background image
TINJAUAN KEPUSTAKAAN
Medical Treatment
of Spinal Tuberculosis
Zuljasri Albar
Rheumatology Division, Department of Internal Medicine, Faculty of Medicine, University of Indonesia
Cipto Mangunkusumo Hospital, Jakarta
Indonesia
INTRODUCTION
Tuberculosis is still a major health problem in developing
countries. Indonesia is the third largest TB population in the
world, after China and India. Extra-pulmonary TB accounts for
17.9% - 19.4% of all tuberculosis cases. About 11% of
extra-pulmonary TB showed osteoarticular involvement; spinal
lesions constitute a major bulk among this osteoarticular TB; it
is the commonest form of osteoarticular tuberculosis and
contributes to about 50% (25-60%) of all cases of skeletal
tuberculosis in various reported series (Tuli et al 1969, Martini
et al 1988) (from Agarwal et al
(2)
; spinal tuberculosis is
relatively an uncommon form of tuberculous infection
occurring in about 1% of patients with tuberculosis.
(3)
Bone and joint TB was found more often in certain
racial/ethnic groups, HIV positive group, immigrants from
countries with high TB prevalence, elderly, children under 15
years of age and other immunocompromised conditions. In
HIV patients, the incidence of tuberculosis is 500 times higher
than that of general population. On the other hand,about
25-50% of new cases of tuberculosis in USA were HIV
positive
(1)
.
DIAGNOSIS
About 80% of tuberculosis infections are caused by
activation of dormant bacteria. Bacteria living in scars left by
the initial infection - usually in the top of one or both lungs -
may begin to multiply. Activation of dormant bacteria can
occur when the person's immune system becomes impaired, for
example from AIDS, the use of corticosteroids or in very
advanced age. Spinal tuberculosis is often the result of
haematogenous dissemination from primary focus, usually in
the lungs. The detection of primary focus or an associated
visceral tuberculous lesion however depends greatly upon the
amount of efforts put into investigations
(1)
.
The disease begins in the anteroinferior portion of the
vertebral body and tends to spread beneath the anterior
longitudinal ligament to involve adjacent vertebral bodies.
Because the anterior portion of a vertebral body is much more
likely involved than the posterior portion, a sharp kyphosis may
occurs. Simultaneous involvement of anterior and posterior
elements of vertebra in spinal tuberculosis is rare. Even with
the resolution of acute infectious process, the kyphosis may
continue to cause anterior compression of the cord and late
neurological sequelae. Multiple sites in affected. Other
investigators found thoracal vertebra is more often affected, and
cervical vertebra is the least often affected. In Cipto
Mangunkusumo Hospital, Jakarta, thoracal vertebra was
involved in about 71% spinal tuberculosis cases. There is
5%-7% incidence of multiple level vertebral involvement,
mostly between 1 to 5 vertebral body with an average 2.51.
Narrowing of the disc space occurs as a late phenomenon. In a
majority of spinal tuberculosis patients, a typical paradiscal
lesion characterised by destruction of adjacent bone end plates
with reduction in disc space is seen. Extension of the infection
into the adjacent paraspinal soft tissues, with abscess formation,
particularly beneath the fascia of the psoas muscle is frequent.
Subligamentous spread and posterior extension into the
epidural space occur less commonly.
Tuberculous spondylitis can have myriad, variable clinical
presentations. Classically, the typical complaint is spine pain
and manifestations of chronic illness including weight loss,
malaise, fever, and/or night sweats.
Physical examination may demonstrate deformity (gibbus),
local tenderness, muscle spasm, restricted motion, a mass in the
groin, thigh or flank and neurologic deficit
(3)
. Neurologic injury
may be caused by pressure on the spinal cord from a paraspinal
abscess, inflammatory vasculitis with thrombosis of spinal
vessels, cord transection from vertebral collapse or spinal root
compression from arachnoiditis or abscess. This situation occur
in 12 to 50 % of cases
(8)
. The most serious complication of
spinal tuberculosis is paraplegia (Pott's paraplegia) which may
occur either early or late in the course of the disease. Butler and
Seddon, working independently, agreed with Sorrel-Dejerine to
divide Pott's paraplegia into two types : 1). Paraplegia of early
onset, coming on during the florid phase of the spinal disease
usually within the first 2 years, and 2). Paraplegia of late onset,
Cermin Dunia Kedokteran No. 137, 2002 29
background image
appearing even many years after the disease has become
quiescent and sometimes without evidence of reactivation
(8)
.
The pathology of Pott's paraplegia was described elsewhere in
the literatures.
