Data regarding the use of immunoglobulins as adjunctive therapy for the treatment of
select infections in the neutropenic cancer patient are primarily limited to case
reports. Patients with pneumonia secondary to CMV may benefit from adjunctive
immunoglobulin therapy (in combination with ganciclovir). In addition, IV
immunoglobulin G should be considered in those patients with
A full list of references for this chapter can be found at
http://thepoint.lww.com/AT11e. Below are the key references and websites for this
chapter, with the corresponding reference number in this chapter found in parentheses
of growing resistance: summary of the 2011 4th European Conference on Infections in Leukemia.
Haematologica. 2013;98:1826–1835. (176)
undergoing hematopoietic stem-cell transplantation. J Clin Oncol. 2012;30:4427–4438. (177)
www.nccn.org. Accessed September 3, 2015. (3)
Oncology Clinical Practice Guideline Update. J Oncol Pract. 2015. (83)
National Comprehensive Cancer Network. www.nccn.org.
American Society of Clinical Oncology. www.asco.org.
COMPLETE REFERENCES CHAPTER 75 PREVENTION
AND TREATMENT OF INFECTIONS IN NEUTROPENIC
neutropenia: the early years. J Antimicrob Chemother. 2009;63(Suppl 1):i3–13.
de Naurois J et al. Management of febrile neutropenia: ESMO Clinical Practice Guidelines. Ann Oncol.
www.nccn.org. Accessed September 3, 2015.
2010 update by the Infectious Diseases Society of America. Clin Infect Dis. 2011;52:427–431.
Ann Intern Med. 1966;64:328–332.
antibacterial therapy. A randomized, controlled trial. Ann Intern Med. 2001;135:412–422.
piperacillin-tazobactam or cefepime. Pharmacotherapy. 2014;34:662–669.
recipients: a global perspective. Biol Blood Marrow Transplant. 2009;15:1143–1238.
transplantation: comparison with anti-thymocyte globulin. Transpl Infect Dis. 2009;11:413–423.
Clin Infect Dis. 1996;22:1064–1068.
patients with cancer and neutropenia. Clin Infect Dis. 2005;40(Suppl 4):S246–S252.
currently isolated pathogens. Clin Infect Dis. 2004;39:S25–S31.
more targeted antibiotic strategy. Clin Infect Dis. 2003;36:149–158.
reference to anaerobes. Med Oncol. 2002;19:267–272.
Thomas CF Jr, Limper AH. Pneumocystis pneumonia. N EnglJ Med. 2004;350:2487–2498.
Diseases Working Party (AGIHO) of the German Society of Hematology and Oncology (DGHO). Ann
patients. Clin Infect Dis. 2003;36:S117–S122.
transplants. Clin Infect Dis. 2001;33:41–47.
America. Clin Infect Dis. 2008;46:327–360.
and solid tumours. Eur J Cancer. 2011;47(1):8–32.
with emphasis on outpatient studies. Clin Infect Dis. 2002;35:1463–1468.
isolation with oral, nonabsorbable antibiotic prophylaxis. Ann Intern Med. 1975;82:351–358.
with leukaemia. Antifungal Prophylaxis Study Group. Eur J Cancer. 1999;35:1208–1213.
neutropenic patients with haematological malignancies. Mycoses. 1993;36:373–378.
invasive fungal infections. Int J Antimicrob Agents. 2006;27(Suppl 1):36–44.
transplant recipients:summary of the ECIL 3—2009 Update. Bone Marrow Transplant. 2011;46(5):709–718.
patients with cancer. Cochrane Database Syst Rev. 2002;(9):CD000026.
intravenous amphotericin B. Cancer. 1994;73:2099–2106.
leukemia and myelodysplastic syndrome. Cancer. 2003;97:450–456.
prophylaxis for neutropenic patients. Clin Infect Dis. 2000;30:300–305.
Program. Gruppo Italiano Malattie Ematologiche dell’ Adulto. Clin Infect Dis. 1999;28:250–255.
trial comparing itraconazole and amphotericin B. Antimicrob Agents Chemother. 2000;44:1887–1893.
Ann Intern Med. 2003;138:705–713.
stem cell transplants. Blood. 2004;103:1527–1533.
cancer patients. Bone Marrow Transplantation Team. Chemotherapy. 1994;40:136–143.
marrow transplantation. N EnglJ Med.1992;326:845–851.
randomized placebo-controlled, double-blind, multicenter trial. Ann Intern Med. 1993;118:495–503.
comprehensive cancer center during the last four decades. Diagn Microbiol Infect Dis. 2002;44:11–16.
conditions in healthy volunteers. Antimicrob Agents Chemother. 2009;53:958–966.
recipients. Antimicrob Agents Chemother. 2006;50:1993–1999.
chemotherapy for acute myelogenous leukaemia (AML). J Infect. 2007;55:445–449.
fungal infection after allogeneic hematopoietic cell transplantation. Blood. 2010;116:5111–5118.
