Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / @xirurgi_2025 / @xirurgi_2025 - 868 - файл
.pdf
354
https://t.me/med1917
T. Ballouz et al.
follow-up counseling, to recognize the anxiety resulting from the exposure incident,
and to provide psychological counseling and stress management if needed. Finally,
it is essential to promote a culture of safety in healthcare settings, which will provide optimal protection and care for all patients and healthcare workers.
References
1. Needlestick transmission of HTLV-III from a patient infected in Africa. Lancet.
1984;2(8416):1376–7.
2. U.S. Department of Labor Occupational Safety & Health Administration. Regulations
(Standards- 29 CFR) bloodborne pathogens [Internet]. p.1910.1030. https://www.osha.gov/
laws- regs/regulations/standardnumber/1910/1910.1030
3. Occupational Safety and Health Administration. Bloodborne pathogens and needlestick
prevention [Internet]. [cited 9 Jul 2019]. https://www.osha.gov/pls/oshaweb/owadisp.
show_document?p_id=10051&p_table=STANDARDS
4. Elseviers MM, Arias-Guillén M, Gorke A, Arens HJ.Sharps injuries amongst healthcare workers: review of incidence, transmissions and costs. J Ren Care. 2014;40(3):150–6.
5. NIOSH.Use of blunt-tip suture needles to decrease percutaneous injuries to surgical personnel. Saf Heal Inf Bull; 2007. http://www.cdc.gov/niosh/docs/2008- 101/pdfs/2008- 101.pdf
6. Makary M, Al-Attar A, Holzmueller CG, Sexton B, Syin D, Gilson MM, etal. Needlestick
injuries among surgeons in training. N Engl J Med. 2007;356(26):2693–9.
7. Mannocci A, De CG, Di BV, Saulle R, Unim B, Nicolotti N, etal. How much do needlestick
injuries cost? A systematic review of the economic evaluations of needlestick and sharps injuries among healthcare personnel. Infect Control Hosp Epidemiol. 2016;37(6):536–646.
8. Cooke CE, Stephens JM.Clinical, economic, and humanistic burden of needlestick injuries in
healthcare workers. Med Devices Evid Res. 2017;10:225–35.
9. Henry K, Campbell S, Jackson B, Balfour H, Rhame F, Sannerud K, etal. Long-term follow up of health care workers with work-site exposure to human immunodeciency virus.
JAMA. 1990;263(13):1765.
10. Armstrong K, Gorden R, Santorella G.Occupational exposure of healthcare workers (HCWs)
to human immunodeciency virus (HIV): stress reactions and counseling interventions. Soc
Work Health Care. 1995;21(3):61–80.
11. Worthington MG, Ross JJ, Bergeron EK.Posttraumatic stress disorder after occupational HIV
exposure: two cases and a literature review. Infect Control Hosp Epidemiol. 2014;27(2):215–7.
12. United States Public Health Service. Updated U.S.Public Health Service guidelines for the
management of occupational exposures to HBV, HCV, and HIV and recommendations for
postexposure prophylaxis. Morb Mortal Wkly Rep [Internet]. 2001;50(RR11):1–42. https://
www.cdc.gov/mmwr/preview/mmwrhtml/rr5011a1.htm
13. Tarantola A, Abiteboul D, Rachline A.Infection risks following accidental exposure to blood
or body uids in health care workers: a review of pathogens transmitted in published cases. Am
J Infect Control. 2005;34(6):367–75.
14. Beltrami EM, Williams IT, Shapiro CN, Chamberland ME. Risk and management of bloodborne infections in health care workers. Clin Microbiol Rev. 2000;13(3):385–407.
15. Kidd-Ljunggren K, Holmberg A, Bläckberg J, Lindqvist B.High levels of hepatitis B virus
DNA in body uids from chronic carriers. J Hosp Infect. 2006;64(4):352–7.
