Guidelines for the management of osteoporosis and fragility fractures
Internal and Emergency Medicine
https://doi.org/10.1007/s11739-018-1874-2
EM - ORIGINAL
Guidelines for the management of osteoporosis and fragility fractures
Ranuccio Nuti1 · Maria Luisa Brandi2 · Giovanni Checchia3 · Ombretta Di Munno4 · Ligia Dominguez5 ·
Paolo Falaschi6 · Carmelo Erio Fiore1 · Giovanni Iolascon3 · Stefania Maggi6 · Raffaella Michieli7 · Silvia Migliaccio2 ·
Salvatore Minisola1 · Maurizio Rossini4 · Giuseppe Sessa8 · Umberto Tarantino8 · Antonella Toselli7 ·
Giovanni Carlo Isaia5
Received: 20 April 2018 / Accepted: 6 May 2018
© The Author(s) 2018
Abstract
The purpose of this document,a result of the harmonisation and revision of Guidelines published separately by the SIMFER,
SIOMMMS/SIR, and SIOT associations, is to provide practical indications based on specific levels of evidence and various grades of recommendations, drawn from available literature, for the management of osteoporosis and for the diagnosis,
prevention, and treatment of fragility fractures. These indications were discussed and formally approved by the delegates of
the Italian Scientific Associations involved in the project (SIE, SIGG, SIMFER, SIMG, SIMI, SIOMMMS, SIR, and SIOT).
Keywords Osteoporosis · Fractures · Therapy
* Salvatore Minisola
1
SIMI, (Italian Society of Internal Medicine), Rome, Italy
2
SIE (Italian Society of Endocrinology), Rome, Italy
3
SIMFER (Italian Society of Physical and Rehabilitation
Medicine), Rome, Italy
4
SIR (Italian Society of Rheumatology), Milan, Italy
5
SIOMMMS (Italian Society for Osteoporosis, Mineral
Metabolism and Bone Diseases), Rome, Italy
6
SIGG (Italian Society of Gerontology and Geriatrics),
Firenze, Italy
7
SIMG (Italian Society of General Medicine and of Primary
Care), Firenze, Italy
8
SIOT (Italian Society of Orthopaedics), Genoa, Italy
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Internal and Emergency Medicine
Definition
Osteoporosis is a systemic skeletal disease characterized by
a reduction in bone mass and qualitative skeletal changes
(macro- and microarchitecture, material properties, geometry, and micro-damage) that cause an increase in bone fragility and higher fracture risk. There are two forms of the
disease: (a) primary osteoporosis, which includes juvenile,
postmenopausal, and male and senile osteoporosis; and (b)
secondary osteoporosis, which is caused by a large number
of diseases and medications.
Fragility fractures may occur in almost all skeletal segments, but the preferential locations are the vertebral column, the proximal ends of the femur and humerus, and the
distal end of the radius (Colles fracture). Trauma due to a
fall is by far the most frequent cause of fractures affecting
long bones (femur, humerus, and radius), while it is more
difficult to determine the cause and the exact time of fragility
fractures of the vertebral body, which often go undiagnosed.
During patient evaluation, there are some clinical history
details that can suggest a vertebral fracture: recent trauma,
prolonged use of corticosteroids, age, structural spinal
deformity, loss of height > 6 cm, and a distance between
the last rib and the iliac crest < 2 fingers. It is, therefore,
advisable to carefully evaluate the presence of dorso-lumbar
pain, progressive loss of height, or dorsal kyphosis, which
may result in alterations of the respiratory or gastrointestinal
functions.
Primary osteoporosis
(a) Juvenile osteoporosis
The expression juvenile osteoporosis is commonly used
to indicate a form of osteoporosis found in childhood and
adolescence: this disease is mostly due to genetic mutations
that can lead to quantitative or qualitative alterations in the
connective tissue component of bone (as in osteogenesis
imperfecta, which is also characterized by extra-skeletal
alterations), or to an altered osteoblastic activity with the
particular involvement of the trabecular bone (as in the autosomal dominant form caused by inappropriate activation of
the Wnt-β catenin signal). It can also be secondary to leukaemia, prolonged immobilisation, or chronic inflammatory
diseases; or it can be due to the chronic administration of
drugs such as anti-epileptics and glucocorticoids. When it
is not possible to identify possible causes of bone loss and
fragility fractures, this condition is referred to as juvenile
idiopathic osteoporosis.
In accordance with the Pediatric Official Positions of the
International Society for Clinical Densitometry (ISCD), the
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diagnosis of osteoporosis in childhood is made on the basis
of a history of one or more vertebral fragility fractures, or of
a history of at least two fractures of the long bones before the
age of 10, or of three or more long bone fractures before the
age of 19 in the absence of local pathologies, high-energy
trauma, and bone mineral density (BMD) Z-score ≤ 2.0
standard deviation (SD) at the lumbar spine or total body
less head (TBLH) scans.
(b) Postmenopausal osteoporosis
Postmenopausal osteoporosis is the most frequent primary form of the pathology, and is due to oestrogen deficiency associated with menopause, which provokes an
acceleration of bone loss due to age. It is characterized by
rapid loss of trabecular bone mass with perforation of the
trabecular bone, while cortical bone is partially spared. This
loss is responsible for fragility fractures due to load bearing, especially by the vertebrae and the distal radius. It is
also generally characterized by a high bone turnover rate,
with bone marrow expansion, and a prevalence of increased
endosteal resorption, and also by inhibition of periosteal
bone formation. BMD as determined by dual-X-ray absorptiometry (DXA) is unanimously considered to be the most
important predictor of osteoporotic fractures, and is indicated, according to Italian Ministerial Decree regulating
Essential Assistance Levels (EAL), in women of any age,
in the presence of a major risk factor (for example, previous fragility fracture caused by minimal trauma, maternal
family history of osteoporotic fracture at less than 75 years
of age, menopause before 45 years of age, body mass index
(BMI) < 19 kg/m2, and prolonged glucocorticoid therapy)
and, for postmenopausal women only, the presence of at
least three or more of the following minor risk factors:
1. Age greater than 65 years
2. Family history of severe osteoporosis
3. Premenopausal amenorrhoea for a period greater than
6 months
4. Inadequate calcium intake (< 1200 mg/day)
5. Smoking > 20 cigarettes/day
6. Alcoholism (> 60 g/day)
(c) Male osteoporosis.
Osteoporosis is a major public health problem for men,
as well; in fact, more than 20% of all hip fractures occur in
males, and the incidence of vertebral fractures is about half
that reported in women. Male osteoporosis is frequently secondary (about two-thirds of cases in males versus one-third
in females), so it is always advisable to exclude other pathological conditions associated with osteoporosis (Table 1).
Moreover, in men, the BMD DXA technique is the method
of choice to d (...truncated)