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Table 2.  Summary of Chelation Interventions

Author, Year
(Quality)
Study DesignType of InterventionYears ConductedNAgeDuration of followupBaseline BLLBLL ResultsSummary of Effect
Rogan, 199860;
Rogan, 200065;
Rogan, 200161;
Liu, 200262;
Dietrich, 200463;
Peterson, 200464; TLC study

(Good)
Randomized multicenter, placebo controlled, double-blind trial DMSA lasting 26 days, dose based on body surface area; treatment repeated up to 3 times for persistently elevated blood lead level; domestic cleaning with HEPA vacuum and damp cloth wiping. NR 1,854 evaluated,
780 randomized

741 of randomized reanalyzed for Liu 2002  (cognitive function)
Children 12-33 months At 12 months following initiation of treatment, test BLL; at 36 months, planned behavioral,  cognitive, and biochemical tests; retest at 72 months (to age 7); also, at 9 and 34 months, test height-weight 20-44 µg/dL DMSA vs. Placebo

1 wk: BLL 11 µg/dL lower in DMSA.

7 wks: 72% vs. 88% of baseline.

First 6 months: BLL 4.5 µg/dL lower in DMSA.

12 months: groups are similar.
DMSA produced short-term reduction in BLL; rebound began at 1 week and 7 weeks.

Followup outcomes do not support the hypothesis that lead-induced cognitive defects are reversible by chelation therapy. DMSA group scored worse on some measures.
Besunder, 199566

(N/A)
Retrospective case series DMSA 10 mg/kg every 8 hours for 5 days, followed by 10 mg/kg every 12 hours for 14 days; and abatement of domestic lead hazards. June 1991 to May 1993 46 treated, 18 excluded,
N=28
Children Age NR 80 days 25-49 µg/dL BLL post-treatment:
18 days: -43% (± 20.8%)
80 days -31% (± 20.2%)

ZPP post-treatment:
18 days: -12% (±21.7%)
80 days: -32% (±21.9%)
No control group. Cannot exclude other intervention effects (abatement of domestic lead hazards).
Chisolm, 200068

(N/A)
Open-label case series DMSA 1,050 mg/m^2/day, divided in three doses for 5 days, followed by 700 mg/m^2/ day, divided in two doses for 21-23 days; and relocation to lead-safe housing. NR 59 Children 12-65 months 21 days 25-70 µg/dL BLL post-treatment:

1 day: below 35% of pretreatment level.

2-3 weeks: rebounded to 58% of pretreatment level
No control group. Cannot exclude other intervention effects (abatement of domestic lead hazards).
O'Connor, 199967

(Fair)
Randomized placebo-controlled double-blind trial DMSA (child weight <15 kg) 1,000 mg tid for 5 days, followed by 100 mg bid for 14 days.

DMSA (child weight >15 kg) 200 mg tid for 5 days, followed by 200 mg bid for 14 days
NR 39 Children 2.5-5 years 6 months 30-45 µg/dL, DMSA group 34.9 ±4.7 µg/dL

Placebo group 33.0 ±6.2 µg/dL
DMSA vs. Placebo

1 month: 27.4 ±7.5 µg/dL vs. 33.2 ± 10.3 µg/dL

6 months: 28.8 ±6.4 µg/dL vs. 25.1 ±6.8 µg/dL
Both treatment and control groups demonstrated significant BLL reductions. Differences between groups were not significant.

Abbreviations: Bid=Two times per day; BLL= Blood lead level; DMSA=Dimercaptosuccinic acid; HEPA=High efficiency particulate air; NR = Not reported; TID=Three times per day; TLC=Treament of Lead-exposed Children Study; ZPP= Zinc protoporphyrin.

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