Erythrocyte sedimentation rate is generally elevated, but is
usually nonspecific
(3)
. The raised CRP serum concentration
were strongly associated with pus formation (Hadi and
Sapardan, 1997). Tuberculin purified protein derivative (PPD)
skin test is usually positive but only indicates a history of
exposure (remote or current). Sputum specimens are positive
only if there is active pulmonary disease. The only laboratory
finding which can absolutely confirm the diagnosis is a positive
culture from a spinal lesion biopsy
(l,5,9,12)
.
Plain radiographs showed rarefaction of the vertebral end
plates, soft-tissue abscess, increasing loss of disc height,
variable degrees of osseous destruction and newbone
formation. In short, classic picture of spinal tuberculosis
showed narrowing of the disc space, vertebral collapse and
paraspinal abscess
(1)
. Computed tomography (CT) scan will
delineate the extent of bony destruction as well as soft tissue
changes around the spine and in the canal. It also helpful for the
guidance of biopsy and in the planning of operative procedures.
Magnetic resonance imaging (MRI) is the imaging modality of
choice because it will delineate soft-tissue masses in both the
sagittal and the coronal plane and for indicating the extent of
disease and the spread of tuberculous debris under the anterior
and posterior ligaments
(l,5,9)
.
Differential diagnosis is broad, including other infections
such as brucellosis or pyogenic bacterial infection, neoplasm
and sarcoidosis
(l)
.
Despite newer modalities of imaging of the spine and
spinal cord, diagnosis is best made by examination of biopsy
material, obtained by CT-guided or open blopsy
(l,3,5,6,8)
.
TREATMENT
The treatment of musculoskeletal tuberculosis is primarily
medical. Operative intervention is an adjunct to appropriate
antituberculous therapy. It is important to recognize and treat
early, before damage to the backbone causes nerve damage and
paralysis. Spinal tuberculosis can be successfully treated with
antituberculous chemotherapy alone, particularly if the
diagnosis is made early prior to gross bone destruction (Fam
and Rubenstein, 1993). With early, complete treatment the
damaged bones will usually heal and the patient may live
normally, although often somewhat hunched over. Treatment
options for spinal tuberculosis are selected based on the
presence or absence of spinal instability, neurologic deficits
and the level of surgical expertise available
(1)
. In countries
where adequate surgical facilities are lacking, an acceptable
alternative is antituberculous chemotherapy combined with a
spinal brace or cast. In Indonesia, however, the problem is not
only in the early treatment, but also in case finding. Among
40.300 estimated tuberculous patients in Central Java
(population 31 million), only 4668 cases (18%) were detected
and undergone therapy for tuberculosis
(13)
(Kompas, March 31,
2001).
The goal of treatment are to eradicate infection, and to
prevent or to treat neurological deficits and spinal deformity.
Use of antituberculosis drugs has virtually eliminated the
severe distortion of the spinal segment occuring late in the
course of the disease, which in the past often produced a
deforming gibbus or severely fixed scoliosis and pelvic
obliquity. Successful medical treatment of tuberculosis requires
the prolonged administration of a minimum of three drugs
susceptible to the organisms, and at least one of these drugs
must be bactericidal.
Isoniazid is the most potent bactericidal drug available and
is particularly effective against actively growing organisms. It
is relatively non-toxic, easily administered and inexpensive.
The usual adult dosage is 3-5 mg/kg/day. Hepatic toxicity is
major side effect. Ten milligrams of pyridoxin/day should be
given in conjunction with isoniazid to prevent peripheral
neuropathy. Rifampicin and pyrazinamide are the most
effective sterilizing drugs, and they are specifically effective
against bacilli that are dormant and undergo periodic burst of
activity. The usual adult dosage for rifampicin is 10 mg/kg/day;
for pyrazinamide, the dosage is generally 20-25 mg/kg/day.
Ethambutol is bacteriostatic. Retrobulbar neuritis is the most
frequent and serious adverse effect of this drug; the dosage is
15-25 mg/kg/day, and discontinued after 2-3 months.
The optimum duration of treatment has been an issue of
considerable debate, and much of the information now
available concerns the treatment of pulmonary disease. Watts
and Lifeso recommend that treatment be continued for a
minimum of twelve months for osteoarticular involvement,
extending to perhaps eighteen months for certain problems.
Parthasarathy et al reported their experience on 235 spinal
tuberculosis patients without paraplegia treated by three
different regimens : a) radical anterior resection with bone
grafting plus six months of daily isoniazid plus rifampicin; b)
ambulant chemotherapy for six months with daily isoniazid
plus rifampicin; c) similar to b), but with chemotherapy for
nine months. Ten years from the onset of treatment, 90% of a),
94% of b) and 99% of c) had a favourable status. They
concluded that ambulant chemotherapy for a period of six
months with daily isoniazid plus rifampicin (b) was an effective
treatment for spinal tuberculosis except in patients aged less
than 15 years with an initial angle of kyphosis of more than 30°
whose kyphosis increased substantially
(15)
.
