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Osteomyelitis

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Osteomyelitis
Other namesBone infection
Osteomyelitis of the 1st toe
SpecialtyInfectious disease, orthopedics
SymptomsPain in a specific bone, overlying redness, fever, weakness[1]
ComplicationsAmputation[2]
Usual onsetYoung or old[1]
DurationShort or long term[2]
CausesBacterial, fungal[2]
Risk factorsDiabetes, intravenous drug use, prior removal of the spleen, trauma to the area[1]
Diagnostic methodBlood tests, medical imaging, bone biopsy[2]
Differential diagnosisCharcot's joint, rheumatoid arthritis, infectious arthritis, giant cell tumor, cellulitis[1][3]
TreatmentAntimicrobials, surgery[4]
PrognosisLow risk of death with treatment[5]
Frequency2.4 per 100,000 per year[6]

Osteomyelitis (OM) is an infection of bone.[1] Symptoms may include pain in a specific bone with overlying redness, fever, and weakness.[1] The feet, spine, and hips are the most commonly involved bones in adults.[2]

The cause is usually a bacterial infection,[1][7][2] but rarely can be a fungal infection.[8] It may occur by spread from the blood or from surrounding tissue.[4] Risks for developing osteomyelitis include diabetes, intravenous drug use, prior removal of the spleen, and trauma to the area.[1] Diagnosis is typically suspected based on symptoms and basic laboratory tests as C-reactive protein and erythrocyte sedimentation rate. This is because plain radiographs are unremarkable in the first few days following acute infection.[7][2] Diagnosis is further confirmed by blood tests, medical imaging, or bone biopsy.[2]

Treatment of bacterial osteomyelitis often involves both antimicrobials and surgery.[7][4] Treatment outcomes of bacterial osteomyelitis are generally good when the condition has only been present a short time.[7][2] In people with poor blood flow, amputation may be required.[2] Treatment of the relatively rare fungal osteomyelitis as mycetoma infection entails the use of antifungal medications.[9] In contrast to bacterial osteomyelitis, amputation or large bony resections is more common in neglected fungal osteomyelitis (mycetoma) where infections of the foot account for the majority of cases.[8][9] About 2.4 per 100,000 people are affected by osteomyelitis each year.[6] The young and old are more commonly affected.[7][1] Males are more commonly affected than females.[3] The condition was described at least as early as the 300s BC by Hippocrates.[4] Prior to the availability of antibiotics, the risk of death was significant.[10]

Signs and symptoms

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Symptoms may include pain in a specific bone with overlying redness, fever, and weakness and inability to walk especially in children with acute bacterial osteomyelitis.[7][1] Onset may be sudden or gradual.[1] Enlarged lymph nodes may be present.[11] In fungal osteomyelitis, there is usually a history of walking bare-footed, especially in rural and farming areas. Contrary to the mode of infection in bacterial osteomyelitis, which is primarily blood-borne, fungal osteomyelitis starts as a skin infection, then invades deeper tissues until it reaches bone.[8]

Cause

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Age group Most common organisms
Newborns (younger than 4 mo) Staphylococcus aureus, Enterobacter species, and group A and B Streptococcus species
Children (aged 4 mo to 4 y) S. aureus, group A Streptococcus species, Haemophilus influenzae, and Enterobacter species
Children, adolescents (aged 4 y to adult) S. aureus (80%), group A Streptococcus species, H. influenzae, and Enterobacter species
Adult S. aureus and occasionally Enterobacter or Streptococcus species
Sickle cell anemia patients Salmonella species are most common in patients with sickle cell disease.[12]

Acute osteomyelitis almost invariably occurs in children who are otherwise healthy, because of rich blood supply to the growing bones. When adults are affected, it may be because of compromised host resistance due to debilitation, intravenous drug abuse, infectious root-canaled teeth, or other disease or drugs (e.g., immunosuppressive therapy).[7] The most commonly affected areas for children are the long bones,[7][failed verification] and for adults, the feet, spine, and hips.[2]

Osteomyelitis is a secondary complication in 1–3% of patients with pulmonary tuberculosis.[13] In this case, the bacteria, in general, spread to the bone through the circulatory system, first infecting the synovium (due to its higher oxygen concentration) before spreading to the adjacent bone.[13] In tubercular osteomyelitis, the long bones and vertebrae are the ones that tend to be affected.[13]

