التهاب السحايا

التهاب السحايا
Meningitis
Illu meninges.jpg
Meninges of the central nervous system: dura mater, arachnoid, and pia mater.
التبويب والمصادر الخارجية
ICD-10G00.–G03.
ICD-9-CM320322
DiseasesDB22543
MedlinePlus000680
eMedicinemed/2613 emerg/309 emerg/390
Patient UKالتهاب السحايا
MeSHD008581
Illu meninges.jpg

Meningitis إلتهاب السحايا هو إلتهاب للغشاء الواقى الذى يغلف المخ و الحبل الشوكى, يعرف أصطلاحا ب إلتهاب السحايا.[1] الإلتهاب ممكن أن تسببه عدوى بفيروس أو فيروسات بفيروس, بكتيريا , أو كائنات دقيقة أخرى,وأقل شيوعا بواسطة أدوية.[2] Bacterial meningitis, وبعض الأسباب الأخرى تعتبر مهددة للحياة لقرب موضع الأتهاب من المخ والنخاع الشوكى ; ولذلك تعتبر تلك الحالة من حالات الطوارىء الطبية a medical emergency.[1][3]

أهم أعراض إلتهاب السحايا الصداع و تصلب العنق مصحوبا ب حمى , تشويش و وعى متقلب , و عدم القدرة على إحتمال الضوء الخوف من الضوء أو الضجيج العالى (الخوف من الضوضاء). , وهذا في الغالب عند الأطفال وصغار السن , , يمكن وجود بعض الأعراض الغير محددة مثل الإضطراب,والدوخة . إذا وجدطفح جلدى , يمكن أن يكون دلالة على نوع محدد من إلتهاب السحايا; مثلا, إلتهاب سحايا ناتج عن الجرثومة السحائية و يمكن أن يترافق مع طفح جلدى مميز.[1][4]

A عينة قطنية بمكن أن تشخص أو تستبعد إلتهاب السحايا. وهذا يشمل غرس إبرة داخل spinal canal لإستخلاص عينة من السائل الشوكى (CSF), السائل الذى يغلف المخ والحبل الشوكى. و CSF يفحص حينئذ في مختبر طبى .[3] العلاج المعتاد لإلتهاب السحايا هو البدء فورا بإعطاء المضادات الحيوية مضاد حيوى و أحيانا [[مضاد للفيروسات . وفى بعض الأحيان, الكورتيكوستيرويدات التى تستعمل لمنع المضاعفات في الإلتهابات الشديدة .[3][4] إلتهاب السحايا يمكن أن تؤدى الى آثار بعيدة المدى مثل الصمم, الصرع, hydrocephalus و العجز الإدراكىوبالأخص عند عدم علاج الحالة quickly.[1][4] مثل إلتهاب السحاياالمصحوبة ب meningococci, Haemophilus influenzae type B, pneumococci أو mumps virus infections) may be prevented by immunization.[1]

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تعريف المرض

الالتهاب السحائي مرض يصيب الأغشية التي تغطي الدماغ والنخاع الشوكي. وهذه الأغشية تعرف باسم السحايا. كما يصيب المرض السائل الدماغي الشوكي الذي يحيط بالدماغ والنخاع الشوكي. ينتج الالتهاب السحائي عن عدوى بوساطة البكتيريا والفيروسات والفطر والميكروبات الأخرى. وسيقتصر الحديث في هذه المقالة عن الالتهاب السحائي البكتيري والفيروسي، وهما أكثر أشكال المرض شيوعاً. يهاجم الالتهاب السحائي الإنسان في كل الأعمار، إلا أن الرضّع والأطفال أكثر تعرضًا للإصابة به. ويتماثل معظم الضحايا للشفاء التام من المرض، غير أن الالتهاب السحائي البكتيري قد يسبب تلفاً حاداً للدماغ، ينتهي بالوفاة. كما قد يؤدي الالتهاب السحائي البكتيري إلى الصمم، والشلل، وضعف العضلات، والتخلف العقلي، والعمى، وتغيرات في السلوك. والإنسان الذي يعاني حالة عضوية تُضعف مقاومة الجسم للعدوى، أكثر تعرضاً للإصابة بالالتهاب السحائي. وتشمل مثل هذه الحالات أنيميا الخلايا المنجلية، وعدم وجود الطحال، ونقص البروتينات المضادة للعدوى والتي تعرف باسم الغُلُوبْيُولينات المناعية.

