Haemophilus influenzae is a gram-negative coccobacillus that colonizes the nasopharyngeal surface and upper respiratory tract of healthy individuals and includes six encapsulated serotypes as well as non-encapsulated, non-typeable strains. Since the widespread use of the Haemophilus influenzae type b (Hib) conjugate vaccine implemented in 1990, the majority of invasive illness now seen in the United States is secondary to capsular serotypes other than type b and non-typeable strains with the largest burden of disease affecting the extremes of age-infants and the elderly. We report a case of acute Haemophilus influenzae type f meningitis in a 12-month-old female who was previously healthy and had been fully immunized. She demonstrated clinical improvement on ceftriaxone, but persistent fever and ear-tugging resulted in obtaining an MRI that displayed bilateral subdural empyemas requiring burr-hole craniotomy, central venous thrombosis requiring anticoagulation, and bilateral sensorineural hearing loss requiring cochlear implants. Immunological studies confirmed immunocompetency and appropriate response to her previous Hib vaccination, suggesting a significant impact of bacterial virulence. These complications, with the exception of sensorineural hearing loss, have not been reported in the literature for Haemophilus influenzae type f and should be considered in the care of these patients despite clinical appearance given the severity of complications and potential for acute decompensation. Despite the success of vaccination in reducing invasive disease, cases of H. influenzae meningitis continue to occur via less common encapsulated serotypes with unknown complications, making the management and treatment of these infections more difficult for practitioners.
Haemophilus influenzae is a gram-negative coccobacillus that colonizes the nasopharyngeal surface and upper respiratory tract of healthy individuals and includes six encapsulated serotypes as well as non-encapsulated, non-typeable strains [1, 2]. Since the widespread use of the Haemophilus influenzae type b (Hib) conjugate vaccine implemented in 1990, the majority of invasive illness in the United States is secondary to capsular serotypes other than type b and non-typeable strains with the largest burden of disease affecting the extremes of age-infants and the elderly [3-5]. We report a case of acute bacterial meningitis in a previously healthy, fully immunized 12-month-old female. The pathogen was identified as Haemophilus influenzae type f and was successfully treated with a four-week course of ceftriaxone.
A 12-month-old, previously healthy, fully immunized female developed cough, congestion, vomiting, and fever with poor oral intake and decreased urine output leading to first presentation at the emergency department. She showed improvement in activity level during the evaluation and was discharged home with a clinical diagnosis of a viral upper respiratory infection. Over the next four days, she had normal oral intake and urine output, but continued to have decreased activity level, congestion, mild cough, and fever despite scheduled antipyretics. Her parents noted that she was fussy, refused to sit up, and was not acting like herself. She developed increased work of breathing which prompted a second presentation to the emergency department. She was noted to be afebrile, awake, and alert but was significantly irritable with nuchal rigidity. Cranial imaging was not performed, but lumbar puncture revealed cloudy cerebrospinal fluid (CSF) concerning for bacterial meningitis. Initial CSF studies revealed: Glucose <4 mg/dL, protein 107 mg/dL, Leukocyte count 4,063 cells/cmm, and 89% neutrophils. She was empirically started on ceftriaxone and vancomycin and admitted for bacterial meningitis.
CSF cultures eventually grew H. influenzae type f sensitive to ceftriaxone. Respiratory swab revealed adenovirus co-infection. She improved clinically in terms of alertness and activity level with down-trending leukocytosis and inflammatory markers but continued to spike fevers despite scheduled antipyretics and was noted to be tugging at her right ear. A magnetic resonance imaging (MRI) scan was obtained, which showed bilateral subdural empyema (SDE), central venous thrombosis, and enhancement of inner ears (Figure 1).
Right-sided burr-hole craniotomy was performed to drain the empyema for further source control; cultures of the purulent drainage were negative. The central venous thrombosis was treated with heparin infusion with transition to enoxaparin. Repeat MRI showed improving empyema (Figure 2), but persistent labyrinthitis (Figure 3). Given the severity of her presentation, immunological studies (Table 1) were performed and confirmed she was immunocompetent and had responded to her previous Hib vaccination. To assess for functional asplenia, a blood smear was performed and showed no Howell-Jolly bodies.