Staphylococcus aureus is the organism most commonly isolated from all forms of osteomyelitis.[13]

Osteomyelitis is often caused by Staphylococcus aureus.[14] In infants, S. aureus, Group B streptococci and Escherichia coli are commonly isolated; in children from one to 16 years of age, S. aureus, Streptococcus pyogenes, and Haemophilus influenzae are common. In some subpopulations, including intravenous drug users and splenectomized patients, Gram-negative bacteria, including enteric bacteria, are significant pathogens.[15]

The most common form of the disease in adults is caused by injury exposing the bone to local infection.[14] Staphylococcus aureus is the most common organism seen in osteomyelitis, seeded from areas of contiguous infection. But anaerobes and Gram-negative organisms, including Pseudomonas aeruginosa, E. coli, and Serratia marcescens, are also common. Mixed infections are the rule rather than the exception.[15]

Systemic mycotic infections may also cause osteomyelitis. The two most common are Blastomyces dermatitidis and Coccidioides immitis.[citation needed]

In osteomyelitis involving the vertebral bodies, about half the cases are due to S. aureus, and the other half are due to tuberculosis (spread hematogenously from the lungs). Tubercular osteomyelitis of the spine was so common before the initiation of effective antitubercular therapy, it acquired a special name, Pott's disease.[citation needed]

The Burkholderia cepacia complex has been implicated in vertebral osteomyelitis in intravenous drug users.[16]

Pathogenesis

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In general, microorganisms may infect bone through one or more of three basic methods

The area usually affected when the infection is contracted through the bloodstream is the metaphysis of the bone.[17] Once the bone is infected, leukocytes enter the infected area, and, in their attempt to engulf the infectious organisms, release enzymes that lyse the bone. Pus spreads into the bone's blood vessels, impairing their flow, and areas of devitalized infected bone, known as sequestra, form the basis of a chronic infection.[13] Often, the body will try to create new bone around the area of necrosis. The resulting new bone is often called an involucrum.[13] On histologic examination, these areas of necrotic bone are the basis for distinguishing between acute osteomyelitis and chronic osteomyelitis. Osteomyelitis is an infective process that encompasses all of the bone (osseous) components, including the bone marrow. When it is chronic, it can lead to bone sclerosis and deformity.[citation needed]

Chronic osteomyelitis may be due to the presence of intracellular bacteria.[19] Once intracellular, the bacteria are able to spread to adjacent bone cells.[20] At this point, the bacteria may be resistant to certain antibiotics.[21] These combined factors may explain the chronicity and difficult eradication of this disease, resulting in significant costs and disability, potentially leading to amputation. The presence of intracellular bacteria in chronic osteomyelitis is likely an unrecognized contributing factor in its persistence.[citation needed]

In infants, the infection can spread to a joint and cause arthritis. In children, large subperiosteal abscesses can form because the periosteum is loosely attached to the surface of the bone.[13]

Because of the particulars of their blood supply, the tibia, femur, humerus, vertebrae, maxilla and the mandibular bodies are especially susceptible to osteomyelitis.[22] Abscesses of any bone, however, may be precipitated by trauma to the affected area. Many infections are caused by Staphylococcus aureus, a member of the normal flora found on the skin and mucous membranes. In patients with sickle cell disease, the most common causative agent is Salmonella, with a relative incidence more than twice that of S. aureus.[12]

Diagnosis

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Mycobacterium doricum osteomyelitis and soft tissue infection. Computed tomography scan of the right lower extremity of a 21-year-old patient, showing abscess formation adjacent to nonunion of a right femur fracture.
Extensive osteomyelitis of the forefoot
Osteomyelitis in both feet as seen on bone scan

The diagnosis of osteomyelitis is complex and relies on a combination of clinical suspicion and indirect laboratory markers such as a high white blood cell count and fever, although confirmation of clinical and laboratory suspicion with imaging is usually necessary.[23]

Radiographs and CT are the initial method of diagnosis, but are not sensitive and only moderately specific for the diagnosis. They can show the cortical destruction of advanced osteomyelitis, but can miss nascent or indolent diagnoses.[23]