كيفية تطورالمرض

توجد البكتيريا والفيروسات التي تسبب الالتهاب السحائي في معظم الحالات في أعضاء الجهاز التنفسي. وتمر الميكروبات في مجرى الدم وتصل إلى الدماغ، حيث تصيب السحايا والسائل الدماغي الشوكي. وتُحدث تغيرات كيميائية مختلفة في الدماغ، الذي قد ينتفخ. هناك أنواع كثيرة من البكتيريا التي تسبب الالتهاب السحائي. إلا أن معظم حالات الالتهاب السحائي البكتيري تنتج عن العدوى عن طريق ثلاثة أنواع من البكتيريا هي النيسرية السحائية والمستدمية النزلية، النوع ب والعقدية الرئوية. كما تسبب عدة فيروسات الالتهاب السحائي.

العلامات والأعراض

الظواهر المرضية

أعراض الالتهاب السحائي البكتيري ـ بصورة عامة ـ أكثر حدة من أعراض الالتهاب السحائي الفيروسي. كما تتفاوت الأعراض باختلاف عمر المريض. فتشمل الأعراض لدى الرضّع والأطفال الحمى والغثيان والقيء وفقدان الشهية والنعاس. كما قد يعاني بعض الأطفال تشنجات أو ارتعاش الأطراف الذي يمكن السيطرة عليه. وكثيراً ماتشمل الأعراض عند الأطفال الأكبر سناً والراشدين الصداع وآلام الظهر وآلام العضلات وحساسية العينين للضوء. وكذلك يعاني بعض المصابين تصلُّبًا في العنق. في البالغين ، فإن الصداع الشديد هو العلامة الأكثر شيوعا لالتهاب السحايا -- تحدث في حوالي 90 ٪ من حالات التهاب السحايا الجرثومي ، تليها جمود nuchal (عجز لثني الرقبة إلى الأمام بشكل سلبي نتيجة لزيادة التصلب في عضلة الرقبة ).[5] الثالوث الكلاسيكي من علامات تشخيصية تتكون من جمود nuchal ، مفاجئ حمى عالية ، وتغيير في الحالة النفسية ، ولكن كل الثلاثة أعراض موجودة فقط في 44-46 ٪ من جميع حالات التهاب السحايا الجرثومي.[5][6] إذا كان أيا من العلامات الثلاثة غير موجودة ، فإن إلتهاب السحايا من غير المرجح أن يوجد.[6] علامات أخرى تترافق عادة مع التهاب السحايا وتشمل الخوف من الضوء (التعصب للضوء الساطع) و phonophobia أو (التعصب للضجيج العالى). الأطفال الصغار في كثير من الأحيان لا تظهر الأعراض المذكورة آنفا لديهم ، ويمكن فقط ظهور العصبي .[1] عند الأطفال الرضع بدأ من 6 أشهر من العمر ، فإن انتفاخ في اليافوخ (البقعة الناعمة على قمة رأس الطفل) قد تكون موجودة. وهى من الخصائص الأخرى التي يمكن أن نميز التهاب السحايا من أمراض أقل خطورة في الأطفال الصغار من آلام الساق ، والأطراف الباردة ، وتغيير طبيعية لون الجلد.[7]

Nuchal جمود أو تصلب يحدث في 70 ٪ من حالات التهاب السحايا الجرثومي للكبار.[6] علامات أخرى من السحائية وتشمل وجود علامة Kernig إيجابية أو و علامة Brudzinski.هو علامة من المقررة مع المريض المنبطح مستلق ، مع توخي المرونة في مفصل الورك والركبة الى 90 درجة. في المريض مع Kernig إيجابية ، وحدود الألم للتمديد السلبي في الركبة. وقال في إشارة إيجابية Brudzinski تحدث عند انثناء العنق تسبب الانثناء اللاإرادي في الركبة والورك. وعلى الرغم من Kernig وBrudzinski هو علامات على حد سواء وتستخدم عادة للكشف عن مرض التهاب السحايا ، و حساسية من هذه الاختبارات هو محدود.[6][8] They do, however, have very good specificity for meningitis: the signs rarely occur in other diseases.[6] Another test, known as the "jolt accentuation maneuver" helps determine whether meningitis is present in patients reporting fever and headache. The patient is told to rapidly rotate his or her head horizontally; if this does not make the headache worse, meningitis is unlikely.[6]

Meningitis caused by the bacterium Neisseria meningitidis (known as "meningococcal meningitis") can be differentiated from meningitis with other causes by a rapidly spreading petechial rash which may precede other symptoms.[7] The rash consists of numerous small, irregular purple or red spots ("petechiae") on the trunk, lower extremities, mucous membranes, conjuctiva, and (occasionally) the palms of the hands or soles of the feet. The rash is typically non-blanching: the redness does not disappear when pressed with a finger or a glass tumbler. Although this rash is not necessarily present in meningococcal meningitis, it is relatively specific for the disease; it does, however, occasionally occur in meningitis due to other bacteria.[1] Other clues as to the nature of the cause of meningitis may be the skin signs of hand, foot and mouth disease and genital herpes, both of which are associated with various forms of viral meningitis.[9]