Intravenous antibiotics were administered for four weeks and discontinued based on resolution of findings previously seen on MRI. Enoxaparin was administered for a total of six weeks. Auditory Brainstem Response testing performed during repeat MRI showed profound bilateral sensorineural hearing loss, requiring bilateral cochlear implants and tympanostomy tubes.
We report a case of a 12-month-old, immunocompetent female that presented with Haemophilus influenza type f meningitis and a clinical course complicated by bilateral subdural empyemas, central venous thrombosis, and bilateral sensorineural hearing loss. Her initial presentation was significant for viral infection positive for adenovirus and recent history of bilateral acute otitis media which may have predisposed her to colonization and infection [6, 7]. Apart from sensorineural hearing loss, these complications have not been reported in the literature for Haemophilus influenzae type f [8, 9] and should be considered in the care of these patients despite clinical appearance given the severity of complications and potential for acute decompensation. In this case, our patient showed clinical improvement in terms of temperament, behavior, and nuchal rigidity after IV antibiotic administration as well as down-trending inflammatory markers. However, subtle findings of ear tugging and persistent fever prompted further investigation leading to MRI imaging and further source control. This serves as a reminder for providers to maintain a high index of suspicion for complications in cases of bacterial meningitis, such as SDE, as symptoms may be subtle .
In infants, bacterial meningitis is the main cause of SDE . Up to 2% of patients with bacterial meningitis will develop SDE . The main features are fever, seizure, and impaired consciousness, which is difficult to discern from meningitis. Thus, imaging is needed to diagnose SDE; cranial ultrasonography is feasible in low resource settings, while high resolution contrast CT and contrast enhanced MRI are the gold standard for diagnosis . Further considerations in the treatment of SDE include a prolonged antibiotic course as well as surgical intervention. Surgical strategies include burr hole drainage as a less invasive approach with comparable clinical outcomes to craniotomy .
Non-type b serotypes of Haemophilus influenza, notably serotype f, are growing in prevalence [13, 14]. In children, pneumonia and meningitis are the most common forms of type f infection, while pneumonia is most common in adults . Additionally, the majority of invasive non-type b Hi cases are seen in immunocompetent patients with no predisposing factors, thereby suggesting a significant impact of bacterial virulence . In response to these growing numbers, non-typable, broad coverage Hi vaccines are currently being developed [17, 18]. In the meantime, this report aims to contribute to the understanding of this decreasingly rare disease, thereby helping in management of these patients.
Despite the success of vaccination in reducing invasive disease, cases of H. influenzae meningitis continue to occur via less common encapsulated serotypes with unknown complications making the management and treatment of these infections more difficult for practitioners. Continued reporting of these non-type b cases will aid in achieving further understanding and appropriate management.
- Ladhani SN, Collins S, Vikers A, Litt DJ, Crawford C, Ramsay ME, Slack MP: Invasive Haemophilus influenzae serotype e and f disease, England and Wales. Emerg Infect Dis. 2012, 18:725-732. 10.3201/eid1805.111738
- Oikonomou K, Alhaddad B, Kelly K, Rajmane R, Apergis G: Haemophilus influenzae serotype f endocarditis and septic arthritis. IDCases. 2017, 9:79-81. 10.1016/j.idcr.2017.06.008
- Bender JM, Cox CM, Mottice S, She RC, Korgenski K, Daly JA, Pavia AT: Invasive Haemophilus influenzae disease in Utah children: an 11-year population-based study in the era of conjugate vaccine. Clin Infect Dis. 2010, 50:41-46. 10.1086/651165
- Macneil JR, Cohn AC, Farley M, et al.: Current epidemiology and trends in invasive Haemophilus influenzae disease - United States, 1989-2008. Clin Infect Dis. 2011, 53:1230-1236. 10.1093/cid/cir735
- Soeters HM, Blain A, Pondo T, et al.: Current epidemiology and trends in invasive Haemophilus influenzae disease - United States, 2009-2015. Clin Infect Dis. 2018, 67:881-889. 10.1093/cid/ciy187
- Berndsen MR, Erlendsdottir H, Gottfredsson M: Evolving epidemiology of invasive Haemophilus infections in the post-vaccination era: results from a long-term population study. Clin Microbiol Infect. 2012, 18:918-923. 10.1111/j.1469-0691.2011.03700.x
- Cardoso MP, Pasternak J, Giglio AE, Casagrande RR, Troster EJ: Meningitis due to Haemophilus influenzae type f. Einstein (Sao Paulo). 2013, 11:521-523. 10.1590/S1679-45082013000400020
- Ronit A, Berg RM, Bruunsgaard H, Plovsing RR: Haemophilus influenzae type f meningitis in a previously healthy boy. BMJ Case Rep. 2013, 2013:bcr2013008854. 10.1136/bcr-2013-008854
- Pincus DR, Robson JMB: Meningitis due to Haemophilus influenzae type f. J Paediatr Child Health. 1998, 34:95-96.
