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CHAPTER 126: Rheumatology in the ICU  1241


                    Reporting Unusual or New Drug Interactions:  MedWatch is a voluntary     • Evans WE, McLeod HL. Drug therapy: pharmacogenomics—drug
                    program sponsored by the Food and Drug Administration for reporting   disposition, drug targets, and side effects. N Engl J Med. 2003;348:538.
                    adverse events and problems with drugs and other products regulated by
                    this agency. Although it is not a direct information source, contributed     • Krishnan V, Corbridge T, Murray P. Critical care pharmacology.
                    data collectively provide continuous new drug information. MedWatch is   In: Hall JB, Schmidt GA, Wood LDH, eds. Principles of Critical
                    a major component of the FDA’s postmarketing drug product surveillance   Care. 3rd ed. New York: McGraw-Hill; 2005:1547.
                    and has identified ADRs that were not apparent during preapproval clini-    • Levey AS, Bosch JP, Lewis JB, et al. A more accurate method to
                    cal trials (eg, cardiotoxic effects of astemizole). Reports are encouraged   estimate glomerular filtration rate from serum creatinine: a new
                    even if the practitioner is not certain the product caused the event and   prediction equation. Modification of Diet in Renal Disease Study
                    whether or not all details are available. The program utilizes a consoli-  Group. Ann Intern Med. 1999;130:461.
                    dated reporting form (FDA form 3500), which may be submitted online     • Matzke GR, Aronoff GR, Atkinson AJ et al. Drug dosing con-
                    or facsimile or mail. Reports can also be made over the phone 24 hours   sideration in patients with acute and chronic  kidney disease-a
                    a day 7 days a week. For more information or to report quality problems   clinical update from Kidney Disease: Improving Global Outcomes
                    call 1-800-FDA-1088 or visit www.fda.gov/safety/MedWatch/default.htm.  (KDIGO). Kidney Int. 2011;80:1122-1137.
                    Drug Manufacturer Information:  The package insert that accompa-    • National Institute of Health Pharmacogenetics Research Network’s
                    nies all products contains FDA-approved information regarding the   PharmGKB: The Pharmacogenetics and the Pharmacogenomics
                    known properties and appropriate use of the drug. Contact infor-  Knowledge Base. www.pharmgkb.org. Accessed on Nov 9, 2014.
                    mation (including toll-free telephone numbers) for pharmaceutical      • Nelson DR. Cytochrome P450 Homepage.  Hum Genomics.
                    companies can also generally be found in this insert or other   2009;4(1):59-65.
                    package labeling or through the hospital drug information center.
                    Pharmaceutical  manufacturing  companies  usually  have  drug  infor-    • Nolin TD, Frye RF, Matzke GR. Hepatic drug metabolism and
                    mation support services that can provide up-to-date information   transport in patients with kidney disease.  Am  J Kidney Dis.
                    pertinent to their products. Manufacturers are required to perform   2003;42:906-925.
                    postmarketing surveillance of their products and to collect informa-    • Stevens LA comparative performance of the CKD epidemiology
                    tion about drug interactions and other ADRs.             collaboration (CKD_EPI) and the modification of diet in renal dis-
                                                                             ease (MDRD) Study equations for estimating GFR above 60ml/min.
                    Computerized Resources in the ICU:  Application of computer technol-  Am J Kidney Dis. 2010;56:486.
                    ogy to medical care can improve efficacy and decrease errors at every
                    step of drug administration. Computers can serve as a repository for
                    references. Availability of textbooks, journals, review services, and for-  REFERENCES
                    mularies may be valuable at the time of drug prescription. While avail-
                    ability of all references by print may be prohibitive, online references   Complete references available online at www.mhprofessional.com/hall
                    are easily accessible, such as Med-line (National Library of Medicine,
                    United  States),  MDConsult  (LLC  Ltd  Liability  Co.,  DE),  Physician
                    Drug References,  and UptoDate (UptoDate Inc, DE), to name a few.
                                112
                     Most institutions in the United States use computers to store patient   CHAPTER  Rheumatology in the ICU
                    medical records. A step further in the integration of computer technol-
                    ogy into medical practice is patient information capture. Real-time    126  Scott Vogelgesang
                    capture of patient data, such as vital signs, pulse oximetry, and   Vijay Raveendran Pottathil
                    laboratory results, aids in the dissemination of information and more   John A. Robinson
                    informed decisions for drug prescription and drug effect monitoring.
                                                                      113
                    Therapeutic drug monitoring can be more effectively regulated with
                    integration of patient data and drug administration.   KEY POINTS
                     Recent advances in handheld devices make all of the aforementioned     • Most ICU admissions for rheumatology patients are prompted by
                    systems  even  more  convenient  and  portable.  Software  for  handheld     infection.
                    devices, such as Epocrates Rx (Epocrates, Inc., CA) and Medcalc, for
                    example, allow for quick and convenient references for patient data     • New-onset rheumatic diseases rarely prompt ICU admission in the
                    interpretation. While computer technology continues to advance, the   absence of a revealing prodrome.
                    major barriers to incorporation of these systems into the medical prac-    • In most patients without a previously established collagen vascular
                    tice include the initial costs of the computer devices and software, the   disease, suspected vasculitis will be explained by an alternative
                    time to install the appropriate software, the education and willingness   diagnosis.
                    of health care professionals to use the technology available, and the     • Serologic assessment of critically ill patients is a double-edged
                    real possibility of technical malfunction. Future trends in computer   sword providing both enlightenment and misleading shadows. All
                    technology in the ICU involve expert systems that can simulate human   serologic testing must be interpreted with a thorough understand-
                    judgment to aid in diagnostic and therapeutic decision making, and data   ing of the patient’s clinical condition.
                    mining that can analyze large amounts of data to recognize relationships
                    that have not been otherwise discovered.                  • Inability to assign specific diagnostic labels to patients with severe
                                                                            life-threatening autoimmune or inflammatory disease should not
                                                                            delay therapeutic intervention.
                                                                              • Not all ischemic skin lesions that appear to be vasculitis are.
                     KEY REFERENCES                                         Vasculopathies of various causes should always be part of the
                        • Boyer EW, Shannon M. The serotonin syndrome. N Engl J Med.   differential diagnosis.
                       2005;352:1112-1120.                                    • Empiric trials with corticosteroids can be a rational approach to
                        • Cox ZL. Adverse drug events during AKI and its recovery. Clin J   patient care when such trials are carried out appropriately and
                       Am Soc Nephrol. 2013;8:1070-1078.                    infection and malignancy have been excluded.









            section11.indd   1241                                                                                      1/19/2015   10:52:13 AM
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