Confirmation is most often by MRI.[24] The presence of edema, diagnosed as increased signal on T2 sequences, is sensitive, but not specific, as edema can occur in reaction to adjacent cellulitis. Confirmation of bony marrow and cortical destruction by viewing the T1 sequences significantly increases specificity. The administration of intravenous gadolinium-based contrast enhances specificity further. In certain situations, such as severe Charcot arthropathy, diagnosis with MRI is still difficult.[23] Similarly, it is limited in distinguishing avascular necrosis from osteomyelitis in sickle cell anemia.[25]

Nuclear medicine scans can be a helpful adjunct to MRI in patients who have metallic hardware that limits or prevents effective magnetic resonance. Generally a triple phase technetium 99 based scan will show increased uptake on all three phases. Gallium scans are 100% sensitive for osteomyelitis but not specific, and may be helpful in patients with metallic prostheses. Combined WBC imaging with marrow studies has 90% accuracy in diagnosing osteomyelitis.[26]

Diagnosis of osteomyelitis is often based on radiologic results showing a lytic center with a ring of sclerosis.[13] Culture of material taken from a bone biopsy is needed to identify the specific pathogen;[27] alternative sampling methods such as needle puncture or surface swabs are easier to perform, but cannot be trusted to produce reliable results.[28][29]

Factors that may commonly complicate osteomyelitis are fractures of the bone, amyloidosis, endocarditis, or sepsis.[13]

Classification

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The definition of osteomyelitis (OM) is broad, and encompasses a wide variety of conditions. Traditionally, the length of time the infection has been present and whether there is suppuration (pus formation) or osteosclerosis (pathological increased density of bone) are used to arbitrarily classify OM. Chronic OM is often defined as OM that has been present for more than one month. In reality, there are no distinct subtypes; instead, there is a spectrum of pathologic features that reflects a balance between the type and severity of the cause of the inflammation, the immune system, and local and systemic predisposing factors.[citation needed]

OM can also be typed according to the area of the skeleton in which it is present. For example, osteomyelitis of the jaws is different in several respects from osteomyelitis present in a long bone. Vertebral osteomyelitis is another possible presentation.[citation needed]

Treatment

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Osteomyelitis often requires prolonged antibiotic therapy for weeks or months. A PICC line or central venous catheter can be placed for long-term intravenous medication administration. Some studies of children with acute osteomyelitis report that antibiotic by mouth may be justified due to PICC-related complications.[30][31] It may require surgical debridement in severe cases, or even amputation. Antibiotics by mouth and by intravenous appear similar.[32][33]

Due to insufficient evidence it is unclear what the best antibiotic treatment is for osteomyelitis in people with sickle cell disease as of 2019.[34]

Initial first-line antibiotic choice is determined by the patient's history and regional differences in common infective organisms. A treatment lasting 42 days is practiced in a number of facilities.[35] Local and sustained availability of drugs have proven to be more effective in achieving prophylactic and therapeutic outcomes.[36] Open surgery is needed for chronic osteomyelitis, whereby the involucrum is opened and the sequestrum is removed or sometimes saucerization[37] can be done. Hyperbaric oxygen therapy has been shown to be a useful adjunct to the treatment of refractory osteomyelitis.[38]

Before the widespread availability and use of antibiotics, blow fly larvae were sometimes deliberately introduced to the wounds to feed on the infected material, effectively scouring them clean.[39][40]

There is tentative evidence that bioactive glass may also be useful in long bone infections.[41] Support from randomized controlled trials, however, was not available as of 2015.[42]

Hemicorporectomy is performed in severe cases of Terminal Osteomyelitis in the Pelvis if further treatment won't stop the infection.[43]

History

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The word is from Greek words ὀστέον osteon, meaning bone, μυελός myelos meaning marrow, and -ῖτις -itis meaning inflammation.

In 1875, American artist Thomas Eakins depicted a surgical procedure for osteomyelitis at Jefferson Medical College, in an oil painting titled The Gross Clinic.[44]

Canadian politician and premier of Saskatchewan Tommy Douglas suffered from osteomyelitis as a child, and in 1910, underwent several surgeries, which the surgeon performed for free in exchange for allowing his medical students to observe the procedures (which Douglas's parents could not have otherwise afforded). This experience convinced him that medical care should be free for everyone.[45] Douglas became known as the Canadian "Father of Medicare."[46]

Fossil record

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Main article: Paleopathology