The Medical Research Council Committee for Research
for Tuberculosis in the Tropics concluded that the treatment of
choice for spinal tuberculosis in developing countries is
ambulatory chemotherapy for 6 or 9 months with isoniazid and
rifampicin. Surgery is reserved for biopsy, management of
myelopathy, abscesses and sinuses and for stabilization to
prevent or correct kyphotic deformity especially if there is an
associated and progressive neurologic deficits.
The recommendations for duration of TB treatment in
HIV-infected persons are the same as for persons not infected
with HIV
(5)
.
Surgical intervention, once the mainstay of management, is
now less frequently required. Indications include diagnostic
biopsy when needle aspiration and biopsy are unsuccessful,
drainage of a large paraspinal abscess and spinal decom-
Cermin Dunia Kedokteran No. 137, 2002
30
background image
pression and fusion in patients with progressive neurologic
deficit, and in those with gross destruction and/or increasing
spinal deformity, particularly of the cervical or thoracic spine.
Another indications for operative intervention have been
proposed by several authors. Watts and Lifeso pointed out
absolute and relative indications for operative intervention.
4.
The Merck Manual of Medical Information - Home Edition. Ch. 181.
5.
Watts HG, Lifeso RM. Tuberculosis of bone and joints. J Bone and Joint
Surg 1996; 78A (2): 288-95.
6. Scully RE (Ed.). Case records of the Massachusetts General Hospital.
NEJM 1996; 334(12): 784-89.
7. Arnadi et al. Spinal tuberculosis profile at Cipto Mangunkusumo
Hospital, Jakarta, Indonesia during 1995-2000. Indonesian Rheumatology
Association, Annual Meeting, 2000.
8. Jones C. The great masquerader. Tuberculous spondylitis. Another
differential diagnosis in back pain.
SUMMARY
Tuberculosis infection is still a major health problem in
developing countries. Indonesia has the third largest TB
population in the world, after China and India. Spinal tuber-
culosis is found in about 1 % of tuberculous infection. Pott's
paraplegia can occur early or late in the course of the disease.
The choice of therapy depends on the condition of the patient,
the stage of the disease, availability of surgical facilities and
trained personnel.
9.
Ytterberg SR. Mycobacterial, fungal, and parasitic arthritis. In Klippel JH
(ed.) Primer on the Rheumatic Diseases. 11
th
ed., Arthritis Foundation,
Atlanta, GA, 1997. p 207-11.
10. Hodgson et al. The pathogenesis of Pott's paraplegia. J Bone and Joint
Surg 1967; 49A: 1147-56.
11. Hadi SA, Sapardan S : The CRP levels in spondylitis TB. Maj Ortopedi
Indon 1997; 25(1): 21-2.
12. Lifeso RN et al. Tuberculous spondylitis in adults. J Bone and Joint Surg
1985; 67A: 1405-13.
13. Kompas, Sabtu, 31 Maret 2001.
14. Anwar IB et al. Sensitifitas dan spesifisitas infecton pada penderita
tuberkulosa tulang belakang di Rumah Sakit Hasan Sadikin Bandung Juli
1998 - Oktober 1999. Maj Ortopedi Indon, Juni 2000; 28 (1): 42-9.
REFERENCES
15. Parthasarathy R et al. A comparison between ambulant treatment and
radical surgery - ten-year report. J Bone and Joint Surg 1999; 81B:
464-71.
1. Mahowald ML. Arthritis due to mycobacteria, fungi and parasites. In
Koopman WJ (eds.) Arthritis and allied conditions ­ A Textbook of
Rheumatology. 14
th
ed., Lippincott Williams & Wilkins, 2001, pp.
2607-28.
16. MRC Working Party on Tuberculosis of the Spine : Five-year assessment
of controlled trials of short-course chemotherapy regimens of 6, 9 or 18
months' duration for spinal tuberculosis in patients ambulatory from the
start or undergoing radical surgery. Fourteenth report of the Medical
Research Council Working Party on Tuberculosis of the Spine. Inter-
national Orthopaedics 1999; 23(2) : 73-81.
2.
Agarwal P, Rathi P, Verma R, Pradhan CG : Tuberculous spondylitis :
`Global lesion'. Special issues on Tuberculosis. Bombay Hospital Journal,
1999.
3.
Fam AG, Rubenstein J. Another look at spinal tuberculosis. J Rheum 20:
10; 1731-40.
Cermin Dunia Kedokteran No. 137, 2002 31