16. Scott RM, Snitbhan R, Bancroft WH, Alter HJ, Tingpalapong M.Experimental transmission
of hepatitis B virus by semen and saliva. J Infect Dis. 1980;142(1):67–71.
17. Irwin GR, Allen AM, Bancroft WH, Karwacki JJ, Brown HL, Pinkerton RH, etal. Hepatitis B
antigen in saliva, urine, and stool. Infect Immun. 1975;11(1):142–5.
18. Victor Feinman S, Berris B, Rebane A, Sinclair JC, Wilson S, Wrobel D. Failure to
detect hepatitis b surface antigen (Hbsag) in feces of hbsag-positive persons. J Infect Dis.
1979;140(3):407–10.

21 “I Got Stuck!” Blood Exposure in the OR: Prevention and Management of Sharp…
https://t.me/med1917
19. Bond WW, Favero MS, Petersen NJ, Gravelle CR, Ebert JW, Maynard JE.Survival of hepatitis
B virus after drying and storage for one week. Lancet. 1981;317(8219):550–1.
20. Centers for Disease Control and Prevention. Prevention of hepatitis B virus infection in the
United States: recommendations of the Advisory Committee on Immunization. Morb Mortal
Wkly Rep. 2018;67
21. Savasi V, Parrilla B, Ratti M, Oneta M, Clerici M, Ferrazzi E.Hepatitis C virus RNA detection in different semen fractions of HCV/HIV-1 co-infected men by nested PCR.Eur J Obstet
Gynecol Reprod Biol. 2010;151(1):52–5.
22. Rey D, Fritsch S, Schmitt C, Meyer P, Lang JM, Stoll-Keller F.Quantitation of hepatitis C
virus RNA in saliva and serum of patients coinfected with HCV and human immunodeciency
virus. J Med Virol. 2001;63(2):117–9.
23. Suzuki T, Omata K, Satoh T, Miyasaka T, Arai C, Maeda M, etal. Quantitative detection of
hepatitis C virus (HCV) RNA in saliva and gingival crevicular uid of HCV-infected patients.
J Clin Microbiol. 2005;43(9):4413–7.
24. Pfaender S, Helfritz FA, Siddharta A, Todt D, Behrendt P, Heyden J, etal. Environmental
stability and infectivity of hepatitis C virus (HCV) in different human body uids. Front
Microbiol. 2018;9(504):1–8.
25. Paintsil E, He H, Peters C, Lindenbach BD, Heimer R.Survival of Hepatitis C virus in syringes:
implication for transmission among injection drug users. J Infect Dis. 2010;202(7):984–90.
26. Hosoglu S, Celen MK, Akalin S, Geyik MF, Soyoral Y, Kara IH.Transmission of hepatitis C
by blood splash into conjunctiva in a nurse. Am J Infect Control. 2003;31(8):502–4.
27. Sartori M, La Terra G, Aglietta M, Manzin A, Navino C, Verzetti G.Transmission of hepatitis
C via blood splash into conjunctiva. Scand J Infect Dis. 1993;25(2):270–1.
28. Henderson DK, Fahey BJ, Willy M, Schmitt JM, Carey K, Koziol DE, etal. Risk for occupational transmission of human immunodeciency virus type 1 (HIV-1) associated with clinical
exposures: a prospective evaluation. Ann Intern Med. 1990;113(10):740–6.
29. Cardo DM, Culver DH, Cieseielski CA, Srivastava PU, Marcus R, Abiteboul D, etal. A casecontrol study of HIV seroconversion in health care workers after percutaneous exposure. N
Engl J Med. 1997;337(21):1485–90.
30. Kuhar DT, Henderson DK, Struble KA, Heneine W, Thomas V, Cheever LW, etal. Updated
US Public Health Service guidelines for the management of occupational exposures to human
immunodeciency virus and recommendations for postexposure prophylaxis. Infect Control
Hosp Epidemiol. 2013;34(9):875–92.
31. World Health Organization. Occupational risks and management of bloodborne pathogens.
In: WHO best practices for injections and related procedures toolkit. Geneva; 2010. p.29–38.