Medical Mycology. J Antimicrob Chemother. 2014;69:1162–1176.
Antimicrobial Therapy Project Group. J Infect Dis. 1984;150:372–379.
factors. Clin Infect Dis. 1992;14:1201–1207.
systematic review and meta-analysis. J Antimicrob Chemother. 2007;59:5–22.
cancer who have received prophylactic norfloxacin. Clin Infect Dis. 1995;20:557–560.
methicillin-sensitive bacteriemia. Int J Antimicrob Agents. 1998;10:55–58.
leukaemia unit. BMJ. 1989;299:294–297.
Study Group. Transpl Infect Dis. 2010;12(5):421–427.
allogeneic hematopoietic stem cell transplant recipients. Int J Hematol. 2009;89:231–237.
following allogeneic stem cell transplantation. Blood. 2006;107:3002–3008.
hematopoietic stem cell transplantation. Bone Marrow Transplant. 2006;37:851–856.
transplantation. Transpl Infect Dis. 2007;9:102–107.
Oncology Clinical Practice Guideline Update. J Oncol Pract. 2015;33(28):3199–3212.
clinical practice guideline. J Clin Oncol. 2006;24:3187–3205.
Oncology NCCNCPGi. Myeloid growth factors (v.1.2010).
http://wwwnccnorg/professionals/physician_gls/pdf/myeloid_growthpdf. Accessed June 21, 2010.
Oncology Group. J Clin Oncol. 1995;13:1632–1641.
Radiat Oncol Biol Phys. 2001;50:1161–1171.
factors: where are we now? Support Care Cancer. 2010;18:529–541.
shock: need for better strategies. J Infect. 2001;42:120–125.
fungal infection in febrile neutropenic patients. Curr Opin Infect Dis. 2010;23(6):567–577.
chemotherapy for acute myeloid leukaemia. Scand J Infect Dis. 2010;42:97–101.
pediatric population with febrile neutropenia and cancer. Pediatr Hematol Oncol. 2009;26:414–425.
management. Ann Oncol. 2008;19:984–989.
diagnosis and treatment. J Antimicrob Chemother. 2009;63(Suppl 1):i31–i35.
study. J Clin Oncol. 2010;28:667–674.
Database Syst Rev. 2013;(10):CD003992.
febrile patients with neutropenia during cancer chemotherapy. N EnglJ Med. 1999;341:305–311.
Kern WV et al. Oral versus intravenous empirical antimicrobial therapy for fever in patients with
randomized controlled trials. J Antimicrob Chemother. 2006;57:176–189.
ceftazidime versus imipenem. J Clin Oncol. 1995;13:165–176.
cancer patients? Cancer. 1998;82:2449–2458.
hematologic malignancies. Clin Infect Dis. 2006;43:447–459.
Infect Dis. 2004;39(Suppl 1):S56–S58.
patients. Am J Med. 1986;80:96–100.
N EnglJ Med. 1987;317:1692–1698.
febrile neutropenic patients: a meta-analysis. Lancet Infect Dis. 2002;2:231–242.
neutropaenia. Cochrane Database Syst Rev. 2002;(2):CD003038.
neutropenic patients compared with standard therapy. Am J Hematol. 1998;58:293–297.
in febrile neutropenic patients. A randomized, double-blind trial. Ann Intern Med. 2002;137:77–87.
for empiric treatment of febrile neutropenic patients. Am J Med. 1989;87:278S–282S.
empiric treatment of fever in neutropenic patients. Antimicrob Agents Chemother. 1989;33:87–91.
patients with cancer. Cochrane Database Syst Rev. 2014;(1):CD003914.
impact of empirical administration of vancomycin. Eur J Cancer. 1996;32A:1332–1339.
autologous peripheral blood stem cell transplants. Bone Marrow Transplant. 1998;21:923–926.
Database Syst Rev. 2005;(3):CD003914.
Antimicrob Agents. 2000;14:129–135.
nephrotoxicity and ototoxicity. Antimicrob Agents Chemother. 1999;43:1549–1555.
patients with and without concomitant piperacillin-tazobactam. Pharmacotherapy. 2014;34:670–676.
vitro. Antimicrob Agents Chemother. 2014;58:1028–1033.
febrile neutropenic patients with cancer. Clin Infect Dis. 2006;42:597–607.
bloodstream infections in cancer patients. Int J Antimicrob Agents. 2010;36:182–186.
