Neurologic Manifestations of Brucellosis Follow-up

  • Author: Robert Stanley Rust Jr, MD, MA; Chief Editor: Karen L Roos, MD   more...
 
Updated: Jan 11, 2010
 

Further Inpatient Care

Follow-up sampling of CSF in order to ensure clearance of evidence for inflammation or the presence of organisms is important in determining the efficacy and duration of antibiotic treatment.

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Further Outpatient Care

Follow-up care is needed to ensure compliance for a full 6-week course of antibiotics and to determine whether a relapse has occurred. In some instances, a relapsing and remitting course similar to MS develops. In such instances, treatment with triple therapy (as noted in Medical Care) may be undertaken for periods as long as 6 months or more.

The prognosis for meningoencephalitis is generally good. Chronic forms tend to have a less favorable prognosis. The granulomatous and arachnoiditic changes tend to respond to antibiotic therapy, but the chronic meningoencephalitic and polyradiculopathic processes are less responsive. Residual deficits, including deafness and weakness, may be found in a fair number of patients.

Relapsing brucellosis must be distinguished from instances in which patients experience reinfection. The degree of immunity induced by an initial attack of brucellosis may be inadequate to prevent reinfection. Second, third, or even more instances of reinfection may occur, especially in veterinarians and others individuals with continual exposure to animals. Some individuals acquire infection-induced hypersensitivity to Brucella antigens. This may result in a severe local reaction due to accidental self-inoculation with Brucella vaccines. Reactions of this sort are especially likely to be experienced by veterinarians and others who are responsible for inoculating animal herds.

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Deterrence/Prevention

Avoid consumption of unpasteurized milk and milk products, as well as raw or undercooked meats. Education may be provided to the patient and family concerning risks and should emphasize avoiding anything identified as a specific cause in the case at hand. Should the identified source be a live animal, the herd or flock from which it came should be investigated.

Scrupulous hygiene may prevent infection, especially when practiced by individuals likely to have close contact with goats, sheep, cows, camels, pigs, reindeer, rabbits, or hares. Obviously, this contact is of greatest importance in areas of endemic disease.

Considerable concern has been harbored by authorities concerning the utilization of Brucella species in biological weapons. Airborne transmission of these bacteria is readily achieved via the mucous membranes of the conjunctivae, nasal passages, oropharynx, and respiratory tract. Infection may occur as the result of lodging of organisms in cuts or abrasions. As few as 10-100 organisms may produce infection via aerosol exposure. The resulting disease may have any of the many various manifestations of which Brucella species are capable.

Bichat guidelines have been established for the management of individuals at risk for or manifesting evidence of brucellosis after bioterroristic exposure. Treatment regimens combining doxycycline with either streptomycin or rifampin are thought adequate in such situations and the combination of ofloxacin with rifampin is also cited. However, currently no evidence exists concerning efficacy of postexposure prophylaxis as a method of preventing brucellosis.[20]

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Complications

Initiation of antibiotic treatment may provoke the Jarisch-Herxheimer reaction with clinical worsening and CSF changes from lymphocytic to polymorphonuclear predominance.

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Prognosis

In uncomplicated cases of acute brucellosis, fever, malaise, and many other manifestations improve rapidly with bed rest, while sustained physical activity may prolong or worsen the degree of illness.

  • Considerable improvement from the symptoms of the acute "toxic" phase of illness occurs in most cases within a few weeks, with or without treatment. In many cases this is followed by complete remission within 2-6 months.
  • Recovery tends to be more rapid in individuals infected with B abortus than in those infected with B melitensis or B suis.

Death seldom occurs as the consequence of acute brucellosis, although it has been reported. Postmortem analysis of such cases confirms that the burden of acute brucellotic infection is borne by tissues of the lymphoreticular system.

Recurrence of symptoms of acute brucellosis is not uncommon. The recurrent disease may be systemic or localized. In some of these patients, the condition evolves into chronic brucellosis, which if untreated may be progressive.

Chronic brucellosis is variously classified, but includes systemic and specific localized forms (including various types of neurobrucellosis), the characteristics of which are discussed in the Clinical section.

  • The various forms of chronic brucellosis, including neurobrucellosis, are due to continued infectious disease, for which additional treatment is indicated and effective.
  • Objective clinical and laboratory evidence for ongoing disease is demonstrable. Patients who do not have such evidence and who complain of occasional mild symptoms similar to those found in acute brucellosis are likely to have psychoneurosis. This complication of acute brucellosis does not usually resolve with anti-brucellosis treatments, although such treatments may exert placebo effects for individual bouts. Psychiatric treatment may be indicated.
  • The likelihood of recurrence is greater in individuals who are not treated or who are inadequately treated for acute brucellosis.
  • Recurrence is possible even in properly treated patients who have had acute brucellosis. Addition of oral rifampicin to oral tetracycline may reduce the recurrence risk for patients who are treated with that combined therapy for acute brucellosis.
  • Chronic brucellosis may continue to trouble patients for as long as 25 years, but such cases are quite rare.