32. Centers for Disease Control and Prevention. CDC guidance for evaluating health-care personnel for hepatitis B virus protection and for administering postexposure management. Morb
Mortal Wkly Rep [Internet]. 2013;62(10). http://www.cdc.gov/mmwr/cme/conted.html
33. Beasley RP, Hwang L-Y, Stevens CE, Lin C-C, Hsieh F-J, Wang K-Y, etal. Efcacy of hepatitis B immune globulin for prevention of perinatal transmission of the hepatitis B virus carrier state: nal report of a randomized double-blind, placebo-controlled trial. Hepatology.
1983;3(2):135–41.
34. Stevens CE, Toy PT, Tong MJ, Taylor PE, Vyas GN, Nair PV, et al. Perinatal hepatitis B virus transmission in the United States: prevention by passive-active immunization.
JAMA. 1985;253(12):1741745.
35. Naggie S, Holland DP, Sulkowski MS, Thomas DL.Hepatitis C virus postexposure prophylaxis in the healthcare worker: why direct-acting antivirals don’t change a thing. Clin Infect
Dis. 2016;64(1):92–9.
36. Krawczynski K, Alter MJ, Tankersley DL, Beach M, Robertson BH, Lambert S, etal. Effect
of immune globulin on the prevention of experimental hepatitis C virus infection. J Infect Dis.
1996;173(April):822–8.
37. Haase AT. Targeting early infection to prevent HIV-1 mucosal transmission. Nature.
2010;464(7286):217–23.
355

356
https://t.me/med1917
38. Irvine C, Egan KJ, Shubber Z, Van Rompay KKA, Beanland RL, Ford N. Efcacy of HIV
postexposure prophylaxis: systematic review and meta-analysis of nonhuman primate studies.
Clin Infect Dis. 2015;60(Suppl 3):S165–9.
39. Otten RONA, Smith DK, Adams DR, Pullium JK, Jackson E, Kim CN, etal. Efcacy of postexposure prophylaxis after intravaginal exposure of pig-tailed macaques to a human-derived
retrovirus (human immunodeciency virus type 2). J Virol. 2000;74(20):9771–5.
40. Tsai C, Emau P, Follis KE, Beck TW, Benveniste RE, Bischofberger N, etal. Effectiveness
of postinoculation (R)-9-(2-Phosphonylmethoxypropyl) adenine treatment for prevention of
persistent simian immunodeciency virus SIVmne infection depends critically on timing of
initiation and duration of treatment. J Virol. 1998;72(5):4265–73.
41. Shih C-C, Kaneshima H, Rabin L, Namikawa R, Sager P, McGowan J, etal. Postexposure
prophylaxis with zidovudine suppresses human immunodeciency virus type 1 infection in
SCID-hu mice in a time-dependent manner. J Infect Dis. 1991;163(3):625–7.
42. Wiboonchutikul S, Thientong V, Suttha P, Kowadisaiburana B, Manosuthi W. Signicant
intolerability of efavirenz in HIV occupational postexposure prophylaxis. J Hosp Infect.
2016;92(4):372–7.
43. U.S. Food and Drug Administration. FDA Drug Safety Communication: FDA to evaluate
potential risk of neural tube birth defects with HIV medicine dolutegravir (Juluca, Tivicay,
Triumeq); 2018.
44. Zash R, Makhema J, Shapiro RL.Neural-tube defects with dolutegravir treatment from the
time of conception. N Engl J Med. 2018;379(10):979–81.
45. Department of Health and Human Services (HHS) Antiretroviral Guidelines Panels.
Recommendations regarding the use of dolutegravir in adults and adolescents with HIV who
are pregnant or of child-bearing potential [Internet]; 2018. https://aidsinfo.nih.gov/news/2109/
recommendations- regarding- the- use- of- dolutegravir- in- adults- and- adolescents- with- hivwho- are- pregnant- or- of- child- bearing- potential
46. Wald J.The psychological consequences of occupational blood and body uid exposure injuries. Disabil Rehabil. 2009;31(23):1963–9.
