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November 2025


Tularemia treatment and prophylaxis recommendations
The graphic shows an image of a neck mass caused by tularemia with text that reads, “Francisella tularensis, the bacteria that causes tularemia, occurs naturally and is a potential bioweapon. Treatment guidelines have been updated.” A chart shows first line therapy options for adults, neonates, and pregnant women.

Tularemia, caused by Francisella tularensis bacteria, occurs naturally in the United States. A person can get tularemia from a bite from an infected arthropod (e.g., ticks and deer flies), contact with infected animals, ingestion of contaminated meat or water, contact with contaminated soil or hay, or inhalation of aerosolized particles. Because F. tularensis has a low infectious inoculum, it is classified as a potential bioterrorism agent that could infect thousands of people if intentionally released. CDC updated clinical guidelines to provide best practices for treatment and prophylaxis of human tularemia for both naturally occurring disease and after a bioterrorism attack.

Notable changes compared to previously published guidelines include:
  • Designation of fluoroquinolones (ciprofloxacin or levofloxacin) and doxycycline as first-line treatment options for outbreaks of any size
  • Identification of third-tier treatment options when first-line and alternative antimicrobials are unavailable or contraindicated for certain patients
  • Recommendations for neonates, breastfeeding infants, lactating mothers, and patients with immunocompromise or who are geriatric
Learn more:

MMWR: Tularemia Antimicrobial Treatment and Prophylaxis: CDC Recommendations for Naturally Acquired Infections and Bioterrorism Response — United States, 2025

CDC: Guidelines, Recommendations and Resources

About Tularemia

 

Hepatitis B and shared glucometers
The image shows a vial of hepatitis B vaccine and a clinician using a blood glucose monitor to check a patient’s blood sugar. Text reads, “Hepatitis B virus (HBV) was transmitted in a nursing home through a shared glucometer. Nursing homes, protect residents who have diabetes: offer routine HBV vaccination; use a dedicated glucometer for each resident. If shared glucometers are used, they should be those designed for use in professional settings and cleaned and disinfected after every use.”

(HBV) was transmitted in a nursing home through a shared glucometer. Nursing homes, protect residents who have diabetes: offer routine HBV vaccination; use a dedicated glucometer for each resident. If shared glucometers are used, they should be those designed for use in professional settings and cleaned and disinfected after every use.”

 In May 2024, the North Carolina Division of Public Health was notified that a hospitalized patient with diabetes had received a diagnosis of acute hepatitis B virus (HBV) infection after being transferred from a skilled nursing facility. The patient’s diabetes management included regular blood glucose monitoring. The patient had no documented history of hepatitis B or hepatitis B vaccination. Investigation revealed that glucometers at the skilled nursing facility were shared among several residents and observed to be disinfected per manufacturer instructions between uses. No other gaps in infection control practices were observed. Hepatitis B testing identified one skilled nursing facility resident with a previously diagnosed and unreported chronic HBV infection who had also received daily assisted blood glucose monitoring during a period that overlapped with the estimated incubation period of the newly infected resident. The newly infected resident repeatedly underwent monitoring <1 minute following the resident with chronic HBV infection, an interval that might not have allowed for adequate disinfection. Whole genome sequencing analysis demonstrated that both residents were infected with a genetically identical HBV strain.

Bottom Line:
  • Sharing glucometers, even when disinfection protocols are followed, can present a risk for HBV transmission.
  • CDC recommends assigning blood glucose monitors (glucometers) to one person.
  • CDC recommends universal hepatitis B vaccination for persons aged <60 years and, based on shared clinical decision making, also recommends hepatitis B vaccination for adults aged ≥60 years at higher risk for hepatitis B, such as those with diabetes.
Learn more:

MMWR: Notes from the Field: Hepatitis B Virus Transmission Associated with Assisted Blood Glucose Monitoring in a Skilled Nursing Facility — North Carolina, 2024

Universal Hepatitis B Vaccination in Adults Aged 19–59 Years: Updated Recommendations of the Advisory Committee on Immunization Practices — United States, 2022

CDC: Considerations for Blood Glucose Monitoring and Insulin Administration

Clinical Care of Plague

Other: Use of hepatitis B vaccination for adults with diabetes mellitus: recommendations of the Advisory Committee on Immunization Practices (ACIP)

 

Influenza vaccines
The image shows a person with a bandage on their upper arm. Text reads, “Fight flu. It’s not too late to vaccinate your patients against influenza.”