التشخيص

يشخِّص الأطباء الالتهاب السحائي من خلال فحص عينة من السائل الدماغي الشوكي للمريض. ويتم الحصول على العينة بإدخال إبرة بين الفقرات في الجزء السفلي من الظهر. وتعرف هذه العملية باسم النقب القطني أو البزل الشوكي. يحوي السائل الدماغي للمصابين بالالتهاب السحائي البكتيري نسبة عالية من البروتين ونسبة منخفضة من الجلوكوز. بينما يحوي سائل معظم مرضى الالتهاب السحائي الفيروسي نسبة عادية أو عالية من البروتين ونسبة عادية من الجلوكوز. ولكي يتم تحديد نوع الجرثومة أو الفيروس المسبب، يتم فحص السائل الدماغي الشوكي للمريض بطرق مختلفة حتى يمكن تحديد نوع الكائن الحي الذي سبب العدوى.

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الوقاية والعلاج

يجب أن يبقى المريض الذي يعاني الالتهاب السحائي تحت رعاية الطبيب. وليس هناك علاج محدد فعّال ضد الالتهاب السحائي البكتيري، ويعالج الالتهاب السحائي البكتيري بالمضادات الحيوية. ومثل هذه المعالجة تقلل كثيراً خطر الوفاة بسبب المرض. يعتمد نوع المضاد الحيوي المستعمل على البكتيريا المسببة. وأكثر أنواع المضادات الحيوية المستخدمة لالتهاب السحايا الجرثومي البنسلين، والأمبيسلين، والكلورامفنيكول. ويتماثل معظم المرضى للشفاء من الالتهاب السحائي خلال عدة أسابيع. بعض أنواع الالتهاب السحائي البكتيري والفيروسي معدية. ويساعد الرفامبسيْن في الحماية من انتشار الالتهاب السحائي الذي تسببه النيسرية السحائية والمستدمية النزلية، النوع ب. يصف الأطباء عادة هذا المضاد الحيوي للأشخاص المتصلين بالمريض. كما تحمي اللقاحات من حدوث أنواع معينة من الالتهاب السحائي البكتيري. وليست هناك وسيلة فعالة للوقاية من الالتهاب السحائي الفيروسي.

Early complications

A severe case of meningococcal meningitis in which the petechial rash progressed to gangrene and required amputation of all limbs. The patient, Charlotte Cleverley-Bisman, managed to survive the disease and became a poster child for a meningitis vaccination campaign in New Zealand.

People with meningitis may develop additional problems in the early stages of their illness. These may require specific treatment, and sometimes indicate severe illness or worse prognosis. The infection may trigger sepsis, a systemic inflammatory response syndrome of falling blood pressure, fast heart rate, high or abnormally low temperature and rapid breathing. Very low blood pressure may occur early, especially but not exclusively in meningococcal illness; this may lead to insufficient blood supply to other organs.[1] Disseminated intravascular coagulation, the excessive activation of blood clotting, may cause both the obstruction of blood flow to organs and a paradoxical increase of bleeding risk. In meningococcal disease, gangrene of limbs can occur.[1] Severe meningococcal and pneumococcal infections may result in hemorrhaging of the adrenal glands, leading to Waterhouse-Friderichsen syndrome, which is often lethal.[10]

The brain tissue may swell, with increasing pressure inside the skull and a risk of swollen brain tissue getting trapped. This may be noticed by a decreasing level of consciousness, loss of the pupillary light reflex, and abnormal positioning.[4] Inflammation of the brain tissue may also obstruct the normal flow of CSF around the brain (hydrocephalus).[4] Seizures may occur for various reasons; in children, seizures are common in the early stages of meningitis (30% of cases) and do not necessarily indicate an underlying cause.[3] Seizures may result from increased pressure and from areas of inflammation in the brain tissue.[4] Focal seizures (seizures that involve one limb or part of the body), persistent seizures, late-onset seizures and those that are difficult to control with medication are indicators of a poorer long-term outcome.[1]

The inflammation of the meninges may lead to abnormalities of the cranial nerves, a group of nerves arising from the brain stem that supply the head and neck area and control eye movement, facial muscles and hearing, among other functions.[1][6] Visual symptoms and hearing loss may persist after an episode of meningitis (see below).[1] Inflammation of the brain (encephalitis) or its blood vessels (cerebral vasculitis), as well as the formation of blood clots in the veins (cerebral venous thrombosis), may all lead to weakness, loss of sensation, or abnormal movement or function of the part of the body supplied by the affected area in the brain.[1][4]

Causes

Meningitis is usually caused by infection by viruses or microorganisms. Most cases are due to infection with viruses,[6] with bacteria, fungi, and parasites being the next most common causes.[2] It may also result from various non-infectious causes.[2]