47. Sohn JW, Kim BG, Kim SH, Han C. Mental health of healthcare workers who experience
needlestick and sharps injuries. J Occup Health. 2006;48(6):474–9.
48. H.R. 5178—106th Congress: Needlestick Safety and Prevention Act [Internet]. 2000 p. HR 3801.
https://www.govinfo.gov/content/pkg/BILLS- 106hr5178enr/pdf/BILLS- 106hr5178enr.pdf
49. Berguer R, Heller PJ. Preventing sharps injuries in the operating room. J Am Coll Surg.
2004;199(3):462–7.
50. Jagger J, Bentley M, Tereskerz P.A study of patterns and prevention of blood exposures in OR
personnel. AORN J. 1998;67(5):979–96.
51. Davis MS.Advanced precautions for today’s O.R.: the operating room professional’s handbook for the prevention of sharps injuries and bloodborne exposures. Atlanta: Sweinbinder
Publications LLC; 1999.
52. American College of Surgeons. American College of Surgeons (ACS) statement [Internet].
https://www.facs.org/about- acs/statements/94- sharps- safety
T. Ballouz et al.

“I’m Missing aSponge!” New Techniques
https://t.me/med1917
inthePrevention ofForeign Body
22
Retention
ScottE.Regenbogen andSamanthaJ.Rivard
Retained surgical items (RSIs) can include any surgical equipment (i.e., sponge,
instrument, needle) unintentionally left inside a patient after an operation. RSIs
result in signicant patient morbidity, possible mortality, and excess healthcare
costs. Over time, many strategies have been utilized to prevent the retention of surgical items. Traditionally, manual surgical counts and intraoperative plain imaging
have served this purpose. More recently, new technologies have emerged, including
bar-coded sponges and radio-frequency technology. This chapter focuses on reviewing RSI epidemiology, risk factors, and prevention methods—both standard practices and new technology.
RSIs are considered by many regulatory organizations to be “never events,” serious reportable incidents thought to be universally preventable, as dened by the
National Quality Forum [1]. Since June 2005, the Joint Commission has classied
RSIs as sentinel events that require immediate reporting, investigation with subsequent root cause analysis, and coordinated institutional response [2]. The Centers
for Medicare and Medicaid Services (CMS) have also included RSIs on its list of
hospital-acquired conditions. Therefore, since 2008, medical care resulting from
RSIs is not reimbursed by CMS [3]. Many state and private health insurers have also
adopted policies to not reimburse care associated with an RSI.
Retained surgical items represent signicant complications for a variety of reasons. They may result in serious, even fatal injuries, and infectious complications,
which require additional medical care, frequently manifested as increased length of
stay, readmissions, and reoperations. Additionally, retained surgical item cases frequently lead to litigation and negatively affect the reputation of clinicians and hospital systems. All of these contribute to substantial healthcare costs.
S. E. Regenbogen (*) · S. J. Rivard
Department of Surgery, University of Michigan, Ann Arbor, MI, USA
e-mail: sregenbo@med.umich.edu
© Springer Nature Switzerland AG 2024
J. J. Hoballah et al. (eds.), Principles of Perioperative Safety and Efciency,
https://doi.org/10.1007/978-3-031-41089-5_22
357

358
https://t.me/med1917
Unfortunately, despite increasing attention to the prevention of RSIs, they remain
the most common sentinel event reported to the Joint Commission, with 124
reported in 2017 and 121in 2018 [4, 5]. Therefore, an understanding of the natural
history, risk factors, and strategies for prevention of RSIs is critical for patient safety
and surgical quality. As a community, we must recognize that while certain patientand operation-specic factors may predispose to RSIs, human, team, and system
factors contribute considerably.