Influenza vaccination protects against influenza and its potential complications. This report updates the 2024–25 recommendations of the Advisory Committee on Immunization Practices (ACIP) concerning the use of seasonal influenza vaccines in the United States for the 2025–26 influenza season. Updates include approval of FluMist (nasal spray live attenuated influenza vaccine) for self-administration or caregiver administration and expansion of the approved age threshold for Flublok (recombinant influenza vaccine) from ≥18 years to ≥9 years.

Bottom Line:
  • Routine annual influenza vaccination is recommended for all persons aged ≥6 months without a contraindication to vaccination to protect against influenza and its complications.
  • Vaccination should continue after October and throughout the influenza season as long as influenza viruses are circulating and unexpired vaccine is available.
Learn more:

MMWR: Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2025–26 Influenza Season

 

Lenacapavir as HIV preexposure prophylaxis
The image shows a patient talking to a clinician. Text reads, “Eligibility for use of injectable lenacapavir for HIV PrEP: Weight 77 pounds or more and with increased chances of getting HIV; No signs or symptoms of acute HIV infection; Negative blood-based HIV antigen/antibody test result within 7 days before first dose; Negative confirmatory HIV RNA test, if available; No known significant drug interactions or contraindications.”

HIV preexposure prophylaxis (PrEP) reduces HIV incidence; however, adherence to available PrEP regimens is suboptimal. In June 2025, FDA approved injectable lenacapavir (LEN) administered every 6 months as HIV PrEP, based on results from two randomized controlled trials (RCTs) that reported LEN efficacy at reducing HIV infection as 100% among females and 96% among a primarily male trial population over a follow-up of 52 weeks. Based on efficacy and safety demonstrated by the two RCTs, the CDC PrEP Guidelines Work Group strongly recommends administering LEN as an HIV PrEP option in persons weighing ≥77 lbs (≥35 kg) who would benefit from PrEP.

Bottom Line:
  • CDC strongly recommends lenacapavir injections every 6 months as an HIV PrEP option in persons weighing ≥77 lbs (≥35 kg) who would benefit from PrEP.
  • LEN has the potential to improve PrEP adherence and thus enhance HIV prevention in the United States.
Learn more:

MMWR: Clinical Recommendation for the Use of Injectable Lenacapavir as HIV Preexposure Prophylaxis — United States, 2025

CDC: Clinical Guidance for PrEP

 

Neisseria meningitidis conjunctivitis

Neisseria meningitidis is an unusual cause of bacterial conjunctivitis. Forty-one cases of N. meningitidis conjunctivitis caused by an unencapsulated (nongroupable) strain of N. meningitidis identified by whole genome sequencing occurred in young, healthy military trainees living in a communal setting; all had received quadrivalent meningococcal vaccine. No source was identified. One patient developed periorbital cellulitis and received intravenous antibiotics; all other patients were treated successfully with topical antibiotics.

Bottom Line:
  • Neisseria meningitidisis an unusual cause of conjunctivitis.
  • When outbreaks of mucopurulent conjunctivitis occur in congregate living settings such as military barracks or school dormitories, culturing exudate can identify outbreak etiology, and whole genome sequencing can help guide treatment and response.
  • Despite the invasive infectious risk posed by nongroupable N. meningitidis conjunctivitis in otherwise healthy persons might be successfully treated with topical antimicrobials.
Learn more:

MMWR: Outbreak of Neisseria meningitidis Conjunctivitis in Military Trainees — Texas, February–May 2025

CDC: Clinical Overview of Pink Eye (Conjunctivitis)


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