Cronin C M, Shapiro C R, Casiro O G, Cheang M S
Section of Neonatology, St Boniface General Hospital, Winnipeg.
Arch Pediatr Adolesc Med. 1995 Feb;149(2):151-8. doi: 10.1001/archpedi.1995.02170140033005.
To test the hypothesis that parental stress associated with long-term morbidity of very low-birth-weight infants (VLBWIs) is long lasting.
Matched case-control study.
High-risk newborn follow-up program, Winnipeg, Manitoba.
Parents of 96 Manitoban VLBWIs born from July 1986 through June 1990, compared with parents of full-term controls matched for age, sex, race, domicile, singleton or multiple pregnancy, and birth order.
Mailed questionnaire, including Stein's Impact on Family Scale, positive impact of parenthood, and attitudes toward treating VLBWIs.
Families were demographically similar. The parents of VLBWIs had higher scores for financial burden, familial/social impact, personal strain, and mastery (P < .0001). The parents of VLBWIs experienced more impact when children had a functional handicap or low adaptive developmental quotient. Scores were highest when the adaptive developmental quotient was 70 to 85. High scores were associated with low family income and less parental education. Impact did not change over time. Only half of the parents in each group felt that "doctors should try to save every baby." The parents of VLBWIs felt more strongly that cost should never enter into the decision to treat a tiny baby (P < .005). The families of VLBWIs expressed a stronger desire for more children (P < .01), but control families were more likely to have given birth again (46.3% vs 28.2%).
The birth and upbringing of a VLBWI is associated with more long-term stress, even for well-educated nuclear families whose health care is financed by government. Caregivers need increased awareness of the needs of these families so that their medical and social needs are met effectively. Support services should be targeted toward low income, poorly educated parents whose children have functional handicaps.
检验极低出生体重儿(VLBWIs)长期患病给父母带来的压力会长期持续这一假设。
匹配病例对照研究。
马尼托巴省温尼伯市的高危新生儿随访项目。
1986年7月至1990年6月出生的96名马尼托巴省极低出生体重儿的父母,与年龄、性别、种族、住所、单胎或多胎妊娠及出生顺序相匹配的足月对照组婴儿的父母进行比较。
邮寄问卷调查,包括斯坦因家庭影响量表、为人父母的积极影响以及对治疗极低出生体重儿的态度。
两组家庭在人口统计学特征上相似。极低出生体重儿的父母在经济负担、家庭/社会影响、个人压力和掌控感方面得分更高(P < .0001)。当孩子有功能障碍或适应性发育商较低时,极低出生体重儿的父母受到的影响更大。当适应性发育商为70至85时得分最高。高分与家庭收入低和父母受教育程度低有关。影响不会随时间变化。每组中只有一半的父母认为“医生应该尽力挽救每个婴儿”。极低出生体重儿的父母更强烈地认为,在决定治疗微小婴儿时费用绝不应成为考虑因素(P < .005)。极低出生体重儿的家庭生育更多孩子的愿望更强烈(P < .01),但对照组家庭再次生育的可能性更大(46.3%对28.2%)。
即使对于由政府资助医疗保健的受过良好教育的核心家庭,极低出生体重儿的出生和养育也会带来更多长期压力。护理人员需要提高对这些家庭需求的认识,以便有效满足他们的医疗和社会需求。支持服务应针对那些孩子有功能障碍、收入低且受教育程度低的父母。