asthma who are inade-
quately controlled despite best available therapy (GINA 2002 step 4
treatment): INNOVATE. Allergy 2005;60:309–316.
Optimal Plan 7. Food and Drug Administration (FDA) 2007. FDA alert: Omalizumab
4.a. Outline an optimal plan of treatment for this patient’s chronic (marketed as Xolair) information 2/2007. Available at: http://
asthma. www.fda.gov/cder/drug/infopage/omalizumab/default.htm.
Outcome Evaluation
5. What clinical parameters are necessary to evaluate the therapy for
achievement of the desired therapeutic effect and to detect or
25
prevent adverse effects?
CHRONIC OBSTRUCTIVE
Patient Education PULMONARY DISEASE
6. What information should be provided to the patient regarding
the use of her asthma medications and how she can use her peak- Quick Fix, Lifetime Risk . . . . . . . . . . . . . . . . . . . Level II
flow readings to better manage her disease? Joel C. Marrs, PharmD, BCPS
■ SELF-STUDY ASSIGNMENTS
1. Review the NIH guidelines on the management of asthma during
pregnancy, and develop a pharmacotherapeutic treatment plan
LEARNING OBJECTIVES
for this patient’s asthma if she were to become pregnant. After completing this case study, the reader should be able to:
2. Review the literature on the impact of chronic inhaled cortico- • Recognize modifiable and nonmodifiable risk factors for the
steroid use on the risk for development of osteoporosis, and development of COPD.
81
• Interpret spirometry readings to evaluate and appropriately ! Meds
stage the severity of COPD for an individual patient.
CHAPTER 25
Metoprolol tartrate 50 mg po BID
• Identify the importance of nonpharmacologic therapy in pa- Salmeterol (Serevent Diskus) 1 inhalation (50 mcg) BID
tients with COPD. Tiotropium (Spiriva) 1 capsule (18 mcg) inhaled once daily
Lisinopril 20 mg po once daily
• Develop an appropriate medication regimen for a patient with Esomeprazole (Nexium) 20 mg po once daily
COPD based on disease severity. Albuterol MDI 1–2 puffs Q 6 h PRN
• Evaluate the role of inhaled and/or oral corticosteroids in the Aspirin 81 mg po once daily
management of COPD.
! All
• Educate patients on the proper use of inhaled medications and
! Physical Examination
PATIENT PRESENTATION Gen
WDWN man appearing in mild respiratory distress after walking to
! Chief Complaint the end of the hall to reach the exam room
“Why can’t I just take prednisone every day? It always works when
I get admitted to the hospital.” VS
BP 138/88, P 85, RR 26, T 37.5°C; Wt 95 kg, Ht 5'11''
! HPI
Skin
Thomas Jones is a 66-year-old man with COPD who is presenting
to the family medicine clinic today to have a 1-month follow-up Warm, dry; no rashes
appointment from his last hospital admission for an acute exacerba-
HEENT
tion of COPD. This last COPD exacerbation is the second hospital
admission in the last 6 months related to TJ’s COPD instability. Normocephalic; PERRLA, EOMI; normal sclerae; mucous mem-
After TJ’s hospitalization, his discharge COPD regimen was branes are moist; TMs intact; oropharynx clear
changed to include tiotropium, 1 inhalation daily in addition to
Neck/Lymph Nodes
salmeterol 50 mcg, 1 inhalation Q 12 h, and an albuterol MDI as
needed. TJ had pulmonary function tests (PFTs) while he was in the Supple without lymphadenopathy
hospital 1 month ago but has yet to have them reassessed after the
Lungs
change in his COPD regimen. He wants to start taking prednisone
every day because he believes this would prevent him from being Tachypnea with prolonged expiration; decreased breath sounds; no
readmitted to the hospital. The patient states that his respiratory rales, rhonchi, or crackles
symptoms are better than when he was admitted 1 month ago, but
CV
he still has shortness of breath every day and a decreased exercise
capacity (e.g., he becomes very short of breath after walking a RRR without murmur; normal S1 and S2
couple of blocks). He states that he is adherent to the new medica-
Abd
tion regimen that was changed on discharge from the hospital. No
other medications were changed at that time that he can recall. His Soft, NT/ND; (+) bowel sounds; no organomegaly
daughter, who is at the appointment today, states that she makes
Genit/Rect
sure he uses his inhalers but often wonders if he is using them
correctly because he still has daily symptoms. No back or flank tenderness; normal male genitalia
! PMH MS/Ext
COPD × 12 years No clubbing, cyanosis, or edema; pulses 2+ throughout
GERD × 5 years
Neuro
HTN × 20 years
CAD (MI 5 years ago) A & O × 3; CN II–XII intact; DTRs 2+; normal mood and affect
! FH ! Labs
Mother died from emphysema 4 years ago at the age of 82. Father Na 135 mEq/L Hgb 12.1 g/dL AST 40 IU/L Ca 8.9 mg/L
K 4.2 mEq/L Hct 38.5% ALT 19 IU/L Mg 3.6 mg/L
has a history of coronary artery disease.
Cl 108 mEq/L Plt 195 × 103/mm3 T. bili 1.1 mg/dL Phos 2.9 mg/dL
CO2 26 mEq/L WBC 6.4 × 103/mm3 Alb 3.1 g/dL
! SH BUN 19 mg/dL Pulse Ox 93% (RA)
He lives with his daughter and her family. His wife died 10 years ago SCr 1.1 mg/dL
Glu 109 mg/dL
from breast cancer. He has a 35 pack-year history of smoking. He
quit smoking approximately 3 months ago but has had occasional
relapses. He states he has not smoked for approximately a week. He ! Pulmonary Function Tests (during Hospital Admission 1 Month Ago)
drinks one to two beers every evening. Prebronchodilator FEV1 = 1.1 L (predicted is 3.1 L)
82
Prebronchodilator FVC = 3.2 L Patient Education
Postbronchodilator FEV1 = 1.6 L
6. What information should be provided to the patient to enhance
SECTION 3