From the Guidelines
Ciprofloxacin is recommended as prophylaxis in allogeneic hematopoietic stem cell transplantation to prevent bacterial infections during the period of neutropenia, with a typical regimen of 500 mg orally twice daily, as it has been shown to reduce the incidence of gram-negative bacteremia and febrile neutropenia episodes in transplant recipients 1.
Key Points
- The use of ciprofloxacin as prophylaxis in allogeneic stem cell transplant patients is supported by guidelines from the Infectious Diseases Working Party of the German Society of Haematology and Oncology 1.
- Ciprofloxacin primarily targets gram-negative bacteria, particularly Pseudomonas aeruginosa and Enterobacteriaceae, which pose significant risks during neutropenia.
- The typical regimen involves administering ciprofloxacin 500 mg orally twice daily, starting at the beginning of conditioning chemotherapy and continuing until neutrophil recovery (ANC >500 cells/μL) or until broad-spectrum antibiotics are initiated for febrile neutropenia.
- Clinicians should be aware of potential side effects including tendon inflammation, QT prolongation, and C. difficile infection, and institutional antibiograms should guide prophylaxis decisions to minimize resistance development and adverse effects.
Considerations
- The emergence of vancomycin-resistant cocci has become an important problem, and the mortality of Gram-positive infections is low, even after marrow transplantation, making additional Gram-positive prophylaxis not generally recommended 1.
- Pneumococcus prophylaxis is recommended for patients with active chronic graft-versus-host disease and lifelong after splenectomy, and patients under pneumocystis carinii pneumonia (PCP)-prophylaxis with trimethoprim/sulfamethoxazole will be protected sufficiently against pneumococci 1.
- The use of intravenous immunoglobulins for anti-infectious prophylaxis is generally not recommended due to controversial results 1.
From the Research
Role of Ciprofloxacin in Prophylaxis for Allogeneic Hematopoietic Stem Cell Transplantation
- Ciprofloxacin is used as prophylaxis to prevent infections in patients undergoing allogeneic hematopoietic stem cell transplantation 2, 3, 4.
- The use of ciprofloxacin as prophylaxis has been shown to reduce the incidence of gram-negative bacterial infections 3.
- However, the widespread use of ciprofloxacin has led to the emergence of resistant isolates, including Escherichia coli bacteremia 3.
- Studies have compared the efficacy of ciprofloxacin with other antibiotics, such as levofloxacin, in preventing infections in hematopoietic stem cell transplantation patients 2, 5.
- Levofloxacin has been shown to be associated with a lower incidence of febrile neutropenia and bacteremia compared to ciprofloxacin in some studies 2, 5.
- Ciprofloxacin prophylaxis has been shown to be effective in reducing the incidence of neutropenic fever and its complications in autologous stem cell transplantation patients 6.
- The use of ciprofloxacin prophylaxis has also been shown to reduce the duration of hospitalization and the incidence of bacteremia in some studies 6.
Comparison with Other Antibiotics
- Levofloxacin has been compared to ciprofloxacin in several studies, with some showing that levofloxacin is associated with a lower incidence of febrile neutropenia and bacteremia 2, 5.
- The choice of antibiotic for prophylaxis may depend on the specific patient population and the prevalence of resistant isolates in the institution 3.
- Further studies are needed to determine the optimal antibiotic prophylaxis regimen for allogeneic hematopoietic stem cell transplantation patients 2, 5.
Clinical Implications
- The use of ciprofloxacin prophylaxis in allogeneic hematopoietic stem cell transplantation patients requires careful consideration of the potential risks and benefits 3.
- Clinicians should be aware of the potential for resistant isolates to emerge with the widespread use of ciprofloxacin 3.
- The choice of antibiotic prophylaxis regimen should be individualized based on the specific patient population and the prevalence of resistant isolates in the institution 2, 5.