Bacterial meningitis

The types of bacteria that cause bacterial meningitis vary by age group. In premature babies and newborns up to three months old, common causes are group B streptococci (subtypes III which normally inhabit the vagina and are mainly a cause during the first week of life) and those that normally inhabit the digestive tract such as Escherichia coli (carrying K1 antigen). Listeria monocytogenes (serotype IVb) may affect the newborn and occurs in epidemics. Older children are more commonly affected by Neisseria meningitidis (meningococcus), Streptococcus pneumoniae (serotypes 6, 9, 14, 18 and 23) and those under five by Haemophilus influenzae type B (in countries that do not offer vaccination, see below).[1][3] In adults, N. meningitidis and S. pneumoniae together cause 80% of all cases of meningitis, with increased risk of L. monocytogenes in those over 50 years old.[3][4]

Recent trauma to the skull gives bacteria in the nasal cavity the potential to enter the meningeal space. Similarly, individuals with a cerebral shunt or related device (such as an extraventricular drain or Ommaya reservoir) are at increased risk of infection through those devices. In these cases, infections with staphylococci are more likely, as well as infections by pseudomonas and other Gram-negative bacilli.[3] The same pathogens are also more common in those with an impaired immune system.[1] In a small proportion of people, an infection in the head and neck area, such as otitis media or mastoiditis, can lead to meningitis.[3] Recipients of cochlear implants for hearing loss are at an increased risk of pneumococcal meningitis.[11]

Tuberculous meningitis, meningitis due to infection with Mycobacterium tuberculosis, is more common in those from countries where tuberculosis is common, but is also encountered in those with immune problems, such as AIDS.[12]

Recurrent bacterial meningitis may be caused by persisting anatomical defects, either congenital or acquired, or by disorders of the immune system.[13] Anatomical defects allow continuity between the external environment and the nervous system. The most common cause of recurrent meningitis is skull fracture,[13] particularly fractures that affect the base of the brain or extend towards the sinuses and petrous pyramids.[13] A literature review of 363 reported cases of recurrent meningitis showed that 59% of cases are due to such anatomical abnormalities, 36% due to immune deficiencies (such as complement deficiency, which predisposes especially to recurrent meningococcal meningitis), and 5% due to ongoing infections in areas adjacent to the meninges.[13]


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Aseptic

The term aseptic meningitis refers loosely to all cases of meningitis in which no bacterial infection can be demonstrated. This is usually due to viruses, but it may be due to bacterial infection that has already been partially treated, with disappearance of the bacteria from the meninges, or by infection in a space adjacent to the meninges (e.g. sinusitis). Endocarditis (infection of the heart valves with spread of small clusters of bacteria through the bloodstream) may cause aseptic meningitis. Aseptic meningitis may also result from infection with spirochetes, a type of bacteria that includes Treponema pallidum (the cause of syphilis) and Borrelia burgdorferi (known for causing Lyme disease). Meningitis may be encountered in cerebral malaria (malaria infecting the brain). Fungal meningitis, e.g. due to Cryptococcus neoformans, is typically seen in people with immune deficiency such as AIDS. Amoebic meningitis, meningitis due to infection with amoebae such as Naegleria fowleri, is contracted from freshwater sources.[2]

Viral meningitis

Viruses that can cause meningitis include enteroviruses, herpes simplex virus type 2 (and less commonly type 1), varicella zoster virus (known for causing chickenpox and shingles), mumps virus, HIV, and LCMV.[9]

Non-infectious

Meningitis may occur as the result of several non-infectious causes: spread of cancer to the meninges (malignant meningitis)[14] and certain drugs (mainly non-steroidal anti-inflammatory drugs, antibiotics and intravenous immunoglobulins).[15] It may also be caused by several inflammatory conditions such as sarcoidosis (which is then called neurosarcoidosis), connective tissue disorders such as systemic lupus erythematosus, and certain forms of vasculitis (inflammatory conditions of the blood vessel wall) such as Behçet's disease.[2] Epidermoid cysts and dermoid cysts may cause meningitis by releasing irritant matter into the subarachnoid space.[2][13] Mollaret's meningitis is a syndrome of recurring episodes of aseptic meningitis; it is now thought to be caused by herpes simplex virus type 2. Rarely, migraine may cause meningitis, but this diagnosis is usually only made when other causes have been eliminated.[2]

Mechanism

The meninges comprise three membranes that, together with the cerebrospinal fluid, enclose and protect the brain and spinal cord (the central nervous system). The pia mater is a very delicate impermeable membrane that firmly adheres to the surface of the brain, following all the minor contours. The arachnoid mater (so named because of its spider-web-like appearance) is a loosely fitting sac on top of the pia mater. The subarachnoid space separates the arachnoid and pia mater membranes, and is filled with cerebrospinal fluid. The outermost membrane, the dura mater, is a thick durable membrane, which is attached to both the arachnoid membrane and the skull.

