It’s with great sadness to let you know that Itzhak passed away peacefully on Jan 10, 2025 from cancer, surrounded by his family at home.
We miss Itzhak dearly; you can read more about his life here.
This site was created by Itzhak Brook MD. It explains the diagnosis, causes, treatment and complications of sinusitis. Dr. Brook is a Professor of Pediatrics at Georgetown University Washington D.C.
It’s with great sadness to let you know that Itzhak passed away peacefully on Jan 10, 2025 from cancer, surrounded by his family at home.
We miss Itzhak dearly; you can read more about his life here.
Intracranial pyogenic complications of sinusitis in children can lead to serious sequelae. Smiljkovic and colleagues from the Hospital for Sick Children, Toronto, Canada; characterized the clinical, epidemiologic and microbiologic characteristics of children with such complications over a 20-year period.
One hundred and four cases of complicated sinusitis were
included after review. The most frequent complications were epidural empyema (n
= 50, 48%), subdural empyema (n = 46, 44%) and Pott's puffy tumor (n = 27,
26%). 52% (n = 54) underwent neurosurgery and 46% (n = 48) underwent
otolaryngological surgery. The predominant pathogen isolated from sterile site
specimens was Streptococcus anginosus (n = 40, 63%), but polymicrobial growth
was common (n = 24; 38%). The median duration of intravenous antibiotic therapy
was 51 days (IQR 42-80). Persistent neurological sequelae (or death, n = 1)
were found in 24% (n = 25) and were associated with the presence of cerebritis
and extensive disease on neuroimaging (P = 0.02 and P = 0.04, respectively).
The authors concluded that Intracranial complications of sinusitis
continue to cause significant morbidity in children. Polymicrobial aerobic anaerobic infections
are common, which reinforces the need for broad-spectrum empiric antibiotic
therapy and cautious adjustment of the antibiotic regimen based primarily on
sterile site cultures. The association of neurologic sequelae with the presence
of cerebritis and extensive intracranial involvement on neuroimaging suggest
that delayed diagnosis may be a contributor to adverse outcome.
In the wake of the ongoing Coronavirus Disease 2019 (COVID-19) pandemic, a new epidemic of COVID associated mucormycosis (CAM) emerged in India.
Early diagnosis and prompt treatment of this deadly disease are of paramount importance in improving patient survival. MRI is the cornerstone of diagnosis of early extrasinus disease, particularly intracranial complications which have traditionally been associated with a high mortality rate.
Sehgal et al from Maulana Azad Medical College and Lok Nayak Hospital, New Delhi India ; presented the sinonasal, perisinus, orbital and intracranial involvement in CAM. The aim of the review is to familiarise the reader with the MR imaging spectrum of CAM with special focus on intracranial complications and a brief account of their impact on patient prognosis in the author's experience.
Special emphasis is made on intracranial disease which is categorized into vascular, parenchymal, meningeal, bony involvement and perineural spread. Vascular complications are the most common form of intracranial involvement. Some unusual yet interesting imaging findings such as nerve abscesses involving the optic, trigeminal and mandibular nerves and long segment vasculitis of the internal carotid artery extending till its cervical segment are also illustrated. In our experience, patient outcome in CAM (survival rate of 88.5%) was better compared to the pre-pandemic era. Presence of intracranial disease also did not affect prognosis as poorly as traditionally expected (survival rate of 82.8%). Involvement of brain parenchyma was the only subset of intracranial involvement that was associated with higher mortality (p value 0.016).
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The US Food and Drug Administration (FDA) has issued
guidelines for the pharmaceutical industry for developing antimicrobials for the
treatment of acute bacterial sinusitis (ABS). The FDA stated that any new drug being studied for ABS should have documenting in-vitro antibacterial activity against the most commonly pathogens associated with ABS. These include Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis. Even though animal models of ABS has been developed, particularly for S. pneumoniae infection, they cannot substitute for clinical trials in patients that must be conducted to evaluate drug safety and efficacy. The FDA recommend that two adequate and well-controlled human trials establishing safety and efficacy be conducted for that indication. However, a single trial for an ABS indication may be appropriate if there is data from other clinical trials demonstrating effectiveness in other respiratory tract diseases such as community acquired bacterial pneumonia.
Additional supportive information like pharmacokinetic and
pharmacodynamic studies demonstrating concentration of the antibacterial drug
in the sinuses at a level expected to be active against the common pathogens
causing ABS would be required. Because direct assessment of ABS symptoms to
support a conclusion of treatment benefit in response to antibacterial drug
therapies is readily measured no surrogate markers of success of therapy are
needed.
Antimicrobials with clinically significant toxicity would not be considered appropriate for study of ABS unless treatment of a more seriously ill patient population is being considered.
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