Rimawi RH et al. Ceftaroline—a cause for neutropenia. J Clin Pharm Ther. 2013;38:330–332.
Varada NL et al. Agranulocytosis with ceftaroline high-dose monotherapy or combination therapy with
clindamycin. Pharmacotherapy. 2015;35:608–612.
Yam FK, Kwan BK. A case of profound neutropenia and agranulocytosis associated with off-label use of
ceftaroline. Am J Health Syst Pharm. 2014;71:1457–1461.
cancer. J Pediatr Hematol Oncol. 2002;24:714–716.
Support Care Cancer. 2000;8:198–202.
neutropenia: a retrospective observationalstudy. J Antimicrob Chemother. 2014;69:2556–2562.
pediatric patients. Infection. 1998;26:396–398.
neutropenic adults. Antimicrob Agents Chemother. 1998;42:849–856.
malignancy. J Antimicrob Chemother. 1994;34:809–812.
Aust N Z J Med. 1998;28:311–315.
systematic review and meta-analysis. J Antimicrob Chemother. 2011;66:251–259.
Cancer Treat Rev. 2004;30:119–126.
Diseases Society of America. Clin Infect Dis. 2009;48:503–535.
of pyrexia of unknown origin in neutropenic patients. Br J Haematol. 1997;98:711–718.
versus amphotericin B lipid complex in the empirical treatment of febrile neutropenia. L Amph/ABLC
Collaborative Study Group. Clin Infect Dis. 2000;31:1155–1163.
patients with neutropenia and persistent fever. N EnglJ Med. 2002;346:225–234.
in the empirical treatment of fever and neutropenia. Clin Infect Dis. 1998;27:296–302.
controlled trial. BMJ. 2001;322:579–582.
cancer patients with prolonged fever and neutropenia. Am J Med. 1998;105:478–483.
therapy of febrile neutropenic patients with cancer. Am J Med. 2000;108:282–289.
persistent fever and neutropenia. N EnglJ Med. 2004;351:1391–1402.
transfusions. Ann Hematol. 2002;81:273–281.
Acute retroviralsyndrome is characterized by nonspecific symptoms,
such as fever, lymphadenopathy, rash, fatigue, and night sweats that
coincide with an initial burst of viremia. These symptoms, as well as the
presence of an opportunistic infection, and high-risk sexual or drug-using
behaviors, warrant human immunodeficiency virus (HIV) testing. With
current antigen/antibody laboratory tests, HIV can be diagnosed as
early as 2 weeks after infection. In patients in whom very early
infection (<2 weeks) is suspected, nucleic acid tests for HIV RNA may
be considered for diagnostic purposes.
HIV RNA viral load is measured to quantify the level of viral replication
in the body and CD4 cell counts are followed to assess immune system
Antiretroviral therapy should be offered to all patients who are willing
and able to commit to lifelong treatment after a discussion of the
benefits and risks of highly active antiretroviral therapy (HAART) and
the importance of adherence. Clinicalsituations which favor more
urgent initiation of HAART include pregnancy; AIDS-defining condition
rapidly declining CD4 count (>100 cells/μL decrease per year); higher
baseline viral load (>100,000 copies/mL); and acute/early HIV infection.
US Department of Health and Human Services (DHHS) guidelines
provide recommendations for optimal antiretroviral therapy.
Goals of antiretroviral therapy include suppression of viral load,
preservation and strengthening of the immune system, limitation of drug
adverse events, promotion of adherence, and prevention of HIV-related
General rules of therapy involve selection of HAART-based regimen,
optimization of the selected agents, and inclusion of quality of life in
After initiating a HAART regimen, short-term goals include resolution of
symptoms, at least a threefold (0.5 log) decrease in HIV RNA at 1
month, a tenfold decrease (1.0 log) in HIV RNA at 2 months, and an
increase in CD4 count at 3 to 4 months. Long-term assessments include
the monitoring of HIV RNA and CD4 count every 3 to 6 months to
identify treatment failures, assessment of medication adherence, and
determination of tolerability and quality of life.
General rules for changing failing regimens include switching to at least
two new active drugs (although all new drugs are preferable), as quickly
as possible after treatment failure to avoid accumulation of resistance
mutations. To avoid the development of further resistance, a single drug
should never be added to a failing regimen. If one drug must be
discontinued, the whole regimen should be stopped simultaneously.
Finally, previously failed regimens should never be restarted because of
No comments:
Post a Comment
اكتب تعليق حول الموضوع