In bacterial meningitis, bacteria reach the meninges by one of two main routes: through the bloodstream or through direct contact between the meninges and either the nasal cavity or the skin. In most cases, meningitis follows invasion of the bloodstream by organisms that live upon mucous surfaces such as the nasal cavity. This is often in turn preceded by viral infections, which break down the normal barrier provided by the mucous surfaces. Once bacteria have entered the bloodstream, they enter the subarachnoid space in places where the blood-brain barrier is vulnerable—such as the choroid plexus. Meningitis occurs in 25% of newborns with bloodstream infections due to group B streptococci; this phenomenon is less common in adults.[1] Direct contamination of the cerebrospinal fluid may arise from indwelling devices, skull fractures, or infections of the nasopharynx or the nasal sinuses that have formed a tract with the subarachnoid space (see above); occasionally, congenital defects of the dura mater can be identified.[1]

The large-scale inflammation that occurs in the subarachnoid space during meningitis is not a direct result of bacterial infection but can rather largely be attributed to the response of the immune system to the entrance of bacteria into the central nervous system. When components of the bacterial cell membrane are identified by the immune cells of the brain (astrocytes and microglia), they respond by releasing large amounts of cytokines, hormone-like mediators that recruit other immune cells and stimulate other tissues to participate in an immune response. The blood-brain barrier becomes more permeable, leading to "vasogenic" cerebral edema (swelling of the brain due to fluid leakage from blood vessels). Large numbers of white blood cells enter the CSF, causing inflammation of the meninges, and leading to "interstitial" edema (swelling due to fluid between the cells). In addition, the walls of the blood vessels themselves become inflamed (cerebral vasculitis), which leads to a decreased blood flow and a third type of edema, "cytotoxic" edema. The three forms of cerebral edema all lead to an increased intracranial pressure; together with the lowered blood pressure often encountered in acute infection, this means that it is harder for blood to enter the brain, and brain cells are deprived of oxygen and undergo apoptosis (automated cell death).[1]

It is recognized that administration of antibiotics may initially worsen the process outlined above, by increasing the amount of bacterial cell membrane products released through the destruction of bacteria. Particular treatments, such as the use of corticosteroids, are aimed at dampening the immune system's response to this phenomenon.[1][4]

Diagnosis

CSF findings in different forms of meningitis[16]
Type of meningitis   Glucose   Protein Cells
Acute bacterial low high PMNs,
often > 300/mm³
Acute viral normal normal or high mononuclear,
< 300/mm³
Tuberculous low high mononuclear and
PMNs, < 300/mm³
Fungal low high < 300/mm³
Malignant low high usually
mononuclear

Blood tests and imaging

In someone suspected of having meningitis, blood tests are performed for markers of inflammation (e.g. C-reactive protein, complete blood count), as well as blood cultures.[3][17]

The most important test in identifying or ruling out meningitis is analysis of the cerebrospinal fluid through lumbar puncture (LP, spinal tap).[18] However, lumbar puncture is contraindicated if there is a mass in the brain (tumor or abscess) or the intracranial pressure (ICP) is elevated, as it may lead to brain herniation. If someone is at risk for either a mass or raised ICP (recent head injury, a known immune system problem, localizing neurological signs, or evidence on examination of a raised ICP), a CT or MRI scan is recommended prior to the lumbar puncture.[3][17][19] This applies in 45% of all adult cases.[4] If a CT or MRI is required before LP, or if LP proves difficult, professional guidelines suggest that antibiotics should be administered first to prevent delay in treatment,[3] especially if this may be longer than 30 minutes.[17][19] Often, CT or MRI scans are performed at a later stage to assess for complications of meningitis.[1]

Lumbar puncture

A lumbar puncture is done by positioning the patient, usually lying on the side, applying local anesthetic, and inserting a needle into the dural sac (a sac around the spinal cord) to collect cerebrospinal fluid (CSF). When this has been achieved, the "opening pressure" of the CSF is measured using a manometer. The pressure is normally between 6 and 18 cm water (cmH2O);[18] in bacterial meningitis the pressure is typically elevated.[3][17] The initial appearance of the fluid may prove an indication of the nature of the infection: cloudy CSF indicates higher levels of protein, white and red blood cells and/or bacteria, and therefore may suggest bacterial meningitis.[3]

Gram stain of meningococci from a culture showing Gram negative (pink) bacteria, often in pairs

The CSF sample is examined for presence and types of white blood cells, red blood cells, protein content and glucose level.[3] Gram staining of the sample may demonstrate bacteria in bacterial meningitis, but absence of bacteria does not exclude bacterial meningitis as they are only seen in 60% of cases; this figure is reduced by a further 20% if antibiotics were administered before the sample was taken, and Gram staining is also less reliable in particular infections such as listeria. Microbiological culture of the sample is more sensitive (it identifies the organism in 70–85% of cases) but results can take up to 48 hours to become available.[3] The type of white blood cell predominantly present predicts whether meningitis is due to bacterial or viral infection (see table).[3]

