| Literature DB >> 18671873 |
Michelle L Bell1, Devra L Davis, Luis A Cifuentes, Alan J Krupnick, Richard D Morgenstern, George D Thurston.
Abstract
BACKGROUND: Greenhouse gas (GHG) mitigation policies can provide ancillary benefits in terms of short-term improvements in air quality and associated health benefits. Several studies have analyzed the ancillary impacts of GHG policies for a variety of locations, pollutants, and policies. In this paper we review the existing evidence on ancillary health benefits relating to air pollution from various GHG strategies and provide a framework for such analysis.Entities:
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Year: 2008 PMID: 18671873 PMCID: PMC2519068 DOI: 10.1186/1476-069X-7-41
Source DB: PubMed Journal: Environ Health ISSN: 1476-069X Impact factor: 5.984
Figure 1Relationship between climate change and air quality policies.
Concentration-response functions used in the assessments listed in Additional file 1
| PM: Adult and infant [ | Lung-cancer, acute and chronic respiratory symptoms, pseudo-croup, asthma [ |
| PM10 (chronic): modified version of Pope et al. 1995 [ | Outpatient visits, emergency room visits, hospital admissions, work loss days, acute respiratory symptoms in children and adults, chronic respiratory symptoms in children and adults, asthma attacks [ |
| PM10 and nitrates (acute) [ | NOx: respiratory symptoms, eye irritation days, phlegm days [ |
| PM10 (acute and chronic): | Respiratory hospital admissions [ |
| Adults [ | |
| Infants [ | |
| O3 (acute) [ | |
| PM10 (acute): Based on previously conducted literature reviews [ | Respiratory hospital admissions, emergency room visits, RAD, MRAD, clinic visits for bronchitis for children <15 years, respiratory symptoms for adults and children, chronic bronchitis, chest discomfort, eye irritation, headaches. Based on previously conducted literature reviews [ |
| Did not apply concentration-response functions. Estimated changes in mortality based on baseline burden. | Respiratory disease and neoplasm. Did not apply concentration-response functions. Estimated changes in morbidity based on baseline burden. |
| PM2.5 (chronic) [ | Respiratory and cardiovascular (CVD) hospitalizations [ |
| PM10 (acute and chronic) [ | Chronic bronchitis [ |
| PM (acute and chronic) [ | Respiratory hospital admissions [ |
| O3 (acute) [ | |
Note: References for health endpoints refer to the concentration-response function applied.
Sample of typically used values for PM-related health impacts (mean estimates) ($2000 PPP-adjusted [197])
| 1,042 | 1,296,552 (premature death) [ | ||||
| VSL: Adults | 6,300,000 | 2,247,191 | 3,480,000 | 1,439,394 | 1,717,241 (1,724,138) [ |
| VSL: Children | 2 × adult | 4088764 (infant) | |||
| VSLY | 134,831 | 70,455 | 118,621 | ||
| 1929.55 (average cost/separation) [ | |||||
| Morbidity: children | 2 × adults | ||||
| Chronic bronchitis | 340,000 | 213,483 | |||
| Chronic asthma | 39,000 | ||||
| Respiratory hospital admission | 14,000 | 2,247 | 1,032 | 2,069 | |
| CVD hospital admission | 21,000 | 2,247 | 1,052 | 2,759 | |
| Emergency room visit | 300 (asthma) | 541 (respiratory) 562 (CVD) | |||
| Doctor's visit | 60 | ||||
| RAD | 106 | 92 (working age) 78 (young, elderly) | 22 | 53 | |
| MRAD | 50 | 43 | |||
| Acute respiratory symptom | 3–24 | ||||
| Use of respiratory medication | 1.12 | ||||
| Asthma day | 32–74 | 43 | 15 | ||
| [ | [ | [ | [ | [ |
Note: *: VSL derived from population-weighted values in the Australian Bureau of Transport and Regional Economics (BTRE) assessment, Table 3 [128]. Population data from the Australian Bureau of Statistic.
Theoretical predictions and empirical results of studies estimating value of mortality risk reductions. Source: Hammitt and Graham (1999) [103]
| Life cycle model: Theory | +, proportional | - | +a | + | -b, + then -c | indeterminate |
| Empirical Studies | ||||||
| Compensating Wage | + | N/A | -d | + | - | N/A |
| Other Revealed Preference | + | N/A | Unknown | + | + | N/A |
| CV | +, not proportional | - | Varies | + | + then -, 0, - | No effect, + |
a. Small "dead anyway" effect: Higher value to benefits while alive than for a bequest [133].
b. With borrowing against future earnings.
c. Inverted U with no borrowing.
d. Self selection by risk tolerant workers
Credibility ratings for approaches to valuing changes in the risk of mortality
| Human Capital | N | M (not recent) | Undervalues non-workers | D |
| COI | Not usually; in principle could be if separate estimates available for pain and suffering | M | Usually underestimates | C |
| Revealed preference: Hedonic Labor Market; others | Y | M | Inappropriate commodity/Population sampled | B |
| CV and choice experiments: health | Y | S | Hypothetical; hard to understand small probability change | B |
| QALYs | N (except under very restrictive conditions) | M | Monetization arbitrary | C |
Credibility ratings for approaches to valuing changes in the risk of chronic morbidity
| COI | Not usually; hospitalization; sometimes labor productivity (which is a revealed preference approach) | M: medical cost studies F: labor productivity studies | Pricing medical services can be difficult where medical care is socialized or subsidized | C-B |
| Revealed preference | Y | Many on injury/accidents; not on morbidity | C | |
| CV and choice experiments: health | Y | F | See above | B |
| QALYs | Y (under very restrictive conditions) | M | Arbitrary monetization | C |
Credibility ratings for approaches to valuing changes in the risk of acute morbidity
| COI | No | M | Pricing medical services can be difficult | C |
| Revealed preference (averting behavior) | Y (under restrictive conditions) | Many for injury and accidents; not for acute respiratory symptoms | C | |
| CV and choice experiments: Health | Y | S | Old methods/studies; some ad hoc estimates; small samples | B |
| QALYs | Y (under very restrictive conditions) | M | Scores insensitive to severity of acute effects | C |