Evidence for osteomyelitis found in the fossil record is studied by paleopathologists, specialists in ancient disease and injury. It has been reported in fossils of the large carnivorous dinosaur Allosaurus fragilis.[47] Osteomyelitis has been also associated with the first evidence of parasites in dinosaur bones.[48]

See also

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References

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  1. ^ a b c d e f g h i j k "Osteomyelitis". NORD (National Organization for Rare Disorders). 2005. Archived from the original on 11 February 2017. Retrieved 20 July 2017.
  2. ^ a b c d e f g h i j k "Osteomyelitis". Genetic and Rare Diseases Information Center (GARD). 2016. Archived from the original on 9 February 2017. Retrieved 20 July 2017.
  3. ^ a b Ferri, Fred F. (2017). Ferri's Clinical Advisor 2018 E-Book: 5 Books in 1. Elsevier Health Sciences. p. 924. ISBN 978-0-323-52957-0. Archived from the original on 2017-09-10.
  4. ^ a b c d Schmitt, SK (June 2017). "Osteomyelitis". Infectious Disease Clinics of North America. 31 (2): 325–38. doi:10.1016/j.idc.2017.01.010. PMID 28483044. S2CID 257184257.
  5. ^ Bennett, John E.; Dolin, Raphael; Blaser, Martin J. (2014). Principles and Practice of Infectious Diseases. Elsevier Health Sciences. p. 2267. ISBN 978-1-4557-4801-3. Archived from the original on 2017-09-10.
  6. ^ a b Hochberg, Marc C.; Silman, Alan J.; Smolen, Josef S.; et al. (2014). Rheumatology E-Book. Elsevier Health Sciences. p. 885. ISBN 978-0-7020-6303-9. Archived from the original on 2017-09-10.
  7. ^ a b c d e f g h El-Sobky, T; Mahmoud, S (July 2021). "Acute osteoarticular infections in children are frequently forgotten multidiscipline emergencies: beyond the technical skills". EFORT Open Reviews. 6 (7): 584–592. doi:10.1302/2058-5241.6.200155. PMC 8335954. PMID 34377550.
  8. ^ a b c El-Sobky, TA; Haleem, JF; Samir, S (2015). "Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy". Case Reports in Pathology. 2015: 129020. doi:10.1155/2015/129020. PMC 4592886. PMID 26483983.
  9. ^ a b van de Sande, Wendy; Fahal, Ahmed; Ahmed, Sarah Abdalla; et al. (10 March 2018). "Closing the mycetoma knowledge gap". Medical Mycology. 56 (suppl_1): S153–S164. doi:10.1093/mmy/myx061. PMID 28992217.
  10. ^ Brackenridge, R. D. C.; Croxson, Richard S.; Mackenzie, Ross (2016). Medical Selection of Life Risks 5th Edition Swiss Re branded. Springer. p. 912. ISBN 978-1-349-56632-7. Archived from the original on 2017-09-10.
  11. ^ Root, Richard K.; Waldvogel, Francis; Corey, Lawrence; Stamm, Walter E. (1999). Clinical Infectious Diseases: A Practical Approach. Oxford University Press. p. 577. ISBN 978-0-19-508103-9.
  12. ^ a b Burnett, M.W.; J.W. Bass; B.A. Cook (1998-02-01). "Etiology of osteomyelitis complicating sickle cell disease". Pediatrics. 101 (2): 296–97. doi:10.1542/peds.101.2.296. PMID 9445507.
  13. ^ a b c d e f g h i j Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; Mitchell, Richard N. (2007). Robbins Basic Pathology (8th ed.). Saunders Elsevier. pp. 810–11 ISBN 978-1-4160-2973-1
  14. ^ a b "Osteomyelitis". Mayo Clinic. 8 November 2022. Retrieved 25 July 2023.
  15. ^ a b Carek, P.J.; L.M. Dickerson; J.L. Sack (2001-06-15). "Diagnosis and management of osteomyelitis". Am Fam Physician. 63 (12): 2413–20. PMID 11430456.
  16. ^ Weinstein, Lenny; Knowlton, Christin A.; Smith, Miriam A. (2007-12-16). "Cervical osteomyelitis caused by Burkholderia cepacia after rhinoplasty". Journal of Infection in Developing Countries. 2 (1): 76–77. doi:10.3855/jidc.327. ISSN 1972-2680. PMID 19736393.