The concentration of glucose in CSF is normally above 40% that in blood. In bacterial meningitis it is typically lower; the CSF glucose level is therefore divided by the blood glucose (CSF glucose to serum glucose ratio). A ratio ≤0.4 is indicative of bacterial meningitis;[18] in the newborn, glucose levels in CSF are normally higher, and a ratio below 0.6 (60%) is therefore considered abnormal.[3] High levels of lactate in CSF indicate a higher likelihood of bacterial meningitis, as does a higher white blood cell count.[18]

Various more specialized tests may be used to distinguish between various types of meningitis. A latex agglutination test may be positive in meningitis because of Streptococcus pneumoniae, Neisseria meningitidis, Haemophilus influenzae, Escherichia coli and group B streptococci; its routine use is not encouraged as it rarely leads to changes in treatment, but it may be used if other tests are not diagnostic. Similarly, the limulus lysate test may be positive in meningitis caused by Gram-negative bacteria, but it is of limited use unless other tests have been unhelpful.[3] Polymerase chain reaction (PCR) uses enzymes to enhance the presence of bacterial or viral DNA in cerebrospinal fluid; it is a highly sensitive and specific test. It may identify bacteria in bacterial meningitis and may assist in distinguishing the various causes of viral meningitis (enterovirus, herpes simplex virus 2 and mumps in those not vaccinated for this).[9] Serology (identification of antibodies to viruses) may be useful in viral meningitis.[9] If tuberculous meningitis is suspected, the sample is processed for Ziehl-Neelsen stain, which has a low sensitivity, and tuberculosis culture, which takes a long time to process; PCR is being used increasingly.[12] Diagnosis of cryptococcal meningitis can be made at low cost using an India ink stain of the CSF; however, testing for cryptococcal antigen in blood or CSF is more sensitive, particularly in persons with AIDS.[20][21][22]

A diagnostic and therapeutic conundrum is the "partially treated meningitis", where there are meningitis symptoms after receiving antibiotics (such as for presumptive sinusitis). When this happens, CSF findings may resemble those of viral meningitis, but antibiotic treatment may need to be continued until there is definitive positive evidence of a viral cause (e.g. a positive enterovirus PCR).[9]

Postmortem

Meningitis can be diagnosed after death has occurred. The findings from a post mortem are usually a widespread inflammation of the pia mater and arachnoid layers of the meninges covering the brain and spinal cord. Neutrophil leucocytes tend to have migrated to the cerebrospinal fluid and the base of the brain, along with cranial nerves and the spinal cord, may be surrounded with pus—as may the meningeal vessels.[23]

Treatment

Initial treatment

Meningitis is potentially life-threatening and has a high mortality rate if untreated;[3] delay in treatment has been associated with a poorer outcome.[4] Thus treatment with wide-spectrum antibiotics should not be delayed while confirmatory tests are being conducted.[19] If meningococcal disease is suspected in primary care, guidelines recommend that benzylpenicillin be administered before transfer to hospital.[7] Intravenous fluids should be administered if hypotension (low blood pressure) or shock are present.[19] Given that meningitis can cause a number of early severe complications, regular medical review is recommended to identify these complications early,[19] as well as admission to an intensive care unit if deemed necessary.[4]

Mechanical ventilation may be needed if the level of consciousness is very low, or if there is evidence of respiratory failure. If there are signs of raised intracranial pressure, measures to monitor the pressure may be taken; this would allow the optimization of the cerebral perfusion pressure and various treatments to decrease the intracranial pressure with medication (e.g. mannitol).[4] Seizures are treated with anticonvulsants.[4] Hydrocephalus (obstructed flow of CSF) may require insertion of a temporary or long-term drainage device, such as a cerebral shunt.[4]

Bacterial meningitis

Structural formula of ceftriaxone, one of the third-generation cefalosporin antibiotics recommended for the initial treatment of bacterial meningitis.