Of note, heterogeneity exists in the terminology used in the published literature,
which complicates the study of RSIs. The following terminology has all been utilized: retained foreign bodies, retained foreign objects, retained surgical equipment,
retained surgical items, and retained sponges and instruments. Gossypiboma specically refers to surgical sponges unintentionally left inside a patient during a surgical procedure. Other terms include textiloma, gauzoma, and muslinoma [6]. For
the remainder of this chapter, the abbreviation RSI will be used to encompass
“retained surgical items,” including any surgical equipment (sponge, instrument,
needle), which was unintentionally left inside a patient.
S. E. Regenbogen and S. J. Rivard
Epidemiology
The true incidence of retained surgical items is unknown and difcult to determine
based on the nature of existing literature, which mainly consists of voluntary incident reporting, insurance and malpractice claims data, and retrospective reviews.
Additionally, postoperative patients are infrequently screened for retained surgical
items, which may take many years to become clinically relevant [6]. This results in
a likely underestimation of true RSI incidence.
A landmark study based on malpractice claims estimated an incidence of 1in
8801 to 18,760 of all inpatient operations [7]. However, this was felt to be an underestimate, and more recent literature cites an incidence of 1in 5500 operations [8].
When focused on abdominal operations, incidence estimates increase to 1in 1000
to 1500 cases [9, 10]. Although the risk of RSI is higher in emergency surgery, most
events occur among elective operations.
The most common RSI is cotton materials, specically sponges (52–69%), followed by surgical instruments (3–43%), and needles (9%) [7, 8, 11, 12]. It is not
surprising that surgical sponges constitute the majority of RSIs as they are small and
commonly used and become camouaged when blood-soaked. Interestingly, needles were found to be a major cause of near misses, but less frequently result in an
RSI [8].
Retained surgical items have been discovered in patients of all ages, within
all body cavities, and throughout all subspecialties. The majority of RSIs are
found in the abdomen or pelvis (46–65%) followed by the thorax (7.4–23%),
vagina (22%), extremities (8%), head/neck (2%), natural orices (mouth, rectum, urinary tract), and elsewhere (17%; including spinal canal, face, brain) [6,
7, 11, 13, 14]. In one series, 27.5% of RSI cases involved uncomplicated vaginal
deliveries [14].

22 “I’m Missing a Sponge!” New Techniques in the Prevention of Foreign Body…
https://t.me/med1917
RSIs can be discovered immediately or take many years until discovery [11].
Throughout the literature, the average time to discovery of an RSI was 6.9years,
ranging from under 3months to over 40years [6]. However, the median time to
discovery was 2.2years because of high likelihood complications that occur within
the rst 2years after surgery. Abdominal and pelvic locations were associated with
signicantly longer intervals to retained item identication and removal [13].
359
Natural History
The majority of patients discovered to have RSI undergo reoperation (65–83%) for
removal of the item to treat or prevent complications [7, 8, 11, 13]. The complications associated with RSIs include adhesions (31%), abscess (24%), stula (20%),
small bowel perforation or obstruction (3–22%), and sepsis (7%) [6, 7, 11, 13]. In
some cases, RSIs result in erosion into the gastrointestinal or genitourinary tracts,
or vasculature [15]. Readmissions and increased length of stay from RSIs have been
reported in 30–59% of cases [7, 8, 11, 13]. Mortality estimates range from 0 to 6%
[7, 12, 13].
Some RSIs are discovered incidentally during the postoperative period, while
others are discovered due to clinical signs and symptoms, and others remain hidden
for years [11]. The majority of RSIs are discovered on imaging (67%) followed by
self-exam or physical exam (24–30%) [7]. The most common imaging detection
methods are CT scans (61%), then radiographs (35–51%), and ultrasound (34%) [7,
13]. Other technologies utilized include MRI, endoscopy, barium enemas, PET-CT,
and mammography [6]. Some (9%) retained surgical items are not found until reoperation for complications [7].