  17. ^ a b Luqmani, Raashid; Robb, James; Daniel, Porter; Benjamin, Joseph (2013). Orthopaedics, Trauma and Rheumatology (second ed.). Mosby. p. 96. ISBN 978-0-7234-3680-5.
  18. ^ Metsemakers, WJ; Morgenstern, M; McNally, MA; et al. (March 2018). "Fracture-related infection: A consensus on definition from an international expert group". Injury. 49 (3): 505–510. doi:10.1016/j.injury.2017.08.040. hdl:1765/101708. PMID 28867644.
  19. ^ Ellington. "Microbial Pathogenesis" (1999).[page needed]
  20. ^ Ellington Journal of Bone and Joint Surgery (2003).[page needed]
  21. ^ Ellington. Journal of Orthopedic Research (2006).[page needed]
  22. ^ King MD, Randall W, Johnson D (2006-07-13). "Osteomyelitis". eMedicine. WebMD. Archived from the original on 2007-11-09. Retrieved 2007-11-11.
  23. ^ a b c Howe, B. M.; Wenger, D. E.; Mandrekar, J; Collins, M. S. (2013). "T1-weighted MRI imaging features of pathologically proven non-pedal osteomyelitis". Academic Radiology. 20 (1): 108–14. doi:10.1016/j.acra.2012.07.015. PMID 22981480.
  24. ^ Arachchige, Arosh S. Perera Molligoda; Verma, Yash (2024-01-03). "State of the art in the diagnostic evaluation of osteomyelitis: exploring the role of advanced MRI sequences—a narrative review". Quantitative Imaging in Medicine and Surgery. 14 (1): 1070085–1071085. doi:10.21037/qims-23-1138. ISSN 2223-4306. PMC 10784094. PMID 38223108.
  25. ^ Delgado, J; Bedoya, M. A.; Green, A. M.; et al. (2015). "Utility of unenhanced fat-suppressed T1-weighted MRI in children with sickle cell disease – can it differentiate bone infarcts from acute osteomyelitis?". Pediatric Radiology. 45 (13): 1981–87. doi:10.1007/s00247-015-3423-8. PMID 26209118. S2CID 7362493.
  26. ^ Termaat, M. F.; Raijmakers, P. G.; Scholten, H. J.; et al. (2005). "The accuracy of diagnostic imaging for the assessment of chronic osteomyelitis: A systematic review and meta-analysis". The Journal of Bone and Joint Surgery. American Volume. 87 (11): 2464–71. doi:10.2106/JBJS.D.02691 (inactive 2024-11-13). PMID 16264122.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  27. ^ Zuluaga AF; Galvis W; Saldarriaga JG; et al. (2006-01-09). "Etiologic diagnosis of chronic osteomyelitis: A prospective study". Archives of Internal Medicine. 166 (1): 95–100. doi:10.1001/archinte.166.1.95. ISSN 0003-9926. PMID 16401816. S2CID 2599315.
  28. ^ Zuluaga, Andrés F; Galvis, Wilson; Jaimes, Fabián; Vesga, Omar (2002-05-16). "Lack of microbiological concordance between bone and non-bone specimens in chronic osteomyelitis: An observational study". BMC Infectious Diseases. 2 (1): 8. doi:10.1186/1471-2334-2-8. PMC 115844. PMID 12015818.
  29. ^ Senneville E, Morant H, Descamps D, et al. (2009). "Needle puncture and transcutaneous bone biopsy cultures are inconsistent in patients with diabetes and suspected osteomyelitis of the foot". Clinical Infectious Diseases. 48 (7): 888–93. doi:10.1086/597263. PMID 19228109. S2CID 28498296.
  30. ^ Keren, Ron; Shah, Samir S.; Srivastava, Rajendu; et al. (2015-02-01). "Comparative Effectiveness of Intravenous vs Oral Antibiotics for Postdischarge Treatment of Acute Osteomyelitis in Children". JAMA Pediatrics. 169 (2): 120–28. doi:10.1001/jamapediatrics.2014.2822. ISSN 2168-6203. PMID 25506733.