Empiric antibiotics (treatment without exact diagnosis) must be started immediately, even before the results of the lumbar puncture and CSF analysis are known. The choice of initial treatment depends largely on the kind of bacteria that cause meningitis in a particular place. For instance, in the United Kingdom empirical treatment consists of a third-generation cefalosporin such as cefotaxime or ceftriaxone.[17][19] In the USA, where resistance to cefalosporins is increasingly found in streptococci, addition of vancomycin to the initial treatment is recommended.[3][4][17] Empirical therapy may be chosen on the basis of the age of the patient, whether the infection was preceded by head injury, whether the patient has undergone neurosurgery and whether or not a cerebral shunt is present.[3] For instance, in young children and those over 50 years of age, as well as those who are immunocompromised, addition of ampicillin is recommended to cover Listeria monocytogenes.[3][17] Once the Gram stain results become available, and the broad type of bacterial cause is known, it may be possible to change the antibiotics to those likely to deal with the presumed group of pathogens.[3]

The results of the CSF culture generally take longer to become available (24–48 hours). Once they do, empiric therapy may be switched to specific antibiotic therapy targeted to the specific causative organism and its sensitivities to antibiotics.[3] For an antibiotic to be effective in meningitis, it must not only be active against the pathogenic bacterium, but also reach the meninges in adequate quantities; some antibiotics have inadequate penetrance and therefore have little use in meningitis. Most of the antibiotics used in meningitis have not been tested directly on meningitis patients in clinical trials. Rather, the relevant knowledge has mostly derived from laboratory studies in rabbits.[3]

Adjuvant treatment with corticosteroids (usually dexamethasone) reduces rates of mortality, severe hearing loss and neurological damage in adults, specifically when the causative agent is S. pneumoniae. The likely mechanism is suppression of overactive inflammation.[24] Professional guidelines therefore recommend the commencement of dexamethasone or a similar corticosteroid just before the first dose of antibiotics is given, and continued for four days.[17][19] Given that most of the benefit of the treatment is confined to those with pneumococcal meningitis, some guidelines suggest that dexamethasone be discontinued if another cause for meningitis is identified.[3][17]

Adjuvant corticosteroids have a different role in children than in adults. Though the benefit of corticosteroids has been demonstrated in adults as well as in children from high-income countries, their use in children from low-income countries is not supported by evidence; the reason for this discrepancy is not clear.[25] Even in high-income countries, the benefit of corticosteroids is only seen when they are given prior to the first dose of antibiotics, and is greatest in cases of H. influenzae meningitis,[3][26] the incidence of which has decreased dramatically since the introduction of the Hib vaccine. Thus, corticosteroids are recommended in the treatment of pediatric meningitis if the cause is H. influenzae and only if given prior to the first dose of antibiotics, whereas other uses are controversial.[3]

Tuberculous meningitis requires prolonged treatment with antibiotics. While tuberculosis of the lungs is typically treated for six months, those with tuberculous meningitis are typically treated for a year or longer.[12] In tuberculous meningitis there is a strong evidence base for treatment with corticosteroids, although this evidence is restricted to those without AIDS.[27]

Other infections

Viral meningitis typically requires supportive therapy only; most viruses responsible for causing meningitis are not amenable to specific treatment. Viral meningitis tends to run a more benign course than bacterial meningitis. Herpes simplex virus and varicella zoster virus may respond to treatment with antiviral drugs such as aciclovir, but there are no clinical trials that have specifically addressed whether this treatment is effective.[9] Mild cases of viral meningitis can be treated at home with conservative measures such as fluid, bedrest, and analgesics.[28] Fungal meningitis, such as cryptococcal meningitis, is treated with long courses of highly dosed antifungals, such as amphotericin B and flucytosine.[20][29]

Prognosis

Untreated, bacterial meningitis is almost always fatal. Viral meningitis, in contrast, tends to resolve spontaneously and is rarely fatal. With treatment, mortality (risk of death) from bacterial meningitis depends on the age of the patient and the underlying cause. Of the newborn patients, 20–30% may die from an episode of bacterial meningitis. This risk is much lower in older children, whose mortality is about 2%, but rises again to about 19–37% in adults.[1][4] Risk of death is predicted by various factors apart from age, such as the pathogen and the time it takes for the pathogen to be cleared from the cerebrospinal fluid,[1] the severity of the generalized illness, decreased level of consciousness or abnormally low count of white blood cells in the CSF.[4] Meningitis caused by H. influenza and meningococci has a better prognosis compared to cases caused by group B streptococci, coliforms and S. pneumoniae.[1] In adults, too, meningococcal meningitis has a lower mortality (3–7%) than pneumococcal disease.[4]

In children there are several potential disabilities which result from damage to the nervous system. Sensorineural hearing loss, epilepsy, learning and behavioral difficulties, as well as decreased intelligence, occur in about 15% of survivors.[1] Some of the hearing loss may be reversible.[30] In adults, 66% of all cases emerge without disability. The main problems are deafness (in 14%) and cognitive impairment (in 10%).[4]

Epidemiology

Demography of meningococcal meningitis.██ meningitis belt██ epidemic zones██ sporadic cases only

