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with those with BLL less than 5μg/dL.  Independent evalua-  symptoms; however, it reflects recent exogenous exposure
                                        33
          tion of the people age 17 years or older in the same cohort (n   (i.e., the past 30 days) more than endogenous equilibration
          = 13,946) found that BLL of at least 3.62μg/dL compared with   from bone stores.  Therefore, BLL is not a reliable indica-
                                                                           41
          BLL less than 1.94μg/dL was associated with a hazard ratio of   tor of cumulative dose, temporality of exposure, or end-organ
          1.55 for cardiovascular mortality and 1.25 for all-cause mor-  toxicity. BLL is superior to lead levels measured using urine,
          tality.  Thorough evaluation of these data has been determined   hair, or other sources, and capillary samples should be avoided
              34
          sufficient to ascribe causal association of lead exposure with   because of skin surface contamination.  Periodic testing or
                                                                                            42
          several specific cardiovascular health effects  and that the rela-  biologic monitoring of BLL demonstrates temporality of ex-
                                           28
          tionship develops at a BLL less than 10μg/dL. 30   posure and may be used to monitor for continued exposure or
                                                             response to treatment.
          Central and peripheral nervous system dysfunction is another
          proven health effect of lead toxicity and may be one of the   Other Tests
          most concerning for SOF. Lead has been shown to affect cog-  A patient diagnosed with lead poisoning may require further
          nitive and psychomotor performance, mood, and the auditory,   testing, such as CBC count, blood smear, urinalysis, and blood
          visual, and balance systems dose dependently.  Increasing con-  urea nitrogen, serum creatinine, hepatic aminotransferases,
                                             3
          centrations of blood lead and patella bone lead (a biomarker   and free erythrocyte protoporphyrin or zinc protoporphyrin
          for cumulative lead exposure) have been correlated with cog-  (ZPP) levels. The Occupational Safety and Health Administra-
          nitive decline and neurologic deficits. A cross-sectional analy-  tion  (OSHA) lead  surveillance  program  requires  ZPP moni-
          sis of lead-exposed workers (n = 803) and unexposed control   toring. CBC count with smear morphology may demonstrate
          subjects (n = 135) found that a BLL increase of 5μg/dL was   hemolytic anemia in the context of acute exposure, basophilic
          equivalent to 1.05 years of cognitive age–related decline, us-  stippling with subacute exposure, and hypochromic, normo-
          ing eight separate measures of the World Health Organization   cytic, or microcytic anemia with chronic poising.  Free eryth-
                                                                                                   43
          Neurobehavioral Core Test Battery.  A longitudinal analysis   rocyte protoporphyrin and ZPP measure the effect of lead on
                                      35
          of men (n = 1,089) in the Normative Aging Study demon-  hemoglobin synthesis. ZPP positivity may lag BLL elevation
          strated that bone lead increases were predictive of worsening   by several weeks and may remain elevated for the life cycle of
          reaction-time  scores on visuospatial  and visuomotor tests.    red blood cells (approximately 120 days). K-shell X-ray fluo-
                                                         36
          Thorough review of current data has shown that lead-related   rescence (KXRF), dual-energy x-ray absorptiometry scans, or
          symptoms can be detected at BLLs as low as 12μg/dL and that   other markers of bone lead are not recommended for clinical
          cognitive effects of lead exposure may be present years after   diagnosis and treatment. KXRF is used for research purposes
          cessation of occupational lead exposure.           only.

          Low-level lead toxicity increasingly has been associated with   Providers who suspect lead poisoning, especially in the pres-
          a host of other maladies, including reproductive dysfunction.   ence of diminished cognitive function and elevated BLL, should
          The fetus and neonate are exposed to lead when it crosses the   include neurobehavioral testing as part of their examination.
          placental barrier or is present in breast milk.  A case-control   Neurobehavioral testing can elucidate deficits characteristic
                                             37
          study of pregnant women (n = 668) found BLLs of 5–9, 10–14,   of lead toxicity in manual dexterity, perceptual motor speed,
          and greater than 15μg/dL to have odds ratios for spontaneous   mood,  and memory. 44,45  Specifically, cognitive  performance
          abortions of 2.3, 5.4, and 12.2, respectively, after matching for   may be measured via simple reaction time, by the Mini-Mental
          age, gestational age, education, and other covariates.  Mater-  State Examination, and by neurobehavioral tests. Signs of pe-
                                                   38
          nal lead exposure has been found to affect children’s physical   ripheral neuropathies may be revealed by measuring the effects
          development prenatally, and multiple prospective studies have   of vibrational perception in the hand and foot.  In addition,
                                                                                                  46
          elucidated deleterious effects on neurobehavioral development   changes in the auditory, visual, and balance systems can be
          throughout early childhood.  Lead has also been associated   correlated with lead toxicity and may require thorough evalu-
                                39
          with abnormal sperm morphology and decreased sperm count   ation and testing.
          in men. 40
                                                             Treatment
          Diagnosis of Lead Poisoning
                                                             Treatment for lead toxicity begins with cessation of exposure.
          Medical practitioners should take a thorough exposure history   The  patient  should be  removed  from  any  work  or training
          from any patient presenting with signs or symptoms of lead   that entails lead exposure, and the necessary decontamination
          poisoning. History should include employment, hobbies, use   should be performed. In the case of acute ingestion, whole-
          of personal protective equipment, hygiene practices, smoking   bowel irrigation and mechanical removal should be consid-
          and eating environments, and previous exposures to lead.  An   ered.  Retained bullets should also be considered for surgical
                                                                 14
                                                      16
          appropriate expectation is that anyone within the Special Op-  removal. Once the patient is no longer exposed and supportive
          erations community is potentially exposed, especially given the   care is provided, chelation therapy may be considered.
          poorly regulated environments found during foreign deploy-
          ments. A thorough physical examination should be conducted   Chelation therapy may accelerate urinary lead excretion and
          to assess for signs that correlate with lead exposure. Indeed, a   reduce blood lead concentrations but will have limited effect
          detailed neurologic examination can reveal the manifestations   on bone and total-body lead levels. Although anecdotal evi-
          of lead toxicity.                                  dence suggests that chelation may treat symptoms and reduce
                                                             mortality  risk,  there  are  no data  from  randomized  trials  of
          BLL is the most common test for monitoring lead exposure   chelation therapy on long-term health outcomes.  Further-
                                                                                                     39
          and toxicity, and can be used to guide clinical management.   more, BLL may equilibrate after chelation, causing a rebound
          At levels above 40–80μg/dL, BLL may correlate with clinical   of blood concentration.


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