  31. ^ Norris, Anne H; Shrestha, Nabin K; Allison, Genève M; et al. (2019-01-01). "2018 Infectious Diseases Society of America Clinical Practice Guideline for the Management of Outpatient Parenteral Antimicrobial Therapya". Clinical Infectious Diseases. 68 (1): e1–e35. doi:10.1093/cid/ciy745. ISSN 1058-4838. PMID 30423035.
  32. ^ Sæterdal, I; Akselsen, PE; Berild, D; et al. (2010). "Antibiotic Therapy in Hospital, Oral Versus Intravenous Treatment". Oslo, Norway: Knowledge Centre for the Health Services at The Norwegian Institute of Public Health. PMID 29319957.
  33. ^ Stengel, D; Bauwens, K; Sehouli, J; et al. (October 2001). "Systematic review and meta-analysis of antibiotic therapy for bone and joint infections". The Lancet. Infectious Diseases. 1 (3): 175–88. doi:10.1016/S1473-3099(01)00094-9. PMID 11871494.
  34. ^ Martí-Carvajal, AJ; Agreda-Pérez, LH (7 October 2019). "Antibiotics for treating osteomyelitis in people with sickle cell disease". The Cochrane Database of Systematic Reviews. 10 (4): CD007175. doi:10.1002/14651858.CD007175.pub5. PMC 6778815. PMID 31588556.
  35. ^ Putland M.D, Michael S., Hyperbaric Medicine, Capital Regional Medical Center, Tallahassee, Florida, personal inquiry June 2008.
  36. ^ Soundrapandian, C; Datta S; Sa B (2007). "Drug-eluting implants for osteomyelitis". Critical Reviews in Therapeutic Drug Carrier Systems. 24 (6): 493–545. doi:10.1615/CritRevTherDrugCarrierSyst.v24.i6.10. PMID 18298388.
  37. ^ "Saucerization".
  38. ^ Kawashima M, Tamura H, Nagayoshi I, et al. (2004). "Hyperbaric oxygen therapy in orthopedic conditions". Undersea and Hyperbaric Medicine. 31 (1): 155–62. PMID 15233171.
  39. ^ Baer M.D., William S. (1 July 1931). "The Treatment of Chronic Osteomyelitis with the Maggot (Larva of the Blow Fly)". Journal of Bone and Joint Surgery. 13 (3): 438–75. Archived from the original on 22 December 2007. Retrieved 2007-11-12.
  40. ^ McKeever, Duncan Clark (June 2008). "The Classic: Maggots in Treatment of Osteomyelitis: A Simple Inexpensive Method". Clinical Orthopaedics and Related Research. 466 (6): 1329–35. doi:10.1007/s11999-008-0240-5. PMC 2384033. PMID 18404291.
  41. ^ Aurégan, JC; Bégué, T (December 2015). "Bioactive glass for long bone infection: a systematic review". Injury. 46 (Suppl 8): S3–7. doi:10.1016/s0020-1383(15)30048-6. PMID 26747915.
  42. ^ van Gestel, NA; Geurts, J; Hulsen, DJ; et al. (2015). "Clinical Applications of S53P4 Bioactive Glass in Bone Healing and Osteomyelitic Treatment: A Literature Review". BioMed Research International. 2015: 684826. doi:10.1155/2015/684826. PMC 4609389. PMID 26504821.
  43. ^ Jeffrey, Janis (2009). "A 25-Year Experience with Hemicorporectomy for Terminal Pelvic Osteomyelitis" (PDF).
  44. ^ Floryan, Meg. "Eakins's The Gross Clinic". Smarthistory. Khan Academy. Archived from the original on October 21, 2020. Retrieved February 11, 2013.
  45. ^ Thomas, Lewis, ed. (1982). The Making of a Socialist: The Recollections of T.C. Douglas. Edmonton: The University of Alberta Press. pp. 6–7. ISBN 978-0-88864-070-3.
  46. ^ Bryan Eneas. "Tommy Douglas honoured as person of national historic significance". CBC News. Retrieved 19 March 2019.
  47. ^ Molnar, R. E. (2001). "Theropod paleopathology: a literature survey". In Tanke, D. H.; Carpenter, K.; Skrepnick, M. W. (eds.). Mesozoic Vertebrate Life. Bloomingon: Indiana University Press. pp. 337–63. ISBN 0-253-33907-3.
  48. ^ Langlois, Jill (18 Nov 2020). "First Evidence of Parasites in Dinosaur Bones Found". Smithsonian Magazine. Retrieved 2020-11-24.
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