Only a minority of patients (19%) report symptoms that prompted retained surgical item discovery. Those presenting with signs and symptoms report pain/irritation
(42%), palpable mass (27%), fever (12%), nausea, emesis, and diarrhea. Of note,
48% of symptomatic RSI patients reported more than one symptom at presentation
[6, 13]. Abdominal and pelvic RSIs were more likely to have clinically signicant
presenting symptoms [13]. Other nonspecic symptomologies included systemic
inammatory response syndrome and lack of expected clinical progress [11].
Therefore, for any patient with nonspecic or unexplained symptoms after surgery,
it is recommended to obtain plain imaging, followed by CT imaging if radiographs
are inconclusive [13].
The natural history of RSIs differs according to the duration that the RSI has
been present. RSIs that have been present for longer periods of time are more likely
to exhibit an inammatory pathological response. Foreign material triggers the
body’s inammatory response, which eventually leads to a brotic response manifesting as adhesions, granulomas, and, eventually, encapsulation. Only 16% of RSIs
removed within 24h were found to have inammatory ndings on pathology, compared to 42% of RSIs discovered between 24h and 1week, and 68% of RSIs discovered more than 6weeks after surgery [13]. Most items retrieved beyond 24h had
one or more abnormal pathology ndings, most commonly exudative reaction,

360
https://t.me/med1917
brosis, and purulence/abscess. Fibrosis was more common in patients whose RSIs
were discovered more than 1week after retention [13].
Similarly, the clinical presentation correlates with the length of time of item
retention. The majority of RSIs that were discovered less than 24h postoperatively
were asymptomatic, but some were acutely symptomatic or discovered incidentally
on imaging [13]. RSIs that were discovered between 24h and 3months after retention were more likely to have inammatory signs and symptoms including fever,
uid collections, abscesses, abnormal wound drainage, and stulas. In a subset of
patients that remained largely asymptomatic for years, RSIs were more likely to be
discovered incidentally on imaging obtained for other reasons, or with new unexplained masses that were mistaken for neoplasms. Chronic manifestations may also
include granuloma formation, tissue erosion, mass, and stula/sinus formation [13].
Thus, early recognition and removal of retained surgical items are recommended to
prevent long-term complications.
Retained surgical items incur a variety of negative consequences beyond the
clinical morbidity, including ligation, negative publicity, and provider distress [7,
14]. The average cost of a retained surgical item is estimated at $95,000, which
includes about $14,701 for unreimbursed readmission and reoperation costs [16].
Legal fees vary widely between states and specic cases, with a range of $37,041 to
$2,350,000, with an average of $52,581 per case [7, 16]. By understanding the risk
factors associated with RSIs and the prevention strategies available, these monetary
gures represent potential healthcare cost savings.
S. E. Regenbogen and S. J. Rivard
Risk Factors
Approaches to the prevention of RSI have begun with attempts to dene important
risk factors. Identication of key risk factors for RSIs could enable additional
screening for the highest risk cases. A meta-analysis of three retrospective, casecontrol studies of RSI risk factors found seven risk factors to be signicantly associated with increased RSI risk, listed in order of highest to lowest risk [17]:
1. Incorrect surgical count
2. Unexpected intraoperative factors
3. More than one surgical team
4. Surgical count not performed
5. More than one sub-procedure
6. Duration of operation
7. Estimated operative blood loss more than 500mL
Specically, incorrect nal sponge counts were associated with a 20-fold
increased RSI risk [12].
Other factors thought to be associated with an increased risk of RSI are changes
in nursing staff, emergency surgery, BMI, and operations performed “after hours.”
In one study, the incidence of RSI was nine times greater in emergency surgery [7].