Neurobrucellosis, a specific subtype of localized chronic brucellosis, has a variable outcome.

  • Recovery of patients with acute brucellotic meningitis, meningoencephalitis, or disseminated encephalomyelitis is typically excellent.
  • The likelihood of an excellent outcome from neurobrucellosis is thought to be increased when effective antimicrobial therapy is started early in the course of illness.
  • There is as yet, however, no agreement on the criterion standard for treatment of neurobrucellosis. The issues involved are considered in the Treatment section.
  • The Herxheimer reaction is either extremely uncommon or unknown in the treatment of neurobrucellosis.
  • The scrupulousness with which seizures and cardiovascular complications are treated and supportive care is undertaken to manage incontinence and to prevent of bedsores is likely also to influence outcome.
  • Some patients with neurobrucellosis manifest permanent deficits. The risk for permanent deficits is higher in certain subgroups of primary or secondary neurobrucellosis.
  • Outcome is worse in cases in which neurobrucellosis is complicated by critical elevations of intracranial pressure. Prompt recognition and effective treatment of raised intracranial pressure usually results in rapid and complete recovery, however. In cases of malignant intracranial hypertension, surgical decompression has been advocated by some authorities as improving outcome and as a method of preventing death due to herniation.
  • Permanent deficits may occur in individuals who have cerebrovascular occlusive strokes secondary to brucellar endocarditis, producing emboli that cause occlusions or prompt the development of intracerebral mycotic aneurysms. Outcome may be poor in cases of intracranial mycotic aneurysm rupture with intracerebral or subarachnoid hemorrhage.
  • The risk for permanent deficits is higher in individuals who develop osteoarthritic forms of brucellosis that compromise spinal cord or spinal roots due to spondylitic compressive myelopathy and radiculopathy. The outcome for peripheral neuritis of the lower spinal nerves, which may be difficult to distinguish from spondylitic myelopathy, may be better than the outcome for disease secondary to musculoskeletal abnormalities.
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Patient Education

  • Education with regard to vectors, consumption of pasteurized or appropriately cooked foods, and hygiene may reduce the risk of contracting brucellosis for family members living in areas of endemic disease.
  • Reassurance concerning recurrent symptoms that are not associated with clinical or laboratory evidence of acute brucellotic disease is important in some instances.
  • For excellent patient education resources, visit eMedicine's Brain and Nervous System Center and Public Health Center. Also, see eMedicine's patient education articles Brain Infection and Foreign Travel.
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Contributor Information and Disclosures
Author

Robert Stanley Rust Jr, MD, MA  Thomas E Worrell Jr Professor of Epileptology and Neurology, Co-Director of FE Dreifuss Child Neurology and Epilepsy Clinics, Director, Child Neurology, University of Virginia; Chair-Elect, Child Neurology Section, American Academy of Neurology

Robert Stanley Rust Jr, MD, MA is a member of the following medical societies: American Academy of Neurology, American Epilepsy Society, American Headache Society, American Neurological Association, Child Neurology Society, International Child Neurology Association, and Society for Pediatric Research

Disclosure: Nothing to disclose.

Specialty Editor Board

Aashit K Shah, MD  Associate Professor of Neurology, Wayne State University; Program Director, Clinical Neurophysiology Fellowship, Department of Neurology, Detroit Medical Center

Aashit K Shah, MD is a member of the following medical societies: American Academy of Neurology, American Clinical Neurophysiology Society, and American Epilepsy Society

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Senior Pharmacy Editor, eMedicine

Disclosure: eMedicine Salary Employment

Florian P Thomas, MD, MA, PhD, Drmed  Director, Spinal Cord Injury Unit, St Louis Veterans Affairs Medical Center; Director, National MS Society Multiple Sclerosis Center; Director, Neuropathy Association Center of Excellence, Professor, Department of Neurology and Psychiatry, Associate Professor, Institute for Molecular Virology, and Department of Molecular Microbiology and Immunology, St Louis University School of Medicine

Florian P Thomas, MD, MA, PhD, Drmed is a member of the following medical societies: American Academy of Neurology, American Neurological Association, American Paraplegia Society, Consortium of Multiple Sclerosis Centers, and National Multiple Sclerosis Society

Disclosure: Nothing to disclose.

Selim R Benbadis, MD  Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, University of South Florida School of Medicine, Tampa General Hospital

Selim R Benbadis, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Clinical Neurophysiology Society, American Epilepsy Society, and American Medical Association

Disclosure: UCB Pharma Honoraria Speaking, consulting; Lundbeck Honoraria Speaking, consulting; Cyberonics Honoraria Speaking, consulting; Glaxo Smith Kline Honoraria Speaking, consulting; Pfizer Honoraria Speaking, consulting; Sleepmed/DigiTrace Honoraria Speaking, consulting

Chief Editor

Karen L Roos, MD  John and Nancy Nelson Professor of Neurology, Professor of Neurological Surgery, Department of Neurology, Indiana University School of Medicine

Karen L Roos, MD is a member of the following medical societies: American Academy of Neurology and American Neurological Association

Disclosure: Nothing to disclose.

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