Although meningitis is a notifiable disease in many countries, the exact incidence rate is unknown.[9] Bacterial meningitis occurs in about 3 people per 100,000 annually in Western countries. Population-wide studies have shown that viral meningitis is more common, at 10.9 per 100,000, and occurs more often in the summer. In Brazil, the rate of bacterial meningitis is higher, at 45.8 per 100,000 annually. In sub-Saharan Africa, large epidemics of meningococcal meningitis occur in the dry season, leading to it being labeled the "meningitis belt"; annual rates of 500 cases per 100,000 are encountered in this area, which is poorly served by medical care. These cases are predominantly caused by meningococci.[6] The most recent epidemic, affecting Nigeria, Niger, Mali and Burkina Faso, started in January 2009 and is ongoing.[31]

Meningococcal disease occurs in epidemics in areas where many people live together for the first time, such as army barracks during mobilization, college campuses[1] and the annual Hajj pilgrimage.[32]

There are significant differences in the local distribution of causes for bacterial meningitis. For instance, N. meningitides groups B and C cause most disease episodes in Europe, while group A meningococci are more common in China and amongst Hajj pilgrims. In the "meningitis belt" of Africa, group A and C meningococci cause most of the outbreaks. Group W135 meningococci have caused several recent epidemics in Africa and during the Hajj.[33] These differences are expected to change further as vaccines against common strains are introduced.[33]

Prevention

For some causes of meningitis, prophylaxis can be provided in the long term with vaccine, or in the short term with antibiotics.

Since the 1980s, many countries have included immunization against Haemophilus influenzae type B in their routine childhood vaccination schemes. This has practically eliminated this pathogen as a cause of meningitis in young children in those countries. In the countries where the disease burden is highest, however, the vaccine is still too expensive.[33][34] Similarly, immunization against mumps has led to a sharp fall in the number of cases of mumps meningitis, which prior to vaccination occurred in 15% of all cases of mumps.[9]

Meningococcus vaccines exist against groups A, C, W135 and Y.[35] In countries where the vaccine for meningococcus group C was introduced, cases caused by this pathogen have decreased substantially.[33] A quadrivalent vaccine now exists, which combines all four vaccines. Immunization with the ACW135Y vaccine against four strains is now a visa requirement for taking part in the Hajj.[32] Development of a vaccine against group B meningococci has proved much more difficult, as its surface proteins (which would normally be used to make a vaccine) only elicit a weak response from the immune system, or cross-react with normal human proteins.[33][35] Still, some countries (New Zealand, Cuba, Norway and Chile) have developed vaccines against local strains of group B meningococci; some have shown good results and are used in local immunization schedules.[35]

Routine vaccination against Streptococcus pneumoniae with the pneumococcal conjugate vaccine (PCV), which is active against seven common serotypes of this pathogen, significantly reduces the incidence of pneumococcal meningitis.[33][36] The pneumococcal polysaccharide vaccine, which covers 23 strains, is only administered in certain groups (e.g. those who have had a splenectomy, the surgical removal of the spleen); it does not elicit a significant immune response in all recipients, e.g. small children.[36]

Childhood vaccination with Bacillus Calmette-Guérin has been reported to significantly reduce the rate of tuberculous meningitis, but its waning effectiveness in adulthood has prompted a search for a better vaccine.[33]

Short-term antibiotic prophylaxis is also a method of prevention, particularly of meningococcal meningitis. In cases of meningococcal meningitis, prophylactic treatment of close contacts with antibiotics (e.g. rifampicin, ciprofloxacin or ceftriaxone) can reduce their risk of contracting the condition, but does not protect against future infections.[17][37]

History

Some suggest that Hippocrates may have realized the existence of meningitis,[6] and it seems that meningism was known to pre-Renaissance physicians such as Avicenna.[38] The description of tuberculous meningitis, then called "dropsy in the brain", is often attributed to Edinburgh physician Sir Robert Whytt in a posthumous report that appeared in 1768, although the link with tuberculosis and its pathogen was not made until the next century.[38][39] It appears that epidemic meningitis is a relatively recent phenomenon.[40] The first recorded major outbreak occurred in Geneva in 1805.[40][41] Several other epidemics in Europe and the United States were described shortly afterward, and the first report of an epidemic in Africa appeared in 1840. African epidemics became much more common in the 20th century, starting with a major epidemic sweeping Nigeria and Ghana in 1905–1908.[40]

The first report of bacterial infection underlying meningitis was by the Austrian bacteriologist Anton Weichselbaum, who in 1887 described the meningococcus.[42] Mortality from meningitis was very high (over 90%) in early reports. In 1906, antiserum was produced in horses; this was developed further by the American scientist Simon Flexner and markedly decreased mortality from meningococcal disease.[43][44] In 1944, penicillin was first reported to be effective in meningitis.[45] The introduction in the late 20th century of Haemophilus vaccines led to a marked fall in cases of meningitis associated with this pathogen,[34] and in 2002 evidence emerged that treatment with steroids could improve the prognosis of bacterial meningitis.[24][25][44]

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