Guideline for Management of Fever and Neutropenia in Children with Cancer and/or Undergoing Hematopoietic Stem Cell Transplantation - Flowchart
Guideline for Management of Fever and Neutropenia in Children with Cancer and/or Undergoing Hematopoietic Stem Cell Transplantation - Flowchart Fever and Neutropenia, Pediatric Patient Fever and Neutropenia, Pediatric Patient
«Flowchart»

Fever (>38.3�C or >38�C sustained for 1 hr), with an ANC of <500 or an ANC expected to fall to <500 in the next 48 hr

Fever (>38.3�C or >38�C sustained for 1 hr), with an ANC of <500 or an ANC expected to fall to <500 in the next 48 hr

Fever (>38.3�C or >38�C sustained for 1 hr), with an ANC of <500 or an ANC expected to fall to <500 in the next 48 hr

Clinical change

Clinical change

Clinical change

Clinical change

Clinical change

Clinical change

Persistent or new fever after >96 hr

Persistent or new fever after >96 hr

Persistent or new fever after >96 hr

Defervescence

Defervescence

Defervescence

Repeat blood and urine cultures every 24 hr
Start empirical fungal treatment with a mold-active antifungal agent
Consider imaging of sinuses, chest, abdomen, and pelvis, looking for an infectious nidus
Biweekly galactomannan levels

Repeat blood and urine cultures every 24 hr
Start empirical fungal treatment with a mold-active antifungal agent
Consider imaging of sinuses, chest, abdomen, and pelvis, looking for an infectious nidus
Biweekly galactomannan levels

Repeat blood and urine cultures every 24 hr
Start empirical fungal treatment with a mold-active antifungal agent
Consider imaging of sinuses, chest, abdomen, and pelvis, looking for an infectious nidus
Biweekly galactomannan levels




Clinically unstable

Cover GP, GN, and anaerobes
Double-cover Pseudomonas
MRSA coverage

Clinically unstable

Cover GP, GN, and anaerobes
Double-cover Pseudomonas
MRSA coverage

Clinically unstable

Clinically unstable

Cover GP, GN, and anaerobes
Double-cover Pseudomonas
MRSA coverage


Pseudomonas

Follow cultures, adjust Abx accordingly.
Continue Abx until count recovery (ANC >200 and rising)

Follow cultures, adjust Abx accordingly.
Continue Abx until count recovery (ANC >200 and rising)

Follow cultures, adjust Abx accordingly.
Continue Abx until count recovery (ANC >200 and rising)


End

End

End

Defervescence

Defervescence

Defervescence

* Antibiotic selection should account for local resistance patterns as well as prior infections with resistant organisms. Commonly used monotherapies include antipseudomonal β-lactams and fourth-generation cephalosporins or carbapenems.

* Antibiotic selection should account for local resistance patterns as well as prior infections with resistant organisms. Commonly used monotherapies include antipseudomonal β-lactams and fourth-generation cephalosporins or carbapenems.

* Antibiotic selection should account for local resistance patterns as well as prior infections with resistant organisms. Commonly used monotherapies include antipseudomonal β-lactams and fourth-generation cephalosporins or carbapenems.

* β

Clinically stable

Broad spectrum GP and GN coverage, including pseudomonal coverage* (minimum of 48 hr)
If HSCT, recent high-dose cyclophosphamide, AML induction or consolidation, ALL relapse induction, intensification, or GVHD, consider MRSA coverage for 48 hr

Clinically stable

Broad spectrum GP and GN coverage, including pseudomonal coverage* (minimum of 48 hr)
If HSCT, recent high-dose cyclophosphamide, AML induction or consolidation, ALL relapse induction, intensification, or GVHD, consider MRSA coverage for 48 hr

Clinically stable

Clinically stable

Broad spectrum GP and GN coverage, including pseudomonal coverage* (minimum of 48 hr)
If HSCT, recent high-dose cyclophosphamide, AML induction or consolidation, ALL relapse induction, intensification, or GVHD, consider MRSA coverage for 48 hr

* *

Defervescence

Defervescence

Defervescence

Persistent or new fever after >96 hr

Persistent or new fever after >96 hr

Persistent or new fever after >96 hr

Thorough physical examination, including oropharynx, skin, lines/port sites, and perianal area
Laboratory tests: CBC + diff, blood cultures, noncatheterized urine culture, electrolytes, and LFTs
Imaging: CXR or abdominal CT as dictated by symptoms

Thorough physical examination, including oropharynx, skin, lines/port sites, and perianal area
Laboratory tests: CBC + diff, blood cultures, noncatheterized urine culture, electrolytes, and LFTs
Imaging: CXR or abdominal CT as dictated by symptoms

Thorough physical examination, including oropharynx, skin, lines/port sites, and perianal area
Laboratory tests: CBC + diff, blood cultures, noncatheterized urine culture, electrolytes, and LFTs
Imaging: CXR or abdominal CT as dictated by symptoms



Clinically stable

Broad spectrum GP and GN coverage, including pseudomonal coverage* (minimum of 48 hr)
If HSCT, recent high-dose cyclophosphamide, AML induction or consolidation, ALL relapse induction, intensification, or GVHD, consider MRSA coverage for 48 hr

Clinically stable

Clinically stable

Broad spectrum GP and GN coverage, including pseudomonal coverage* (minimum of 48 hr)
If HSCT, recent high-dose cyclophosphamide, AML induction or consolidation, ALL relapse induction, intensification, or GVHD, consider MRSA coverage for 48 hr

* *
Clinically stable

Clinically unstable

Cover GP, GN, and anaerobes
Double-cover Pseudomonas
MRSA coverage

Clinically unstable

Clinically unstable

Cover GP, GN, and anaerobes
Double-cover Pseudomonas
MRSA coverage


Pseudomonas Pseudomonas
Clinically unstable