- Muzumdar D, Biyani N, Deopujari C: Subdural empyema in children. Childs Nerv Syst. 2018, 34:1881-1887. 10.1007/s00381-018-3907-6
- Liu ZH, Chen NY, Tu PH, Lee ST, Wu CT: The treatment and outcome of postmeningitic subdural empyema in infants. J Neurosurg Pediatr. 2010, 6:38-42. 10.3171/2010.4.PEDS09433
- Agrawal A, Timothy J, Pandit L, Shetty L, Shetty JP: A review of subdural empyema and its management. Infect Dis Clin Pract. 2007, 15:149-153. 10.1097/01.idc.0000269905.67284.c7
- Whittaker R, Economopoulou A, Dias J, et al.: Epidemiology of invasive Haemophilus influenzae disease, Europe, 2007-2014. Emerg Infect Dis. 2017, 23:396-404. 10.3201/eid2303.161552
- Rubach MP, Bender JM, Mottice S, et al.: Increasing incidence of invasive Haemophilus influenzae disease in adults, Utah, USA. Emerg Infect Dis. 2011, 17:1645-1650. 10.3201/eid1709.101991
- Urwin G, Krohn JA, Deaver-Robinson K, Wenger JD, Farley MM: Invasive disease due to Haemophilus influenzae serotype f: clinical and epidemiologic characteristics in the H. influenzae serotype b vaccine era. The Haemophilus influenzae Study Group. Clin Infect Dis. 1996, 22:1069-1076. 10.1093/clinids/22.6.1069
- Resman F, Ristovski M, Ahl J, et al.: Invasive disease caused by Haemophilus influenzae in Sweden 1997-2009; evidence of increasing incidence and clinical burden of non-type b strains. Clin Microbiol Infect. 2011, 17:1638-1645. 10.1111/j.1469-0691.2010.03417.x
- Prymula R, Schuerman L: 10-valent pneumococcal nontypeable Haemophilus influenzae PD conjugate vaccine: Synflorix™. Expert Rev Vaccines. 2009, 8:1479-1500. 10.1586/erv.09.113
- Murphy TF: Vaccine development for non-typeable Haemophilus influenzae and horaxella catarrhalis: progress and challenges. Expert Rev Vaccines. 2005, 4:843-853. 10.1586/14760522.214.171.1243
Haemophilus influenzae Type f Meningitis Complicated by Bilateral Subdural Empyema, Central Venous Thrombosis, and Bilateral Sensorineural Hearing Loss in an Immunocompetent 12-month-old
Ethics Statement and Conflict of Interest Disclosures
Human subjects: Consent was obtained by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Cite this article as:
Abou-Hanna J, Panning K, Mehta H (June 06, 2019) Haemophilus influenzae Type f Meningitis Complicated by Bilateral Subdural Empyema, Central Venous Thrombosis, and Bilateral Sensorineural Hearing Loss in an Immunocompetent 12-month-old. Cureus 11(6): e4850. doi:10.7759/cureus.4850
Received by Cureus: April 29, 2019
Peer review began: May 07, 2019
Peer review concluded: May 29, 2019
Published: June 06, 2019
© Copyright 2019
Abou-Hanna et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 3.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.