22 “I’m Missing a Sponge!” New Techniques in the Prevention of Foreign Body…
https://t.me/med1917
Some studies suggest that the presence of surgical trainees reduced the risk of RSI
by as much as 70% [11, 12]
361
Prevention
Every member of the perioperative team shares the responsibility for patient safety,
with the ultimate goal of eliminating patient adverse events. Observational studies
have identied team or system errors in more than 90% of cases of RSI, whereas
isolated human error was responsible in only a small minority [13]. This nding
suggests that, rather than individual culpability, RSI prevention requires interventions focused on team training and highly reliable systems. Many different institutional policies exist with the goal of preventing the occurrence of retained foreign
bodies. Institutional policies differ in their components of surgical team training,
manual surgical counts, traditional wound sweeps, use of intraoperative radiology,
and technological advances.
Manual Surgical Count
Manual surgical counting has been used for decades as the main defense against
retained surgical items. It is truly a multidisciplinary endeavor, relying on multiple
team members, including circulating nurse, scrub technician, and surgeons. This
process is highly prone to human error as it is a “simple task” performed in a complex environment, with multiple distractions and competing tasks [8]. The more
times a count is performed, the incidence of possible error increases exponentially [8].
For standardization of the process, the Association of periOperative Registered
Nurses (AORN) rst published surgical count guidelines in 1976, which have
undergone multiple revisions, with the most recent update in 2015 with the
“Guideline for Prevention of Retained Surgical Items.” The AORN standard practices recommend counting sponges, sharps, instruments, and miscellaneous items
on all procedures with the possibility that a foreign object could be retained. They
recommend that all cotton sponges be radiopaque. Counting practices are required
to be audible and performed by two individuals, including the circulating nurse.
Surgical counts should occur before the procedure for a baseline, when new items
are added to the eld, before closure of a cavity within a cavity (e.g., bladder), when
wound closure begins, when skin closure begins or at the end of the procedure, at
the time of permanent relief of either the RN circulator or the scrub person, and any
time a discrepancy is suspected.
AORN further recommends proper steps for resolving an incorrect count, which
include the certied surgical technologist and/or circulator informing the surgeon of
incorrect count, visual search of the surgical eld, and the surgeon performing thorough exploration of operative cavity. If item is not found, it is recommended to
obtain an intraoperative X-ray, read by a radiologist, before surgical wound is closed

362
https://t.me/med1917
S. E. Regenbogen and S. J. Rivard
and patient leaves the OR.All sponge, sharp, and instrument counts, as well as any
additional procedures taken during a miscount, should be documented in the intraoperative record and patient’s chart [18].
While manual surgical counting has remained the mainstay of RSI prevention for
decades, many call into question its reliability due to dependence on human consistency and accuracy in a complex environment plagued with interruptions, time pressures, and multitasking. In retrospective studies, 62–88% of retained surgical items
occur in operations for which a nal count was erroneously documented as correct
[6–8, 11, 12, 14]. In one study evaluating the value of counting, the observed sensitivity of manual surgical counts was 77.27%, specicity was 99%, and positive
predictive value was 1.6%, owing to the low incidence of RSIs [19]. The positive
likelihood ratio of an incorrect count was 113.3, indicating that cases with incorrect
counts were over 100 times more likely to result in an RSI [19]. While these statistics point to a higher value of counting then found in the literature, surgical teams
should be careful to assume a correct surgical count as protective against a retained
surgical item, as it can lead to a false sense of security [8].
Another criticism of manual surgical counting relates to the time it takes to perform counting activities, which divert the attention of ancillary staff from the activities of the surgeon. A mean of 16.6 counting episodes occur per operation, each
requiring an average of 8.6min to perform, consuming up to 14% of operative time
[20]. In many institutions, this increased operative time correlates with increased
healthcare expenditures.
While retained surgical items are rare, count discrepancies are more common,
occurring in about 1in 145 operations or 0.69% of surgical procedures [19]. Count
discrepancies are dened as any event in which a subsequent count does not agree
with a previous one, indicating that there is no accurate representation of the number of sponges, needles, and instruments [20]. A prospective observational eld
study by Greenberg etal. in 2008 found that 1in 8 operations incurred an intraoperative count discrepancy. Unresolved count discrepancies require thorough manual
wound exploration, intraoperative radiographs, or both, which increase the operative time and therefore cost. After a discrepancy occurs, an average of 13min is
required to reconcile the discrepancy [20].
The majority of count discrepancies involve sponges (45%), followed by instruments (34%) and needles (21%). Most (59%) result from misplaced items, which
are eventually found in the body, on the surgical eld, or elsewhere in the
OR. Alternatively, 38% of discrepancies result from errors in the written record
[12]. Cases with personnel change, specically circulating nurse or surgical technician, are three times more likely to have a discrepancy [20].
Count discrepancies are associated with prolonged surgery time, increasing 2.7fold for every additional 2h of surgery, as well as with operations later in the day,
as well as those with a higher number of nursing teams involved [19]. Count accuracy also depends on the complexity and urgency of the operation, as well as the
surgical team’s fatigue and workload [19]. Count discrepancies were most common
in transplantation (10.2%), cardiothoracic surgery, and neurosurgery (2–3%) [19].
In coronary artery bypass graft (CABG) surgery, each count discrepancy was

22 “I’m Missing a Sponge!” New Techniques in the Prevention of Foreign Body…
https://t.me/med1917
associated with $932 of excess cost, associated with diagnostic testing and increased
time spent in the OR.Extrapolating these expenses, the national cost of count discrepancies in CABG alone would be $24million annually [19].
Recognizing that the majority of count discrepancies represent actual misplaced
items, all count discrepancies warrant a thorough search and reconciliation [20].
Despite the inability of manual counts to prevent all RSIs, the role for manual surgical counts still exists because standard counting detects 82% of possible RSIs [21].
If no counting was performed, the incidence of retained surgical sponges might be
as high as 67 per 100,000 operations [21].
363
Radiographs
Guidelines for use of radiographic detection of RSI vary widely between institutions. Some hospitals require radiographs in every open surgical case, while others
selectively require radiographs in high-risk cases or only in those with discrepant
counts. Some hospitals do not have radiography policies at all [7, 8, 22].
Intraoperative or dedicated postoperative plain radiographs are not completely
protective. Radiographs do not appear to be reliable enough to prevent RSI, as intraoperative radiographs may have sensitivity as low as 67% [6, 8]. Up to 48% of RSIs
have been missed on initial intraoperative radiographs, which contributes to a false
sense of security [12].
This is attributed to the poor imaging quality of intraoperative radiographs and
variable appearance of surgical sponges on plain lms. The radiopaque threads on
sponges are likely to be distorted and have been mistaken as sternal sutures, monitor
wires, valve rings, and even linear tube markers, such as nasogastric tubes [23].
Cases have also been reported when an RSI was out of radiograph’s view, which
indicates that multiple lms may be necessary. Therefore, an intraoperative radiograph reported as negative for a retained surgical item when counts are incorrect
should not be taken as a denitive test [8].
The literature suggests that sponges and instruments are much easier to detect on
imaging than needles [8]. Overall mean accuracy of intraoperative radiographs for
needles is 74% and specicity is 80% for plain radiographs in the detection of
retained surgical needles. While the overall reported sensitivity of 69% for needle
detection on intraoperative radiographs appears higher than the sensitivity for any
RSI detection on intraoperative radiograph, this statistic is misleading because it is
highly dependent on needle size. Sensitivity for needles 25mm or more in length
was 99% compared to needles of 11–24mm, which was 84%, and needles ≤10mm,
which was 29%. For reference, the length of a CTX needle on a 0 suture is 48mm
in length, an SH needle on a 3-0 suture is 26mm, and a BV needle on a 6-0 suture
is 11mm. Some suggest that radiographs for lost needles smaller than 13mm pose
unnecessary radiation risk for little or no gain, as the clinical signicance is debatable [11, 24].
In one institution that requires high-resolution postoperative survey lm prior to
patients being brought to the recovery room, 59% of RSIs were discovered through
Соседние файлы в папке @xirurgi_2025
